Sep 152021
 
 September 15, 2021  Posted by at 8:40 am Finance Tagged with: , , , , , , ,  64 Responses »


Vincent van Gogh Café, le soir, Arles 1888

 

The Meaning of the FDA Resignations (Tucker)
Considerations In Boosting Covid-19 Vaccine Immune Responses (Lancet)
1 In 7 Vaccinated Americans Have Dumped Friends Over Covid-19 Jabs (RT)
Unvaccinated US Covid Patients Cost $5.7 Billion To Treat In Last 3 Months (F.)
Ordeal by Narrative (Kunstler)
Nearly Half Of ‘COVID Hospitalizations’ This Year Have Been Mild Or Asymptomatic (ZH)
Israel Health Ministry Chief Says Covid Spread Reaching Record Heights (ToI)
Israel Increases Hospital Staff to Fight COVID Surge (Haaretz)
Suspensions Put Strain On Greek Health System (K.)
France Health Worker Vaccine Mandate Comes Into Effect (G.)
Bring In Measures Soon Or Risk 7,000 Daily Covid Hospitalisations – Sage (G.)
Harrowing Account Of NSW ‘Hospital At Home’ Program (News.au)
White House: 75% Of Adults Have At Least One Covid-19 Vaccine Dose
Contaminated Pfizer Vaccines Reported In Several Japanese Cities (ZH)
Milley Secretly Called Chinese Officials Out Of Fear Trump Would ‘Attack’ (Fox)
CNN and WaPo Finger Milley as Leader of Military Coup Against Trump (CTH)

 

 

 

 

 

 

Something’s afoot. Can’t imagine these two will be the only ones.

“This is a deep problem for actual scientists working within the bureaucracy because they know for sure that all of this is a pretense and that the government cannot win this war on the virus.”

The Meaning of the FDA Resignations (Tucker)

Now to the striking resignation of two top officials at the FDA who were in charge of vaccine safety and administration. It was the Director and Deputy Director of the Office of Vaccines Research, Marion Gruber and Phillip Kause. They gave no reason for their departure, which is scheduled for October and November. The case is fascinating because 1) people rarely resign cushy government jobs unless a higher-paying, higher-prestige job in the private sector awaits, or 2) they are being pushed out. It’s rare for anyone in a position like to to resign over a principled matter of science. When I first read that they were going, I figured something else was up. These days, extremely weird things are going on within the Biden administration.

Even though his approval ratings are sinking, the president has to pretend that he has all the answers, that the science behind his mandates and virus war is universally settled, that anyone who disagrees with him is really just a political enemy. He has gone so far as to denounce, demonize, and legally threaten red-state governors who disagree with him. This is a deep problem for actual scientists working within the bureaucracy because they know for sure that all of this is a pretense and that the government cannot win this war on the virus. They simply cannot preside over more false promises, especially when the whole of their professional training is about accessing the safety and effectiveness of vaccines. So what can they do? In this case, it appears they had to get away before they dropped a bombshell.

The bombshell is called “Considerations in boosting COVID-19 vaccine immune responses.” It appears in the prestigious British medical journal The Lancet. The two top officials are among the authors. The article recommends against the Covid booster shot that the Biden administration, following Fauci’s advice, is suggesting as the key to making the vaccines work better and finally fulfill their promise. Fauci and company are pushing boosters because they know what is coming. Essentially we are going the way of Israel: most everyone is vaccinated but the virus itself is not being controlled. More and more among those hospitalized and dying are vaccinated. This same trend is coming to the US. The boosters are a means by which government can save face, or so many believe.

The trouble now is that the top scientists at the FDA disagree. Further, they think that the push for boosters is courting problems. They think the current regime of one or two shots is working as well as one can expect. Nothing is gained on net from a booster, they say. There just isn’t enough evidence to take the risk of another booster, and another and another. The authors knew this article was appearing. They knew that signing it under the FDA affiliation would lead to a push for their resignations. Life would get very difficult for both of them. They got ahead of the messaging and resigned before it came out. Very smart.

The signed article goes even further to warn of possible downsides. They point out that boosters might seem necessary because “variants expressing new antigens have evolved to the point at which immune responses to the original vaccine antigens no longer protect adequately against currently circulating viruses.” At the same time, there are possible side effects that could discredit all vaccines for a generation or more. “There could be risks,” they write, “if boosters are widely introduced too soon, or too frequently, especially with vaccines that can have immune-mediated side-effects (such as myocarditis, which is more common after the second dose of some mRNA vaccines, or Guillain-Barre syndrome, which has been associated with adenovirus-vectored COVID-19 vaccines.”)

Read more …

Here’s the article Jeffrey Tucker was talking about.

Among the authors are Marion Gruber and Philip Krause, director and deputy director of the Office of Vaccines Research and Review at FDA’s Center for Biologics Evaluation and Research (CBER), who just resigned.

Conclusion: boosters are not needed. But take a look at Gamma in that graph.

Question: why did they resign only after approving Pfizer?

Considerations In Boosting Covid-19 Vaccine Immune Responses (Lancet)

A new wave of COVID-19 cases caused by the highly transmissible delta variant is exacerbating the worldwide public health crisis, and has led to consideration of the potential need for, and optimal timing of, booster doses for vaccinated populations.1 Although the idea of further reducing the number of COVID-19 cases by enhancing immunity in vaccinated people is appealing, any decision to do so should be evidence-based and consider the benefits and risks for individuals and society. COVID-19 vaccines continue to be effective against severe disease, including that caused by the delta variant. Most of the observational studies on which this conclusion is based are, however, preliminary and difficult to interpret precisely due to potential confounding and selective reporting. Careful and public scrutiny of the evolving data will be needed to assure that decisions about boosting are informed by reliable science more than by politics.

Even if boosting were eventually shown to decrease the medium-term risk of serious disease, current vaccine supplies could save more lives if used in previously unvaccinated populations than if used as boosters in vaccinated populations. Boosting could be appropriate for some individuals in whom the primary vaccination, defined here as the original one-dose or two-dose series of each vaccine, