Dec 052021
 


Rembrandt van Rijn Study of the Head and Clasped Hands of a Young Man as Christ in Prayer 1655

 

1 In 2680 Young Men In Hong Kong Get Acute Myocarditis From Comirnaty (Malone)
120 Children Hospitalized In Vietnam Pfizer Vaccine Batch Suspended (Vne)
Twitter: Research On Potential Heart Risks Of Covid Vaccine ‘Unsafe’ (JTN)
WHO: Omicron in 38 Countries, No Deaths Reported (ET)
Do You Know Why There Isn’t An EUA For Fluvoxamine? (Kirsch)
‘Wall Of Secrecy’ In Pfizer Contracts As Company Accused Of Profiteering (G.)
Australian Children Aged 5 To 11 Set To Receive Pfizer Covid Vaccine
Molnupiravir Set For UK At-Home Trials (G.)
EU Chief Calls For Throwing Out Nuremberg Code (PM)
Hundreds Of NY Corrections Officers Put On Leave For Refusing Covid Jab (NYP)
Joe Biden Warns Vladimir Putin Not to Invade Ukraine (GR)
Obituary for Russiagate (Patrick Lawrence)

 

 

So we don’t blame them

 

 

Below is an article by Robert Malone about myocarditis in Hong Kong, which says 37.32 per 100,000 = 1 in 2680 young men are afflicted.

But Eric Topol says there are no cases among 5 million kids in the US. At the same ratio (and why shouldn’t there be), there should be 1,850. Irresponsible nonsense, Topol. 2nd hand car salesman.

Topol
https://twitter.com/EricTopol/status/1467242562285092865

 

 

“..Under conditions of terror most people will comply but some people will not, just as the lesson of the countries to which the Final Solution was proposed is that “it could happen” in most places but it did not happen everywhere.” – Hannah Arendt

 

 

They never found a cure for the “common” cold because the cold IS the cure.

 

 

“37.32 per 100,000 = 1 in 2680 young men who develop myocarditis/pericarditis within two weeks of their second vaccination..”

1 In 2680 Young Men In Hong Kong Get Acute Myocarditis From Comirnaty (Malone)

Strong data from a peer reviewed article in the journal of Clinical Infectious Disease shows that there is a significant increase in the risk of myocarditis/pericarditis following Comirnaty vaccination among Chinese male adolescents, especially after the second dose. Onset of myocarditis was a median of 2 days after vaccination. The clinically significant (acute and/or “mild”) myocarditis/pericarditis incidence rate came in at one out of every 2680 young males. The results conclude with : “Among male adolescents, the incidence after the first and second doses were 5.57 (95% CI 2.38-12.53) and 37.32 (95% CI 26.98-51.25) per 100,000 persons vaccinated.”

Analysis: 37.32 per 100,000 = 1 in 2680 young men who develop myocarditis/pericarditis within two weeks of their second vaccination (median time to disease: 2 days). This study was an analysis of hospital records of myocarditis/pericarditis, so did not include adolescents who may have developed the disease but did not seek medical attention. Many pediatric cardiologists including my colleague and friend Dr. Kirk Milhoan, MD, PhD (MD board certified in pediatric cardiology, PhD. in vascular inflammation) assert that there is no such thing as “mild” myocarditis in children. Myocarditis causes heart damage. Heart damage is for life – the heart does not heal by replacing damaged cells. It scars. Scars in the heart can lead to changes in electrical conduction in heart muscle, which in turn can result in “sudden death” due to changes in heart beat regularity and muscular contraction of the heart. These events may happen at any time, particularly when the heart is stressed in some way.

Results (from the abstract) Between 14 June 2021 and 4 September 2021, 33 Chinese adolescents who developed acute myocarditis/pericarditis following Comirnaty vaccination were identified. 29 (87.88%) were males and 4 (12.12%) were females, with a median age of 15.25 years. 27 (81.82%) and 6 (18.18%) cases developed acute myocarditis/pericarditis after receiving the second and first dose, respectively. All cases are mild and required only conservative management. The overall incidence of acute myocarditis/pericarditis was 18.52 (95% Confidence Interval [CI], 11.67-29.01) per 100,000 persons vaccinated. The incidence after the first and second doses were 3.37 (95%CI 1.12-9.51) and 21.22 (95%CI 13.78-32.28 per 100,000 persons vaccinated, respectively. Among male adolescents, the incidence after the first and second doses were 5.57 (95% CI 2.38-12.53) and 37.32 (95% CI 26.98-51.25) per 100,000 persons vaccinated.

Conclusion from the Abstract “There is a significant increase in the risk of acute myocarditis/pericarditis following Comirnaty vaccination among Chinese male adolescents, especially after the second dose.”

Read more …

Just a batch? Let’s see the follow-up.

120 Children Hospitalized In Vietnam Pfizer Vaccine Batch Suspended (Vne)

Thanh Hoa has suspended the use of a Pfizer Covid-19 vaccine batch after over 120 students were hospitalized following their inoculation. Since November 30, the central province has been vaccinating children aged 15-17 with the Pfizer Covid-19 vaccine. However, over 120 of the children were admitted to hospitals after exhibiting symptoms like nausea, high fever or breathing difficulties, the provincial Center for Disease Control (CDC) said Thursday. Of these, 17 had severe reactions, but their health has stabilized and they continue to be monitored at the hospital, the center said. The cause of their symptoms has yet to be confirmed by Thanh Hoa authorities.

Thanh Hoa CDC director Luong Ngoc Truong said the province has stopped using the current vaccine batch. “We still have other batches, also Pfizer vaccines, so we will continue vaccinating the children,” he said. The suspended batch would be put into storage and could be used later for other groups like adults, Truong added. Vu Van Chinh, director of the Ha Trung District General Hospital, said side-effects following vaccination was normal, but are more likely to happen in children than adults. “Those who have reactions or faint need to be separated so no chain reaction occurs,” said Chinh.

The Thanh Hoa CDC has distributed around 117,000 Covid-19 vaccine doses to 27 districts and towns. Over 56,700 doses have been administered. Over the past week, three children have died following their vaccination with the Pfizer Covid-19 vaccine in Bac Giang, Hanoi and Binh Phuoc. The cause of death has been determined as “overreaction to the vaccine.” Last week, four workers in Thanh Hoa’s Kim Viet Shoe factory died following their Vero Cell Covid-19 vaccination, also due to “overreaction.”

Read more …

It’s not the vaccine that’s unsafe, it’s the research.

Twitter: Research On Potential Heart Risks Of Covid Vaccine ‘Unsafe’ (JTN)

Twitter this week ignited controversy when it slapped an “unsafe” label on a research abstract regarding potential heart effects arising from the use of COVID-19 mRNA vaccines. The abstract in question, “Mrna COVID Vaccines Dramatically Increase Endothelial Inflammatory Markers and ACS Risk as Measured by the PULS Cardiac Test: a Warning,” claims that research suggests those vaccines “dramatically increase inflammation on the endothelium and T cell infiltration of cardiac muscle” and that the purported side effects “may account for the observations of increased thrombosis, cardiomyopathy, and other vascular events following vaccination.” The abstract, published in the American Heart Association-affiliated journal Circulation, drew an “expression of concern” from the AHA’s Committee on Scientific Sessions Program.


That statement claimed that, within the article, “there are several typographical errors, there is no data in the abstract regarding myocardial T-cell infiltration, there are no statistical analyses for significance provided, and the author is not clear that only anecdotal data was used.” Twitter subsequently applied the “unsafe” warning to the original article, with users who click through to the abstract being told that the research “could” constitute, among other potential categories, “violent or misleading content that could lead to real-world harm.” The original abstract was published by controversial American cardiac surgeon Steven Gundry, who has been criticized for his theories on the link between heart inflammation and lectins.

Read more …

Some people must be disappointed. They’ll find a way.

WHO: Omicron in 38 Countries, No Deaths Reported (ET)

The World Health Organization (WHO) on Friday said the COVID-19 omicron variant is now in 38 countries, up from 23 two days ago, suggesting that the variant may be more contagious than Delta. During a news conference, WHO official Maria Van Kerkhove said the U.N. health body has seen “an increasing growth rate,” and “we see increasing numbers of Omicron being detected.” No deaths have been reported so far in connection to the COVID-19 strain, another WHO spokesperson told reporters Friday. “There is a suggestion that there is increased transmissibility, what we need to understand is if it’s more or less transmissible compared to Delta,” Van Kerkhove said. The Delta variant is the dominant strain throughout the world, she said.

In the United States, at least six U.S. states have confirmed Omicron cases so far, including a fully vaccinated male who traveled from an anime convention in New York City to Minnesota this week, according to health officials, who said the individual had mild symptoms and recovered. The first American case was detected in California’s San Francisco Bay Area. A previous update from WHO said Omicron has numerous mutations to its spike protein, which is what it uses to bind to human cells, which may lead to higher transmission rates. It’s not yet clear, however, officials have cautioned. But whether the new strain causes more severe disease or not is unclear, Van Kerkhove said. Early reports from South Africa and Israel suggest many patients experience mild symptoms.

Van Kerkhove said that the first Omicron cases were based on a cluster of college students, noting that younger people tend to experience milder symptoms than older people. A top South African doctor this week told news outlets that the symptoms were unusual but “extremely mild.” “There was initial reports that it tended to be more mild, but it’s really too soon,” Van Kerkhove said. “Everybody who is infected with SARS-CoV-2 regardless of what variant will always start out with a mild disease. And so maybe it will stop there with mild, some people are asymptomatic of course, but it may stop with mild disease or it may take some time.”

Read more …

“Basically, the system is set up so that only proprietary drugs that can kill you are approved.”

Do You Know Why There Isn’t An EUA For Fluvoxamine? (Kirsch)

The reason is simple. We tried. And after 6 weeks of waiting, we were told that to get an EUA for a repurposed drug, you have to partner with a drug company in the EUA application. Because no drug company will partner with us, even if we pay all the filing costs, there won’t be an EUA. Ever. So most doctors will never prescribe it for COVID, even thought it works better than anything else. And the NIH won’t do anything with fluvoxamine either like add it to their guidelines. It will never be upgraded on the NIH COVID treatment guidelines. It is currently sitting at “NEUTRAL” after two trials where it had a 100% risk reduction in both trials without any downside risk. In short, if deployed it would likely save a lot of lives and there is no risk of deployment since the risks of the drug are well known.

It’s a very safe drug when properly prescribed. I took it myself and I couldn’t tell I was on it the side-effects were so negligible. When the fluvoxamine Phase 3 study published in Lancet showed the drug worked better than any other drug (including the new antiviral pills from Merck and Pfizer), the NIH simply ignored the study. They didn’t even mention it. Even 60 Minutes which did a story on fluvoxamine didn’t mention the Phase 3 study proved it worked when the study came out (normally, they’d do this at the end of a show to let their audience know they got it right). Fluvoxamine provides a 12-fold reduction in death if you started the drug early, but the NIH basically said “Ho hum. Only 12X reduction in death? That’s better than anything including the vaccines (which according to the Pfizer 6 month Phase 3 study was only a 2X reduction in mortality).

So not even worth mentioning in the guidelines. It would save too many lives. Best to ignore it. And if we ignore it, no doctor in America will dare to prescribe it. So the vaccine will be the only option just like we planned.” Cliff Lane, who heads the guidelines committee, reports to Fauci. Cliff simply isn’t going to allow the NIH recommendation to be modified no matter what the science says. This is not about saving lives. It never was. When the key opinion leader (KOL) panel of NIH, CDC, FDA and academia experts recommended fluvoxamine be used back in January 2021, the NIH ignored that too. Jeffrey Klausner, who convened the panel, wrote a great op-ed about it in the Washington Post right after the meeting so everyone would know. Doctors ignored it.

Klausner shopped the KOL meeting notes to 10 journals, all of whom refused to publish it. Truly stunning! Life saving drug and nobody would publish the recommendation of an expert panel to use it. Wow. When the KOL meeting notes were finally published in the peer-reviewed medical literature on December 1, 2021, only 12 months after the meeting, the NIH again did absolutely nothing, ignoring the advice of these key experts, even though now they have more data from the Together trial showing it works. Basically, the system is set up so that only proprietary drugs that can kill you are approved.

Read more …

The Guardian turns on Pfizer?

‘Wall Of Secrecy’ In Pfizer Contracts As Company Accused Of Profiteering (G.)

Ministers have agreed a secrecy clause in any dispute with the drugs manufacturer Pfizer over Britain’s Covid vaccine supply. Large portions of the government’s contracts with the company over the supply of 189m vaccine doses have been redacted and any arbitration proceedings will be kept secret. The revelation comes as Pfizer is accused by a former senior US health official of “war profiteering’’ during the pandemic. In a Channel 4 Dispatches investigation to be broadcast this week, Tom Frieden, who was director of the US Centers for Disease Control and Prevention under Barack Obama, said: “If you’re just focusing on maximising your profits and you’re a vaccine manufacturer … you are war profiteering.”

Zain Rizvi, research director at Public Citizen, a US consumer advocacy organisation which has examined Pfizer’s global vaccine contracts, said: “There is a wall of secrecy surrounding these contracts and it’s unacceptable, particularly in a public health crisis.” Rizvi said the UK needed to explain why it had agreed to secret arbitration proceedings. He said: “It’s the only high-income country we have seen that has agreed to this provision. It allows pharmaceutical companies to bypass domestic legal processes. “The UK government has allowed the drug firms to call the shots. How did we end up in a situation where a handful of drug firms were able to exert so much control over the most powerful governments in the world? It points to a broken system.”

Pfizer has won plaudits for its vaccine delivery programme, but the US multinational faces growing scrutiny over the scale of its profits and the proportion of doses it has delivered to low-income countries. While AstraZeneca agreed to sell its vaccine at cost during the pandemic, Pfizer wanted to secure its profits. The Pfizer/BioNTech vaccine, which now has the brand name Comirnaty, will be one of the most lucrative drugs in pharmaceutical history. The Channel 4 investigation reveals analysis by one biological engineering expert claiming the Pfizer vaccine costs just 76p to manufacture for each shot. It is reportedly being sold for £22 a dose to the UK government.

The estimated manufacturing costs do not include research, distribution and other costs, but Pfizer says its profit margin as a percentage before tax are in the “high-20s”. Pfizer expects to deliver 2.3bn vaccines this year with predicted revenues of $36bn (£26.3bn).

Read more …

Big trial. Population wide.

Australian Children Aged 5 To 11 Set To Receive Pfizer Covid Vaccine

Australian children aged five to 11 could receive the Pfizer vaccine against Covid as soon as 10 January, following provisional approval by the country’s drugs regulator. The Therapeutic Goods Administration (TGA) green light, announced by the federal health minister, Greg Hunt, on Sunday will likely be followed by an independent recommendation from the Australian Technical Advisory Group on Immunisation (Atagi) to use the vaccine in that age group. Hunt told reporters the provisional approval was “about keeping our kids safe, keeping our families safe, keeping all Australians safe”. “From 10 January, Australian children will have access to Pfizer vaccines, and it is recommended for children right across Australia,” he said in Melbourne.

Hunt said the TGA was also considering children’s doses of Moderna, the other mRNA vaccine, and will form a view on that “in the coming weeks”. The head of the TGA, Prof John Skerritt, said the Pfizer vaccine had been “extensively clinically tested” including a trial of 2,500 children aged five to 11. “The response of the body, the immune response, was identical to that in young adults,” he said. “There were … no safety problems identified in those trials. The children had some of the same things that adults get – tiredness, sore arms, headache and so forth – but these tended to be brief and fairly short-lived.” Skerritt said the children’s Pfizer was the “same vaccine” but “formulated differently for children” – using one-third of an adult dose.

[..] Hunt said 92.8% of Australians aged 16 and over have now had a first dose of a Covid-19 vaccine and 88% were double-dosed. Since vaccinations were opened to the 12 to 15 age group in September, more than three quarters (76.7%) in that cohort have received a first dose while two-thirds (67.8%) have had two doses.

Read more …

We know Molnupiravir doesn’t work. But:

“The UK has proven itself to be a world leader in identifying and rolling out effective treatments for Covid-19..”

Yeah, they have humor..

Molnupiravir Set For UK At-Home Trials (G.)

The first at-home treatment for Covid-19 could reportedly be offered to UK patients before Christmas as an attempt to protect the most vulnerable from the Omicron variant. The Sunday Telegraph reported that Sajid Javid is set to launch a national pilot of the Molnupiravir antiviral pill, marketed as Lagevrio. The newspaper said that under the plans, the NHS was expected to deliver courses of the tablet to clinically vulnerable and immunosuppressed patients within as little as 48 hours of them testing positive for Covid. It said hospitals and GPs had been told a series of Covid medicines delivery units were being established to ensure the treatment gets to patients as quickly as possible once it is confirmed they have the virus. Last month, the UK became the first country in the world to license its use – a move described as a “gamechanger” by Javid, the health secretary.


But just over a week ago, England’s chief medical officer, Prof Chris Whitty, warned its use may have to be reconsidered in the light of the emergence of Omicron. “I think we probably need to do a rethink of it just to make sure with the new variant, we’re targeting in the right direction.” A Department of Health and Social Care spokesman said: “The UK has proven itself to be a world leader in identifying and rolling out effective treatments for Covid-19, including through government-backed national trials. “The government’s antivirals taskforce was launched to identify treatments for UK patients who have been exposed to Covid-19 to take at home, stopping the infection spreading and speeding up recovery time. “There are a number of exciting opportunities in the pipeline and we will provide further details in due course.”

Read more …

This warrants a lot more scrutiny.

EU Chief Calls For Throwing Out Nuremberg Code (PM)

Ursula Van Der Leyen, the head of the EU commission, told the press on Wednesday that she is in favour of scrapping the long-standing Nuremburg Code and forcing people to get vaccinated against COVID. In an interview she gave to the BBC, the EU chief said that it was “understandable and appropriate” to consider vaccine mandates, especially due to the new Omicron variant of COVID 19, which has been now detected in 12 different member nations of the EU. “How we can encourage and potentially think about mandatory vaccination within the European Union? This needs discussion. This needs a common approach, but it is a discussion that I think has to be led,” commented Van Der Leyen to the BBC.


The WHO, however, has strongly encouraged countries not to enact travel bans because of Omicron, and further iterated that early data points to the fact that most Omicron cases are not severe. Most of the world’s governments are not paying attention to the WHO’s guidelines on this occasion, however. The Nuremberg Code was enacted in 1947, immediately after the Second World War to prevent many of the egregious human rights abuses enacted by the Nazis and the Imperial Japanese during the war. Especially were at issue the performance of medical procedures on subjects without their consent. These procedures, often performed under the command of people such as Dr. Josef Mengele or Hideki Tojo, often were akin to the worst kinds of torture. Since then, full and proactive ongoing consent has been required.

Read more …

It’s all about safety.

Hundreds Of NY Corrections Officers Put On Leave For Refusing Covid Jab (NYP)

More than 500 officers with the already depleted city Department of Corrections are still refusing to get vaccinated against COVID-19 and remain on unpaid leave. New data released by the city shows 17% of DOC uniform officers had yet to receive at least one jab as of Thursday night – two days after a deadline imposed by Mayor Bill de Blasio kicked in requiring proof of inoculation for them to continue working. Most city workers had until Oct. 29 to get vaccinated or be placed on unpaid leave until they provide proof of vaccination. However, de Blasio gave uniformed correction officers extra time — until Dec. 1 — to receive their first jab, because of the ongoing staffing shortage at the troubled Rikers Island jail complex.


Although the DOC’s 83% vaccination rate is the lowest of any city agency, the DOC has seen its rate rise significantly from 46% when de Blasio’s October mandate went into effect, and 77% when the correction officer deadline recently kicked in. Another 9% of DOC uniformed staff who have applied for medical or religious exemptions are continuing to report to work as the city reviews their cases, meaning 92% of the uniformed workforce is active. Councilman Keith Powers (D-Manhattan), who chairs the criminal justice committee that oversees city jails, said the mandates are working, adding “we still have work to do, but the current numbers present progress.” The mayor gave the DOC permission to assign 12-hour shifts and “any other measures necessary to address the current staffing shortage” earlier this week as the agency prepared for an employee shortage.

Read more …

Russia invading Ukraine is a story the US made up. So it can warn against it.

Joe Biden Warns Vladimir Putin Not to Invade Ukraine (GR)

President Joe Biden said on Friday that he and his administration have plans to make it “very, very difficult” for Russian President Vladimir Putin to invade Ukraine. Biden and his team are creating a new set of initiatives to check Russia and make sure Ukraine is protected. But Biden made sure to calmly issue a warning to Putin before any of said initiatives become necessary. The U.S. President is primarily concerned with an increased presence of Russian troops at the Ukrainian border. The Kremlin has also boasted war-ready rhetoric in its recent language. “What I am doing is putting together what I believe will be the most comprehensive and meaningful set of initiatives to make it very, very difficult for Mr. Putin to go ahead and do what people are worried he may do,” Biden told the press.

There are indications that the tensions are high enough that a meeting between the White House and the Kremlin may be held as soon as next week. Putin’s foreign affairs adviser Yuri Ushakov told the press that the Kremlin had been organizing a call between the two leaders in the next coming days. Will Biden has made sure not to name any specific consequences he is considering, Russian Foreign Minister Sergey Lavrov said that he believes that Biden will put pressure on Russia with new sanctions. Lavrov spoke with U.S. Secretary of State Antony Blinken in Stockholm, Sweden on Thursday, where Blinken said that the U.S. would “have to respond” if Russia acted on Ukraine:

“We don’t know President Putin’s intent. We don’t know if he’s made a decision to take renewed, aggressive action against Ukraine, but what we do know is that he’s putting in place the capacity to do so and to do so on short, on short notice,” Blinken said in a statement to Euronews following the meeting. But Lavrov seemed unshaken by Blinken’s remark and Biden’s warning, saying that “If the new ‘sanctions from hell’ come, we will respond. We can’t fail to respond.”

Read more …

Anybody can write one of these now. But how, looking at the fall-out, can you leave out the Covid hysteria? It’s lessons learned from Russiagate, on steroids.

Obituary for Russiagate (Patrick Lawrence)

There is, of course, the more dangerous world Russiagate has done so much to create. In the culture of unreason, the Deep State has a discouraging record of success in gaining wide public support for any aggressive campaign against any nation or people it wishes to act against. In this dimension, Russiagate has destroyed the Democrats as a party willing to stand against the imperial project in its late phase. A war with China over the Taiwan question is now spoken of as a logical possibility. Washington is now raising the temperature on the Ukraine–Russia border, just as it did when it cultivated the 2014 coup in Kiev, and this is put across as a Democratic administration’s sound policy. Rampant Russophobia is a direct consequence of the Russiagate ruse, Sinophobia its uglier sibling — uglier for its racist subtext.

We have active subversion operations in Nicaragua, Venezuela, Cuba and Peru, all progressive states in the true meaning of this term, and Democrats of all stripes — including “progressives” with the necessary quotation marks — cheer on every one of them. We cannot view this as distinct from the elevation of institutions dedicated to campaigns of covert subterfuge — chiefly but not only the C.I.A. — to wholly inappropriate positions of respect. The damage Russiagate has done to the press … let me rephrase this. The damage the press has inflicted upon itself in the cause of Russiagate is so extensive it is hard to calculate with any precision. We watch now as their credibility collapses in real time. Those running the mainstream newspapers and networks seem to understand this, as they rush to protect what remains of their reputations with rearguard actions to obscure their grossly irresponsible conduct.

The long list of those who caved to the Russiagate orthodoxy includes some stunning names. Among publications that should have known better we find Mother Jones, The Nation, The Intercept, and Democracy Now! Was it conformity, pressure from donors or Democratic Party ventriloquists, or some combination of ideology, ignorance and inexperience that caused them to flip? The Atlantic, The New Yorker, the major dailies, the networks — they have all sustained one or another degree of discredit, left either to craven rewrites in their archives, denial in the Corn–Frum mode, or silence. None will do: They will never regain lost ground without first acknowledging what they have done, and this appears out of the question.

Read more …

 

 

 

 

 

 

Melbourne
https://twitter.com/i/status/1466965416283029506

 

 

Vienna

 

 


This photo is the most detailed model of a human cell to date, obtained using X-ray, NMR, and cryo-electron microscopy data sets

 

 

Support the Automatic Earth in virustime; donate with Paypal, Bitcoin and Patreon.

 

Nov 262021
 


Pablo Picasso Bather on the beach 1920

 

Ignorant and Afraid (eugyp)
Ex-England Star Wonders If Football Player Collapses Linked To Vaccine (RT)
Ethics of Vaccine Refusal (BMJ)
WHO Calls Special Meeting To Discuss New Covid Variant (CNBC)
Former WHO Director Warns Making Vaccines Mandatory Could Cause Riots (SN)
COVID-19 Vaccine For Babies And Toddlers Could Be Approved Early 2022 (CBC)
Media Tells Americans to Check Vaccine Status of Thanksgiving Dinner Guests (SN)
EU Moves To Place Covid Booster Jabs At Heart Of Travel Rules (G.)
No, You Cuck. This Is How (Denninger)
FDA Report Finds All-Cause Mortality Higher Among Vaccinated (INN)
Marines Face Defining Moment Ahead of Vaccine Mandate Deadline (USN)
Missouri Judge Says Covid-19 Public Health Orders Must Be Lifted (Hill)
Pfizer Vaccine Linked To 26 New Cases Of Myocarditis In Australia (DT)
365 Studies Prove the Efficacy of Ivermectin and HCQ in Treating COVID-19 (GP)
Centrist Dems Sink Biden’s Nominee For Top Bank Regulator (Axios)

 

 

 

 

Heart attacks

 

 

Mount Sinai Long Beach hospital
https://twitter.com/i/status/1463610474482872320

 

 

“Merkel’s remarkable virus paranoia, quietly acknowledged by the press now for months, explains her fixation on social isolation, closures and curfews as the only acceptable pandemic policies.”

Ignorant and Afraid (eugyp)

I’ve mentioned this episode a few times: On 11 March 2020, Angela Merkel held a press conference where she remarked that the best hope was to slow the spread of SARS-2, and that 70% of Germans could be infected. The Italian lockdown was only a few days old, and it was plainly not Merkel’s intent to go down the path of mass containment. The United Kingdom, Germany, Sweden and likely a few other countries too still planned for an ordinary approach to Corona, with minimal mitigations. All the while, though, Team Lockdown was hard at work behind the scenes, to bend policy in their direction. As a leaked email from 20 March shows, German medical bureaucrats deputised by the Ministry of the Interior were soon consulting experts on how best to instil “fear and a willingness to obey in the population.”

Because Western governments doubted their capacity to enforce Chinese-style lockdowns outright, fomenting mass panic became a non-pharmaceutical intervention in its own right. The histrionic media messaging has continued to this day, and it has contributed to a profoundly important division in our society: There are on the one hand those people in essential roles, who have endured exposure to Corona from the beginning, and most of whom have had the virus by now. And there are on the other hand those in Martin Kulldorf’s “laptop class,” that is to say well-off urban professionals, who have spent most of the last 21 months at home, hiding from a virus that many of them believe is approximately as dangerous as SARS. Mass infections among these people are only starting to happen right now.

As members of this privileged, sheltered class, politicians and bureaucrats have absorbed the virus hysteria that they helped seed in their social milieu. In the beginning, Merkel did not especially fear the possibility of mass infections in Germany. Six months of press hysteria later, in October 2020, she had grown accustomed to carrying two plastic envelopes in her bag. One was for the careful, hygienic disposal of used surgical masks. The other carried precious new ones, whenever she judged her current mask had reached a dangerous state of virus saturation. [..] Merkel’s remarkable virus paranoia, quietly acknowledged by the press now for months, explains her fixation on social isolation, closures and curfews as the only acceptable pandemic policies.

She is a 67 year-old sedentary woman who likely suffers from one or more undisclosed health problems. And she is surrounded by other older, unfit government officials, like 73 year-old interior minister Horst Seehofer, who nearly died of a B19 virus infection in 2002, and so has a reason to fear viral infection. For months and months, all of these people have been taking every possible personal precaution – including house-arresting the entire domestic populations of the countries they govern – in the vain hope of escaping Corona. You could feel their collective relief when the vaccines were rolled out. All of them eagerly accepted vaccination. Merkel even provided pictures of her personal yellow vaccine pass to the press, with the stamp documenting her first dose of AstraZeneca. (Her purpose, in part, was to allay public concerns over the propensity of AstraZeneca to cause blood clots.)

Read more …

Not allowed to ask.

Ex-England Star Wonders If Football Player Collapses Linked To Vaccine (RT)

Former England and Manchester City player Trevor Sinclair has been criticized online after asking if the recent collapse of a professional footballer may have been linked to the Covid vaccine.Sinclair won 12 caps for England and is remembered for a 14-year stint in the Premier League that began at his most associated club, Queens Park Rangers. Now acting as a pundit in his post-playing days, he made controversial remarks on popular UK radio station TalkSport. On Tuesday, Scottish Sheffield United star John Fleck was rushed to hospital after a scare in his team’s 1-0 victory over Reading. The following evening, in a Champions League clash against Real Madrid, Sheriff Tiraspol’s winger Adama Traore went to the turf clutching his chest and had to be helped off the pitch by medical staff.

Elsewhere, Barcelona’s Sergio Aguero is tipped to retire after a heart incident earlier this month, while Danish midfielder Christian Eriksen suffered a high-profile incident at the European Championships in the summer. But even though there has been no evidence that these occurrences were connected to the Covid vaccine, Sinclair seemingly suggested a link. “I think everyone wants to know if he has had the Covid vaccine,” the 48-year-old began on Fleck. Later on Twitter, he also added: “Everyone I speak to about these heart problems suffered by footballers (which worryingly seem to be happening more regularly) are they linked to Covid vaccines or not??”. Sinclair was widely-attacked for the comments. “This is an inappropriate place to ask that question,” Sinclair was informed.”You are begging for conspiracy theories. Ask a doctor. Ask a medical researcher.

“Do your own research online, being careful of the reliability of the sources. Everything I’ve read says NO.” “Pretty irresponsible stuff to post, Trevor,” said another do-gooder.”If vaccines had anything to do with this, then surely millions of us would be having new heart problems every day all over the world. And we’re not.””Eh, so you came up with an idea and are now asking people on social media if your imagination is reality,” was another criticism.But not everyone jumped on the bandwagon. “We don’t know Trevor as TalkSport cut you off when you asked,” came one reply to his Twitter post.

“Fair play to you for having the balls to ask the question. “Yes Trevor, don’t ask questions or think for yourself ever again,” it was suggested in support, after another user told him to think before he tweets.”All these comments are trying to be politically correct, grow a pair and say it how it is,” demanded another outspoken voice. “One major side effect of the vaccine is inflammation of the heart. Yet we’re supposed to think these sudden cases are a coincidence.”

https://twitter.com/i/status/1463966084428709900

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“Restrictions on freedoms can be justified only if they are reasonably necessary to preserve what makes human life worth living, because freedom is a necessary condition of a life worth living and, therefore, worth preserving.”

Ethics of Vaccine Refusal (BMJ)

Arguments in favour of mandatory universal vaccination rely on the premise that everyone who can be vaccinated has a moral obligation to do so for the sake of those who cannot be vaccinated due to age or certain immune system disorders, or because the public health benefits of universal vaccination are so profound that to refuse vaccination would be unethical. This line of reasoning underpins the ‘obligation to vaccinate’ (OTV) range of arguments. Brennan1 formulates a broadly representative OTV-type argument in terms of an ‘enforceable moral principle that prohibits people from participating in the collective imposition of unjust harm or risk of harm’.

Brennan begins by positing that (A) certain vaccines have a low incidence of side effect and are effective at preventing serious illness; (B) it would be a disaster if a large majority of individuals failed to receive various vaccines; (C) individual freedoms can be overridden to prevent a disaster; therefore, (D) ‘it is permissible to force individuals to receive certain vaccines against dangerous illnesses’. The argument seems to imply that non-vaccination is a sufficient condition of a disaster (would make the disaster imminent) that mandating mass vaccination is a sufficient condition of preventing the disaster, and that the overriding of individual freedoms could not result in a disaster of a different kind. None of these conditions can be assumed to be true.

We could also infer from the above premises that anything conceived of as harm could be classified as a ‘disaster’ and this would automatically give someone a legitimate right to override the freedoms of others, but this is absurd. We must, therefore, conclude that C is false: individual freedoms cannot be overridden just to prevent a disaster. Restrictions on freedoms can be justified only if they are reasonably necessary to preserve what makes human life worth living, because freedom is a necessary condition of a life worth living and, therefore, worth preserving. This is a conceptually appealing formula, but since the criterion of reasonable necessity is as elastic as the notion of disaster, it does not tell us much about practical moral obligations.

Brennan sidesteps this problem by proceeding to hone an OTV-type argument just in virtue of preventing ‘the collective imposition of unjust harm or risk of harm’. The reference to unjust harm makes his moral premise intuitively true but also compels us to identify the underlying injustice. Given that the existing vaccination technology is not risk-free (even if serious adverse reactions are rare) the alleged moral OTV implies that we have an obligation to reduce the risk to the health of others by accepting an increased or unknown health risk to ourselves. If I must accept an increased risk to myself in order to reduce the risk to others, because everyone has a moral obligation to do so, then justice demands that others must also accept an increased risk to themselves in order to reduce the risk to me, therefore, contradiction. This impasse can be resolved only by taking into account what set of ‘risk-permitting rules would tend to benefit everyone as individuals’1; a crucial question to which I will return.

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Very little is known, which is a great reason to panic.

WHO Calls Special Meeting To Discuss New Covid Variant (CNBC)

The World Health Organization is monitoring a new variant with numerous mutations to the spike protein, scheduling a special meeting Friday to discuss what it may mean for vaccines and treatments, officials said Thursday. The variant, called B.1.1.529, has been detected in South Africa in small numbers, according to the WHO. “We don’t know very much about this yet. What we do know is that this variant has a large number of mutations. And the concern is that when you have so many mutations, it can have an impact on how the virus behaves,” Dr. Maria Van Kerkhove, WHO’s technical lead on Covid-19, said in a Q&A that was livestreamed on the organization’s social media channels. The monitoring of the new variant comes as Covid cases surge around the world heading into the holiday season, with the WHO reporting hot spots in all regions and particularly in Europe.

South African scientists have detected more than 30 mutations to the spike protein, the part of the virus that binds to cells in the body, South African scientist Tulio de Oliveira said in a media briefing hosted by the South Africa Department of Health on Thursday. The B.1.1.529 variant contains multiple mutations associated with increased antibody resistance, which may reduce the effectiveness of vaccines, along with mutations that generally make it more contagious, according to slides he presented at the briefing. Other mutations in the new variant haven’t been seen until now, so scientists don’t yet know whether they are significant or will change how the virus behaves, according to the presentation. The variant has spread rapidly through the Gauteng province, which contains the country’s largest city of Johannesburg.

“Especially when the spike happens in Gauteng, everybody travels in and out of Gauteng from all corners of South Africa. So it’s a given that in the next few days, the beginning of rising positivity rate and numbers is going to be happening. It’s a matter of days and weeks before we see that,” South Africa Minister of Health Joe Phaahla said during the briefing. The variant has also been detected in Botswana and Hong Kong, Phaahla said. “Right now, researchers are getting together to understand where these mutations are in the spike protein and the furin cleavage site, and what that potentially may mean for our diagnostics or therapeutics and our vaccines,” Van Kerkhove said. She said there are fewer than 100 full genome sequences of the new mutation.

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Not could, will. Just try.

Former WHO Director Warns Making Vaccines Mandatory Could Cause Riots (SN)

Former World Health Organization director Anthony Costello warns that making COVID-19 vaccines mandatory could cause “riots.” Costello, a professor of global health and sustainable development at University College London, made the comments in response to numerous European countries continuing to experience COVID case surges. Although insisting that mandatory vaccinations is a “debate we can have,” Costello said it might sweep up more of the “indifferent” people, but that there were potentially explosive ramifications. “But you will repel a lot of people who lack trust in government and in vaccines. And you may start to see the unpleasant civil disobedience and riots they’ve had across Europe,” he added.


Meanwhile, WHO official Robb Butler called for other European countries to consider making vaccines mandatory. Doing so “can, but does not always, increase uptake,” argued Butler, adding, “We believe it’s time to have that conversation from both an individual and a population-based perspective. It’s a healthy debate to have.” Numerous countries have already seen large scale civil unrest in response to attempts by governments to impose new lockdowns and compulsory vaccinations. Austrians face fines and even prison time if they refuse to get jabbed after a February deadline.

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Warped “logic”: immune systems must fight off the vaccine.

“Children do have a robust immune system and I expect that they will mount a good immune response to the vaccine as well..”

COVID-19 Vaccine For Babies And Toddlers Could Be Approved Early 2022 (CBC)

Canada’s chief public health officer says COVID-19 vaccines for babies and toddlers could be approved early in the new year, depending on how clinical trials play out. In an interview with CBC Radio-Canada, Dr. Theresa Tam said a vaccine for some of Canada’s youngest people could be a turning point in the fight against COVID-19. “Children do have a robust immune system and I expect that they will mount a good immune response to the vaccine as well,” she said. “And for their parents as well, it’s sort of offering them some further hope.” In a major vaccine milestone, children aged five to 11 started to receive their first doses this week after Health Canada approved Pfizer-BioNTech’s vaccine for that age group. Meanwhile, that company is running clinical trials for those aged six months to just under five years.


Moderna is waiting for Health Canada approval on its COVID-19 vaccine for children aged six to 11, and is also in the midst of recruiting younger children for a clinical trial. “I can’t tell you exactly when those results will be available,” Tam said of the trials. “It depends on how many people they recruit and how fast the trials go. But I think all of that is well underway.” Tam said she anticipates seeing results from Pfizer-BioNTech for those aged two to five first. The doctor said she’s hoping to see some trial data toward the end of this year. “Which means for the youngest age group, the most likely timeline is optimistically at the beginning of next year,” she said.

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“..millions of households may need their own Thanksgiving bouncer..”

Media Tells Americans to Check Vaccine Status of Thanksgiving Dinner Guests (SN)

On the eve of Thanksgiving, media outlets urged Americans to perform COVID tests and check the vaccination status of Thanksgiving dinner guests before allowing them into their homes.Yes, really. During a segment on CBS Mornings, psychologist Lisa Damour was asked how nervous Thanksgiving hosts should bring up the subject of vaccination status when welcoming friends and family. “It might be a difficult conversation before people step into your house to say, ‘whoa, wait a minute, where’s your card, what’s your status?’ before you walk into my home,” the host of the show said. “This is tough because people are all over the map on this,” responded Damour. “They’re also all over the map with their risk tolerance. But the rapid tests have made this a lot easier. Whatever people’s vaccination status is, we can actually confirm safety on the spot.”

“If the situation feels weird, maybe make it kind of fun,” she added. “And say, ‘we’re going to start with hors d’oeuvres in the garage. You know, we’ll have drinks, we’ll do our rapid tests, and then come on in,’ right?” You can make it playful, make it fun, and then be able to enjoy the holiday because you’re not worried about safety.” Let’s just take a moment to sympathize with people who are attending Thanksgiving dinner today at a relative’s house who is so paranoid about a virus with a 99.9% survival rate, they want to perform medical tests on their own family members before letting them in. Good luck to those people.

Meanwhile, Axios published an article suggesting that hosts should deploy “Thanksgiving bouncers” to deal with people who fail to comply. “No one really wants this job, but millions of households may need their own Thanksgiving bouncer. The cover charge is a negative COVID test, done ahead of arrival or outside the front door,” the article states. “Normalizing rapid tests is a practical way to help extended families feel a little more normal around the holiday dinner table.” The piece went on to encourage hosts to inform guests ahead of time that they will “be testing everyone at the door for their own safety.” No thanks, think I’ll be staying home this year.

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“The current system, under which countries are added and removed from a safe list, will be dropped, a change officials think offers more certainty.” Huh?

EU Moves To Place Covid Booster Jabs At Heart Of Travel Rules (G.)

People hoping to travel to the European Union next year will have to get a booster jab once their original Covid vaccines are more than nine months old, under new proposals from Brussels. On Thursday, the European Commission proposed a nine-month limit for vaccine validity that would apply for travel within and to the EU. If the plans are approved by EU ministers, from 10 January 2022 non-EU travellers will be required to show proof of an EU-approved booster jab once their original vaccine status is more than nine months old. Similarly, travellers between the member states would have to meet the same requirement to avoid Covid tests, quarantine and other restrictions. The Commission hopes to avoid a confusing mixture of rules across the 27 member states, as governments scramble to tighten restrictions on everyday life following a surge in coronavirus infections.

The plans were unveiled on Thursday as the European Medicines Agency approved the use of the Pfizer-BioNTech vaccine for children aged five to 11, opening the way for governments to extend vaccination campaigns. The EU regulator recommended two injections three weeks apart in the upper arm for primary-school children, at one-third of the adult dose. The latest EU proposals prioritise vaccinated people, as Brussels moves to classify travellers according to individual health and vaccine status, rather than their country of departure. From 1 March 2022, EU member states would only permit entry to vaccinated, recovered or essential travellers, such as lorry drivers. The current system, under which countries are added and removed from a safe list, will be dropped, a change officials think offers more certainty.

The recommendation to make booster jabs necessary after nine months for non-EU non-essential travellers is part scientific advice, part practical policy. Immunity wanes after six months, but EU officials added an extra three to allow governments to get booster-shot programmes up and running. The EU executive also wants to allow entry for travellers with non-EU approved vaccines that are recognised by the World Health Organization, such as China’s Sinopharm and Sinovac and the AstraZeneca vaccine made by the Serum Institute of India. The EU has only approved four vaccines: Pfizer-BioNTech, AstraZeneca (produced in Europe), Janssen (Johnson & Johnson) and Moderna. Most EU member states only permit entry to people with EU-approved vaccines. Under the new proposals, travellers to the EU with a WHO-approved vaccine that is not EU approved, could enter the EU, but would have to produce a negative Covid-test.

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“Hospitals cannot be allowed to become prisons where patients are denied rights they would otherwise have.”

No, You Cuck. This Is How (Denninger)

**** you Daniel. “The family of Sun Ng will definitely have a meaningful Thanksgiving this year thanks to an attorney, a judge, and a doctor who bucked the system and enabled him to get ivermectin when he was at death’s doorstep. Imagine how many thousands of others are missing at this year’s Thanksgiving dinner thanks to the satanic effort to block this lifesaving drug – both outpatient and for those close to death?” It’s not just Ivermectin. These *******s are filling people with Remdesivir, which I remind you failed three times previously, including in a clinical trial for Ebola, a virus that kills half of those who get it. Distribution of patients into that treatment arm was stopped because of safety problems; in other words it was killing people more than the virus itself did, so they stopped using it partway through.

Today hospitals are being paid bounties — yes, actual bonuses — if they use this drug on all Covid-19 patients. So the answer isn’t this: “There is an immediate need for every attorney general to do battle with these hospitals and every legislature to pass a law specifically barring hospitals from blocking any patient from seeking the use of an FDA-approved drug at the direction of a physician to treat COVID. Hospitals cannot be allowed to become prisons where patients are denied rights they would otherwise have.” The way you stop it is simple: Charge the hospital administrators with felony manslaughter for each and every Covid-19 patient who dies and is either (1) denied medication they, their family or their physicians want to use OR (2) is given Remdesivir, which generates a rebuttable presumption that the drug killed them and not the virus.

Said presumption can be rebutted by autopsy if and only if their kidneys and liver are not damaged, which is what the drug does. Charge the hospital administrators with felony manslaughter for everyone they kill this way and watch their tune change immediately. Oh, and people will stop dying of Covid-19 too. Until and unless you advocate and in fact demand that **** you Mr. Auschwitz.

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The winter of excess deaths is coming. And nobody knows why.

FDA Report Finds All-Cause Mortality Higher Among Vaccinated (INN)

The clinical trials of Pfizer’s coronavirus vaccine found that the all-cause mortality rate of the vaccinated group was higher than that of the control group, months after the trials were launched, according to a recently released FDA report. According to the report, which was released by the US Food and Drug Administration to provide background information on its August 2021 decision to grant full approval for the Pfizer-BioNTech coronavirus vaccine after offering limited emergency authorization of use in last December, six months after the vaccine’s clinical trial began, the total number of deaths reported in the vaccinated group was nearly one-quarter higher than the number of deaths in the placebo group. The report emphasized that “None of the deaths were considered related to vaccination.”

Just under 22,000 participants were included in each group, with half receiving the coronavirus vaccine, and half receiving a saline solution injection. The initial results of the clinical trials suggested a high-level of efficacy for the vaccine in preventing symptomatic cases of COVID-19, an in particular, serious illness from COVID – but lacked significant data on all-cause mortality, due to the short time-frame and small number of total deaths. A follow-up assessment of participants completed on March 13th of this year looked at the overall health outcomes of the trial participants, six months after they received either the COVID vaccine or the saline solution injection. While Pfizer in July released partial data on the outcomes from the six-month assessment ending March 13th, the new FDA report includes more comprehensive data, and shows a significantly higher number of all-cause fatalities among the vaccinated cohort.

The Pfizer report in late July of this year showed effectively equal all-cause fatality rates between the vaccine and placebo cohorts six months after the tests were conducted, with 15 deaths among the nearly 22,000 vaccine recipients, versus 14 deaths among the nearly 22,000 placebo recipients. Most of the total 29 deaths in both groups were not related to the coronavirus; of the deaths in both groups, three fatalities were listed as being related to the virus; two in the placebo group and one in the vaccinated group. The FDA report, however, revealed a larger number of deaths by all causes in both groups, with 17 deaths among the control group and 21 in the vaccinated cohort.

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“The idea of rejecting an order, that’s counter to Marine Corps culture.”

Marines Face Defining Moment Ahead of Vaccine Mandate Deadline (USN)

The Marine Corps faces a defining moment leading up to its Monday deadline for all Marines to have received a coronavirus vaccine, with reports of a significant number who have refused the shot clashing with the service’s meticulously crafted image as the military’s most disciplined fighting force – and its most potent. Roughly 10,000 of its 186,000-strong active duty force are positioned to miss the deadline the Department of the Navy set for all Marines and sailors to become fully vaccinated, according to the latest data, representing the highest proportion of any of the military services potentially to violate direct orders from the chain of command. Even those who may have waited until the final weeks to begin the vaccination process will ultimately miss the deadline, which requires Marines to have completed the two-week vaccination process.

The 38,000 Marine Corps reservists face a later deadline of Dec. 28. Marine Corps headquarters has so far declined to say how many have applied for or been granted exemptions – a bureaucratic process to accommodate religious, medical or administrative concerns that has taken on outsized relevance in the age of coronavirus vaccine skepticism – or how it will punish those who outright refuse to receive the shot. A spokesman says it continues to study the scope of the issue. But those with deep experience in the corps and its place in the wider military say it has already suffered from the initial refusals, with the potential for greater damage after next week. “For decades the Marine Corps has been about the expeditionary force and readiness.

‘First to Fight,’ ‘Send the Marines’ – all those slogans about how they have to be ready to go on a moment’s notice,” says David Lapan, a former Marine Corps officer and later a spokesman for the Pentagon and Department of Homeland Security. “The Marine Corps prides itself on its discipline and following orders,” he adds. “The idea of rejecting an order, that’s counter to Marine Corps culture.” The Navy, by comparison, facing the same deadlines neared 100 percent vaccination early this month – matching a trend it has maintained in recent months following the catastrophic fallout of outbreaks that sidelined Navy ships early in the pandemic. The Office of Management and Budget revealed Wednesday that 92 percent of the entire federal workforce – including the military – had been vaccinated, with 4 percent receiving exemptions. The mandate takes on a different meaning for the Defense Department, however, as it was issued as a formal order by each service member’s chain of command.

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“.. Among those who filed the lawsuit was Ben Brown, who is running for state Senate in Missouri and owns Satchmo’s Bar and Grill..”

Missouri Judge Says Covid-19 Public Health Orders Must Be Lifted (Hill)

A Missouri judge ruled that local health officials can no longer issue COVID-19 safety orders, which he said infringe upon the constitutional separation of powers between branches of government, reported the St. Louis Post-Dispatch. The ruling from Cole County Circuit Court Judge Daniel Green means local health regulations throughout Missouri are struck down and rendered obsolete, reported the Post-Dispatch. “This case is about whether Missouri’s Department of Health and Senior Services regulations can abolish representative government in the creation of public health laws, and whether it can authorize closure of a school or assembly based on the unfettered opinion of an unelected official. This court finds it cannot,” said Green, according to the Post-Dispatch.


“Missouri’s local health authorities have grown accustomed to issuing edicts and coercing compliance. It is far past time for this unconstitutional conduct to stop,” added Green, a Republican who was first elected as county judge in 2010. The lawsuit was originally filed in 2020 and claimed that state health officials were overstepping their authority by issuing coronavirus mitigation measures such as quarantines and business closures, reported the Post-Dispatch. Among those who filed the lawsuit was Ben Brown, who is running for state Senate in Missouri and owns Satchmo’s Bar and Grill, which he fought to keep open during the pandemic against St. Louis County officials’ orders, reported the Post-Dispatch. Brown posted about the ruling on Tuesday on his Twitter account, where he wrote, “The age of mandates and forced quarantine of students by local health departments in our state is over!” and “Freedom wins!”

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Be open about it. It’s the only thing that will work.

Pfizer Vaccine Linked To 26 New Cases Of Myocarditis In Australia (DT)

The number of cases of heart inflammation linked to the Pfizer Covid vaccine in Australia has risen to 341 from about 23.9 million doses. There were 26 new cases of the rare side effect known as myocarditis reported in the week ending November 21. There was also one new blood clots case linked to the AstraZeneca vaccine following a first dose. It involved a 67-year-old woman from Victoria. The new case increased the total Thrombosis with thrombocytopenia syndrome (TTS) or blood clots cases to 164 out of 13.4 million doses. Of these 148 (81 confirmed, 62 probable) related to a first dose and 21 to a second dose (six confirmed, 15 probable).


Eight people have died as a result of blood clots – six of these were women. There have also been a total of 150 reports of suspected Guillain-Barre Syndrome (GBS) occurring after vaccination with AstraZeneca, a rare but sometimes serious immune disorder affecting the nerves. And a total of 90 reports of suspected immune thrombocytopenia (ITP) following vaccination with AstraZeneca, a rare immune reaction that can occur after a viral infection or vaccination when platelets, which help blood to clot, are mistakenly destroyed. [..] Myocarditis is reported in one to two in every 100,000 people who receive Pfizer, although it is more common in young men and teenage boys after the second dose (five to 11 cases per 100,000 doses).

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Poorly written, but still..

365 Studies Prove the Efficacy of Ivermectin and HCQ in Treating COVID-19 (GP)

There have now been 67 Ivermectin COVID-19 controlled studies that show a 67% improvement in COVID patients. [..] Dr. Robert Malone, the inventor of the mRNA vaccines, accused Dr. Fauci and others of lying and causing the death of over 500,000 Americans by preventing HCQ and Ivermectin, and other treatments from COVID-19 patients. Dr. Malone is right. It is well documented that Dr. Fauci and top US doctors conspired to disqualify and condemn hydroxychloroquine as a COVID-19 treatment. Millions died as a result of this. As TGP reported earlier — It wasn’t just Fauci but all of the top US medical leaders who were in on the hydroxychloroquine lie. Dr. Meryl Nass, MD, broke this story in The Defender. According to Dr. Nass, the top health officials were all in on the conspiracy against hydroxychloroquine.

“Fauci runs the NIAID, Collins is the NIH director (nominally Fauci’s boss) and Farrar is director of the Wellcome Trust. Farrar also signed the Lancet letter. And he is chair of the WHO’s R&D Blueprint Scientific Advisory Group, which put him in the driver’s seat of the WHO’s Solidarity trial, in which 1,000 unwitting subjects were overdosed with hydroxychloroquine in order to sink the use of that drug for COVID. Farrar had worked in Vietnam, where there was lots of malaria, and he had also been involved with SARS-1 there. He additionally was central in setting up the UK Recovery trial, where 1,600 subjects were overdosed with hydroxychloroquine.

Even if Farrar didn’t have some idea of the proper dose of chloroquine drugs from his experience in Vietnam, he, Fauci and Collins would have learned about such overdoses after Brazil told the world about how they mistakenly overdosed patients in a trial of chloroquine for COVID. The revelation was made in an article published in the JAMA in mid-April 2020. Thirty-nine percent of the subjects in Brazil who were given high doses of chloroquine died, average age 50.Yet the Solidarity and Recovery hydroxychloroquine trials continued into June, stopping only after their extreme doses were exposed. Fauci made sure to control the treatment guidelines for COVID that came out of the NIAID, advising against both chloroquine drugs and ivermectin. Fauci’s NIAID also cancelled the first large-scale trial of hydroxychloroquine treatment in early disease, after only 20 of the expected 2,000 subjects were enrolled.”

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A curious story. She wants big changes.

Centrist Dems Sink Biden’s Nominee For Top Bank Regulator (Axios)

Five Democratic senators have told the White House they won’t support Saule Omarova to head the Office of the Comptroller of the Currency, effectively killing her nomination for the powerful bank-regulator position. The defiant opposition from a broad coalition of senators reflects the real policy concerns they had with Omarova, a Cornell University law professor who’s attracted controversy for her academic writings about hemming in big banks. Their opposition also hints at a willingness of some Democratic senators to buck the White House on an important nomination, even if it hands Republicans a political — and symbolic — victory. Republicans have attacked the Kazakh-born scholar in remarkably personal terms, and turned her nomination into a proxy battle over how banks should be regulated.


In phone call on Wednesday, Sens. Jon Tester (D-Mont.) Mark Warner (D-Va.) and Kyrsten Sinema (D-Ariz.), all members of the Senate Banking Committee, told Sen. Sherrod Brown (D-Ohio) — the panel’s chairman — of their opposition. They’re joined in opposing her by Sens. John Hickenlooper (D-Colo.) and Mark Kelly (D-Ariz.). Biden officials also have heard directly from the senators. They’re aware of their deep opposition and know Omarova faces nearly impossible odds for confirmation. Still, they continue to back her publicly. “The White House continues to strongly support her historic nomination,” a White House official told Axios. “Saule Omarova is eminently qualified for this position,” the official said. “She has been treated unfairly since her nomination with unacceptable red-baiting from Republicans like it’s the McCarthy era.”

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STD

 

 

Temples of the Holy Spirit

 

 

Support the Automatic Earth in virustime; donate with Paypal, Bitcoin and Patreon.

 

Nov 242021
 
 November 24, 2021  Posted by at 9:44 am Finance Tagged with: , , , , , , ,  140 Responses »


Jean-Francois Millet The Young Shepherdess 1870-73

 

SARS-CoV-2 Spike Protein Disrupts Human Cardiac Pericytes Function (CS)
Vaccine Data Transparency at the FDA (Kheriaty)
Fauci Speaks Of ‘Unfinished Business’ Before He Can Retire (RT)
Judge Tells Hospital: “Step Aside”, Give a Dying Man Ivermectin (Pfeiffer)
Kansas Governor to Allow Broad Exemptions to COVID-19 Vaccine Requirements (ET)
New Zealand To Stay Closed To Foreigners For Another Five Months (MSN)
Scottish Govt Vax Passport Sends People’s Private Data To Amazon, Microsoft (S)
Covid Deaths In Europe To Top 2 Million By March, Says WHO (G.)
The Health Effects Of Vitamin D Supplementation (Nature)
US to Require Vaccines for All Border Crossers in January (AP)
Americans Got Richer Thanks To Vaccines & Covid Policies, Biden Claims (RT)
US, Russia Military Chiefs Hold Urgent “Deconfliction” Call On Ukraine (ZH)

 

 

 

 

Denmark pressure
https://twitter.com/M_B_Petersen/status/1463036582345248768

 

 

https://www.fda.gov/media/153409/download
Vaccines and Related Biological Products Advisory Committee October 26, 2021
No data. 5 Years of Study Needed.

 

 

Full title: “The SARS-CoV-2 Spike protein disrupts human cardiac pericytes function through CD147-receptor-mediated signalling: a potential non-infective mechanism of COVID-19 microvascular disease.”

SARS-CoV-2 Spike Protein Disrupts Human Cardiac Pericytes Function (CS)

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a broad range of clinical responses including prominent microvascular damage. The capacity of SARS-CoV-2 to infect vascular cells is still debated. Additionally, the SARS-CoV-2 Spike (S) protein may act as a ligand to induce non-infective cellular stress. We tested this hypothesis in pericytes (PCs), which are reportedly reduced in the heart of patients with severe coronavirus disease-2019 (COVID-19). Here we newly show that the in vitro exposure of primary human cardiac PCs to the SARS-CoV-2 wild type strain or the Alpha and Delta variants caused rare infection events.

Exposure to the recombinant S protein alone elicited signalling and functional alterations, including: (1) increased migration, (2) reduced ability to support endothelial cell (EC) network formation on Matrigel, (3) secretion of pro-inflammatory molecules typically involved in the cytokine storm, and (4) production of pro-apoptotic factors causing EC death. Next, adopting a blocking strategy against the S protein receptors angiotensin-converting enzyme 2 (ACE2) and CD147, we discovered that the S protein stimulates the phosphorylation/activation of the extracellular signal-regulated kinase 1/2 (ERK1/2) through the CD147 receptor, but not ACE2, in PCs.

The neutralisation of CD147, either using a blocking antibody or mRNA silencing, reduced ERK1/2 activation, and rescued PC function in the presence of the S protein. Immunoreactive S protein was detected in the peripheral blood of infected patients. In conclusion, our findings suggest that the S protein may prompt PC dysfunction, potentially contributing to microvascular injury. This mechanism may have clinical and therapeutic implications.

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55 years till you know if the vaccine is safe enough to take. Till the, you’re on your own.

Vaccine Data Transparency at the FDA (Kheriaty)

In September I organized 30 distinguished academic physicians and scientist colleagues to form Public Health and Medical Professionals for Transparency. This group included, among other luminaries, my friends Harvey Risch of Yale, Andrew Bostom of Brown, Joseph Ladapo of UCLA (who has since been appointed Surgeon General of Florida), Paul Alexander, formerly of HHS and WHO, Aditi Bhargava of UCSF, and other scientists from the U.S., Canada, Denmark, Australia, Germany, and the University of Oxford in the U.K. With the help of my lawyers, Aaron Siri and Elizabeth Brehm, we submitted a FOIA request to the FDA for all the data relied upon to authorize Pfizer’s Covid vaccine. While this information was not available while the vaccine was only approved under Emergency Use Authorization (EUA), under federal law, the FDA was required to make this data publicly available once it received full approval, which happened in August.


The law is crystal clear on this point: our FOIA request was not at all legally complicated, and the FDA’s lawyers at the Department of Justice are well aware of this. As we describe on our website: “The organization takes no position on the data other than that it should be made publicly available to allow independent experts to conduct their own review and analyses. Any data received will be made public.” This is likewise uncontroversial, since transparency is widely regarded as a core ethical principle of all public health initiatives. It is one of the central ethical principles articulated, for example, in the University of California’s “Allocation of Scarce Critical Resources under Crisis Standards of Care,” the ventilator triage policy that I helped draft for the UC’s hospitals last year (see 3.f below):

[..] I look forward to seeing the DOJ lawyers in court, and will keep you updated on this story as the legal proceedings unfold.

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As long as he’s useful for Pfizer.

Fauci Speaks Of ‘Unfinished Business’ Before He Can Retire (RT)

Top White House Covid adviser Anthony Fauci insisted his long career as a federal bureaucrat is far from over, saying retirement is simply out of the question as he looks to wrap up “unfinished business” in the world of medicine. Asked whether he is thinking of leaving his long-held leadership post at the National Institute of Allergy and Infectious Diseases (NIAID), the 80-year-old health official said he’s “not even remotely contemplating that right now.” “There’s a lot of unfinished business right now, so I’m not even thinking about walking away,” Fauci told Reuters in an interview on Tuesday, adding that he would like to see the end of the coronavirus pandemic, and even further progress on eradicating HIV and AIDS, before he steps away from his work.

The White House adviser also reiterated calls for the “overwhelming majority” of fully-vaccinated American adults to receive booster shots, noting that the additional dose could eventually become standard in defining what it means to be ‘fully’ immunized. “Right now, officially, fully vaccinated equals two shots of the mRNA and one shot of the J&J, but without a doubt that could change. That’s on the table for discussion,” he said, referring to Pfizer and Moderna’s vaccines which use messenger-RNA, and Johnson & Johnson’s one-dose formulation.

While an FDA advisory panel initially voted overwhelmingly against booster doses for all healthy Americans – instead greenlighting additional shots only for the elderly and certain at-risk groups – the FDA itself decided to cut the panel out of the process entirely and authorized boosters on its own last week. A similar panel with the Centers for Disease Control and Prevention (CDC), however, did give its blessing, with CDC Director Rochelle Walensky quickly signing off on the decision.

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“..the hospital system filed notice that it would appeal the order that had already been carried out. It did this even though Sun Ng seemed to have benefited greatly.”

Judge Tells Hospital: “Step Aside”, Give a Dying Man Ivermectin (Pfeiffer)

Sun Ng, a retired contractor from Hong Kong, traveled to Illinois to celebrate his only granddaughter’s first birthday. He got covid and was near death in a Chicago-area hospital. All other options were exhausted, but the hospital refused to give Mr. Ng a generic, FDA-approved drug with an extraordinary safety record that a doctor believed could safe his life. Finally, a judge asked the right question about ivermectin. “What’s the downside?” Put another way: If a man is dying of covid in an ICU and all else has been tried, why not order a hospital to give a safe, last-ditch drug? Edward Hospital, located near Chicago, offered three arguments as to why Sun Ng, seventy-one, should not be given ivermectin: There could be side effects. Ordering ivermectin would violate its policies. Forcing the issue would be “extraordinary” judicial overreach.

On each argument, DuPage County Circuit Court Judge Paul Fullerton firmly disagreed. “I can’t think of a more extraordinary situation than when we are talking about a man’s life,” he said in a November 5 decision that is a model of rational decision-making in an irrational era. “I am not forcing this hospital to do anything other than to step aside,” he continued in a Zoom hearing. “I am just asking—or not asking—I am ordering through the Court’s power to allow Dr. Bain to have the emergency privileges and administer this medicine.” The hospital ultimately stepped aside. Dr. Alan Bain, an internist, administered a five-day course of 24 milligrams of ivermectin, from November 8 through November 12. Ng, who with his wife, Ying, had come from Hong Kong to celebrate their granddaughter’s birthday, was able to breathe without a ventilator within five days—he, in fact, removed the endotracheal himself.

He left the ICU Tuesday, November 16, and, although confused and weak, was breathing Sunday without supplemental oxygen on a regular hospital floor. “Every day after ivermectin, there was accelerated and stable improvement,” said Dr. Bain, who administered the drug in two previous court cases after hospitals refused. “Three times we’ve shown something,” he told me. “There’s a signal of benefit for ventilator patients.” Ng’s remarkable progress stands in sharp relief to the repeated attempts by Edward-Elmhurst Health, the hospital’s managing system, to thwart the use of ivermectin. It succeeded in having the court’s initial November 1 order dismissed by claiming Ng was in better health than his lawsuit contended (he wasn’t). It then defied the November 5 order, saying Dr. Bain was not vaccinated (a negative test resolved the issue).

Moreover, after Ng’s treatment was complete, the hospital system filed notice that it would appeal the order that had already been carried out. It did this even though Sun Ng seemed to have benefited greatly. The patient’s improvement, or condition generally, did not seem to matter.

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And she’s a Democrat.

Kansas Governor to Allow Broad Exemptions to COVID-19 Vaccine Requirements (ET)

The governor of Kansas has said she intends to sign a measure that will force businesses that require COVID-19 vaccination to give broad exceptions to workers who don’t want to get the vaccine. Kansas Gov. Laura Kelly, a Democrat, said in a one-sentence Nov. 22 statement that she will sign the legislation “when it reaches my desk.” Derek Schmidt, Kansas attorney general and a Republican, also said he would sign it if he were governor. Schmidt is challenging Kelly in the Kansas gubernatorial race. The Republican-controlled state House of Representatives and state Senate approved House Bill 2001 earlier on Nov. 22 during a special session. The Senate vote was 24–11 and the House vote was 78–41.

The legislation states that any employer who imposes a COVID-19 vaccine requirement must exempt workers if they submit a written waiver request stating that complying with the requirement would endanger the life or health of the waiver applicant or somebody they live with or if receiving the vaccine violates a sincerely held religious belief. Any workers punished or terminated due to violation of the law would be able to file a complaint with state officials, who would be mandated to investigate each complaint and issue an order on each case within 60 calendar days.

An employer who is found to have violated the law would face civil action in a bid to fine them up to $10,000 per violation if they have fewer than 100 employees or up to $50,000 per violation if they have 100 or more employees. The employer would avoid legal action if they reinstate the worker. Another major component of the legislation requires that workers who get laid off due to vaccination requirements be eligible for unemployment benefits. Kansas Senate President Ty Masterson, a Republican, said the measure will “protect the rights of Kansans who are facing impending deadlines from the Biden administration that would force them to choose between their livelihood and their religious freedom or their livelihood and advice from their own physician.”

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Like a lab experiment.

New Zealand To Stay Closed To Foreigners For Another Five Months (MSN)

New Zealand said Wednesday it will not reopen to foreign travellers for at least another five months, as it slowly relaxes some of the world’s toughest pandemic border restrictions. The Pacific nation’s Covid-19 Response Minister Chris Hipkins said New Zealanders stranded in Australia could return home from mid-January and Kiwis travelling from elsewhere would be allowed in a month later. But foreign nationals must wait until the end of April under the blueprint for a phased reopening unveiled Wednesday. “We acknowledge it’s been tough, but the end of heavily restricted travel is now in sight,” Hipkins told reporters. New Zealand closed its borders in March last year, requiring all international arrivals to undergo two weeks of hotel quarantine, a period that was recently cut to seven days.


Hipkins said under the new regime, travellers would self isolate for seven days provided they were fully vaccinated and passed a series of Covid-19 tests. The move comes amid mounting pressure from overseas-based New Zealanders frustrated at being unable to book spots in the overstretched hotel quarantine system. Local media regularly carry reports of Kiwis unable to return home to see visit dying relatives because there are no available quarantine rooms. The border announcement comes as New Zealand prepares to revamp its domestic Covid-19 response to scrap lockdowns in recognition that the highly contagious Delta variant is now firmly embedded in the community.

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And why not….

Scottish Govt Vax Passport Sends People’s Private Data To Amazon, Microsoft (S)

As if the liberty erasing connotations of vaccine passports were not enough on their own, it has been revealed that the Scottish government has allowed data from the scheme to be shared with private companies including Amazon. The Daily Record reports, “We have learned the NHS mobile phone app which presents the personal medical information in the form of a QR Code shares data with companies including Amazon, Microsoft, ServiceNow, Royal Mail and an AI facial recognition firm.” Users of the vaccine passport app were not informed their data would be shared, according to the report.

Commenting on the findings, Sam Grant of privacy advocate group Liberty warned “Vaccine passports create a two-tier society and already many people in Scotland have been coerced into getting a vaccine passport in order to attend events and access certain parts of society.” Grant added, “It’s extremely concerning that, in doing so, data has been shared with third parties without people having the option to opt out or without even being made aware that this is happening. This only furthers the wide concerns people already have around vaccine passports.”

The leader of the Scottish Liberal Democrat party, Alex Cole-Hamilton, also stated that his party “have repeatedly warned the Government that data protection is virtually non-existent – a simple screenshot was enough to bypass whatever ‘security measures’ the system had in place.” “The launch was a shambles and the IT system struggled to cope,” Cole-Hamilton explained, adding “Everyone has the right to medical privacy; nobody should ever have to provide part of their medical history to a bouncer or a series of private companies. That is just simply absurd.”

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The WHO itself is the cause.

Covid Deaths In Europe To Top 2 Million By March, Says WHO (G.)

Total deaths across Europe from Covid-19 are likely to exceed 2 million by March next year, the World Health Organization (WHO) has said, adding that the pandemic had become the number one cause of death in the region. Reported deaths have risen to nearly 4,200 a day, double the number being recorded in September, the agency said, while cumulative reported deaths in the region, which includes the UK, have already surpassed 1.5 million. Describing the situation as “very serious”, the WHO said it expected “high or extreme stress” on hospital beds in 25 of the region’s 53 countries, with intensive care units in 49 countries set to come under similar strain. On current trends, the region’s cumulative death toll would surpass 2.2 million by 1 March, it said.

As Europe again becomes the centre of the pandemic, with tighter controls mainly on the unvaccinated and heated debate in several countries about making vaccination obligatory, Austria this week became the first west European country to re-enter lockdown since inoculation began earlier this year. The increase in cases was being driven by the highly transmissible Delta variant which is now dominant across the region, the WHO said, fuelled by a widespread relaxation of preventive measures, such as mask wearing and physical distancing, since the summer. With more and more people gathering indoors in the colder late-autumn weather, a large number still not vaccinated, and vaccine efficacy against severe forms of the disease waning, “many people are left vulnerable to the virus”.

Dr Hans Kluge, the WHO’s regional director for Europe, said it was essential that countries adopted a “vaccine plus” approach. “This means getting the standard doses of vaccine and taking a booster if offered,” he said, “but also incorporating preventive measures into our normal routines.”

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Published: 23 November 2021. Daily intake: 400 IU of vitamin D. Not in good faith. There was a UK report in early 2020 that did the same thing.

The Health Effects Of Vitamin D Supplementation (Nature)

There is consensus that daily intake of 400 IU of vitamin D can prevent nutritional rickets in infants and children1. However, the skeletal effects of vitamin D deficiency in adults and older adults (aged >65 years), and the potential extra-skeletal effects of vitamin D are more controversial. Some people consider that vitamin D supplementation is futile2. By contrast, others have suggested that the vitamin D intake requirement is much higher than currently achieved by the general population and that people should aim to achieve 25-hydroxyvitamin D (25OHD, the major marker of vitamin D status) concentrations similar to those found in certain tribes in equatorial Africa with a sun exposure lifestyle that might be similar to that of early humans.


The potential extra-skeletal effects of the vitamin D endocrine system (which refers to vitamin D in its active form, its precursors and metabolites, and vitamin D receptor) are based on several arguments. For example, the vitamin D receptor (VDR) and CYP27B1 (the enzyme primarily responsible for producing the active form of vitamin D, 1,25-dihydroxyvitamin D or 1,25(OH)2D3) are widely expressed, including in tissues that are not involved in calcium or phosphate transport (Fig. 1). In addition, ~3% of the human and mouse genomes are under the direct or indirect control of 1,25(OH)2D3 (refs8,9). Finally, many diseases and illnesses in humans are associated with a poor vitamin D status, as measured by low serum levels of 25OHD. Therefore, one of the major clinical questions in the field is whether poor vitamin D status plays a causal role in the diseases and conditions associated with low 25OHD levels, such as cancer, impaired muscle strength and falls, and immune, metabolic or cardiovascular diseases. Furthermore, if the link is causal, the threshold serum level of 25OHD below which the risk of these diseases is increased must be identified.

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There’ll be no truckers left.

US to Require Vaccines for All Border Crossers in January (AP)

President Joe Biden will require essential, nonresident travelers crossing U.S. land borders, such as truck drivers, government and emergency response officials, to be fully vaccinated beginning on Jan. 22, the administration planned to announce Tuesday. A senior administration official said the requirement, which the White House previewed in October, brings the rules for essential travelers in line with those that took effect earlier this month for leisure travelers, when the U.S. reopened its borders to fully vaccinated individuals. Essential travelers entering by ferry will also be required to be fully vaccinated by the same date, the official said. The official spoke to The Associated Press on the condition of anonymity to preview the announcement.

The rules pertain to non-U.S. nationals. American citizens and permanent residents may still enter the U.S. regardless of their vaccination status, but face additional testing hurdles because officials believe they more easily contract and spread COVID-19 and in order to encourage them to get a shot. The Biden administration pushed back the requirement for essential travelers by more than two months from when it went into effect on Nov. 8 for non-essential visitors to prevent disruptions, particularly among truck drivers who are vital to North American trade. While most cross-border traffic was shut down in the earliest days of the pandemic, essential travelers have been able to transit unimpeded.

Even with the delay, though, Norita Taylor, spokeswoman for the trucking group Owner-Operator Independent Drivers Association, criticized the vaccination requirement, calling it an example of “how unnecessary government mandates can force experienced owner-operators and independent truckers out of business.” “These requirements are another example of how impractical regulations will send safe drivers off the road,” she said.

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Does he believe it? Quite possible.

Americans Got Richer Thanks To Vaccines & Covid Policies, Biden Claims (RT)

US citizens are wealthier 20 months after the Covid-19 pandemic than they were before, President Joe Biden has insisted, as many in the country check their pockets and find them still empty. The president praised his economic leadership during a press conference on Tuesday, declaring the US was the only country whose residents could count themselves richer than they had been before the pandemic. However, while the Federal Reserve may have printed up a (digital) storm of new money to keep the economy afloat, ordinary Americans haven’t seen much of it. “America’s the only major economy, the only one in the world, where the economy is bigger today, and families have more money in their pockets today, than before the pandemic hit,” Biden boasted during a Monday press conference, adding that his calculations already took inflation into account.

Not only could “none of our competitors internationally […] say that,” the president continued, but it was a “testament to the effectiveness of the vaccines and our vaccination effort,” as well as “a testament to the economic policies we’ve fought so hard to pass.” While government responses to the Covid-19 pandemic have indeed sent some people’s wealth soaring skyward, much of that growth – a whopping $2.1 trillion – has gone to the billionaires. Tesla tycoon and world’s richest man Elon Musk alone made $209 billion as of October. However, some 89 million ordinary Americans have lost their jobs.

Meanwhile, income inequality continues to swell to preposterous levels – anything but closing the massive gap that already yawned between rich and poor in 2019. Data shows the poor have stayed poor, and the middle-class are rapidly joining them at the bottom of the income ladder. While Biden might have tried to appear sanguine regarding inflation, that monetary force continues to send the price of consumer goods skyward, and most of the federal unemployment benefits that kept out-of-work Americans comfortable during the first year of the pandemic have evaporated, meaning Americans now need to find a job and pay their rent or find themselves out in the cold.

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“..coming the same day CNN reported the Biden administration is now mulling additional weapons and military trainers for Ukraine.”

US, Russia Military Chiefs Hold Urgent “Deconfliction” Call On Ukraine (ZH)

The heads of the Russian and United States militaries held a rare and urgent phone call on Tuesday in efforts to deescalate soaring tensions in eastern Europe, with both sides cryptically confirming it was to discuss “current” international security issues. Russia’s most senior military general, Valery Gerasimov, held the call with US Chairman of the Joint Chiefs of Staff Mark Milley, in which the two top generals talked about “pressing issues of international security”. The past days have witnessed heightening rhetoric and threats being exchanged between Moscow and Washington over tensions in Ukraine and Belarus, especially given recent reports from US media over a Russian force build-up and planned “invasion” of eastern Ukraine, reports which the Kremlin has vehemently denied.

The US side’s readout of the call acknowledged it was for the purpose of rapid “de-confliction” between the two superpowers, also coming the same day CNN reported the Biden administration is now mulling additional weapons and military trainers for Ukraine. No additional details or specifics of the military-to-military call were revealed; however, it was without doubt related to a building new Ukraine crisis, following the US allegations of a massive Russian troop build-up near Ukraine for a potential imminent invasion. At the start of this week it was revealed that the Biden administration was reported to have briefed the European partners that Russia on the supposed planned invasion of eastern Ukraine. The Kremlin has been fierce in its response rejecting the accusations, with some thinly-sourced Western reports suggesting as many as 100,000 active duty Russian troops and reservists were being mustered for a major offensive operation.

A report in US News and World Report that tensions are fast approaching a breaking point, leading to the potential for a ‘Ukraine crisis 2.0’ amid the tit-for-tat accusations: “Through a series of public statements and posts through its state news services, leaders in Russia on Monday presented the unified case that Ukraine was needlessly deploying its military forces to challenge Russia’s sovereignty and its nearby interests, that rising concern in the West of military action by Moscow represents only an attempt by Kyiv to mask its own intentions to do so, that the Western-backed peace process for the conflict in Ukraine is broken and that Kyiv’s allies in Europe and North America are not prepared to back up their pledges of support.”

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Melbourne

 

 

4th Turning

 

 

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Nov 152021
 
 November 15, 2021  Posted by at 9:43 am Finance Tagged with: , , , , , ,  85 Responses »


Francisco Goya Fire at night 1793-94

 

Is Vaccine Efficacy A Statistical Illusion? (Fenton)
What They Didn’t Tell You (Denninger)
New Pfizer Drug and Ivermectin (Campbell)
COVID-19 Vaccine-Myocarditis Paper To Be Permanently Removed: Elsevier (RW)
Delta Variant Displays Moderate Resistance To Neutralizing Antibodies (bioRxiv)
Patient Trajectories Among Hospitalised Covid-19 Patients (medRxiv)
The Media’s Epic Fail On The Steele Dossier (Axios)
Alan Dershowitz: Kyle Rittenhouse ‘Should Be Acquitted’ And Sue Media (JTN)
Was Rittenhouse’s Possession of the AR-15 Unlawful? (Turley)

 

 

The 1905 SCOTUS case Jacobson v Massachusetts held that mandates can only be considered to “prevent the spread of contagious disease.”


As all studies show the shots don’t stop transmission, Covid mandates are obviously illegal.

 

 

The Miracle Vaccine Nobody Will Talk About: Covax-19

 

 

 

 

Can’t catch it well in this format, do read it. He shifts reporting of deaths by just a week, and the world looks entirely different.

Norman Fenton is Professor in Risk Information Management

@profnfenton: “Turns out that, simply by delayed reporting of deaths by 1 week, it’s inevitable a placebo will appear to reduce mortality in those who receive it compared to those who don’t..”

Is Vaccine Efficacy A Statistical Illusion? (Fenton)

Suppose we want to examine and compare the mortality rates of the unvaccinated and vaccinated cohorts based on the data in Table 2. Figure 1 shows this comparison, and we can see that the mortality rate is consistently lower for the vaccinated than that for the unvaccinated throughout the roll out of the vaccination programme and it reduces as soon as vaccination nears population saturation at close to 100%.


Figure 1 Reported weekly mortality rates vaccinated against unvaccinated

We might conclude that those who remain unvaccinated look to be suffering much higher levels of mortality than the vaccinated. The reporting delay therefore creates a completely artificial impression that the vaccine must be highly effective. In fact, it looks like a magic ‘cure all’ wonder drug! The fact that the mortality rate of the unvaccinated peaks when the percentage of those vaccinated peaks should ring some alarm bells that something strange is going on (unless there is independent evidence that the virus was peaking at the same time).


While the placebo vaccine example was purely hypothetical, Figure 2 shows the vaccinated against unvaccinated mortality using the data in the latest ONS report mortality in England by Covid-19 vaccination status (weeks 1 to 38)[1], complemented by NIMS vaccination survey data (up to week 27 only). Here we show other-than covid mortality to remove the virus signal.


Figure 2 Reported weekly other-than covid mortality rates for vaccinated versus unvaccinated for 60-69 age group for weeks 1-38 2021

Note that we see the same features as the shifted graph in Figure 1. In other words, a perfectly reasonable explanation for what is observed here could be that there is no difference in mortality rates between vaccinated and unvaccinated and the mortality differences are simply a result of a delay in death reporting. Moreover, given we have removed covid deaths (which were only a small percentage of all-cause deaths in the reported data) we get a near identical result for non-covid mortality to that which would result if the vaccine were a placebo! Thus, we appear to have created a statistical illusion of vaccine efficacy.

If this is not a statistical illusion how is it possible that the unvaccinated are dying from non-covid causes at a higher rate than vaccinated? Also how is it possible that, at the time vaccination rates are ramped up to nearly 100% of the population, the nonvaccinated are dying from non-covid deaths at almost twice the rate of those who are vaccinated?

These same patterns are also observable in the 70-79 and 80+ age groups (with the mortality peaks for the unvaccinated appearing at different weeks because these age groups received vaccinations earlier). This strongly suggests that what we are observing is a genuine statistical illusion unexplainable by any real impact of the vaccine on mortality rates. There could, of course, be reasons other than just delays in death reporting or misclassification. For example, any systematic underestimation of the actual proportion who remain unvaccinated would lead to a higher mortality rate for unvaccinated higher than that for the vaccinated, even if the mortality rates were equal in each category.

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“It can’t happen if there are no susceptible people. But it is. So there are susceptible people. How did they become susceptible when they weren’t before in any material size? We jabbed them.”

What They Didn’t Tell You (Denninger)

This study is a bit dense — but has been peer-reviewed, and makes clear that indeed, what I hypothesized was true — and had to be, given the circumstances with Diamond Princess and elsewhere, in fact validates by scientific fact. “In summary, RTC regions like polymerase, expressed in the first stage of the viral life cycle, are highly conserved among HCoV and are preferentially targeted by T-cells in pre-pandemic and SN-HCW samples. A subset of T-cells from donors able to abort infection could cross-recognise SARS-CoV-2 and HCoV sequences at individual RTC epitopes, pointing to prior infection with HCoV as one source of pre-existing cross-reactive T-cells. ” “SN-HCW” are health-care workers who were repeatedly exposed and while they did not get sick or seroconvert “(SeroNegative)” showed very rapid response to Covid-19 from cross-reaction as a result of other coronavirus exposures.

Remember that Diamond Princess only had about 20% of the population on board that got sick despite all of them being confined together over an extended period, and even more-telling, there were multiple instances where one member of a cabin pair (husband and wife, usually) got seriously ill while the other did not only not get ill they did not test positive either. This also occurred among a couple I know early in the pandemic; one (the husband) was killed by the virus, the other (the wife) never got sick. What’s even more damning is that by May of this year about 20% of the population, according to a NEJM study that I wrote on, had seroconverted. This strongly implies that statistically everyone who could get Covid-19 and have a serious problem with already had done so.

So how is that we had a “surge” this summer and continue to see infections this fall? It can’t happen if there are no susceptible people. But it is. So there are susceptible people. How did they become susceptible when they weren’t before in any material size? We jabbed them. The CDC and hospitals do not count someone who gets Covid before 2 weeks after their last jab as “vaccinated.” So if you have a cycle of 28 days from first to second from the first jab to a period of time six weeks later if you get Covid-19 you’re considered “unvaccinated.” Every place where we’ve had very high vaccination uptake as the uptake occurred we have seen material spikes in infection contemporary with the jabs, even out of regular season with normal respiratory viral patterns.

Why? The reasonable hypothesis is that the jabs are destroying pre-existing resistance that formerly was sufficient to prevent significant, seroconverting infections in about 8 out of 10 people, but post-jab that resistance is suppressed either temporarily or permanently and thus they are able to get significantly infected.

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‘No one’s saying that the information [about ivermectin’s efficacy] has been deliberately hidden away while millions of people have died’

New Pfizer Drug and Ivermectin (Campbell)

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Lots of Pfizer ads? How many millions on a yearly basis?

COVID-19 Vaccine-Myocarditis Paper To Be Permanently Removed: Elsevier (RW)

A paper claiming that cases of myocarditis spiked after teenagers began receiving COVID-19 vaccines that earned a “temporary removal” earlier this month will be permanently removed, according to a publisher at Elsevier. As we reported last week, the article, “A Report on Myocarditis Adverse Events in the U.S. Vaccine Adverse Events Reporting System (VAERS) in Association with COVID-19 Injectable Biological Products,” was published in Current Problems in Cardiology on October 1. Sometime between then and October 17, the article was stamped “TEMPORARY REMOVAL” without explanation other than Elsevier’s boilerplate notice in such cases:


“The Publisher regrets that this article has been temporarily removed. A replacement will appear as soon as possible in which the reason for the removal of the article will be specified, or the article will be reinstated. The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy.” In an email to co-author Peter McCullough, Elsevier publisher Diana Goetz said that “the journal is not willing to publish the paper.” Here’s the entire email:

Goetz did not respond to requests for comment from Retraction Watch about whether a retraction notice explaining the move would appear. Elsevier’s policy on such matters has changed slightly over the years, but the central lack of transparency on their “withdrawals” has been the subject of our coverage since 2013. Jessica Rose, the other author of the paper, told Retraction Watch: “We are very motivated to get the information in our paper to the public: pediatricians, parents and policy-makers alike. This is why we decided to publish in the first place. It is extremely frustrating for us to face such censorship when professionals are in need of scientific data and discourse on the subject of myocarditis in children in these very strange times.” Rose’s affiliation on the removed version of the paper is the Institute of Pure and Applied Knowledge’s Public Health Policy Initiative, and McCullough’s is the Truth for Health Foundation in Tucson.


As we noted in our previous post, IPAK is “..a group that has been critical of vaccines and of the response to COVID-19 and has funded one study that was retracted earlier this year… Last month, Baylor Scott & White obtained a restraining order against McCullough — whom Medscape says “has promoted the use of therapies seen as unproven for the treatment of COVID-19 and has questioned the effectiveness of COVID-19 vaccines” — for continuing to refer to an affiliation with the health care institution despite a separation agreement. “Since the Baylor suit, the Texas A&M College of Medicine, and the Texas Christian University (TCU) and University of North Texas Health Science Center (UNTHSC) School of Medicine have both removed McCullough from their faculties,” Medscape reported at the time.”

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Variants of variants.

Delta Variant Displays Moderate Resistance To Neutralizing Antibodies (bioRxiv)

The SARS-CoV-2 B.1.617 lineage variants, Kappa (B.1.617.1) and Delta (B.1.617.2, AY) emerged during the second wave of infections in India, but the Delta variants have become dominant worldwide and continue to evolve. The spike proteins of B.1.617.1, B.1.617.2, and AY.1 variants have several substitutions in the receptor binding domain (RBD), including L452R+E484Q, L452R+T478K, and K417N+L452R+T478K, respectively, that could potentially reduce effectiveness of therapeutic antibodies and current vaccines. Here we compared B.1.617 variants, and their single and double RBD substitutions for resistance to neutralization by convalescent sera, mRNA vaccine-elicited sera, and therapeutic neutralizing antibodies using a pseudovirus neutralization assay.

Pseudoviruses with the B.1.617.1, B.1.617.2, and AY.1 spike showed a modest 1.5 to 4.4-fold reduction in neutralization titer by convalescent sera and vaccine-elicited sera. In comparison, similar modest reductions were also observed for pseudoviruses with C.37, P.1, R.1, and B.1.526 spikes, but seven- and sixteen-fold reduction for vaccine-elicited and convalescent sera, respectively, was seen for pseudoviruses with the B.1.351 spike. Four of twenty-three therapeutic neutralizing antibodies showed either complete or partial loss of neutralization against B.1.617.2 pseudoviruses due to the L452R substitution, whereas six of twenty-three therapeutic neutralizing antibodies showed either complete or partial loss of neutralization against B.1.617.1 pseudoviruses due to either the E484Q or L452R substitution.

Against AY.1 pseudoviruses, the L452R and K417N substitutions accounted for the loss of neutralization by four antibodies and one antibody, respectively, whereas one antibody lost potency that could not be fully accounted for by a single RBD substitution. The modest resistance of B.1.617 variants to vaccine-elicited sera suggest that current mRNA-based vaccines will likely remain effective in protecting against B.1.617 variants, but the therapeutic antibodies need to be carefully selected based on their resistance profiles. Finally, the spike proteins of B.1.617 variants are more efficiently cleaved due to the P681R substitution, and the spike of Delta variants exhibited greater sensitivity to soluble ACE2 neutralization, as well as fusogenic activity, which may contribute to enhanced spread of Delta variants.

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Hard to speak in clear terms when you’re scientists, but:

“We observed no difference in [..] odds of in-hospital death between vaccinated and unvaccinated patients.”

Dr Anthony Hinton: “Norway Study Finds ZERO Vaccine Effectiveness Against Death for Covid Hospital Patients. The Pfizer trial never made this claim they only claimed symptom reduction.”

Patient Trajectories Among Hospitalised Covid-19 Patients (medRxiv)

Objectives With most of the Norwegian population vaccinated against COVID-19, an increasing number and proportion of COVID-19 related hospitalisations are occurring among vaccinated patients. To support patient management and capacity planning in hospitals, we estimated the length of stay (LoS) in hospital and odds of intensive care (ICU) admission and in-hospital mortality among COVID-19 patients ≥18 years who had been vaccinated with an mRNA vaccine, compared to unvaccinated patients.

Methods Using national registry data, we conducted a cohort study on SARS-CoV-2 positive patients hospitalised in Norway between 1 February and 30 September 2021, with COVID-19 as the main cause of hospitalisation. We used a Cox proportional hazards model to examine the association between vaccination status and LoS. We used logistic regression to examine the association between vaccination status and ICU admission and in-hospital mortality.

Results We included 2,361 patients, including 70 (3%) partially vaccinated and 183 (8%) fully vaccinated. Fully vaccinated patients 18–79 years had a shorter LoS in hospital overall (adjusted hazard ratio for discharge: 1.35, 95%CI: 1.07–1.72), and lower odds of ICU admission (adjusted odds ratio: 0.57, 95%CI: 0.33–0.96). Similar estimates were observed when collectively analysing partially and fully vaccinated patients. We observed no difference in the LoS for patients not admitted to ICU, nor odds of in-hospital death between vaccinated and unvaccinated patients.

Conclusions Vaccinated patients hospitalised with COVID-19 in Norway have a shorter LoS and lower odds of ICU admission than unvaccinated patients. These findings can support patient management and ongoing capacity planning in hospitals.

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Axios: “A reckoning is hitting news organizations for years-old coverage of the 2017 Steele dossier, after the document’s primary source was charged with lying to the FBI.”

The Media’s Epic Fail On The Steele Dossier (Axios)

A reckoning is hitting news organizations for years-old coverage of the 2017 Steele dossier, after the document’s primary source was charged with lying to the FBI. Why it matters: It’s one of the most egregious journalistic errors in modern history, and the media’s response to its own mistakes has so far been tepid. Outsized coverage of the unvetted document drove a media frenzy at the start of Donald Trump’s presidency that helped drive a narrative of collusion between former President Trump and Russia. It also helped drive an even bigger wedge between former President Trump and the press at the very beginning of his presidency.

Driving the news: In wake of the key source’s arrest and further reporting on the situation, The Washington Post on Friday corrected and removed large portions of two articles. To The Post’s credit, its media critic, Erik Wemple, has written at length about the mistakes made by The Post and other media outlets in their coverage of the dossier. BuzzFeed News, which made waves in 2017 by publishing the entire dossier, says it has no plans to take the document down. It’s still online, accompanied by a note that says “The allegations are unverified, and the report contains errors.” Ben Smith, who was BuzzFeed’s editor-in-chief at the time and is now a media columnist at The New York Times, told Axios, “My view on the logic of publishing hasn’t changed.”

BuzzFeed defended the decision in a 2018 lawsuit by arguing that because the FBI opened an investigation into the Trump campaign’s ties to Russia, the dossier itself was newsworthy, whatever the merits of its contents turned out to be. It won that case. Other outlets that gave the document outsized coverage have so far been less forthcoming. CNN and MSNBC did not respond to requests for comment about whether they planned to revisit or correct any of their coverage around the dossier. Mother Jones Washington bureau chief David Corn began reporting about the dossier prior to the 2016 election. Asked by Wemple whether he planned to correct the record, Corn said,” My priority has been to deal with the much larger topic of Russia’s undisputed attack and Trump’s undisputed collaboration with Moscow’s cover-up.”

The Wall Street Journal told Axios, “We’re aware of the serious questions raised by the allegations and continue to report and to follow the investigation closely.” Axios was among the outlets that did not publish the dossier or original reporting based on its contents. What to watch: The Steele screwup will undoubtedly cause an even bigger rift in trust between Democrats and Republicans.

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“It’s CNN who is involved in vigilante justice. It’s The New Yorker that’s guilty of vigilante justice.”

Alan Dershowitz: Kyle Rittenhouse ‘Should Be Acquitted’ And Sue Media (JTN)

Alan Dershowitz, the famed Harvard law professor emeritus, said Kyle Rittenhouse “should be acquitted” of injuring a man and killing two others in Kenosha, Wis., and sue media outlets that are claiming he’s guilty of vigilante justice. “If I were a juror, I would vote that there was reasonable doubt [and] that he did act in self-defense,” Dershowitz told Newsmax on Saturday.”Then he’ll bring lawsuits, and that’s the way to answer… vigilante justice is what CNN is doing, not what a 17-year-old kid under pressure may have done right or wrong. It’s CNN who is involved in vigilante justice. It’s The New Yorker that’s guilty of vigilante justice.”


Dershowitz referenced then-Kentucky high school student Nicholas Sandmann and how he sued and settled with CNN and The Washington Post for defamation as they accused him of being racist following viral videos of an encounter he had with a Native American activist in Washington, D.C. “The idea is to make the media accountable for deliberate and willful lies,” he said. Dershowitz added that “the left-wing media … is attacking this judge for trying to be fair. They want an outcome. They want a result and if they don’t get their results and you know this seeps through to the jury, and I worry that the jury could be influenced by the fear that if they vote to acquit, they’ll be called racist and they’ll be attacked.”

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Judge: “I have been wrestling with this statute with, I’d hate to count the hours I’ve put into it, I’m still trying to figure out what it says, what’s prohibited. I have a legal education.”

Was Rittenhouse’s Possession of the AR-15 Unlawful? (Turley)

In covering the motions hearing last week in the trial of Kyle Rittenhouse, I noted a surprising comment from Judge Bruce Schroeder that he had “spent hours” with the Wisconsin gun law and could not state with certainty what it means in this case. The statement could effectively knock out the misdemeanor gun possession count — the one count that could still be in play for the jury after the prosecution’s case on the more serious offense appeared to collapse in court. A close examination of that provision reveals ample reason to question not just its meaning but its application to this case. The unlawful possession of the gun has been a prominent fact cited not only by the prosecutors but the press. At trial, however, prosecutor Thomas Binger at points seemed to be learning the governing law from Rittenhouse.

For example, he pressed Rittenhouse on why he did not just purchase a handgun rather than an AR-15. Rittenhouse replied he could not possess a hand gun at his age. Binger then asked in apparent disbelief that the law allowed him to have an AR-15 but not a handgun and Rittenhouse said yes. Binger then moved on after seemingly drawing out a point for the defenseThe exchange was all the more baffling because it drew attention to the fact that one of Binger’s alleged “victims” was an adult named Gaige Grosskreutz who also decided to bring a handgun to the protests and pointed his .40 caliber Glock at the head of Rittenhouse when he was shot in the arm. However, the most damaging moment came outside of the presence of the jury when the judge drilled down on the law.

He told the prosecutors “I have been wrestling with this statute with, I’d hate to count the hours I’ve put into it, I’m still trying to figure out what it says, what’s prohibited. I have a legal education.” He added that he failed to understand how an “ordinary citizen” could understand what is illegal. It is hard to understand how the count could be given to the jury without a clear understanding of what it means. It is also hard to instruct a jury on an ambiguous statute. Criminal laws are supposed to be interpreted narrowly. It is called the “rule of lenity” and has been around in the English system for centuries. For example, in 1547, the court was faced with a law making it a felony to steal “Horses, Geldings or Mares.” Given the use of plural nouns, the court ruled that it did not apply to stealing just one horse.

The problem with the Wisconsin statute is not a problem of pluralization but definition. It is not clear that the statute actually bars possession by Rittenhouse. Indeed, it may come down to the length of Rittenhouse’s weapon and the prosecutors never bothered to measure it and place it into evidence. In Wisconsin, minors cannot possess short-barreled rifles under Section 941.28. Putting aside the failure to put evidence into the record to claim such a short length, it does not appear to be the case here. Rittenhouse used a Smith & Wesson MP-15 with an advertised barrel length of 16 inches and the overall length is 36.9 inches. That is not a short barrel.

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Nov 102021
 


Francis Tattegrain La ramasseuse d’épaves (The Beachcomber) 1880

 

Frontline Health Workers In England To Get New Vaccine Guidelines (RT)
Whistleblowers To Play Key Role In Enforcing Biden Vaccine Rule (CBS)
Singapore To Start Charging Covid Patients Who Are ‘Unvaccinated By Choice’ (G.)
More Than Half Of Border Patrol Agents May Be Fired For Being Unvaccinated (SN)
Feds Seek to Block Promotion of a Nasal Spray Against COVID-19 (ET)
French Health Authority Warns Men Under 30 To Avoid Moderna Jab (ZH)
Naturally Immune Federal Workers Lodge Class-Action Over Vaccine Mandate (ET)
FDA Pfizer Doc Suggests Myocarditis From Shot Bigger Threat Than Covid (Bl.)
Doctors Will Never Regain The Public’s Trust After Covid (Huffman)
John Durham Is Getting Close to the Jugular (RCP)
Durham Exposes New Links To Clinton Campaign in Russian Collusion (Turley)
‘Out Of Control’ Pandemic Waste Spewed Into Oceans (RT)

 

 

Tucker OSHA

 

 

That’s it. British health workers get another 5 months to get jabbed. Any sense of urgency or emergency is gone. They won, and they know it. “..Up to 100,000 healthcare staff in England are unvaccinated..”

Frontline Health Workers In England To Get New Vaccine Guidelines (RT)

England’s frontline NHS workers will have to be fully inoculated against Covid-19 by April 1 as a mandatory condition of their employment, Heath Secretary Sajid Javid has said, as tens of thousands of staff are still not jabbed. Speaking on Tuesday to Parliament, Javid confirmed that “all those working in the NHS and social care will have to be vaccinated.” “We must avoid preventable harm and protect patients in the NHS, protect colleagues in the NHS and of course protect the NHS itself.” The deadline set for next spring – April 1 – will give all staff enough time to complete the Covid vaccination course. Up to 100,000 healthcare staff in England are unvaccinated, according to the head of NHS Providers Chris Hopson. Javid also said there would be exemptions for people who cannot be vaccinated for medical reasons, or for those not in face-to-face positions with patients.


The decision comes after consultations began in September on whether to make Covid and flu jabs mandatory for frontline NHS and care workers. The flu vaccine, however, will not be made mandatory just yet, but will be kept under review. Health Secretary Sajid Javid told Sky News last month that he was “leaning towards” mandatory vaccination for NHS staff, but Downing Street was yet to make a final decision. The prospect of mandatory vaccinations for NHS staff has raised concerns that the move could adversely impact an already overstretched health service. Hopson insisted that the government must work closely with NHS trusts to avoid a mass exodus of unvaccinated staff: “We understand why people are vaccine-hesitant. We need to win the argument with them rather than beat them around the head,” he told BBC Radio 4’s Today show.

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A nation of snitches. Well done. “Ther are Jews hiding in that building!”

Whistleblowers To Play Key Role In Enforcing Biden Vaccine Rule (CBS)

To enforce President Joe Biden’s new COVID-19 vaccine regulation, the Labor Department is going to need a lot of help. Yet its Occupational Safety and Health Administration (OSHA) doesn’t have nearly enough workplace safety inspectors to do the job. The 490-page regulation will cover American businesses with at least 100 workers, or about 84 million employees in all. So the government will rely upon a corps of informers to identify violations of the order: Employees who will presumably be concerned enough to turn in their own employers if their co-workers go unvaccinated or fail to undergo weekly tests to show they’re virus-free.

What’s not known is just how many employees will be willing to accept some risk to themselves — or their job security — for blowing the whistle on their own employers. Without them, though, experts say the government would find it harder to achieve its goal of requiring tens of millions of workers at large businesses to be fully vaccinated by January 4 or be tested weekly and wear a mask on the job. “There is no army of OSHA inspectors that is going to be knocking on employers door or even calling them,” said Debbie Berkowitz, a former OSHA chief of staff who is a fellow at Georgetown University’s Kalmanovitz Initiative for Labor and the Working Poor. “They’re going to rely on workers and their union representatives to file complaints where the company is totally flouting the law.”

Under the regulation, businesses must maintain records on workers’ vaccination statuses. But for workplaces where employees aren’t required to be vaccinated, workers will need to get weekly tests and wear masks. OSHA said it plans to check on compliance with the latter by doing spot-checks of businesses, and will also rely on complaints the agency receives about businesses that aren’t following the regulation. “We will have our staff available and responsive to complaints, which is a No. 1 way we hear about problems in a workplace,” said Jim Frederick, the acting chief of OSHA, on a conference call with reporters. He also said the agency will focus on job sites “where workers need assistance to have a safe and healthy workplace.”

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Test site for bankrupting ordinary people.

Singapore To Start Charging Covid Patients Who Are ‘Unvaccinated By Choice’ (G.)

Singapore will no longer pay the Covid-19 medical bills for people “unvaccinated by choice”, the government said, as the country grapples with a surge in cases. The government currently covers the full Covid medical costs for all Singaporeans, as well as permanent residents and long-term visa holders, unless they test positive soon after returning home from overseas. However from 8 December, the government said it will “begin charging Covid-19 patients who are unvaccinated by choice”. It said unvaccinated people “make up a sizeable majority of those who require intensive in-patient care and disproportionately contribute to the strain on our healthcare resources”. Covid-related medical bills will still be paid for people who aren’t eligible for a vaccine.


The government will also foot the bill for individuals who are partially vaccinated until 31 December, giving them time to get a second dose. Singapore has among the highest coverage rates in the world, with 85% of the eligible population fully vaccinated. Yet the city state is struggling with rising Covid infections and last month warned its healthcare system was at risk of being “overwhelmed” by surging cases. It came a day after the country expanded quarantine-free travel as part of a shift in its approach to dealing with the pandemic. The prime minister, Lee Hsien Loong, previously said the global business hub could not remain closed indefinitely, and Singapore has moved from a zero-tolerance strategy with lockdowns and closed borders to living with Covid-19.

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“..48 percent of agents have not registered their vaccination status, and of the 52 percent who have done that, ten percent are unvaccinated.”

More Than Half Of Border Patrol Agents May Be Fired For Being Unvaccinated (SN)

An internal report from within the US Customs and Border Protection agency suggests that more than half the border patrol workforce remains unvaccinated, and that if vaccine mandates are implemented it could leave just 8000 officers on duty. The document, obtained by Fox News, notes that 48 percent of agents have not registered their vaccination status, and of the 52 percent who have done that, ten percent are unvaccinated. Former chief operating officer of CBP Mark Morgan, who obtained the internal report, told Fox News that Biden’s vaccine mandate is “going to take an agency that’s already gone through an unbelievable catastrophic crisis on the southwest border and deplete its resources further.”

Morgan also provided a screenshot from the report showing tables of different scenarios of depletion within the CBP. The screenshot highlights that “in the worst-case scenario, agents who have not reported their status have done so because they refuse to take the jab, and so they will be terminated (scenario 3). In that case, net attrition could exceed 11,523 agents, leaving a mere 8,013 border agents on patrol.” If this scenario unfolds, it is likely that the border patrol would lose 59 percent of its workforce. Imagine how that would affect the already rampantly out of control border crisis.

If the 10,000 or so border patrol agents who have yet to register their vaccination status do not do so this week, they will be offered counseling, then suspension, then termination, Morgan further noted, emphasising how the document “illustrates the potential impact that this mandate could have on the workforce.” “So, an agency that is dealing with 1.7 million apprehensions, 400,000 got-aways, at that very moment, the same resources are going to be pulled away and distracted to deal with this mandate nonsense,” Morgan urged, adding that the counseling involves further “critical resources,” because border patrol leadership is involved.

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They have to block anything that might work. It’s in their Pfizer contract.

Feds Seek to Block Promotion of a Nasal Spray Against COVID-19 (ET)

The leading U.S. manufacturer of xylitol-based products says the federal government is deliberately trying to conceal a nasal spray it developed that it says has been scientifically proven to be effective in treating and preventing COVID-19. The U.S. Department of Justice filed a lawsuit in federal court against Utah-based company Xlear on Oct. 28, saying it has deceptively advertised its nasal spray as a treatment and preventative of COVID-19. The lawsuit asks a federal court to permanently ban the company from promoting the nasal spray as a treatment for COVID-19 and also asks that monetary penalties be levied against it. COVID-19 is the disease caused by the CCP virus, commonly known as the novel coronavirus.

The DOJ filed the complaint on behalf of the Federal Trade Commission, which alleges the company has violated the Federal Trade Commission Act and the Consumer Protection Act by making false claims about the benefits. The spray’s main ingredients are saline, grapefruit seed extract, and xylitol, a plant-derived sweetener commonly used in oral care products. “Companies can’t make unsupported health claims, no matter what form a product takes, or what it supposedly prevents or treats,” said Samuel Levine, director of the trade commission’s Bureau of Consumer Protection, said in a press release on the lawsuit. “That’s the lesson of this case and many others like it, and it’s why people should continue to rely on medical professionals over ads.” The commission and the Justice Department declined to make any further comment.

Xlear’s attorney Robert Housman, of the Washington firm Book Hill Partners, told The Epoch Times that the commission is “flat out lying” about the company’s claims being unsupported. Housman pointed out that the National Institute of Allergy and Infectious Diseases (NIAID)—along with the National Institutes of Health (NIH), an arm of the Department of Health and Human Services—funded clinical studies of the use of nasal sprays like Xlear’s and published findings last year that found they were an effective treatment and method of prevention for COVID-19. “When Xlear tells people about scientific studies, even ones republished by the NIH, we are somehow misleading people and making false claims. It’s nonsensical,” Housman told The Epoch Times. “Rather than embrace nasal interventions, the government is trying to eliminate their use because they don’t fit the government’s highly flawed, vaccine-only agenda.”

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Have they published the victims’ numbers and accounts?

French Health Authority Warns Men Under 30 To Avoid Moderna Jab (ZH)

The bad news for Moderna just keeps coming. In the wake of a weak earnings report that sent Moderna shares cratering last week, French health authorities have just released a new advisory recommending that people under 30 don’t get the Moderna vaccine, recommending that they choose the Pfizer-BioNTech jab instead. The decision draws on recently released data showing that the risk of heart inflammation from Pfizer’s jab “appears to be around five times lesser…compared to Modera’s spikevax jab”, per an opinion published by the HAS. Cases of myocarditis mostly manifest within 7 days of vaccination, typically after the second dose has been given.

Most patients who experience side effects are typically men under the age of 30, according to the HAS, which cited research studies. HAS acts as an advisor to the French health sector but it doesn’t have the power to ban medicines or vaccines. The recommendation will apply to first and second doses, as well as a any “booster shot” doses available while the agency awaits additional data. For French men and women aged 30 and over, however, HAS says it sees no problem with administering Moderna’s Spikevax in this group, stating that its efficacy was slightly higher than Pfizer-BioNTech’s jab. Last month saw a handful of Nordic nations place varying restrictions on Moderna’s vaccine.

Tiny Iceland, meanwhile, has banned the Moderna jab from being used across the entire population. Initially. Stockholm announced it would pause the use of Moderna for all of its population born in 1991 or after. Helsinki followed suit, but halted the jabs for young, male Finns only based on a study involving Finland, Denmark, Norway, and Sweden which found that men under 30 had a slightly higher risk of developing heart inflammation. Oslo also suggested that young Norwegian men should consider choosing Comirnaty, the Pfizer jab, over Moderna’s or any of the other options.

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A half year discussion, going nowhere.

Naturally Immune Federal Workers Lodge Class-Action Over Vaccine Mandate (ET)

Federal workers who have recovered from COVID-19 have filed a class-action lawsuit against Dr. Anthony Fauci and other government officials over a COVID-19 vaccine mandate that still forces them to get a jab. The government not only failed to offer a carve-out exemption for naturally immune workers, or those who have recovered, but neither President Joe Biden’s executive order nor the guidance explaining it outlines why naturally acquired immunity isn’t an acceptable alternative to vaccination, the lawsuit states. “Because they already have natural immunity, there is no coherent purpose for the federal government to require them to undertake a medical procedure to be vaccinated if they choose not to, or be terminated from their employment, their careers,” Robert Henneke, general counsel at the Texas Public Policy Foundation and one of the lawyers representing the government workers, told The Epoch Times.


Plaintiffs say the mandate violates the Administrative Procedure Act, which allows courts to overturn government actions deemed “arbitrary, capricious, or an abuse of discretion.” They quoted Dr. Scott Gottlieb, a former Food and Drug Administration commissioner who now sits on the board of Pfizer. During recent television appearances, Gottlieb described natural immunity as “durable” and “robust” and said that government officials should start assimilating it into policy discussions. They also cited Dr. Hooman Noorchashm, an immunologist who has said it is medically unnecessary for the recovered to get vaccinated. Dozens of studies have shown that people who survived COVID-19 have strong immunity against re-infection from the virus that causes it, with some indicating the protection is similar to or higher than that provided by vaccines. Workers tried communicating concerns about the mandate but those “have completely fallen on deaf ears, which is why we’ve turned to litigation,” Henneke said.

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So many things we’ve known forever, that still need to be pointed out every day.

FDA Pfizer Doc Suggests Myocarditis From Shot Bigger Threat Than Covid (Bl.)

In Pfizer’s FDA briefing document prepared for the Oct. 25 meeting was an admission that even according to the company’s own unverified and misleading math, there is a scenario where there would be more hospitalizations among children for myocarditis — just one side effect — than from COVID. “Under Scenario 3 (lowest incidence), the model predicts more excess hospitalizations due to vaccine-related myocarditis/pericarditis compared to prevented hospitalizations due to COVID-19 in males and in both sexes combined,” states Pfizer in page 33 of the document. How in the world could there be any universe where we would approve a shot, much less promote and force it in many settings, when there is a possibility of greater harm than benefit, when the harm is man-made and the virus is left to chance?


They know quite well that this approval will eventually lead to soft and hard mandates, which have already begun in California schools. The document concludes by expressing the same callous attitude toward those raising concerns as toward all their interventions from day one. “However, in consideration of the different clinical implications of hospitalization for COVID-19 versus hospitalization for vaccine-associated myocarditis/pericarditis, and benefits related to prevention of non-hospitalized cases of COVID-19 with significant morbidity, the overall benefits of the vaccine may still outweigh the risks under this lowest incidence scenario.” In other words, sure, we have no clue what’s going to happen, but it’s always better to err on the side of shoving this on children who have a 99.9% recovery rate.

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They have 60% of the people’s trust right now. But what will happen when booster 3,4,5 come along?

Doctors Will Never Regain The Public’s Trust After Covid (Huffman)

One undeniable outcome of the pandemic is that the public’s faith in scientific and medical authorities is perhaps at its lowest point in living memory – and no objective observer can truly be surprised. At the beginning of the Covid-19 pandemic, the US President’s Chief Medical Adviser Dr Anthony Fauci and US Surgeon General Dr Jerome Adams told us not to wear masks, until they instructed us to wear one everywhere we went. The Covid vaccines were declared to be effective at preventing the spread of disease, until breakthrough cases around the globe proved that wasn’t so, and that effectiveness was downgraded to “against hospitalization and death.”

Both The Lancet and the New England Journal of Medicine, two of the most prestigious medical journals in the world, have issued embarrassing retractions to widely publicized papers eventually found to have too little validity to be published. Anyone who suggested that the pandemic originated in a Wuhan laboratory and not a Chinese wet market was labeled a conspiracy theorist by official sources who later had to admit they were possibly correct. The same proved true for everyone who accused Fauci and the National Institutes of Health of funding gain-of-function research at the lab: they were crazy, until they were right.

The US Centers for Disease Control and Prevention and the American College of Obstetricians and Gynecologists urged all pregnant women to be vaccinated, asserting that the new injections were completely safe. Now, a new review of that same data suggests that one in eight women spontaneously aborted her pregnancy after getting the jab. Even medical terms – such as ‘herd immunity’, and the word ‘vaccine’ itself – have literally been redefined over the past few months. All this has shocked a great number of informed, educated people around the world. Should it, though? In fact, a brief glance through the history of science demonstrates that scientists being completely and utterly wrong – in retrospect, often comically so – is the norm, not an aberration. It’s long past time for modern scientific researchers to discover a proper sense of humility and to step down from the pedestal of secular priesthood they’ve ascended.

Stories about an advisory panel’s recommendation to the Food and Drug Administration to approve a Moderna booster shot contained a quote that most might find truly incredible. “It’s more a gut feeling rather than based on really truly serious data,” said biochemistry professor Dr Patrick Moore. “The data itself is not strong, but it is certainly going in the direction that is supportive of this vote.” How can a scientific advisory panel make such a recommendation while admitting it’s based on feeling, not fact? In fact, it happens all the time. ‘Medical consensus’ is a term that carries an authoritative denotation, yet it simply means that a bunch of experts got together and decided amongst themselves what’s correct. The problem is that, today and in the past, those experts – in virtually every field – are so often wrong.

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The jugular is Hillary and Obama. How close can he get?

John Durham Is Getting Close to the Jugular (RCP)

The Clinton team launched this operation with professional expertise. The goal was to produce a powerful anti-Trump story, using whatever materials they could, then share it with the media (to smear Trump) and the FBI (to launch a major investigation and ensnare Trump). Ideally, the campaign’s involvement would be hidden, removed from the damning report by several layers of lawyers, opposition researchers, camp followers, and flacks. To provide that insulation, the campaign used attorney Marc Elias, then at Perkins Coie law firm in Washington (where the recently indicted Michael Sussmann was a colleague), to hire an opposition-research firm, Fusion GPS.

That firm, headed by former reporters Glenn Simpson and Peter Fritsch, in turn hired Steele, a Brit who had formerly worked for his country’s intelligence services, to produce the damning dossier. To translate some Russian materials, Fusion GPS hired Nellie Ohr, whose husband, Bruce, learned how biased Steele was and told the FBI to treat Steele and his information warily. Bureau agents ignored that early warning and all the others. They quickly learned Steele’s material was a mirage, thanks to their interviews with Danchenko. They also confirmed that Steele’s dossier depended on Danchenko, so its claims of “Russian sourcing” were false. By interviewing Danchenko’s own sources, they learned that their third-hand statements, which were used in the dossier, were mainly rumors and “bar talk.”

The prosecutorial team assembled by Robert Mueller should have known all this, too. They had complete access to this exculpatory FBI material on day one and ignored it. A year and a half later, when Mueller himself finally testified before Congress, he didn’t even know what Fusion GPS was. By that point, Mueller seemed to have genuine difficulty remembering the details of his own investigation. His team of attorneys had no such excuse. Hired by Mueller’s top deputy, Andrew Weissmann, they were among the country’s sharpest and toughest prosecutors — and the most partisan. The more Durham uncovers, the worse the Mueller team will look.

Reviewing this evidence, Kimberly Strassel of the Wall Street Journal has concluded the Steele dossier is misnamed. It should be called the “Clinton dossier,” she says, since Hillary commissioned it, paid for it, and had her aides feed it to the media, the State Department, and the FBI. It was a full-scale disinformation campaign — coherent, well-organized, and well-funded. It was rotten to the core. The question now is whether John Durham can find enough evidence to charge the ones who planned and executed it. The charging documents he filed for Danchenko and Sussmann are far more extensive than the necessary minimum. They suggest that Durham has compiled extensive evidence about a broader conspiracy. Will he settle for the capillaries now that he has the jugular in view?

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“Durham clearly seems to be making a meticulous case that the Steele dossier was a political hit job orchestrated by Clinton operatives.”

Durham Exposes New Links To Clinton Campaign in Russian Collusion (Turley)

“To my good friend … A Great Democrat.” Those words written to a Russian figure in Moscow, inside a copy of a Hillary Clinton autobiography, may be the defining line of special counsel John Durham’s investigation. The message reportedly was written by Charles Dolan, a close Clinton adviser and campaign regular whom news reports identify as the mysterious “PR-Executive 1” in the latest Durham indictment, this time of Igor Danchenko. Danchenko, 43, was a key figure in the compilation of the infamous Steele dossier that led to the now discredited investigation of alleged collusion between the Trump campaign and the Russian government during the 2016 presidential race. But Danchenko, a Russian emigre living in the U.S., seems unlikely to be the Durham investigation’s apex defendant. In fact, Durham describes him at points more like a shill than a spy, an “investigator” who was fed what to report by Clinton operatives such as Dolan.

Durham is known as a methodical, apolitical and unrelenting prosecutor. Thus far, his work seems to betray a belief that the FBI got played by the Clinton campaign to investigate the Trump team. The question is whether Durham really wants to indict just the figurative tail if he can get the whole dog — a question that now may weigh heavily on a number of Washington figures, just as it did following Durham’s indictment in September of Clinton campaign lawyer Michael Sussmann. Danchenko’s indictment on five counts of lying to the FBI serves two obvious purposes. First, these counts — with a possible five years in prison on each — are enough to concentrate the mind of any defendant about possibly flipping for the prosecution. Second, indicting Danchenko “hoists the wretch” for potential targets to see and consider that there but for the grace of God — and Durham — go they.

The background details of Durham’s three indictments so far have assembled an impressive list of “great Democrats” who contributed directly or indirectly to the creation of the Russia collusion scandal. Indeed, the collusion case increasingly is taking on a type of “Murder on the Orient Express” feel, in which all of the suspects may turn out to be culprits. While the statute of limitations may protect some, Durham has shown that he can use the crime of lying to federal investigators (18 U.S.C. 1001) as a handy alternative. Targets must admit to prior misconduct or face a new charge. Thus, Durham clearly seems to be making a meticulous case that the Steele dossier was a political hit job orchestrated by Clinton operatives. His latest indictment connects Danchenko to several intriguing figures and groups that, in turn, relate to the Clinton campaign.

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Mass madness.

‘Out Of Control’ Pandemic Waste Spewed Into Oceans (RT)

A new report claims that 25,000 tons of masks, gloves, and other pandemic-related plastic waste has ended up in our oceans since Covid-19 first emerged. Hospitals, rather than individuals, are the chief culprit. “The recent Covid-19 pandemic has led to an increased demand for single-use plastic, intensifying pressure on this already out-of-control problem,” a team of Chinese and American researchers wrote in a paper published by the US National Academy of Sciences. “More than eight million tons of pandemic-associated plastic waste have been generated globally, with more than 25,000 tons entering the global ocean,” they added. The study is not the first to link the glut of Personal Protective Equipment (PPE) produced during the pandemic to a rise in pollution.

The ubiquitous face masks that now litter beaches and high streets can take centuries to decompose, leaching harmful microplastics as they break down. With an estimated 129 billion face masks and 65 billion gloves used globally each month, scientists have already called for the use of more environmentally friendly materials in the production of PPE. The latest study, however, identifies the source and destinations of most of this waste. Hospitals account for nearly 90% of discarded PPE, with individuals responsible for only 7%. The majority of the waste (79%) enters the global ocean via just 10 rivers. Overall, Asian rivers are responsible for 73% of waste discharge, followed by European rivers with 11%.

Once in the ocean, most of this waste remains close to its source, with East and South Asia, South Africa, and the Caribbean identified as hotspots. 13 percent floats in the seawater, 16% sinks to the seabed, and 71% is washed up on the shore. The researchers warned that as “the pandemic will not be completely controlled in a couple of years,” a further 34,000 tons of discarded PPE will end up in the oceans, with much of it adding to huge “garbage patches” in the North and South Atlantic and Pacific Oceans, as well as the Indian Ocean.

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Nov 092021
 


Pablo Picasso Group of dancers. Olga Kokhlova is lying in the foreground 1919

 

NBA Wants Covid-19 Vaccine Boosters For Players Jabbed Just 2 Months Prior (RT)
Expert Committee Member Calls For Booster Covid Shot After 4 Months (K.)
COVID Boosters Likely to Be Annual ‘For the Foreseeable Future’ (ET)
Medicine Wants to Kill You (Kunstler)
Will You Ever Care To SOLVE The Problem? (Denninger)
3CLPro Inhibitors As Potential Anti-SARS-CoV-2 Agents (Nature)
Applying Brakes On ‘Warp Speed’ Covid-19 Vaccinations For Children (WT)
Vaccine Passports: Institutionalized Segregation (BI)
UK Health Expert: Vaccine Passports Make No Sense (DR)
The Cause of Myocarditis: COVID19 or COVID19 Vaccination? (BI)
Marines Chief Blames ‘Disinformation’ For Remaining Unvaccinated Troops (WE)

 

 

Dr Robert Malone – MRNA Vaccines Explained For Real

 

 

Dressen
https://twitter.com/i/status/1457829975680245769

 

 

It’s a countdown now. At what point will we realize that boosters are the end of mass vaccination? 2 months, ha ha ha.

NBA Wants Covid-19 Vaccine Boosters For Players Jabbed Just 2 Months Prior (RT)

The NBA has reportedly urged players to get Covid-19 booster shots. Some vaccinated players may face game-day testing by December if they refuse. The NBA told the players the new rules on Sunday, according to AP, and stressed that those who initially received the Johnson & Johnson Covid-19 vaccine are most in need of a booster shot. Citing its waning efficacy over time, the league called on players, coaches, and referees who received the vaccine more than two months ago to roll up their sleeves for a booster of a different vaccine, namely Pfizer’s or Moderna’s. Those who were vaccinated with either the Pfizer or Moderna vaccine were told that they will need a booster shot six months after initial vaccination.

Depending on which vaccine a player was originally given and when that vaccination took place, some players may already face repercussions for refusing a booster dose by next month. “In some cases, those who are vaccinated but elect to not receive a booster would be subjected to game-day testing again starting Dec. 1,” AP reported. The announcement angered opponents of Covid-19 restrictions, including figures in the sports industry. “Wake up, sheep. The NBA is already mandating the vaccine booster now. This won’t ever end,” tweeted sports commentator Clay Travis, who founded the sports journalism website OutKick. Travis also questioned whether the industry was “going to make 100% healthy people get covid shots every six months for the rest of their lives.”

Sports journalist Jason Whitlock protested that the news was “just the tip,” while Inner Sports founder Garret Kramer wrote, “On what planet do we continue to mandate drugs for people who are not sick? Say NO.” “This world and league is getting more asinine by the day,” golf champion Steve Flesch said. The NBA recommendation found support among proponents of vaccine mandates, however. “The NBA is doing the right thing here,” Jerome Michael Adams, the former surgeon general who served in the Donald Trump administration, tweeted, arguing that “in hindsight this should’ve been billed as a 3 dose (2 for J&J) series anyway.” The NBA already has strict Covid-19 policies for its players, which include unvaccinated players not being able to eat with vaccinated players. Unvaccinated NBA players are also required to socially distance themselves from vaccinated players and must wear face masks.

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A Greek expert says 4 months. He should talk to the NBA.

Expert Committee Member Calls For Booster Covid Shot After 4 Months (K.)

People who have been vaccinated against the novel coronavirus should get their booster shot four instead of six months after their last dose to stem transmission and the possibility of serious illness, a member of the committee of experts advising the government on the pandemic, said on Tuesday. “When the vaccines first came out, they had this incredible effectiveness that we believed would last for some time. I had also said that we should be covered for six months. But new studies have shown that their effectiveness starts to wane after four months, mainly for mild infections, which do not lead to death but are still a transmission risk,” Theodoros Vassilakopoulos, an Athens University professor of pulmonary and critical care medicine, told Skai television.


The booster “needs come sooner,” he said, warning that “the worst obviously still lies ahead,” after Greece on Monday broke a new record with 7,335 new infections in 24 hours. He added that while being vaccinated protects most people from serious illness, this is not the case for people over the age of 60, who are particularly vulnerable. “The vaccinated need to be protected by having the option of getting their booster shot earlier, at four months at least,” he said. “Science is a process of seeking the truth through experimentation and study. We have to rethink or adjust what we know as new evidence emerges,” said Vassilakopoulos.

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Yeah, 3-5 times annual, that is.

COVID Boosters Likely to Be Annual ‘For the Foreseeable Future’ (ET)

From Nov. 8, COVID booster shots will be available for all adult Australians six months after they got their second dose. Around 1.7 million people will be eligible for a booster dose by 2022, a move making Australia the second country in the world after Israel to offer boosters to all ages. Australia has reached the 80 percent full vaccination rate last week, with Prime Minister Scott Morrison praising it as “another magnificent milestone.” At the state level, however, only New South Wales, Victoria, and the Australian Capital Territory have reached this number. The Therapeutic Goods Administration (TGA), the country’s medicine and therapeutics regulator have approved Pfizer as a booster dose. Pfizer booster shots will be given to people even if they had other vaccines for their first two doses.


For those who have an allergic or adverse reaction to Pfizer, the AstraZeneca vaccine will be given instead. While boosters are not required for international travel, states and territories will decide whether to make it mandatory for residents to be fully vaccinated. Victorian Premier Daniel Andrews suggested last month that booster shots may be needed for those who are fully vaccinated to retain their freedoms. “A month before your six months is up, then you will get a message and your vaccination certificate, the thing that gets you the green tick. You’ll be prompted to go and book a time to go and have your booster shot,” Andrews said. “There may be state clinics in that or it might be all done through GPs and pharmacies, that hasn’t been worked through yet. We’re happy to play our part, though. So it’ll be about the maintenance of your vaccination status.”

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Ideally, it wants you to be sick your entire life.

Medicine Wants to Kill You (Kunstler)

It bears repeating that whatever Covid-19 actually is or where it came from, it’s a disease not a whole lot more deadly in the general population than the flu in a bad season; that in the natural course of things, it would have probably only killed mostly the very old and already sick, and that the rest of the population would have soldiered through it and acquired a sturdy natural immunity superior to anything the vaxxes might confer (even in theory). My own doctor tried to persuade me to get vaxed-up during a routine physical in October. I asked him if he was aware of the thousands of deaths and disabling adverse events reported on the CDC’s VAERS system. He said the numbers were not true and went on to say that he had “one hundred percent confidence in the vaccines.”

He’s always appeared to be a smart and capable person. A year or so ago he was enlisted to act as an executive administrator in the health care org he practices in, and now only sees patients two days a week. Perhaps that leaves him no time to follow the news. Or maybe he has no inclination to follow any news except what comes from sources like cable TV channels, which are almost entirely sponsored by the Pharma industry. The bottom line for me is that he has compromised my faith in his judgment. I wonder how many other people feel that way about their doctors. The medical profession was already in trouble before Covid came on the scene. It had entered into a demonic symbiotic relationship with the insurance industry that amounted to pervasive racketeering. (Just imagine the hospital bills of all those people with adverse vax reactions that the doctors affected to be mystified by, and ran countless, fruitless tests on.)

The good news for now is that a federal court has stayed the “Joe Biden” vax mandates. The government is expected to dispute that decision today (Monday Nov 8). Meanwhile, the rumor of a general strike against vaccine tyranny, set for today through Thursday, is in the air and we’ll have to stand by to see if anything happens. We should also be standing by in the weeks ahead to see how many more people begin to show symptoms of developing serious bodily disorders from the multiple shots they have been suffered to take.

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“..the bottom line is this: You take a jab because you believe it will protect you. That’s the beginning and end of it. There is never any other argument available because the risk of adverse events is always yours.”

Will You Ever Care To SOLVE The Problem? (Denninger)

I came of age in the early 1980s. Anyone who says that there have been all these “mandates” to get shots on a durable basis, and that everyone has had to prove it, is 100% full of crap. It’s a flat-out lie. I went to college on my own — both enrolling in a community college while still in High School to take a couple of classes and in college generally until I quit, making more money than it was costing to go to school. I was never asked for any evidence that I had received a single vaccination of any sort. Never. I’ve never been asked to prove my vaccination status for any disease ever in my life. Not once since I became sentient have I, or anyone in my family, ever been asked to prove I’d been immunized against anything. Want to know why? Because there was a hell of a hangover from the mid to late 1970s mess at the time where once again pharma lied, people died and nobody was going anywhere near that bull****.

Yes, by the year 2000 things had changed. People forgot what had happened and who had gotten away with it. The schools wanted evidence my daughter had the “routine” childhood shots. I objected to exactly none of them so there was no foul. All, in my opinion, were in fact safer than the disease and effective in preventing it. Thus administration was voluntary. So let’s solve the problem. No mandates. Period. Zero. Not for measles, DTaP, HIB, nothing. Recommendations, yes. Strong ones. But folks, the bottom line is this: You take a jab because you believe it will protect you. That’s the beginning and end of it. There is never any other argument available because the risk of adverse events is always yours. If the shot harms or kills you that’s on you, so the case to make is that it is less dangerous for you to take the shot than risk the disease. If you can’t make that case on a conclusive basis then sit down and shut up.

Manufacturers are required to publish true and accurate statistics on so-called “breakthroughs” and all adverse events. Health providers are required by law to report all adverse events as they are now, but failure to do so gets you 10 years in prison and permanent revocation of your medical license throughout the US — no ifs, ands or buts. Manufacturers are held to strict liability at the letter of their claims. If you can’t make the case that it is safer to take the shot while telling the truth then you don’t sell any shots. If you lie you are fully legally accountable, period. All medication has risks so as long as the risk is truthfully disclosed in terms of outcomes and odds, and the person chooses to take it, that’s their decision and it’s fine. The NCVIA and PREP Act are both repealed. This is not a request, by the way. It’s demand we are willing to enforce by destroying every firm along with all of the directors and officers shielded by these acts, physically if necessary, if refused.

And, since we’re dealing with this mess, I want to add another provision: Any competent adult may purchase any drug, allegedly “prescription”, over the counter against medical advice and a pharmacist may not refuse to fill it, for any other than a DEA-scheduled controlled substance being purchased beyond reasonable personal use limits, save in one instance: They are able to document, by scientific evidence, a direct contraindication as a result of conflict with some other drug the person is consuming. Such an “AMA” purchase shall absolve the pharmacist along with any physician or other medical facility involved in all liability for the outcome of such consumption If I want to take HCQ and/or Ivermectin if I get the Coof, and add Budesonide to that, I can irrespective of whether a pharmacist or physician likes it or not. If I kill myself doing it that’s on me.

My physician (and pharmacist) is thus returned to their rightful role: That of a paid expert who issues recommendations but under no circumstance can they prohibit or mandate any particular course of action, including the use or withholding of a treatment or drug, for a given condition. It is my ass and thus must be my choice.

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Big stories about molnupiravir as a 3CLPro Inhibitor. We don’t need it.

3CLPro Inhibitors As Potential Anti-SARS-CoV-2 Agents (Nature)

Emerging outbreak of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection is a major threat to public health. The morbidity is increasing due to lack of SARS-CoV-2 specific drugs. Herein, we have identified potential drugs that target the 3-chymotrypsin like protease (3CLpro), the main protease that is pivotal for the replication of SARS-CoV-2. Computational molecular modeling was used to screen 3987 FDA approved drugs, and 47 drugs were selected to study their inhibitory effects on SARS-CoV-2 specific 3CLpro enzyme in vitro.


Our results indicate that boceprevir, ombitasvir, paritaprevir, tipranavir, ivermectin, and micafungin exhibited inhibitory effect towards 3CLpro enzymatic activity. The 100 ns molecular dynamics simulation studies showed that ivermectin may require homodimeric form of 3CLpro enzyme for its inhibitory activity. In summary, these molecules could be useful to develop highly specific therapeutically viable drugs to inhibit the SARS-CoV-2 replication either alone or in combination with drugs specific for other SARS-CoV-2 viral targets.

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“The potential consequences of vaccines crossing the natural blood-brain barrier in children’s developing brains are of the utmost concern to all future humanity.”

Applying Brakes On ‘Warp Speed’ Covid-19 Vaccinations For Children (WT)

One of the worst medical disasters was diethylstilbestrol (DES) which was commonly prescribed as an anti-miscarriage medication in the 1940s. It was recalled 30 years later after it was connected to a rare tumor that appeared in the next generation of daughters of women who had taken it. We rarely know everything about a new drug when it’s approved, and we must brace ourselves for side effects we may only learn of years later. The history of medicine documents time and time again tragic examples of new drugs causing unsuspected problems discovered after release. The challenge for researchers to identify new COVID-19 viral target proteins and then to adapt existing manufacturing platforms already shown to be safe for vaccines against other pathogens is already a daunting endeavor.

However, using a new, rapid, but previously untested manufacturing technology (mRNA or DNA) introduced a second variable. Herein lies the problem that every science student is taught to avoid: changing two variables simultaneously in a single experiment. This violates the classic scientific method. In this case, the vaccines generated were comprised of active (COVID-19 viral sequences) and inactive components (manufacturing ingredients, including any impurities), neither of which had a prior favorable safety track record in healthy adults or children. But how likely is the risk of an epidemic of long-term medical complications worse than the pandemic itself, say five years from now?

RNA-based vaccines (Pfizer and Moderna) could trigger any number of autoimmune diseases, which can take years to manifest. This is because the resulting combination of viral and normal self-proteins expressed by any cell, which takes up mRNA, creates a brand-new target on normal cells, which the immune system potentially recognizes as foreign and attacks. mRNA also activates danger sensors in the primal immune system, which in turn indirectly promotes the release of pro-inflammation factors, specifically interferons, which have been associated with autoimmunity. This issue is underscored by a clinical trial of an mRNA lung cancer vaccine in 2019, in which blood tests revealed elevated indicators for autoimmunity concerns in 20% of patients.

Immune responses directly against RNA molecules themselves cause autoimmune diseases, such as systemic lupus. In 2014 in the early days of the technology, an mRNA COVID-19 vaccine inventor published on this potential long-term concern of mRNA vaccines. Finally, none of the mRNA vaccines has a built-in “off” switch to control where they travel in the body and how long they persist there. Published animal safety studies showed traces of COVID-19 spike protein in the brain, heart, and other vital organs, and the European Medicines Agency’s assessment report acknowledged that low levels of mRNA itself were detected in most tissues. The potential consequences of vaccines crossing the natural blood-brain barrier in children’s developing brains are of the utmost concern to all future humanity.

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“What should we anticipate? Children of different ages being barred from mingling. Children being bullied, ridiculed and mocked, with taunts using terms like “covidiot.”

Vaccine Passports: Institutionalized Segregation (BI)

Increasingly, vaccination is no longer a matter of choice. Hundreds, perhaps thousands, of workplaces and schools are instituting COVID-19 vaccine mandates, with more expected following formal FDA licensure of the vaccines. But mandating people and their children who have consciously chosen not to get vaccinated — a group that tends to be younger, less educated, Republican, non-white and uninsured — is a recipe for creating new and deeper fractures within our society, the kind of fractures we may profoundly regret in hindsight. Let’s not sugarcoat it: This is a new form of institutionalized segregation. Yes, some unvaccinated adults may swallow this bitter pill and comply as a way of doing their part in making America safer.

But many will see it — along with requirements that the unvaccinated wear masks or undergo regular COVID testing — as a thinly veiled attempt at public shaming. After all, if the goal is to maximize the interruption of spread, then surely all people should be masked irrespective of vaccination status. Forced compliance will come with future consequences. The ensuing anger, resentment and loss of trust forms a ticking time bomb waiting to go off. Are we ready to add this mandate to the list of issues helping erode the fabric of our society? These practices diverge substantially from the historical norm of equal opportunity. For all other required vaccines, religious and philosophical exemptions allow unvaccinated children to enjoy the same educational experience as the vaccinated.

This is because exemptions reflect a social value that in the United States, there are valid reasons for refusing treatments or vaccines, and these reasons will be respected. Once exempt, there are no sanctions experienced in everyday life. But with COVID vaccine mandates, even those with exemptions are being sanctioned, sending another clear message: We really don’t care about your reasons. And in schools, where a child’s experience will be shaped by their parents’ decisions and those of policymakers, the situation could become tragic. If schools invite vaccinated children to lose their masks, what was once an act of social responsibility could morph into a mark of disease. What should we anticipate? Children of different ages being barred from mingling. Children being bullied, ridiculed and mocked, with taunts using terms like “covidiot.”

Differential treatment toward unvaccinated children by some teachers (who are, just like everyone else, individuals with their own views about COVID vaccines). And families deciding to withdraw from formal education, choosing instead to home-school. Vaccinate-or-mask policies will drive a wedge between children and parents, cause daily psychological harm, carrying long lasting consequences for future generations. Some might see mandate resistance as a symptom of vaccine misinformation. But considering most of these individuals have complied with mandates for routine vaccines such as mumps and measles, diseases of far less societal consequence than COVID, is it not worth listening to their objections against COVID vaccine mandates?

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“When you are imposing a measure which restricts liberty and undermines human rights, the measure should be necessary and proportionate. Vaccine passports are not.”

UK Health Expert: Vaccine Passports Make No Sense (DR)

One of the UK’s most respected public health experts has called on the Scottish Government to scrap its “ridiculous and discriminatory” vaccine passport scheme. Professor Allyson Pollock spoke out after a study by The Lancet medical bible found double-jabbed people can be just as likely to pass on Covid-19. The research appears to blow a hole in the argument for controversial new laws in Scotland requiring proof of vaccination to enter football grounds and nightclubs. The Scottish Government forged ahead with the scheme, along with a mobile phone app, despite Westminster ditching its plans. Pollock, a clinical professor of public health at Newcastle University, said: “Vaccine passports don’t make public health sense. Your vaccination status tells us nothing about whether you’re infectious or transmitting at that moment in time.

“Even if you’re vaccinated, you may well become infected or re-infected and you may also transmit the virus. “So passports make no sense. They are a ridiculous, discriminatory and disproportionate measure because they tell you nothing about the individual’s risk or what the background prevalence of infection is. “It is very surprising that Scotland has chosen to introduce them given the First Minister claims to be a strong believer in human rights. When you are imposing a measure which restricts liberty and undermines human rights, the measure should be necessary and proportionate. Vaccine passports are not.” Pollock – an ex-member of Covid advisory panel Independent SAGE – spoke out in the wake of the Lancet study last week. Researchers discovered that while vaccines do an excellent job of preventing serious Covid illness and deaths, they are less good at stopping infections.

This is understood to be particularly true since the emergence of the more infectious Delta variant, which is dominant in the UK. Pollock added: “The question that has to be asked is why has the Scottish Government implemented vaccine passports. “Is it to stop transmission and infection or is it a coercive measure to make people have a vaccine. “You really need to be very clear about why are you doing this and that is what parliaments in Edinburgh and Westminster should be debating. “My advice to Nicola Sturgeon would be simple – stop using passports. “If you think that having lots of mass gatherings – nightclubs and things like that – are going to be to too dangerous, then you need to take a decision not to have them. “Clearly there has been pressure to open up the economy and perhaps it is thought vaccine passports offer a reassurance but it is a false reassurance, not a public health measure.

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There are no data on myocarditis from Covid.

The Cause of Myocarditis: COVID19 or COVID19 Vaccination? (BI)

Which causes more myocarditis: COVID19 or COVID19 vaccination? This question should be answered easily, yet here you are, reading this. First, let us agree to the terms: We want to know the rate of myocarditis after COVID19 or vaccination for individuals. Since we know age and gender, it would be useful to know these rates by age and gender. For instance, what is the rate of myocarditis in a boy between the ages of 12-15 if they get COVID19 vs. if they get the vaccination, or alternatively, what are those rates in a 40-45 year old woman? Lumping everyone together— from 12 year old boys to 80 year old women—would be silly. Let us be honest. This is not asking for the moon. It is a simple question. The answer should be very clear. In fact, one could present it as a table.

Second, let’s be very clear about the fraction we are after. When it comes to myocarditis after COVID19 we want the following: Number of cases of myocarditis within 14 or 21 days after vaccination (excess) / Number of vaccinations given For rates of myocarditis after COVID19 we want the following: Number of cases of myocarditis within 14 or 21 days after COVID19 (excess) / Number of infections of COVID19. When it comes to the former, the FDA has given us a clear number for boys aged 12 to 15 and 16 to 18 (orange bars). This is FDA’s slide; the data come from OPTUM health This translates into a risk of myocarditis of 179 per million in boys aged 12 to 15, and 196 per million in boys aged 16 to 18. That is a rate of 1 in 5,600 and 1 in 5,100 respectively. (Note: I am not citing a preprint here, I am citing the FDA’s own slides)

Now what about the rate of myocarditis after COVID19? To perform this calculation you need the numerator of excess myocarditis cases after infection and divide that by the number of people who have been infected. While many publications have reported the numerator, the denominator requires serologic testing. You need to know people who were infected who may not have even showed symptoms. You cannot use cases presenting to health care systems as the denominator, as that is is not the totality of infections. A reader can correct me if I am wrong but, I have not seen ANY analysis that uses the denominator of infections. Many papers model this denominator, but the correct method would be to perform seroprevalence of a large cohort. Can anyone provide a link to such a paper— one that uses a denominator of seroprevalence?

Read more …

“We have to be ready to go every day, all the time,” Berger explained. “We are the ready force. We have to be ready to go.”

That’s exactly the problem, isn’t it?

Marines Chief Blames ‘Disinformation’ For Remaining Unvaccinated Troops (WE)

Marine Corps Commandant Gen. David Berger cited “disinformation” as the reason there are thousands under his leadership who have not yet been vaccinated for the coronavirus. Berger said Thursday during the Aspen Security Forum that the force is being “challenged by disinformation … that still swirls around about where the genesis, how did this vaccine get approved, is it safe, is it ethical — all that swirls around on the internet, and they see all that, they read all that.” As of last Monday, 93% of Marines were partially or fully vaccinated against the coronavirus, according to Pentagon spokesman John Kirby. Each Marine must be vaccinated by Nov. 28, but troops are not considered fully vaccinated until two weeks after the final dose of a two-shot vaccine or that same time period after a one-shot dose.


This means the final shot will actually have to be given by this Sunday. “We have to be ready to go every day, all the time,” Berger explained. “We are the ready force. We have to be ready to go.” He also noted that there are more than a dozen non-COVID-19 vaccinations that troops are required to receive, though some are specific to troops in certain locations. “Just to get through boot camp, you got to get 12 vaccinations,” he said. If the vaccination rate of the Marines remains the same until the deadline, it would leave more than 12,500 Marines unvaccinated, according to Military.com. The Nov. 28 deadline for the Marines is the same for the Navy, which has reported that active-duty sailors have a 99% vaccination rate. The Air Force is the only military branch whose vaccination deadline has passed, being last Tuesday. Slightly less than 96% was vaccinated in time, while roughly 8,500 remain unvaccinated.

Read more …

 

 

 

 

Galloway
https://twitter.com/i/status/1457243550366773252

 

 

Support the Automatic Earth in virustime; donate with Paypal, Bitcoin and Patreon.

 

Nov 072021
 


Pablo Picasso Sleeping peasants 1919

 

US Appeals Court Blocks Biden’s Federal Covid-19 Vaccine Mandate (NYP)
Federal Appeals Court Blocks Biden’s ‘Big-Company’ Vaxx-Mandate (ZH)
Pfizer “Vaccine”: Kill 200 To ‘Save’ One? (OffG)
How Long Does Vaccine Based Immunity Last? (SRMD)
Pfizer Board Member Gottlieb: Pandemic Could Be Over In US By January (CNBC)
Bootleggers, Baptists, and Vaccine Mandates (AIER)
Scientific Journals Censor Science: Removal of Myocarditis report in VAERS (TSN)
Feds Pay Zero Claims For COVID-19 Vaccine Injuries/Deaths (ZH)
When Pandemics Collide: The Interplay Of Obesity And Covid-19 (PMC)
Assange, Fiancee Sue Uk For ‘Preventing Them From Marrying In Prison’ (DM)

 

 

“Because the petitions give cause to believe there are grave statutory and constitutional issues with the Mandate, the Mandate is hereby STAYED pending further action by this court.”

 

 

 

 

“Something very dark is going on.”
https://twitter.com/i/status/1457002810063609859
https://twitter.com/i/status/1457032388232597505

 

 

Big win. Key line:

“Because the petitions give cause to believe there are grave statutory and constitutional issues with the Mandate, the Mandate is hereby STAYED pending further action by this court.”

US Appeals Court Blocks Biden’s Federal Covid-19 Vaccine Mandate (NYP)

A federal appeals court in Louisiana has blocked the Biden administration’s latest COVID-19 vaccination mandate, giving the government until Monday afternoon to submit a response. An emergency stay, issued Saturday from the United States Court of Appeals for the Fifth Circuit, prevents the White House from requiring all full and part-time workers at private-sector companies with 100 or more employees to be vaccinated or get tested weekly and wear face masks. In its decision, the court cited “grave statutory and constitutional” concerns about the government’s mandate, which is scheduled to take effect on January 4. The mandate — issued Thursday under a new rule by the U.S. Department of Labor’s Occupational Safety and Health Administration (OSHA) — would apply to some 84 million Americans.

It has been challenged in court by more than two dozen states, including Texas, Missouri and Louisiana. Employers who don’t comply could face fines of up to $14,000 per infraction, according to the government’s guidelines. “We will have our day in court to strike down Biden’s unconstitutional abuse of authority,” Texas Gov. Greg Abbott tweeted after news of the stay was announced Saturday afternoon. A petition filed by Missouri Attorney General Eric Schmitt and representing 10 other states, declared the vaccine mandate is “unconstitutional, unlawful and unwise.” It also challenges OSHA authority, claiming the agency does not have the jurisdiction to implement the regulations.

“Its unlawful mandate will cause injuries and hardship to working families, inflict economic disruption and staffing shortages on the states and private employers,” reads the petition. In September, the president promised to impose a flurry of vaccine mandates after the Delta variant led to a spike in COVID-19 infections, ending what Biden called the “summer of freedom” from the deadly virus. “A distinct minority of Americans supported by a distinct minority of elected officials are keeping us from turning the corner,” Biden said in a White House address. “We’ve been patient, but our patience is wearing thin, and your refusal has cost all of us.” The government has until Monday at 5 pm to challenge the stay.

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Will need to read a number of reports to get the relevant details. Note: there will be as many appeals as cases brought.

Federal Appeals Court Blocks Biden’s ‘Big-Company’ Vaxx-Mandate

A federal court has issued a temporary victory in a lawsuit against the Biden administration’s coronavirus vaccine mandate issuing a stay on the controversial federal government regulation in Texas. “Yesterday, I sued the Biden Admin over its unlawful OSHA vax mandate,” Texas’ Republican Attorney General Ken Paxton tweeted Saturday. “WE WON. Just this morning, citing “grave statutory and constitutional issues,” the 5th Circuit stayed the mandate. The fight is not over and I will never stop resisting this Admin’s unconstitutional overreach!” As Fox News reports, earlier in the week, Paxton sued the Biden administration over the mandate and argued that the move to force workers at companies with over 100 employees to be vaccinated or undergo weekly testing is “flatly unconstitutional.”

“Biden’s new vaccine mandate on private businesses is a breathtaking abuse of power,” Paxton tweeted Friday. “OSHA has only limited power & specific responsibilities. This latest move goes way outside those bounds. This ‘standard’ is flatly unconstitutional. I’m asking the Court to strike it down.” The Wall Street Journal reports that the New Orleans-based Fifth Circuit said it would quickly consider whether to issue an injunction against the vaccine and testing requirements, ordering the Biden administration to file initial legal papers by late Monday afternoon. A number of trade groups have issued warnings about the mandate, saying that it would exacerbate supply chain bottlenecks and staffing shortages nationwide. The White House remains confident the mandate will stand up to legal challenges.

“We are very confident that it can,” White House Deputy Press Secretary Karine Jean-Pierre said. “As for the legal side of this, let me be crystal clear to avoid what appears to be possible misinformation or disinformation around the emergency temporary standard being a vaccine mandate. That would be on its face incorrect as has been explicit for months. It is a standard for safe workplace to either comply with weekly testing or to be vaccinated.”

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“It’s literally the worst NNTV in the history of vaccination.”

Pfizer “Vaccine”: Kill 200 To ‘Save’ One? (OffG)

This is the absolute risk reduction for Pfizer/BioNtech (each group had over 18,000 people):
Injection Group: 8/18,198 = 0.04%
Placebo Group: 162/18,325 = 0.88%
Absolute risk reduction = 0.84%

From the “absolute risk reduction”, you can then calculate the “number needed to vaccinate” (NNTV). This is the rough number of people you need to inject in order to definitely prevent one case/death. To continue the example above, if your vaccine reduces the odds of infection from 10% to 1% (an ARR of 9%), you need to vaccinate eleven people to prevent one infection, giving you an NNTV of 11. Again, the NNTV of the Covid vaccines are much, much, MUCH higher than 11. Estimates range from between 88 and 700 to prevent a single case, and anything up to 100,000 to prevent one solitary death. And remember, all this data was for adults. Children are at a far lower risk from Covid – both in terms of hospitalisation and death. In the US, children aged 5-11 have a 99.992% chance of surviving “Covid” – so it naturally follows the NNTV for this group will be far, far higher than for adults.

But, now that the FDA has approved Pfizer’s “vaccine” for emergency use on children aged 5-11, “far, far higher” is not good enough. We need to calculate an actual figure for the “number needed to vaccinate” in order to hypothetically protect one child from dying “with Covid”. Fortunately for us, someone else has already done it. Writing on his Substack, economist Toby Rogers PhD has collated the numbers from Pfizer’s own trials, the FDA and the CDC and done a very thorough write up. You can read the whole thing here, we’ll just present you with some of the highlights: As of October 30, 2021, the CDC stated that 170 children ages 5 to 11 have died of COVID-19-related illness since the start of the pandemic. (That represents less than 0.1% of all coronavirus-related deaths nationwide even though children that age make up 8.7% of the U.S. population).

The Pfizer mRNA shot only “works” for about 6 months (it increases risk in the first month, provides moderate protection in months 2 through 4 and then effectiveness begins to wane, which is why all of the FDA modeling only used a 6 month time-frame). So any modeling would have to be based on vaccine effectiveness in connection with the 57 (170/3) children who might otherwise have died of COVID-related illness during a 6-month period.At best, the Pfizer mRNA shot might be 80% effective against hospitalizations and death. That number comes directly from the FDA modeling. I am bending over backwards to give Pfizer the benefit of considerable doubt because again, the Pfizer clinical trial showed NO reduction in hospitalizations or death in this age group.

So injecting all 28,384,878 children ages 5 to 11 with two doses of Pfizer (which is what the Biden administration wants to do) would save, at most, 45 lives (0.8 effectiveness x 57 fatalities that otherwise would have occurred during that time period = 45). So then the NNTV to prevent a single fatality in this age group is 630,775 (28,384,878 / 45). But it’s a two dose regimen so if one wants to calculate the NNTV per injection the number doubles to 1,261,550. It’s literally the worst NNTV in the history of vaccination. 630,000 children injected with 1.2 million doses to save one life. That’s incredibly inefficient. However, it could be even worse than that. As we covered last week, according to statistics cited at the VRBPAC meeting, only 94 children from the 5-11 age group have died. If this lower figure is correct, the NNTV to prevent a single death jumps up to 915,641.

In other words, in order to hypothetically prevent a single child from dying over a six month period, you would have to inject nearly one million children with almost two million doses of the Pfizer vaccine.

Read more …

We need solid research into this.

How Long Does Vaccine Based Immunity Last? (SRMD)

It’s unfortunate that the drug companies decided to end their trials early, by giving active covid vaccine to the members of the placebo group after just a few months. It means that there is no long term follow-up of the covid vaccines from randomized trials, and there never will be. This means that we are instead forced to rely entirely on observational data as we try to understand how safe and effective the vaccines are over the longer term. That is why a recent study out of Sweden is so very interesting. It is currenly available as a pre-print and can be found here. The purpose of the study was to determine how effective the vaccines are at protecting against covid over the longer term (i.e. after more than a few months). This was a registry based study, so it’s not surprising that it is coming out of Sweden. Sweden is generally acknowledged as being better than any other country at collecting and sorting large quantities of population data and using it to produce these types of studies.

The authors of the study began by identifying all people residing in Sweden who had been fully vaccinated against covid-19 by late May 2021. At that time, three different vaccines were being used in Sweden: Moderna, Pfizer, and AstraZeneca. The vaccinated people were then matched individually against people of the same age and gender, and living in the same municipality, who hadn’t been vaccinated. In total, 1,684,958 individuals were included in the study. They were followed until October to see if they developed covid-19. So, what did the study show? As would be expected, the vaccines were very effective at preventing symptomatic covid around two months out from vaccination. This is what the randomized trials showed, and it’s the reason the vaccines were approved for use. Overall, the reduction in relative risk at 31-60 days out from vaccination was 89%.

However, after those first two months, there was a rapid decline in efficacy. At four to six months, the vaccines were only reducing the relative risk of infection by 48%! This is pretty interesting when we consider that governments had initially set the bar for approving the vaccines at a 50% relative risk reduction. So, if the trials had been required to run for six months before presenting results instead of only running for two months, then the vaccines would have been considered too ineffective to be worth bothering with, an would never have been approved. Well, that’s not quite true. One vaccine did still provide a better than 50% relative risk reduction at six months – the Moderna vaccine. At four to six months, the relative risk reduction with the Moderna vaccine was 71%. Pfizer was at the same time point only offering a 47% reduction in risk, and AstraZeneca was at that point not doing anything whatsoever to lower risk.

It makes sense that the Moderna vaccine would offer better protection than the Pfizer vaccine. Although the vaccines are virtually identical, the dose in the Moderna vaccine is three times higher. This is likely the reason why Moderna has been associated with much higher rates of myocarditis, which is why it is no longer approved for use in people under the age of 30 here in Sweden.

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But only if you consume our products.

Pfizer Board Member Gottlieb: Pandemic Could Be Over In US By January (CNBC)

The Covid-19 pandemic could be over in the U.S. by the time President Joe Biden’s workplace vaccine mandates take effect in early January, Pfizer board member Dr. Scott Gottlieb told CNBC’s “Squawk Box” on Friday. The vaccine requirements from the Occupational Safety and Health Administration begin on Jan. 4 for any company with at least 100 employees. Some 84 million private sector workers must get either their second Moderna or Pfizer shot or one dose from Johnson & Johnson by that date or face regular testing for the virus. “These mandates that are going to be put in place by Jan. 4 really are coming on the tail end of this pandemic,” said Gottlieb, who’s also a former commissioner of the Food and Drug Administration.

“By Jan. 4, this pandemic may well be over, at least as it relates to the United States after we get through this delta wave of infection. And we’ll be in a more endemic phase of this virus.” All companies complying with OSHA’s new rules must also start enforcing indoor mask mandates for unvaccinated employees starting Dec. 5. Those personnel must also begin submitting weekly negative Covid tests after Jan. 4 to enter the workplace, and anyone who tests positive should quarantine. The federal mandate contains exemptions for religious and medical reasons. Employees who work exclusively outdoors, at home or in settings where others aren’t present are also exempt from the rules.

OSHA’s guidance doesn’t mandate that businesses pay for their employees’ Covid tests or masks, but any company caught dodging the rules could face fines of anywhere between $13,653 to $136,532 for intentional noncompliance. Gottlieb’s comments came in the wake of data from Pfizer that indicated its Covid antiviral pill, when paired with an HIV medication, slashed the potential for hospitalization or death by 89% in adults at risk for severe complications. Combining the pill with an HIV medication slowed the metabolism, allowing the Covid antiviral to work longer in the body. Pfizer CEO Albert Bourla said in an interview Friday morning with “Squawk Box” before Gottlieb spoke that the company will submit data on the therapeutic to the FDA before Thanksgiving.

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“The Bootleggers supported the ban, too, but only because they would enjoy a thriving black market on those days and profit from illegal alcohol sales.”

Bootleggers, Baptists, and Vaccine Mandates (AIER)

In 1983, economist Bruce Yandle developed the Bootleggers and Baptists framework to explain his belief that durable government action tends to come about with the support of two types of interest groups: those with moral interests and those with financial interests. Yandle appeals to early twentieth-century blue laws, which prohibited the sale of alcohol on Sundays. Baptists, the moralists, were motivated by their beliefs that Sundays should be respected as a day of prayer and rest, not drinking. The Bootleggers supported the ban, too, but only because they would enjoy a thriving black market on those days and profit from illegal alcohol sales. Durable government action, according to Yandle, tends to emerge with the support of coalitions that share a common goal even if they don’t share common motivations.

In a global pandemic, it has not been difficult to find a plethora of public health pieties. Nor has it been hard to find profiteers, especially pharma. I doubt that Anthony Fauci has any financial interests in the Moderna/NIAID vaccine — though investigators should look. He’s in it for the glory. Still, the Moderna/NIAID partnership puts the Bootleggers and Baptists on the same team. Fauci, President Biden, and all the MSM sentinels are the moralists in this equation, that is, if Prof. Yandle will permit a not-so-bright line between moralism and savior complex. They want to be known as the ones who beat the pandemic. One might even say Fauci has been planning for this his whole career. Now he graces us with his presence daily on SAHM programs such as The View, basking in the lamps, reminding us to wear our masks and get our vaccines.

The decrepit Biden, though he needs help getting up on that high horse, once bestride it, holds his mighty executive pen aloft and commands the multitudes to get the jab or else. Waiting in the wings are shadowy corporate figures, such as Moderna’s Bancel, prepared to execute these technocratic plans using billions of dollars inked in red. Though howls against Big Pharma were once prominent in the Progressive Playbook, those have mysteriously been redacted like Anthony Fauci’s FOIA’d emails. When one stops to think that these billions will have to be repaid by the very children who won’t have a choice but to get these vaccines, much less likely Covid, she might find the idea nauseous. A considerably more disturbing thought, though, is that Fauci probably suspected all along that NIH funding led to the creation and (accidental) release of a virus that has killed 5 million people as of this writing.

Anthony Fauci is a monopsony on funding for infectious disease research. He clearly does not want to be known as the guy in charge of funding the pandemic, even inadvertently. His defensiveness, his untruths before Congress, and his moth like draw to camera lights — all seem to reveal a man who, in his moralism, refuses to acknowledge that his agency had any hand in the damage Covid dealt. He wants to be America’s doctor, and his grand plan has always been to vaccinate the world. In his favored scenario, he would not be viewed not as a negligent bureaucrat but a savior. And he wants to keep it that way. The researchers? The intermediaries? The pharma execs? They’re in it for the money upon which their careers depend.

My hypothesis, therefore, tentative but bold, is that economist Bruce Yandle must have seen this coming a mile away. The vaccine mandates of 2020-2021 is a story of Bootleggers colluding with Baptists. The only question that remains, then, is whether we’re going to let them get away with it.

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Cancelling McCullough.

Scientific Journals Censor Science: Removal of Myocarditis report in VAERS (TSN)

Dr Peter McCullough, MD, one of the most cited physicians in the world, an eminent practitioner of internal medicine, a cardiologist and epidemiologist, co-wrote a report with Dr Jessica Rose, Ph.D., a virologist and epidemiologist in Canada, called ‘A Report on Myocarditis Adverse Events in the U.S. Vaccine Adverse Events Reporting System (VAERS) in Association with COVID-19 Injectable Biological Products.’

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Paying means acknowledging damage. Look at the restrictions…

Feds Pay Zero Claims For COVID-19 Vaccine Injuries/Deaths (ZH)

In fiscal year 2021, the U.S. government paid $246.9 million in claims for vaccine-related injuries and deaths. Not a single payout was related to Covid-19 vaccines. Each person with a “provable” injury from a Covid vaccine could claim up to $379,000 from a special Covid vaccine fund set up by the federal government. The payout for death could be as high as $370,376. However, according to an OpenTheBooks.com investigation, the federal government didn’t pay a penny for Covid-vaccine claims. The special fund for these claims is called the Countermeasures Injury Compensation Program (CICP). There were only 1,357 claims filed that alleged “injuries/deaths from the Covid vaccines,” and 53 were listed as deaths, according to recent reporting by the U.S. Department of Health and Human Services (HHS).

By contrast, the self-reporting Vaccine Adverse Reporting System (VAERS) lists 16,310 deaths related to Covid vaccines. Of these, “5,326 of the deaths occurred on Day 0, 1,or 2 following vaccination[.]” The low number of applicants to the CICP fund for injuries or death from the Covid vaccine suggests that people don’t know the special fund exists. The “normal” vaccine fund, the National Vaccine Injury Compensation Program (VICP), has existed since 1988 and provides compensation for injuries or deaths associated with most vaccines routinely administered in the United States (such as pediatric and seasonal influenza vaccines), according to the Congressional Research Service. Last year, this fund paid out $246.9 million in vaccine-related injuries and deaths. Payouts include $250,000 for a vaccine-caused death and $250,000 “for pain and suffering and emotional distress.”

A special vaccine court handles these claims. However, in the case of Covid-19 vaccines developed and approved under Project Warp Speed, deaths resulting from a Covid vaccine would pay out through the CICP and would pay more money than a vaccine-related death in normal times. Since the benefit for a death caused by a Covid-19 vaccine is $370,376 for fiscal year 2021 and $50,000 per year for lost employment income (with a lifetime cap to be “generally $379,000”). So, the death benefit is $120,376 higher than for other vaccines ($250,000). However, there is no equivalent to the VICP’s $250,000 “for pain and suffering and emotional distress” under the current Covid-19 parameters. Here are some other differences between the two vaccine-injury funds:

• No attorney fees. The Covid fund is not authorized to provide reimbursement for attorneys’ fees. Therefore, lawyers have less incentive to represent claims.
• Injured children receive small payouts. A Covid vaccine-injured child would only be reimbursed for “reasonable medical expenses.” Since the child survived and isn’t employed, there’s no other compensation.
• Narrow window to file a claim. The Covid fund allows a one-year window to file a claim whereas the regular vaccine fund has a three-year window.
• And sure enough, the CICP fund hasn’t paid out a dime in Covid-vaccine claims. HHS bluntly states online, “As of October 1, 2021, the CICP has not compensated any Covid-19 countermeasures claims.”

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A good bit on inflammation, something I find sorely lacking in most reports. There’s no way chronic and systemic inflammation is not a huge factor in Covid.

When Pandemics Collide: The Interplay Of Obesity And Covid-19 (PMC)

Among 20,133 patients hospitalized with SARS-CoV-2 infection across 208 hospitals in the United Kingdom, obesity was identified in 10.5% [2]. Worse, obesity was a strong predictor of mortality (HR 1.33; 95% confidence interval (CI): 1.19 to 1.49) after adjusting for other comorbidities. Between March 1 and April 8, 2020, 5279 patients at NYU Langone Health tested positive for SARS-CoV-2 [3]. Of these, 2741 (51.9%) required hospitalization, 990 (36.1%) developed critical illness requiring intensive care unit (ICU) services, and 665 (24.3%) died. In multi-variate analysis, obesity (especially a BMI>40 kg/m2) emerged as a risk factor for both hospital admission (OR 2.5; 95% CI:1.8 to 3.4) and critical illness requiring ICU services (OR 1.5; 1.0 to 2.2).


In another report from New York City, among 3615 individuals who tested positive for SARS-CoV-2, 775 (21%) had a BMI of 30 34 kg/m2 and 595 (16%) had a BMI of 35 kg/m2 or higher [4]. Among patients under 60 years old, those with a BMI of 30 34 kg/m2 were 2.0 (1.6 2.6) times as likely to be admitted to the hospital and 1.8 (1.2 2.7) times as likely to be admitted to the ICU, as compared to those with normal range BMI. In a cohort from Mexico of 51,633 SARS-CoV-2 positive cases and 5332 related deaths (10.3%), the obese, as compared to non-obese, had a higher rate of mortality (13.5% versus 9.4%), critical illness (5.0% versus 3.3%), and ventilator support (5.2% versus 3.3%) [5]. Data from France found a higher rate of obesity in those SARS-CoV-2 patients who were critically ill and required mechanical ventilation (Odds ratio of 7.36 [1.63 33.14] comparing BMI e”35 vs. <25) [6″ ].

These data highlight the devastating impact of one pandemic (obesity) on another (COVID-19). Obese individuals may have a compounded risk for acquiring more severe COVID-19 disease. First, individuals who are obese undergo gross structural and cellular level changes which puts them at greater risk for ischemic heart disease, diabetes, cancer, and respiratory disease, which are themselves risk-factors for acquiring COVID-19 disease. Second, obesity-specific structural changes can make caring for obese patients who acquire COVID-19 disease logistically challenging. Finally, there may be a link between obesity and SARS-CoV-2 specific receptors found in adipose tissue, possibly rendering obese individuals more susceptible to acquiring more severe disease.

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“The wedding stand-off began in May when Stella approached the prison chaplain to ask about arranging a ceremony. After an initial response, no further help was forthcoming. On October 7, Assange formally asked the Governor’s office to agree to a Belmarsh wedding, but he has had no reply.”

Assange, Fiancee Sue Uk For ‘Preventing Them From Marrying In Prison’ (DM)

Julian Assange and his fiancee Stella Moris are bringing legal action against Justice Secretary Dominic Raab and the Governor of Belmarsh Prison, accusing them of preventing the couple from marrying behind bars. They fear the obstacles put in the way of their wedding by UK authorities are linked to a US-backed political war against the Wikileaks publisher and campaigner. In September it was revealed the CIA had drawn up plans to kidnap or kill Assange during his seven years exiled in the Embassy of Ecuador in London. The agency also spied on his family and friends and led a campaign of misinformation against him. Stella, 38, a lawyer, said: ‘Those catch-or-kill plans were not implemented but other hostile measures were and this is the sting in the tail.

‘It’s part of an enormous conspiracy against Julian which makes itself felt in all that we try to do. ‘A wedding would be a moment of happiness, a bit of normality in insane circumstances. Julian needs things to hold on to because daily life is a struggle for him in Belmarsh and there is so much uncertainty about his future. ‘Our love for each other is the one thing which has carried us through and being married would be another bulwark in our emotional defences. ‘There is no reason for political interference in what is a basic human right. The CIA revelations show the lengths some agencies are willing to go to in their persecution of Julian.’ Assange, 50, and his fiancee have been engaged for five years, have two children and are both practising Catholics. They have been asking since May for help to arrange their wedding in Belmarsh.

[..] Stella is adamant their wedding ceremony would have no legal impact on extradition since his right to a family life in the UK is determined by the fact that their sons Gabriel, four, and Max, two, are British citizens. She also has rights of residency, having lived in Britain for 20 years, although she was born in South Africa. On Friday, the couple opened legal action paving the way for a judicial review. The case is brought against the Justice Secretary and Belmarsh Governor Jenny Louis. The wedding stand-off began in May when Stella approached the prison chaplain to ask about arranging a ceremony. After an initial response, no further help was forthcoming. On October 7, Assange formally asked the Governor’s office to agree to a Belmarsh wedding, but he has had no reply.

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“Any system you contrive without us will be brought down.”
— Leonard Cohen
https://twitter.com/i/status/1401284243733594119

 

 

The sights I have to look at every day.

 

 

Support the Automatic Earth in virustime; donate with Paypal, Bitcoin and Patreon.

 

Nov 032021
 
 November 3, 2021  Posted by at 9:55 am Finance Tagged with: , , , ,  63 Responses »


Pablo Picasso Harlequin and woman with necklace 1917

 

80% Of Women Vaxxed In 1st 20 Weeks Of Pregnancy Has Spontaneous Abortion (IP)
Italy Health Department Revises Covid Deaths Down From 130,000+ To 3783 (IT)
CDC Recommends Vaccines for 5 to 11-year-olds, Jabs Start Tomorrow (CTH)
CDC Emails: Our Definition of Vaccine is “Problematic” (Techno Fog)
Researcher Fingers Data Integrity Issues In Pfizer’s Vaccine Trial (BMJ)
Dr. Paul Offit Is Lying To Us About Myocarditis Rates (Steve Kirsch)
German Companies Creating Segregated Canteens For Vaxxed and Unvaxxed (SN)
The Disaster That Never Came (Anderberg)

 

 

“Name one other disease for which: governments & medical boards prohibit doctors from prescribing prophylactic & early treatment meds to patients & threaten them with jail sentences, fines, disciplinary proceedings & termination of their medical license.”

 

 

 

 

I spent a long time thinking about this, the physical stress, the emotional pain, all just a for an experiment. This concerns millions of women just in America alone. And yes, the “natural” spontaneous abortion rate may be high, maybe 20% or so, so a doctor can just say: it’s not abnormal…. try again!

Get the jab! It’s safe and effective! Don’t risk endangering your child!

80% Of Women Vaxxed In 1st 20 Weeks Of Pregnancy Has Spontaneous Abortion (IP)

An important peer-reviewed study looked at the CDC’s data on pregnancy losses following the mRNA injections, and found that more than 80% of those who got the injections during the first 5 months of pregnancy ended up with a spontaneous abortion (which is 7- to 8-times higher than the expected baseline of around 11%)


The study indicates that at least 81.9% (≥104/127) experienced spontaneous abortion following mRNA exposure before 20 weeks, and 92.3% (96/104) of spontaneous abortions occurred before 13 weeks’ gestation (Table 4, footnotes).[4] This is a very high proportion of pregnancy loss observed in those exposed to the mRNA vaccination before 20 weeks’ gestation, ranging from 81.9–91.2% (n = 114–127), which is significantly different to baseline estimates from other studies (11.3%, n = 79,978 [6]; p < 0.001), being 7- to 8-fold higher than expected (p < 0.001).

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Google translate.

Everyone copy the methodology, and apply locally.

Italy Health Department Revises Covid Deaths Down From 130,000+ To 3783 (IT)

According to the new report (which had not been updated since July) from the Higher Institute of Health on mortality from Covid, the virus that brought the world to its knees would have killed far less than a common flu. It seems a bizarre and no vax statement, but according to the statistical sample of medical records collected by the institute, only 2.9% of the deaths registered since the end of February 2020 would be due to Covid 19. So of the 130,468 deaths registered by official statistics at the time of preparation of the new report only 3,783 would be due to the power of the virus itself. Because all the other Italians who lost their lives had from one to five diseases which, according to the ISS, therefore already left them little hope. Even 67.7% would have had more than three contemporary diseases together, and 18% at least two together.


Now I personally know many people, but none who have the misfortune of having five serious illnesses at the same time. I would like to trust our scientists, then I go to read the ailments listed which would be no secondary reason for the loss of so many Italians and I begin to feed some profane doubts. According to the ISS, 65.8% of Italians who are no longer there after being infected with Covid were ill with arterial hypertension, that is, they had high blood pressure. 23.5% were also demented, 29.3% added a little diabetes to their ailments, 24.8% also atrial fibrillation. And that’s not all: 17.4% already had sick lungs, 16.3% had had cancer in the last 5 years; 15.7% suffered from heart failure, 28% had ischemic heart disease, 24.8% suffered from atrial fibrillation, more than one in ten were also obese,

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They should put signs at the airports: “Welcome To Guinea Pig Nation”.

CDC Recommends Vaccines for 5 to 11-year-olds, Jabs Start Tomorrow (CTH)

Center for Disease Control (CDC) Director Rochelle P. Walensky has given the authorization for vaccinations to begin in 5 to 11-year-olds starting tomorrow. You can review the CDC press release HERE. According to the CDC announcement, Walensky states: “We know millions of parents are eager to get their children vaccinated and with this decision, we now have recommended that about 28 million children receive a COVID-19 vaccine.” Unfortunately, the CDC authorization now gives cover to various blue state democrats who will likely mandate COVID-19 vaccinations for public school children. However, despite the CDC position, it is worth noting the recent survey by NBC showing only 27% of parents would vaccinate their kids under 12:


… 64% of people with children under age 11 say they would not vaccinate their kids or would wait to see more data on long term consequences. Only 27% of respondents said they would immediately vaccinate their children with the untested COVID vaccine. (more) It is very reasonable for parents to question the FDA approval and the political intents of the CDC in authorizing this vaccination for children 3 to 11. The risk to children from the virus itself is virtually nonexistent. However, despite the low risk the government is recommending, perhaps soon to be mandating, a little tested vaccine for a population that is not at any significant level of health risk. If the Virginia election result teaches the Biden administration that protecting kids is important to parents on the issue of education…. they haven’t seen anything yet, when it comes to the response from parents to vaccinating kids with an untested vaccine. Madness.

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So we change the definition. If anyone asks, it’s because of The Science. Any more questions, ask Fauci.

CDC Emails: Our Definition of Vaccine is “Problematic” (Techno Fog)

The CDC caused an uproar in early September 2021, after it changed its definitions of “vaccination” and “vaccine.” For years, the CDC had set definitions for vaccination/vaccine that discussed immunity. This all changed on September 1, 2021. The prior CDC Definitions of Vaccine and Vaccination (August 26, 2021): • Vaccine: A product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease. Vaccines are usually administered through needle injections, but can also be administered by mouth or sprayed into the nose. • Vaccination: The act of introducing a vaccine into the body to produce immunity to a specific disease.

The CDC Definitions of Vaccine and Vaccination since September 1, 2021: • Vaccine: A preparation that is used to stimulate the body’s immune response against diseases. Vaccines are usually administered through needle injections, but some can be administered by mouth or sprayed into the nose. • Vaccination: The act of introducing a vaccine into the body to produce protection from a specific disease. People noticed. Representative Thomas Massie was among the first to discuss the change, noting the definition went from “immunity” to “protection”.

To many observers, it appeared the CDC changed the definitions because of the waning effectiveness of the COVID-19 vaccines. For example, the effectiveness of the Pfizer vaccine falls over time, with an Israeli study reported in August 2021 as showing the vaccine being “only 16% effective against symptomatic infection for those individuals who had two doses of the shot back in January.” The CDC recognizes the waning effectiveness, thus explaining their promotion of booster shots.

Of course, the usual suspects defended the CDC. The Washington Post, for example, cast doubt that the CDC changed the definition because of issues with the COVID-19 vaccines. The CDC tried to downplay the change, stating “slight changes in wording over time … haven’t impacted the overall definition.”

CDC emails we obtained via the Freedom of Information Act reveal CDC worries with how the performance of the COVID-19 vaccines didn’t match the CDC’s own definition of “vaccine”/“vaccination”. The CDC’s Ministry of Truth went hard at work in the face of legitimate public questions on this issue.

In one August 2021 e-mail, a CDC employee cited to complaints that “Right-wing covid-19 deniers are using your ‘vaccine’ definition to argue that mRNA vaccines are not vaccines…”

After taking some suggestions, the CDC’s Lead Health Communication Specialist went up the food chain to propose changes to the definitions: “I need to update this page Immunization Basics | CDC since these definitions are outdated and being used by some to say COVID-19 vaccines are not vaccines per CDC’s own definition.”

Getting no response, there was a follow-up e-mail a week later: “The definition of vaccine we have posted is problematic and people are using it to claim the COVID-19 vaccine is not a vaccine based on our own definition.”

The change of the “vaccination” definition was eventually approved on August 31. The next day, on September 1, they approved the change to the “vaccine” definition from discussing immunity to protection (seen below).

There you have it. Affirmative action for the multinational corporations. Why have them improve their vaccines when you can just change the definition of vaccine to fit their ineffective vaccines?

Read more …

From the British Medical Journal.

Researcher Fingers Data Integrity Issues In Pfizer’s Vaccine Trial (BMJ)

In autumn 2020 Pfizer’s chairman and chief executive, Albert Bourla, released an open letter to the billions of people around the world who were investing their hopes in a safe and effective covid-19 vaccine to end the pandemic. “As I’ve said before, we are operating at the speed of science,” Bourla wrote, explaining to the public when they could expect a Pfizer vaccine to be authorised in the United States. But, for researchers who were testing Pfizer’s vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety. A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial.

Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails. On its website Ventavia calls itself the largest privately owned clinical research company in Texas and lists many awards it has won for its contract work. But Jackson has told The BMJ that, during the two weeks she was employed at Ventavia in September 2020, she repeatedly informed her superiors of poor laboratory management, patient safety concerns, and data integrity issues.

Jackson was a trained clinical trial auditor who previously held a director of operations position and came to Ventavia with more than 15 years’ experience in clinical research coordination and management. Exasperated that Ventavia was not dealing with the problems, Jackson documented several matters late one night, taking photos on her mobile phone. One photo, provided to The BMJ, showed needles discarded in a plastic biohazard bag instead of a sharps container box. Another showed vaccine packaging materials with trial participants’ identification numbers written on them left out in the open, potentially unblinding participants. Ventavia executives later questioned Jackson for taking the photos. Early and inadvertent unblinding may have occurred on a far wider scale.

According to the trial’s design, unblinded staff were responsible for preparing and administering the study drug (Pfizer’s vaccine or a placebo). This was to be done to preserve the blinding of trial participants and all other site staff, including the principal investigator. However, at Ventavia, Jackson told The BMJ that drug assignment confirmation printouts were being left in participants’ charts, accessible to blinded personnel. As a corrective action taken in September, two months into trial recruitment and with around 1000 participants already enrolled, quality assurance checklists were updated with instructions for staff to remove drug assignments from charts. In a recording of a meeting in late September2020 between Jackson and two directors a Ventavia executive can be heard explaining that the company wasn’t able to quantify the types and number of errors they were finding when examining the trial paperwork for quality control. “In my mind, it’s something new every day,” a Ventavia executive says. “We know that it’s significant.”

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Just wait till the 5-11 numbers come in.

Dr. Paul Offit Is Lying To Us About Myocarditis Rates (Steve Kirsch)

The New York Times recently reported that Dr. Paul Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia and member of the FDA outside advisory committee for vaccines, said that COVID-19 is much more likely to cause myocarditis than the vaccine. He’s lying. It’s the exact opposite. The FDA and CDC committee members are all misinformed and clueless just like our friend Paul. We know that because hospitals are filling up with kids who are vaccine injured. That never happened before we had vaccine rollouts for kids. But you don’t have to believe me because now the proof is in plain sight thanks to one slide Pfizer mistakenly showed at the last FDA meeting. All my data sources for this proof are the CDC and The NY Times and that one Pfizer slide.

[..] Let’s look at 16 year old boys so we can compute some concrete numbers using trusted data sources to see if Offit’s myocarditis claim is true or false. We use a COVID catch rate of 37 cases per 100,000 per week. We use a myocarditis incident rate of 2.3%. Both numbers are from the NY Times. So multiplying that out for 6 months (which is 24 weeks) we get 37*24*.023=20.4 cases per 100,000 in 6 months or 204 case per million over 6 months. Easy peasy. Here are the screen shots from the two NY Times articles to save you some time:


For the Pfizer vaccine, we have 76.7 cases per million vaccinated male teens from John Su’s chart (see slide 13). This is caused by the vaccine and the vaccines last 6 months so it’s a total amount over 6 months. Just 77 cases per million over 6 months. This is a very conservative estimate since it is based only on reports in the first 7 days and we know these myocarditis cases can show up much later than the first 7 days.

Here’s the slide from the Pfizer presentation at the October 26, 2021 VRBPAC meeting. This slide shows, without a doubt, that VAERS is underreporting myocarditis cases by at least a factor of 5. Now as we’ve said before, VAERS is underreported by more than 41, but that would require you believe me. For this one, you do not have to believe me at all. You just look at Pfizer’s slide and compare 22 with 106:

So now instead of 204>77, we have to multiply the right side by at least 5 since we now have a reference that shows definitively that VAERS is at least 5X under reported. 77*5 is 385. And 385 > 204. Which means that you are worse off taking the vaccine, which is exactly the opposite of what Dr. Offit claimed. So there you have it.

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Jim Crow.

German Companies Creating Segregated Canteens For Vaxxed and Unvaxxed (SN)

Major companies in Germany are segregating their employees by creating canteens for vaccinated people and separate areas for the unvaccinated, who will be forced to continue to follow social distancing and mask mandates. Pharmaceuticals giant Bayer, energy company Eon, and travel company Alltours are all set to impose the new rules, which will see the unvaccinated treated like second class citizens. “In the ‘2G’ areas for vaccinated and recovered people, employees would be allowed to eat together under completely normal conditions, while those who are not vaccinated or do not provide information about their vaccination status would have to continue to live with rules on social distancing, mask wearing and partitions during meals,” reports the Local.

Bayer also announced that its employees have also started forming work groups that “exclude unvaccinated staff.” People visiting Christmas markets in Berlin who haven’t been vaccinated will also be denied entry. As we previously highlighted, despite facing brazen discrimination, 90 per cent of Germans who haven’t had the vaccine say they have no plans to get it in the near future. As we highlighted back in January, German authorities announced that COVID lockdown rulebreakers would be arrested and detained in refugee camps located across the country. Earlier this summer it was also confirmed that the unvaccinated would be deprived of basic lifestyle activities like visiting cinemas and restaurants.

The editor-in-chief of Germany’s top newspaper Bild shocked some people by apologizing for the news outlet’s fear-driven coverage of COVID, specifically to children who were told “that they were going to murder their grandma.” During a meeting with other world leaders in Rome, Angela Merkel engaged in COVID security theater by briefly wearing a mask when she exited her vehicle, only to remove it as soon as she entered the building.

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Google translate.

The Disaster That Never Came (Anderberg)

It’s almost hard to remember it now, but for most of 2020, the word ‘experiment’ had a negative connotation. It was one that we Swedes were exposed to, when we – compared to the rest of the world – maintained some form of normality. This experiment was condemned by the outside world early on as “a disaster” (Time Magazine), a “moral history” (New York Times), “deadly folly” (The Guardian) and so on. The more influential a newspaper was, the stronger the invective seemed to become. In Germany, Focus called it all “laxity”, Italian La Repubblica said that “the Nordic model country” made a dangerous mistake. That’s what it looked like. The description of the Swedish line as an experiment was not really wrong. In both theory and practice, Swedes lived very differently compared to, above all, Americans and other Europeans.

One could object that it was Italy, France, Germany, the United States, the United Kingdom and the other countries that were conducting an experiment, that they were testing completely new ways to prevent the spread of a virus. But the word choice is less important. It is clear that Sweden chose one path, the rest of Europe another. One could see it as if the outside world formulated a hypothesis. It was that freedom in Sweden would be costly. The absence of restrictions, the open schools, the reliance on recommendations in violation of laws and police interventions, would result in higher death rates than in other countries. And – consequently – that the freedom that the citizens of the other countries experienced would save lives.Many Swedes agreed with that hypothesis.

“Shut down Sweden to protect Sweden,” wrote Dagens Nyheter’s Peter Wolodarski, who in his double power of both opinion leaders and head of Sweden’s most influential newsroom, must be described as the country’s most powerful journalist. He was far from alone in demanding a tougher grip. Renowned infection control experts, microbiologists, epidemiologists – from all over the country were warned of the consequences. Researchers from Uppsala University, Karolinska Institutet and the Royal Institute of Technology in Stockholm connected supercomputers and calculated that 96,000 Swedes would die before the summer of 2020. At this time , it was not an unreasonable theory that Swedish freedom was expensive. In the US, with its powerful shutdowns, the death toll – measured per capita – was significantly lower than in Sweden throughout the spring of 2020. And on the sites where the ravages of the pandemic could be followed in real time [..] it was clear that Sweden had higher death rates than most other countries.

But the experiment continued. During the year that followed, the virus ravaged the world and several of the shut down countries now passed Sweden’s death toll – one by one. Great Britain, USA, France, Poland, Portugal, Czech Republic, Hungary, Spain, Argentina, Belgium – countries that blocked playgrounds, forced their children to wear mouth guards, closed schools, fined citizens for hanging on the beach, guarded parks with drones – all have they been hit worse than Sweden. At the time of writing, over 50 countries have a higher proportion of deaths in covid. If you measure excess mortality for the whole of 2020, Sweden, according to Eurostat, will end up in 21st place out of 31 European countries.

Read more …

 

 

 

 

 

Ithaka

 

 

Mullis

 

 

 

 

Support the Automatic Earth in virustime; donate with Paypal, Bitcoin and Patreon.

 

Oct 262021
 


M. C. Escher Relativity Lattice 1953

 

Who Will They Blame When Everyone is Vaccinated?
Concerns About Suboptimal Vaccine Antibodies Erasing Natural Immunity (Blaze)
Informed Consent Disclosure To Vaccine Trial Subjects (NIH)
Why Won’t The CDC or FDA Reveal The VAERS URF? (Kirsch)
200,000 Grannies, No Problem. A Few Puppies? (Denninger)
Consider the Lowly Sandflies (Kunstler)
The Age of Exterminations (VI): The Great Famine to Come (Ugo Bardi)
Biden’s “C’mon, Man” Defense Will Not Fly on Religious Freedom (Turley)
Hertz Orders 100,000 Teslas For Rental Cars (Byte)
‘Unthinkable’ For High Court To Lift US Extradition Ban On Julian Assange (DM)
Allegation Of CIA Murder Plot Game-changer In Assange Extradition Hearing (R.)
A Guide To The US Appeal In The Assange Extradition Case (Gosztola)

 

 

 

 

 

 

Scott Jensen
https://twitter.com/i/status/1452753030391246854

 

 

They will always find a witch to burn, or drown.

Problem is, how are we going to tell the vaxxed that they are in grave danger?

Who Will They Blame When Everyone is Vaccinated?

A question we have been asking for several months: Who are the political officials going to blame for rising COVID infection and hospitalization rates when the vaccination rates are well over 90 percent? What happens on a sociological scale when a vaxxed society realizes there is no magic panacea afforded by the vaccination narrative? Author Jack Cashill takes those questions head-on in a Spectator article noting we only need to look at Waterford, Ireland, to see the dynamic where an almost completely obedient and vaccinated population of 99.7% is facing rising COVID infection rates despite their good citizenship:


Cashill – […] “The arbitrary evolution of Irish COVID policy over the past 18 months has made it clear that public health officials and government policy makers have no idea what they are doing. If proof were needed, County Waterford provides it. According to data published on October 21, Waterford City South has the nation’s highest 14-day incidence rate at 1,486 cases per 100,000 and Tramore-Waterford City West has the third highest at 1,122 cases per 100,000. This is despite internal travel bans and the county’s more than 90 percent vaccination rate. Although Waterford is running three times the rate of the nation writ large, Ireland as a whole is not faring particularly well, especially given its draconian restrictions. In the seven days preceding October 21, Ireland reported 2,026 new cases. To put that number in perspective, wide-open Florida had 2,262 cases during that same period with a population more than four times greater than the Irish Republic’s.”

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More vaccines -> More Covid.

Concerns About Suboptimal Vaccine Antibodies Erasing Natural Immunity (Blaze)

In many areas of life, half a loaf is better than no loaf at all. But when it comes to vaccines, the opposite is true. Half-baked antibodies injected throughout the entire population can make the virus even stronger and negate people’s natural immunity. Thus, all the defenses of the leaky vaccine suggesting that it at least conveys “some” protection are actually extremely concerning, a point driven home by a nugget in the most recent surveillance report from Public Health England (PHE). On page 23 of PHE’s “COVID-19 vaccine surveillance report Week 42,” British health officials report a shocking finding. They believe their serology tests are underestimating the number of people with prior infection due to “recent observations from UK Health Security Agency (UKHSA) surveillance data that N antibody levels appear to be lower in individuals who acquire infection following 2 doses of vaccination.”

In other words, the vaccine might be reducing the all-important N antibodies that one generates from natural infection. Kudos to former NYT reporter Alex Berenson for discovering this important point. Until now, we’ve been operating under the assumption that those with prior infection don’t need the vaccine to boost immunity and taking the shots would only expose them to the growing risk of side effects. However, what if the shots are actually sliding back the natural immunity generated in those with previous infection? What if that is related to the macro concern that a narrow-spectrum vaccine with suboptimal antibodies that only recognize the “S” (spike) protein of the virus but not the “N” (nucleocapsid) of the virus will cause B cells in those with the vaccine to learn to produce only S antibodies, which are slower-acting and less sterilizing (don’t stop transmission) than N antibodies, which are faster-acting and are more effective in their protection against the virus?

It’s not like we weren’t confronted with some other warning signs that the vaccine could perhaps negate some of the immunity acquired from prior infection. In March, researchers from Mount Sinai in New York and Hospital La Paz in Madrid posted a preprint study indicating that at least the second Pfizer shot might weaken T cell immunity. In a shocking discovery after monitoring a group of vaccinated people both with and without prior infection, they found “in individuals with a pre-existing immunity against SARS-CoV-2, the second vaccine dose not only fail to boost humoral immunity but determines a contraction of the spike-specific T cell response.” They also note that other research has shown “the second vaccination dose appears to exert a detrimental effect in the overall magnitude of the spike-specific humoral response in COVID-19 recovered individuals.”

Thus, mass vaccinating with leaky suboptimal antibody production could serve as a Trojan horse and make people more susceptible to an ever-enhanced virus. It’s not like we had no warning about the possibility of viral enhancement through waning and suboptimal vaccine-mediated antibodies. On page 52 of Pfizer’s “Emergency Use Authorization (EUA) for an Unapproved Product Review Memorandum,” it is admitted that antibody dependent disease enhancement was a possibility in the long run with waning efficacy. “However, risk of vaccine-enhanced disease over time, potentially associated with waning immunity, remains unknown and needs to be evaluated further in ongoing clinical trials and in observational studies that could be conducted following authorization and/or licensure,” write the FDA regulators in the memo.

[..] According to PHE data, 86% of all U.K. residents over age 12 have received at least one shot, including nearly everyone in a vulnerable age bracket. Yet the summer and early fall curve, as presented by Worldometer, has blown out the magnitude of the case curve last year when nobody was vaccinated, and the daily numbers are reaching close to their winter peak.

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Vaccines killing off antibodies is not a new idea. This is from March 2021.

“Informed consent disclosure to vaccine trial subjects of risk of COVID-19 vaccines worsening clinical disease.”

Informed Consent Disclosure To Vaccine Trial Subjects (NIH)

Aims of the study: Patient comprehension is a critical part of meeting medical ethics standards of informed consent in study designs. The aim of the study was to determine if sufficient literature exists to require clinicians to disclose the specific risk that COVID-19 vaccines could worsen disease upon exposure to challenge or circulating virus.

Methods used to conduct the study: Published literature was reviewed to identify preclinical and clinical evidence that COVID-19 vaccines could worsen disease upon exposure to challenge or circulating virus. Clinical trial protocols for COVID-19 vaccines were reviewed to determine if risks were properly disclosed.

Results of the study: COVID-19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved, and the data generated in the development and testing of these vaccines suggest a serious mechanistic concern: that vaccines designed empirically using the traditional approach (consisting of the unmodified or minimally modified coronavirus viral spike to elicit neutralising antibodies), be they composed of protein, viral vector, DNA or RNA and irrespective of delivery method, may worsen COVID-19 disease via antibody-dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID-19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials.

Conclusions drawn from the study and clinical implications: The specific and significant COVID-19 risk of ADE should have been and should be prominently and independently disclosed to research subjects currently in vaccine trials, as well as those being recruited for the trials and future patients after vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent.

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Steve keeps pushing.

Why Won’t The CDC or FDA Reveal The VAERS URF? (Kirsch)

VAERS is the Vaccine Adverse Event Reporting System. It is the official system relied upon by the FDA and CDC for adverse event tracking. For example, if you report an adverse event in V-Safe, the app they told you about when you got vaccinated, you are told to file a VAERS report. It is essentially the mother of all adverse event reporting systems for vaccine events in the US. There is nothing more comprehensive than VAERS. The most important thing to know about VAERS is that it is always underreported. This is widely known. To properly interpret any safety data, you must know the underreporting factor (URF). For example, the famous Lazarus report estimated the VAERS URF to be over 100:

“Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA). Likewise, fewer than 1% of vaccine adverse events are reported. Low reporting rates preclude or slow the identification of “problem” drugs and vaccines that endanger public health.” The Baker paper, Advanced Clinical Decision Support for Vaccine Adverse Event Detection and Reporting, showed that “the odds of a VAERS report submission during the implementation period were 30.2 (95% confidence interval, 9.52–95.5).” In other words, the VAERS URF was at least 30 (since the system wasn’t perfect, 30 is a lower bound of the URF in that study), but they estimated that it was likely between 9.5 and 95.

The URF is normally calculated for very serious events since these are required to be reported for all vaccines by healthcare workers. That URF can then be applied to less serious events to create a conservative estimate of the true incidence rate (since less serious events would have a higher URF). The method for calculating the URF is well known. Sadly, the CDC has erroneously assumed that Vaccine Safety Datalink represents a fully reported comparator. This is clearly false as can be seen from slide 13 in ACIP Chair Grace Lee’s presentation delivered on August 30, 2021:

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“Fauci slaughtered tens of thousands of AIDS sufferers by blocking Bactrim in HIV+ persons for years, arguing he needed “controlled trials” first to “prove” that it worked to prevent PCP.”

“.. in the case of HIV it was AZT. This time its intentionally falsely labeled drugs that are called “vaccines” yet are not, along with a new drug from Merck that may be even more dangerous than the jabs.”

200,000 Grannies, No Problem. A Few Puppies? (Denninger)

If you want to know why God is sipping on a cold one and laughing at the evil in our nation and indeed the world you need nothing more. Fauci slaughtered tens of thousands of AIDS sufferers by blocking Bactrim in HIV+ persons for years, arguing he needed “controlled trials” first to “prove” that it worked to prevent PCP. We already knew it did, by the way, having learned that in the late 1970s with Leukemia patients — it cut the mortality rate of people with Leukemia during chemo by a huge amount. Fauci claimed that wasn’t good enough. 30,000, roughly, Americans got shoved in the hole, dead from PCP, as a result. This time around Fauci proclaimed that we had “insufficient evidence” to recommend that people use HCQ, Ivermectin, Budesonide and a whole host of other things at first indication of Covid-19.

The answer was “vaccines”, which did not exist for 11 months, and were not rolled out in size for a full year. In both cases pharmaceutical companies made billions; in the case of HIV it was AZT. This time its intentionally falsely labeled drugs that are called “vaccines” yet are not, along with a new drug from Merck that may be even more dangerous than the jabs. Two hundred thousand Grannies and Grandpas, mostly, died during the last 18 months without even being able to say goodbye to their loved ones, having been denied drugs that might have worked and might not have — but which were almost certainly better than being dead. If they did nothing, so what? Dead is dead, right? Well, neither Ivermectin or Budesonide killed me. I used both when I got Covid in August.

I do not know if Ivermectin appreciably impacted the course of the disease because I hit it early and hard and thus perhaps it did nothing (hard to prove otherwise, isn’t it?) but the budesonide reversed symptom progression within 12 hours of initiation of use. I cannot attribute that change to mere chance. Is it proof? No. But do I believe it worked? You bet. And I’m still here; neither killed me, nor did either do any harm I can detect (nor did the virus itself) to my cardiopulmonary function from pre-infection baseline. Will any of these drugs work for everyone? Nope. Does vaccination? Nope.

St. Elizabeth’s, as of 10/22, makes quite clear that people winding up in the hospital, ICU or with a tube down their throat on a vent happens all the time in fully-vaccinated people. None of that is “rare” and, I remind you, this is a major hospital chain all over NE KY along with a couple of other states. Do the jabs “reduce the risk”? Probably. Do they work as well as using drugs at first hint of trouble? Since these “breakthroughs” that land people in the hospital, ICU or on a vent are hardly RARE — they’re extraordinarily common despite the lies the media, CDC and other hospitals have told — I maintain that I made the correct choice as I did not wind up in a hospital at all and now I have presumptive immunity that actually works unlike these “jabs” which, on the data certainly appear to NOT.

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“Dr. Fauci is ever more emblematic of the American predicament: maniacs and doofuses in charge of powerful institutions strategically positioned to wreck the country.”

Consider the Lowly Sandflies (Kunstler)

Some flinched when Dr. Fauci commanded the children of America to take the mRNA shots fraught with deadly side effects, but now it’s out that the agency he has controlled for decades like a Byzantine despot, the NIAD, gave a $1.6 million grant to a lab in Tunisia — that world-beating center of the bio-sciences — to study what happens when puppy-dogs are pinned down so that ravenous sandflies can chew their snouts off. I guess it didn’t go to well for the puppies. (And doesn’t one wonder exactly what was learned doing that?) We are not Tunisia, of course, at least not yet. We are the mighty USA, a nation imbued with the moral spirit of Walt Disney, and for us this puppy-dog caper might just be an experiment-too-far.

We’ll have to stand by months, maybe years, to find out what the effects are of mRNA shots in human children, but two known possibilities stand out: inflammation and scarring of the heart (myocarditis + sequelae), and an incrementally disabled immune system. Do you really want those shots in your children? — America might ask. And how does Dr. Fauci imagine the child vaxx program would be carried out? In the schools, I suppose, where the subjects of the experiment can be conveniently rounded-up every day. Would you suppose that roughly half the parents in the land would then withdraw their kids from the public school system and, if so, what becomes of the system when they’re gone? Not anything good, I promise you.

But consider that it is already a rotten system ever more incapable of turning out citizens who can speak English, write a coherent sentence, and add up a column of figures, let alone name the capital of Tunisia (warning: trick question!). Dr. Fauci is ever more emblematic of the American predicament: maniacs and doofuses in charge of powerful institutions strategically positioned to wreck the country. For now, they strangely enjoy protection within this matrix of captive institutions while carrying out their nefarious missions. So, the question arises: do Americans wish to live in a wrecked country?

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Seneca.

The Age of Exterminations (VI): The Great Famine to Come (Ugo Bardi)

Note how, in the calculation, the world population decline starts around 2050, some three decades after the start of the crash of the industrial and agricultural systems. Why is it that the population keeps growing while people are starving? Unlikely, to say the least. It is hard to quantify people’s intention to have children or not have them, so the modelers used past data on birthrates as a function of the gross domestic product (GDP). It was equivalent to “running in reverse” the demographic transition that took place in the 1960s when natality had collapsed in many regions of the world in parallel with an increase of the GDP per capita. The result was that a contraction of the GDP would cause people to have more children? These assumptions were later reconsidered and different results were obtained in 2004.

Now, the population starts declining around 2030, less than a decade after that food production starts collapsing, and that looks much more reasonable. Yet, even this curve has problems: would you really believe that in the midst of the great turmoil of the global collapse the result would be such a gentle decline? More likely, all the four horsemen of the apocalypse would enter the game and generate a disastrous general crash. This is called the “Seneca Effect.” You see the typical shape of the Seneca Curve in the figure: decline is much faster than growth. Models such as the one used for the “Limits to Growth” cannot reproduce a really sharp Seneca Curve because they do not consider the many possible “tipping points” that may affect the world system. But the historical data tell us that the Seneca shape is the typical behavior of population collapses. Here is the example of the data for the great famine in Ireland (From Ugo Bardi’s book “The Seneca Effect.”) You can clearly see the “Seneca Shape” of the curve, with a sharp decline following growth.

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“..the federal government must show that the burden imposed furthers a “compelling governmental interest” and is “the least restrictive means” of furthering that interest.”

Biden’s “C’mon, Man” Defense Will Not Fly on Religious Freedom (Turley)

“Come on, man,” seems to be President Biden’s signature response to any uncomfortable question. The phrase is meant to be both dismissive and conclusive in ending inquiries, frequently used to counter reporters before often walking away. Indeed, it is so often repeated that it appears on T-Shirts or coffee mugs and in remixes. This week, however, it was not the pesky press but freedom itself that got hit with a version of the comeback. When asked during a CNN town hall program about those still objecting to taking COVID vaccines, Biden mocked them and their claimed rights with “Come on, ‘freedom.’ ” He then called for any police officers, firefighters, medical personnel or other first responders to be fired en masse if they refuse to be vaccinated.

Biden’s response to the question was applauded by the CNN audience, as if to say “Freedomm Ptff, that is so last century.” And he reduced any vaccine refusals to claiming “I have the freedom to kill you with my COVID.” He is not alone in such rhetoric. Chicago’s Mayor Lori Lightfoot declared that police officers refusing to take vaccines are insurrectionists. The problem is that the courts already recognize some religious exemption arguments. Those arguments are based on both the constitutional protection of religious values but also laws like Title VII of the Civil Rights Act, 42 U.S.C. §2000e-2(a), which declares unlawful any “employment practice for an employer … to fail or refuse to hire or to discharge any individual, or otherwise to discriminate against any individual with respect to his compensation, terms, conditions, or privileges of employment because of such individual’s … religion.”

The federal government also is subject to the Religious Freedom Restoration Act (RFRA), which prohibits the government and other covered entities like the District of Columbia from “substantially burden[ing]” a person’s exercise of religion. Under RFRA, there is no “Come on, man,” defense. Instead, the federal government must show that the burden imposed furthers a “compelling governmental interest” and is “the least restrictive means” of furthering that interest. There is a move in many states to refuse to allow such exemptions, but courts have pushed back. In New York, the state is appealing a preliminary injunction against its refusal to allow religious exemptions to its vaccine mandate. A lower court found the governor’s mandate “has effectively foreclosed the pathway to seeking a religious accommodation that is guaranteed under Title VII.”

Likewise, the Sixth Circuit Court of Appeals this month affirmed such a preliminary injunction against Western Michigan University. The university allowed students to ask for individual exemptions but failed to grant religious exemptions under its discretionary policy.

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“The deal caused Tesla’s market valuation to hit the $1 trillion mark.”

“It’s a striking decision given that Hertz filed for bankruptcy last year..”

Hertz Orders 100,000 Teslas For Rental Cars (Byte)

Rental car company Hertz has ordered 100,000 Tesla Model 3s as part of a massive push to electrify its fleet — the largest purchase of electric vehicles ever, according to Bloomberg. It’s a massive deal reportedly worth $4.2 billion, pushing the automaker’s valuation past the $1 trillion mark for the first time ever. Shares were just two dollars shy of reaching the $1,000 mark on Monday, a new record for the Elon Musk-led company. Musk’s own net value soared in response to the news as well, crossing the quarter trillion mark. “Electric vehicles are now mainstream, and we’ve only just begun to see rising global demand and interest,” Hertz interim CEO Mark Fields told Reuters.


It’s a striking decision given that Hertz filed for bankruptcy last year as a result of the COVID-19 pandemic. But the company’s market value has recovered, Bloomberg reports. Even more so, it’s a major win for Tesla, giving vast numbers of potential customers a first-hand look at the electric carmaker’s offerings when they travel. Bloomberg reports that Hertz is hoping to push maintenance and refueling costs down by switching to electric cars, as well as planning to build out a customers-only charger network. To celebrate the deal, Hertz hired quarterback celeb Tom Brady for a cheesy ad, showing off its new Tesla fleet. Now, the ball is in Tesla’s court to deliver the vehicles. “There is quite an execution journey ahead of us,” Tesla CFO Zachary Kirkhorn told Reuters.

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“‘It would be such a stain on the system in this country that I certainly hope there will be enough pressure and realisation of how devastating it would be for this country ..”

‘Unthinkable’ For High Court To Lift US Extradition Ban On Julian Assange (DM)

The editor-in chief of WikiLeaks believes it would be ‘unthinkable’ for the High Court to lift a US extradition ban on website founder Julian Assange. Speaking ahead of a crunch hearing at the High Court this week, Kristinn Hrafnsson said would be ‘totally unacceptable’ for judges to overturn a decision blocking the extradition of the Australian activist. The High Court is due to hear an appeal this week against a January decision not to extradite the 50-year-old to face charges relating to WikiLeaks’ publication of secret military files due to concerns that he would be a suicide risk in a US prison. And Mr Hrafnsson told a press briefing in London on Monday: ‘It is unthinkable that the High Court will come to any other decision but to uphold the magistrates’ court decision. Anything else is totally unacceptable.


‘It would be such a stain on the system in this country that I certainly hope there will be enough pressure and realisation of how devastating it would be for this country if somehow the judge comes to the decision of reversing the magistrates’ court decision.’ The briefing panel, which also included Mr Assange’s lawyer and partner Stella Moris and director of international campaigns at Reporters Without Borders (RSF) Rebecca Vincent, said the forthcoming hearing follows an investigation, published by Yahoo News, which alleged plots to abduct or kill Mr Assange. A security firm, under investigation in Madrid, is also alleged to have spied on Mr Assange on behalf of the CIA while he was in the Ecuadorian embassy in London and been part of the alleged plot. Ms Moris said: ‘This is a game-changer going into the appeal because it shows the true nature, the true origins, the true criminality of the US actions against Julian and it completely taints any semblance of legality of this appeal going into it.’

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It certainly should be.

Allegation Of CIA Murder Plot Game-changer In Assange Extradition Hearing (R.)

The partner of Julian Assange said on Monday a media report that the CIA had plotted to kill or kidnap the WikiLeaks founder was a game-changer in his fight against extradition from Britain to the United States. U.S. authorities will this week begin their appeal against a British judge’s refusal to extradite Assange – who is wanted on 18 criminal charges including breaking a spying law – because his mental health problems meant he would be at risk of suicide. Last month, Yahoo News reported CIA officials had drawn up options for former U.S. President Donald Trump’s administration for dealing with Assange while he was holed up in the Ecuadorean embassy in London, including assassinating or kidnapping him.

[..] “This (Yahoo report) is a game changer going into the appeal because it shows the true nature, the true origins, the true criminality of the U.S. actions against Julian,” his fiancee Stella Moris, with whom Assange has had two children, told reporters. WikiLeaks came to prominence when it began to publish thousands of secret classified files and diplomatic cables in 2010. Soon afterwards Sweden sought Assange’s extradition from Britain over allegations of sex crimes. When he lost that case against extradition in 2012, he fled to the Ecuadorean embassy. He was finally dragged out from the embassy in April 2019 and jailed for breaching British bail conditions, although the Swedish case against him had already been dropped.

U.S. authorities then sought his extradition. Although the British judge on Jan. 4 rejected Assange’s arguments that the case was political and an assault on freedom of speech, Moris said there was a real risk that, if found guilty, he would be held in a maximum security prison in almost total isolation. That would lead him to attempting suicide, Moris concluded. U.S. lawyers aim to challenge the ruling against U.S. extradition and the evidence given by a key expert at a two-day High Court appeal hearing in London starting on Wednesday. No result is immediately expected, and Moris said the process could be fast, with Assange extradited by next summer, or it could take years. “Both prospects are terrifying,” she said. Currently, Assange is being held at London’s top security Belmarsh Prison where Moris visited him on Saturday, saying he looked very thin. “He was looking very unwell,” she said.

Read more …

Kevin Gosztola spells it all out.

A Guide To The US Appeal In The Assange Extradition Case (Gosztola)

On October 27, the High Court of Justice in the United Kingdom will hear the Crown Prosecution Service argue on behalf of the United States government that a lower court improperly blocked the U.S. from extraditing WikiLeaks founder Julian Assange. The proceedings in London are expected to last two days and will involve five grounds for appeal that were previously approved by the High Court of Justice. (Two were reinstated by the court after a hearing on August 11.) District Court Judge Vanessa Baraitser ruled on January 4 that Assange’s mental health was such that it would be “oppressive to extradite him” to the U.S. But two days later, she accepted the U.S. government’s objections and ordered him to remain in jail while her decision was appealed.

Assange is detained at Her Majesty’s Prison Belmarsh in London, a high-security prison where he has been held since he was expelled from the Ecuador Embassy on April 11, 2019. He faces 18 charges—17 of which are charges under the Espionage Act. The Espionage Act is a U.S. law passed in 1917 that the Justice Department has increasingly wielded against media sources who share “classified” documents or talk about sensitive information with journalists. Because Assange is the first publisher to be charged under the law, press freedom organizations around the world have roundly condemned the political prosecution. It also is part of a troubling development where the U.S. government increasingly seeks to impose its domestic laws on foreign nationals. Assange is an Australian citizen and has no ties whatsoever to the United States.

Each of the charges, aside from a conspiracy to commit a computer crime offense, solely relate to the documents that were submitted by U.S. Army whistleblower Chelsea Manning to WikiLeaks in 2010: the Iraq and Afghanistan War Logs, the U.S. State Embassy cables, and the Guantanamo Files. The general allegations in the indictment against Assange directly criminalize the publication of information.

Read more …

 

 

 

 

 

Still eating
https://twitter.com/i/status/1452481253647785996

 

 

 

 

You may have noticed that: 13 x 13 = 169 and 31 x 31 = 961 which makes the two operations true even if read in reverse.
But this is not the only case.

 

 

Support the Automatic Earth in virustime; donate with Paypal, Bitcoin and Patreon.

 

Oct 082021
 
 October 8, 2021  Posted by at 8:58 am Finance Tagged with: , , , , , , ,  56 Responses »


Pablo Picasso Swimming 1908

 

Why Is Pfizer Pushing An Untested Vaccine On Children? (TF)
Judge Orders Gov’t To Provide Evidence To Justify Vaccinating Children (TE)
Moderna: A Company “In Need Of A Hail Mary” (Whitney Webb)
Molnupiravir Was Made Possible By Government-funded Innovation (STAT)
Myocarditis Adverse Events in VAERS (SD)
Stop This NOW (Denninger)
The Cult of the Vaccine Neurotic (Taibbi)
The Problems With Censoring Doctors Over Their COVID-19 Stances (RCS)
Biden Keeps Pushing Nonexistent Worker Vaccine Mandate (CTH)
Poland’s Top Court Rules Polish Law Takes Presedence Over The EU (ZH)
Prosecution Of Alleged WikiLeaks Vault 7 Source Hits Multiple Roadblocks (Y!)

 

 

 

 

Biden speech

 

 

“Boys between 16 and 19 years of age had the highest incidence of myocarditis after the second dose . . . The risk of heart problems in boys of that age was about nine times higher than in unvaccinated boys of the same age.”

Why Is Pfizer Pushing An Untested Vaccine On Children? (TF)

The face of Pfizer – Pfizer board member (and former FDA commissioner) Scott Gottlieb, MD – was on CBS Face the Nation today estimating the upcoming availability of the Pfizer vaccine for kids aged 5-11. His key quote: “The FDA has said the review is going to be a matter of weeks, not months. . . that could give you a vaccine by Halloween.” Perhaps more concerning is the fact that Gottlieb is confident Pfizer will get FDA approval. This concern is based on the questionable safety and effectiveness of the Pfizer vaccine for kids aged 5-11, as well as questions over whether there is a need for an emergency use authorization for that segment of the American population.

Pfizer tested the vaccine on a small sample of “2,268 participants 5 to <12 years of age.” Pfizer concluded that the results demonstrated “strong immune response in this cohort of children one month after the second dose.” Pay attention to that last part: “one month after the second dose.” Is that it – is Pfizer pushing this vaccine on children after just one month of efficacy data? (The benefit of the emergency use authorization – studies can be limited.) By now it’s clear this is Pfizer’s pattern: they say the vaccine’s “duration of protection” is “unknown” while data demonstrates its effectiveness wanes over time. Compare the Comirnaty Fact Sheet to the latest reporting on the Pfizer vaccine: One would rightfully assume that the effectiveness of the vaccine will wane in children as it has done in other populations.

One would also be correct to assume this is the rationale for Pfizer to submit its current (one month) data to the FDA, hoping for approval from its friends in government before its study group shows the vaccine has diminishing returns. All that has to do with effectiveness. Now we get to the question of safety. This has always been a pandemic of the oldest among us. According to CDC data, children aged 5-14 years-old have accounted for only 161 COVID-19 deaths since the start of the pandemic. In comparison, this same group has experienced 194 pneumonia deaths. To put these numbers into perspective, the CDC cites over 530,000 COVID-19 deaths for the ages 65 years and up. As New York Magazine observed, “The Kids Were Safe from COVID the Whole Time.”

Those numbers are important when we start to look at the necessity of a vaccine for kids. As with all vaccines, there is a cost-benefit analysis that must be made: do the benefits of the vaccine outweigh the cost? (This is something the FDA and CDC have drilled to the American public – that the benefits of the vaccines outweigh the costs.) Looking at the data, a 17 year-old teenager might properly disregard the vaccine while a 75 year-old might seriously consider it. This is expected. Considerations of costs and benefits get us to the safety of the vaccine for kids aged 5-12. Pfizer proudly announces the vaccine’s side effects for 5-12 year olds is “generally comparable to those observed in participants 16 to 25 years of age.” That’s not good. If you’ve been paying attention, you know why those numbers (ages 16-25) matter. It’s because young people – especially young men – in that age range have an increased risk of developing heart problems after the second Pfizer dose. The younger they are, the greater the risk: “Boys between 16 and 19 years of age had the highest incidence of myocarditis after the second dose . . . The risk of heart problems in boys of that age was about nine times higher than in unvaccinated boys of the same age.”

Read more …

“..since teens over the age of 15 had been given the Covid-19 vaccine deaths among the age group had increased by 47%..”

Judge Orders Gov’t To Provide Evidence To Justify Vaccinating Children (TE)

A Judge has ordered the UK Goverment to submit evidence that justifies Covid-19 vaccination of children, giving them a deadline of Monday 11th October. The order from The Hon. Mr Justice Jay is most welcome after we exclusively revealed Thursday 30th September that since teens over the age of 15 had been given the Covid-19 vaccine deaths among the age group had increased by 47% compared to the same period in 2020. We also then delved back into the Office for National Statistics data due to a suspicion we would find the majority of those deaths had been among teenage boys due to the risk of myocardtis, inflammation of the heart muscle, associated with the Pfizer vaccine and mainly occurring in younger males, as well as a correlation with a rise in emergency calls requesting an ambulance due to cardiac arrest, found in Public Health England data.

Unfortunately our fears were confirmed, as we exclusively revealed on Monday 4th October that deaths among teenage boys have increased by 63% in the UK since they started getting the Covid-19 vaccine. To add to that we then exclusively revealed on Tuesday 5th October that Chris Whitty’s decision to overrule the Joint Committee on Vaccination and Immunisation and advise the Government to offer the Covid-19 vaccine to all healthy secondary school children, has so far led to a 400% increase in deaths among male children compared to the same period in 2020. (See here) However, people have been fighting in court to overturn the decision of the Chief Medical Officer for England that children should be given an experimental Covid-19 injection, but unfortunately to no avail so far.


The ‘Covid-19 Assembly’ and lawyer Francis Hoar had an application for an urgent hearing to pause the Covid-19 roll-out to under 18’s denied for a second time on September 2nd. The Claimants had asked for just half a day for the Court to listen to oral argument to consider whether to pause the roll out of injections of experimental mRNA vaccine technology, producing increasing reports of clotting and other adverse effects including death, still under emergency authorisation and never before given to humans, to the whole of the healthy population of children aged 12-17. The Court’s view was that to delay consideration of the Claimants’ application for 14 days to allow the government to prepare its response was not in fact a refusal. However, that delay had the practical effect of denying the urgent relief sought and left the full resources and machinery of the state to be put into gear.

Read more …

“..without the approval of its booster, which has caused great controversy even among the country’s top vaccine officials, Moderna faces a massive financial reckoning.”

Moderna: A Company “In Need Of A Hail Mary” (Whitney Webb)

Not only did the COVID-19 crisis obliterate hurdles that had previously prevented Moderna from taking a single product to market, it also dramatically reversed the company’s fortunes. Indeed, from 2016 right up until the emergence of COVID-19, Moderna could barely hold it together, as it was shedding key executives, top talent, and major investors at an alarming rate. Essentially, Moderna’s promise of “revolutionizing” medicine and the remarkable salesmanship and fund-raising capabilities of the company’s top executive, Stéphane Bancel, were the main forces keeping it afloat. In the years leading up to the COVID-19 crisis, Moderna’s promises—despite Bancel’s efforts—rang increasingly hollow, as the company’s long-standing penchant for extreme secrecy meant that—despite nearly a decade in business—it had never been able to definitively prove that it could deliver the “revolution” it had continually assured investors was right around the corner.

This was compounded by major issues with patents held by a hostile competitor that threatened Moderna’s ability to turn a profit on anything it might manage to take to market, as well as major issues with its mRNA delivery system that led them to abandon any treatment that would require more than one dose because of toxicity concerns. The latter issue, though largely forgotten and/or ignored by media today, should be a major topic in the COVID-19 booster debate, given that there is still no evidence that Moderna ever resolved the toxicity issue that arose in multi-dose products.

In this first installment of a two-part series, the dire situation in which Moderna found itself immediately prior to the emergence of COVID-19 is discussed in detail, revealing that Moderna—very much like the now disgraced company Theranos—had long been a house of cards with sky-high valuations completely disconnected from reality. Part 2 will explore how that reality would have come crashing down sometime in 2020 or 2021 were it not for the advent of the COVID-19 crisis and Moderna’s subsequent partnership with the US government and the highly unusual processes involving its vaccine’s development and approval. Despite the emergence of real-world data challenging the claims that Moderna’s COVID-19 vaccine is safe and effective, Moderna’s booster is being rushed through by some governments, while others have recently banned the vaccine’s use in young adults and teens due to safety concerns.

As this two-part series will show, safety concerns about Moderna were known well before the COVID crisis, yet they have been ignored by health authorities and the media during the crisis itself. In addition, in order to stave off collapse, Moderna must keep selling its COVID-19 vaccine for years to come. In other words, without the approval of its booster, which has caused great controversy even among the country’s top vaccine officials, Moderna faces a massive financial reckoning. While the COVID-19 crisis threw the company a lifeboat, the administration of its COVID-19 vaccine, in which the US government has now invested nearly $6 billion, must continue into the foreseeable future for the bailout to be truly successful.

Read more …

Yup, it’s a horse drug. Priceless.

Barron’s behind paywall:
Beware of the new Merck drug: Wall Street Cheered Merck’s Covid Pill. Some Scientists Are Highlighting Its Potential Dangers. Researchers say the drug could integrate itself into patients’ DNA, theoretically leading to cancer. Merck says its tests show that isn’t an issue.

Molnupiravir Was Made Possible By Government-funded Innovation (STAT)

The story behind molnupiravir is intriguing and a testament to government-funded innovation. Molnupiravir, also known as EIDD-2801 or MK-4482, came out of Drug Innovation Ventures at Emory (DRIVE), a not-for-profit LLC owned by Emory University. It had previously demonstrated broad-spectrum activity against other viruses such as influenza, Ebola, and the Venezuelan equine encephalitis virus. The work goes back to 2004, when Emory researchers were studying a related compound known as EIDD-1931/NHC. Before it was tested for Covid-19, EIDD-2801 had accrued millions of dollars of federal funding. In 2019, the National Institute of Allergy and Infectious Diseases (NIAID) gave the Emory Institute for Drug Development a $16 million contract to test the drug for influenza.

It had previously garnered funding from several other NIAID grants, as well as funding from the Defense Threat Reduction Agency (DTRA), as disclosed by Emory. When attention turned to Covid-19, Emory received pledges of more than $30 million from NIAID and the Department of Defense to cover development of the drug. Jumping on an opportunity to develop a promising drug therapy for Covid-19, Ridgeback Biotherapeutics licensed the drug from DRIVE in March 2020. Ridgeback was founded by Wayne and Wendy Holman, both former investment managers. Within just three months, Ridgeback licensed worldwide rights for EIDD-2801 for Covid-19 to Merck, for which Ridgeback received an undisclosed upfront payment plus milestone payments and shared profits.

But before signing on with Merck, Ridgeback had tried to negotiate a deal with the Biomedical Advanced Research and Development Authority (BARDA), one that was specifically mentioned in the explosive whistleblower complaint by Rick Bright, the former director of BARDA. In his complaint, Bright wrote that George Painter, the CEO of the Emory Institute for Drug Development, and Ridgeback cofounder Wendy Holman sought a contract first from ASPR Next and then from BARDA to develop EIDD-2801 for $100 million, and they personally lobbied the authority to get more financial aid. BARDA denied the request due to a lack of adequate documentation for the request. Even before 2020, Bright had been reluctant to give BARDA funding to EIDD-2801, saying they already had $30 million of support from NIAID and the Department of Defense.

Merck eventually backed Ridgeback and took on development of the drug. Molnupiravir then received even more federal funding: In September 2021, BARDA procured 1.7 million courses of the five-day regimen for $1.2 billion, or $700 per treatment course.

Read more …

Exhaustive study by Jessica Rose and Peter McCullough.

Myocarditis Adverse Events in VAERS (SD)

The fact that the VAERS reporting of myocarditis is 6X higher in 15-year-olds following dose 2 may be indicative of a cause-effect relationship. If we assume that following dose 1, a certain percentage of healthy young males who lack co-morbidities or co-factors experience cardiac-related AEs mild enough so as not to dissuade them from receiving dose 2 (ie: pallor, chest pain and shortness of breath, for example), then it is not difficult to imagine that they may have been experiencing symptoms of myocarditis. If a percentage of young males had experienced primary damage to the heart as a result of inflammation following dose 1, then dose 2 may have induced a much more noticeable clinical impact, or cardiac ‘insult’.


In other words, these young males may receive a definitive diagnosis of myocarditis only following dose 2. What this implies, based on these assumptions, is that if there is a causal relationship then it might manifest with overlooked/unreported AEs following dose 1 and a diagnosis of myocarditis following dose 2. It is noteworthy that ‘Vaccine-induced myocarditis’ was in fact used as the descriptor by medical professionals as the reason for the myocarditis in the VAERS database. During phase III clinical trials for the mRNA COVID-19 products, safety was assessed based on a maximum observation period of 6 months. This is not adequate to assess long-term safety outcomes as it is a requirement, even in an accelerated timeline setting, to spend up to 9 months in Phase III trials.

Read more …

Karl’s take on that study.

Stop This NOW (Denninger)

VAERS is known to materially under-report adverse events. We do not know what the multiplication factor for these findings is as a consequence of that. Note that in the context of all prior years this basically never happens statistically. The average over the three previous years associated with any vaccination is four. Further, an extraordinary level of cardiac adverse events are associated with these jabs. This is not uncommon or “rare” as claimed; there are in fact, as of July 9th, nearly 130,000 such reports for Covid-19 jabs. If we accept the CDC’s numbers for the number of Americans jabbed this puts the rate of cardiac adverse events are right around one in a hundred! What’s nasty is that while the myocarditis incidence is skewed heavily toward males under 30 the cardiac incidence is not; it is centered in the 20-70 range, or roughly “right up the middle” for the people in the nation as a whole.

Indeed, given the known under-reporting in VAERS a 1-in-100 incidence for a category of serious adverse events is extraordinarily significant. There is every reason to believe we may be causing cardiac injury to as many as one in 25 people who get these shots! Whether those injuries spontaneously resolve without permanent compromise or worse, degenerate progression is completely unknown as nobody is following up these individual cases to measure blood levels (e.g. troponins, EKGs, etc.) in an attempt to determine whether these events are transient or result in permanent impairment or worse. “The only way to understand how common myocarditis is after COVID-19 vaccination, is to perform a prospective cohort study where all vaccinated individuals undergo clinical assessment, ECG, and troponin measurement at regular intervals post-administration.”

Which is not being done, on purpose. Incidentally the markers indicating potential trouble were present in the original studies. They were not followed up and the reason for not doing is obvious: It would have prevented issuance of the EUAs on the original desired schedule. As a result the firms involved and the FDA deliberately ignored that signal in the original studies and we have now jabbed somewhere around 200 million Americans — and may have screwed as many as several million of them with irreversible, or even worse degenerate cardiac damage. We do not know because we intentionally did not look. “COVID-19 injectable products are novel and have a genetic, pathogenic mechanism of action causing uncontrolled expression of SARS-CoV-2 spike protein within human cells. When you combine this fact with the temporal relationship of AE occurrence and reporting, biological plausibility of cause and effect, and the fact that these data are internally and externally consistent with emerging sources of clinical data, it supports a conclusion that the COVID-19 biological products are deterministic for the myocarditis cases observed after injection.”

Again, as we knew and as I have documented before these jabs were first released for widespread use — and again, deliberately ignored. While this paper describes a specific risk with regard to myocarditis in young people the larger issue of cardiac events must not be ignored. While it is certainly true that it in healthy young people the risk from Covid-19 infection itself is minuscule and thus appears on the data to be outweighed by the risks of the jab even without accounting for incomplete reporting in my opinion the 900lb Gorilla in the china shop does not simply lie there.

Read more …

It’s a sales job. Always has been.

The Cult of the Vaccine Neurotic (Taibbi)

Yesterday, I ran a story that had nothing to do with vaccines, about the seeming delay of the development of a drug called molnupiravir (see the above segment with the gracious hosts of The Hill: Rising for more). In the time it took to report and write that piece, conventional wisdom turned against the drug, which is now suspected of ivermectinism and other deviationist, anti-vax tendencies, in the latest iteration of our most recent collective national mania — the Cult of the Vaccine Neurotic. The speed of the change was incredible. Just a week ago, on October 1st, the pharmaceutical giant Merck issued a terse announcement that quickly became big news. Molnupiravir, an experimental antiviral drug, “reduced the risk of hospitalization or death” of Covid-19 patients by as much as 50%, according to a study.

The “first draft of history” stories that rushed out in the ensuing minutes and hours were almost uniformly positive. AP called the news a “potentially major advance in efforts to fight the pandemic,” while National Geographic quoted a Yale specialist saying, “Having a pill that would be easy for people to take at home would be terrific.” Another interesting early reaction came from Time: Vaccines will be the way out of the pandemic, but not everyone around the world is immunized yet, and the shots aren’t 100% effective in protecting people from getting infected with the COVID-19 virus. So antiviral drug treatments will be key to making sure that people who do get infected don’t get severely ill. This is what news looks like before propagandists get their hands on it. Time writer Alice Park’s lede was sensible and clear. If molnupiravir works — a big if, incidentally — it’s good news for everyone, since not everyone is immunized, and the vaccines aren’t 100% effective anyway. As even Vox put it initially, molnupiravir could “help compensate for persistent gaps in Covid-19 vaccination coverage.”

Within a day, though, the tone of coverage turned. Writers began stressing a Yeah, but approach, as in, “Any new treatment is of course good, but get your fucking shot.” A CNN lede read, “A pill that could potentially treat Covid-19 is a ‘game-changer,’ but experts are emphasizing that it’s not an alternative to vaccinations.” The New York Times went with, “Health officials said the drug could provide an effective way to treat Covid-19, but stressed that vaccines remained the best tool.” If you’re thinking it was only a matter of time before the mere fact of molnupiravir’s existence would be pitched in headlines as actual bad news, you’re not wrong: Marketwatch came out with “‘It’s not a magic pill’: What Merck’s antiviral pill could mean for vaccine hesitancy” the same day Merck issued its release. The piece came out before we knew much of anything concrete about the drug’s effectiveness, let alone whether it was “magic.”

Bloomberg’s morose “No, the Merck pill won’t end the pandemic” was released on October 2nd, i.e. one whole day after the first encouraging news of a possible auxiliary treatment whose most ardent supporters never claimed would end the pandemic. This article said the pill might be cause to celebrate, but warned its emergence “shouldn’t be cause for complacency when it comes to the most effective tool to end this pandemic: vaccines.” Bloomberg randomly went on to remind readers that the unrelated drug ivermectin is a “horse de-worming agent,” before adding that if molnupiravir ends up “being viewed as a solution for those who refuse to vaccinate,” the “Covid virus will continue to persist.”

Read more …

“Your hospital is reluctant to change their well-established protocols. Most of your intubated patients are dying. What do you do?”

The Problems With Censoring Doctors Over Their COVID-19 Stances (RCS)

Everyone has a right to their opinion. The question is: does everyone have a right to voice their opinion? Increasingly, in these strange times, it seems that we physicians have the right to voice only certain opinions, when it comes to discussing Covid-19. Wanting to hit the mute button on physicians who choose to challenge the public health narrative, especially in regard to vaccination for Covid-19, is understandably tempting. We carry a bit more authority than lawyers or statisticians when we share our thoughts about medical matters; and quite a few physicians seem to have little interest in toeing the party line. However, appealing as it might be to silence these voices, succumbing to the temptation of censorship might end up costing our society more than it gains.

Imagine this: you’re a physician in charge of opening an intensive care unit in New York City for Covid-19 patients in March 2020 as the disease is tearing through the city. You notice that the standard protocols your hospital follows for intubated patients seem to be failing, perhaps injuring, your patients with Covid-19. Rumblings from Chinese intensivists, and publications from Italian physician Luciano Gattitoni, imply that intubation and ventilator management should be reconsidered in this new disease. Your hospital is reluctant to change their well-established protocols. Most of your intubated patients are dying. What do you do? Dr Cameron Kyle-Sidell experienced this dilemma — and then posted a video on YouTube on March 31, 2020, watched nearly a million times, in which he described his experiences caring for Covid-19 patients in respiratory failure.

In the video, Kyle-Sidell shared that existing treatment protocols for patients with severe pneumonia did not seem to apply to Covid-19 patients with dangerously low oxygen levels — they could be intubated later, and their lungs were less stiff and required lower ventilation pressures, than typical severe pneumonia patients. His warning was part of an alarm that was raised by others, as well, which did indeed lead to a rapid shift in management of severely ill Covid-19 patients. He also ended up stepping down from his leadership of the ICU due to disagreement with hospital management; and some of those hundreds of thousands of viewers of his YouTube video concluded that his perhaps poorly-worded comparison of Covid-19 lung disease to high altitude sickness was cause to consider the pandemic a hoax.

Was Dr Kyle-Sidell a hero for sticking his neck out and challenging the prevailing dogma, in a sincere attempt to improve outcomes for severely ill Covid-19 patients? Or should his video have been censored, and perhaps his medical license threatened, for questioning the conventional narrative in ways that could be co-opted by conspiracy theorists?

Read more …

“..without an actual policy or regulation visibly in place, state attorneys general cannot file a lawsuit or request an injunction..”

Biden Keeps Pushing Nonexistent Worker Vaccine Mandate (CTH)

Joe Biden did it again today. A month after the first announcement, the White House occupant claimed again a Dept of Labor rule (via OSHA) is forthcoming, yet no such process appears to be taking place. This ploy now seems very purposeful, because without an actual policy or regulation visibly in place, state attorneys general cannot file a lawsuit or request an injunction. As long as Biden keeps threatening a DOL worker vaccination rule sometime in the future, many employers will take action to require worker vaccination. This seems to be the actual strategy; bolstered by White House Press Secretary Jen Psaki caught off-guard last week when asked about it. Psaki had no idea how to answer the question about any OSHA activity not taking place.

Obviously Psaki didn’t expect the question, but it was also obvious that no background conversation had ever taken place amid the White House communication team. Perhaps responding to an awakening on that issue, Joe Biden gave a speech today begging people to get vaccinated and again warning that a federal vaccine mandate for all workers was coming: TRANSCRIPT – […] The Labor Department is going to shortly issue an emergency rule — which I asked for several weeks ago, and they’re going through the process — to require all employees [employers] with more than 100 people, whether they work for the federal government or not — this is within a — in the purview of the Labor Department — to ensure their workers are fully vaccinated or face testing at least once a week. In total, this Labor Department vaccination requirement will cover 100 million Americans, about two thirds of all the people who work in America. These requirements work. […] And as the Business Roundtable and others told me when I announced the first requirement, that encouraged businesses to feel they could come in and demand the same thing of their employees.”

Biden then went on to praise companies who are doing it on their own. Others are starting to notice as this article in the Federalist notes: […] According to several sources, so far it appears no such mandate has been sent to the White House’s Office of Information and Regulatory Affairs yet for approval. The White House, the Occupational Safety and Health Administration (OSHA), and the Department of Labor haven’t released any official guidance for the alleged mandate. There is no executive order. There’s nothing but press statements. Despite what you may have been falsely led to believe by the media fantasy projection machine, press statements have exactly zero legal authority.

Read more …

“The primacy of constitutional law over other sources of law results directly from the Constitution of the Republic of Poland..”

Poland’s Top Court Rules Polish Law Takes Presedence Over The EU (ZH)

In a stinging rebuke to Europe’s unelected bureaucrats, and a major escalation in the rule of law crisis between Warsaw and Brussels, Poland’s constitutional court ruled on Thursday that Polish law can take precedence over EU law amid an ongoing dispute between the European bloc and the eastern European member state. The decision by the Constitutional Tribunal came after Polish Prime Minister Mateusz Morawiecki requested a review of a decision by the EU’s Court of Justice (ECJ) that gave the bloc’s law primacy. Two out of 14 judges on the panel dissented from the majority opinion. “The attempt by the European Court of Justice to involve itself with Polish legal mechanisms violates … the rules that give priority to the constitution and rules that respect sovereignty amid the process of European integration,” the ruling said, in an outcome that could have wide-reaching consequences for Europe when the next crisis hits.

Meanwhile, Brussels considers the Constitutional Tribunal illegitimate due to the political influence imposed upon Poland’s judiciary by the ruling Law and Justice party (PiS). As the FT’s Henry Foy notes, it is “Hard to overstate the importance of this ruling.” He goes on to note that “Poland is *the* EU success story of eastern enlargement, and the biggest recipient – by a long long way – of EU taxpayer money since 2004. And now it is saying that it refuses to recognize a fundamental part of the whole project.” As DW reports, the court had looked specifically at the compatibility of provisions from EU treaties, which are used by the European Commission to justify having a say in the rule of law in member states, with Poland’s constitution.

A ruling by the ECJ in March said that the EU can force member states to disregard certain provisions in national law, including constitutional law. The ECJ says that Poland’s recently implemented procedure for appointing members of its Supreme Court amounts to a violation of EU law. The ruling from the ECJ could potentially force Poland to repeal parts of the controversial judicial reform. Meanwhile, the EU is withholding billions of euros of aid for post-pandemic rebuilding in Poland over concerns that the rule of law is being degraded in the country. “The primacy of constitutional law over other sources of law results directly from the Constitution of the Republic of Poland,” PiS government spokesman Piotr Muller wrote on Twitter after the court’s decision. “Today (once again) this has been clearly confirmed by the Constitutional Tribunal.”

However, the EPP group, the center-right bloc in the European Parliament to which PiS belongs, come out strongly against the court’s ruling: “It’s hard to believe the Polish authorities and the PiS Party when they claim that they don’t want to put an end to Poland’s membership of the EU. Their actions go in the opposite direction. Enough is enough,” Jeroen Lenaers, MEP and spokesperson for the group, said. “The Polish Government has lost its credibility. This is an attack on the EU as a whole,” he added. Previously, the European Parliament called on Morawiecki to cancel the court case in a resolution passed last month. It stressed the “fundamental nature of primacy of EU law as a cornerstone principle of EU law”, which however now is put in doubt.

Read more …

Scapegoat?

“Schulte, who had worked at an elite CIA hacking unit, said that whoever leaked the Vault 7 documents “deserved to be executed” and that “no traitors ever came from Texas”..”

Prosecution Of Alleged WikiLeaks Vault 7 Source Hits Multiple Roadblocks (Y!)

The prosecution of the former CIA operative accused of providing WikiLeaks with the biggest theft of agency documents in U.S. history continues to be mired in delays and legal issues, drawing out a painful chapter for the agency. WikiLeaks’ publication in 2017 of documents that included CIA hacking tools, which it called Vault 7, so enraged some senior officials, including then-CIA Director Mike Pompeo, that it sparked discussions within the agency and the Trump White House about kidnapping or even killing WikiLeaks founder Julian Assange, according to a Yahoo News investigation. The first trial of Joshua Schulte, the former CIA programmer accused of transmitting the documents to WikiLeaks, ended in a hung jury in March 2020. (Schulte was, however, convicted of related minor charges and remains jailed.)

It was a stinging defeat for federal prosecutors in New York’s Southern District, who vowed to retry the former agency operative. The retrial, which has already been repeatedly postponed, was last scheduled for late October. In September, Schulte, who is now representing himself in court, asked for another delay. The parties are now supposed to confer on a new trial date by Nov. 1, as Inner City Press first reported, but it is unclear precisely when the alleged WikiLeaks source will face another jury. WikiLeaks began publishing Vault 7 documents in March 2017. The leak was “instantly devastating,” said the prosecutor in the case, causing “critical intelligence gathering operations all over the world” to come to “a crashing halt.” Agency investigators later called the leak “the largest data loss in CIA history.”

Before WikiLeaks began publishing the Vault 7 materials, the CIA had no idea they had even been taken. The leak set off a furious search for the culprit. The CIA would soon determine that the files had been stolen in the spring of 2016 by Schulte, a disgruntled agency employee who quit his job within the CIA four months before WikiLeaks began releasing Vault 7 materials. FBI officials, who code-named Schulte “Kinetic Piranha” or “Kinetic Panda,” confronted him in March 2017 in the New York City office lobby of his new employer, Bloomberg LP. In subsequent interviews with bureau officials, Schulte, who had worked at an elite CIA hacking unit, said that whoever leaked the Vault 7 documents “deserved to be executed” and that “no traitors ever came from Texas” (he is a native of Lubbock, Texas).

Schulte has continued to deny any wrongdoing. Interviewing him at a restaurant across from Grand Central Terminal, FBI agents presented Schulte with a grand jury subpoena and a separate subpoena to seize his phone. Bureau personnel then also executed a search warrant of his apartment. Schulte was first arrested in August 2017 after investigators said they had found “approximately ten thousand images and videos of child pornography” while searching his electronic devices. In June 2018, prosecutors charged him with providing the materials to WikiLeaks.

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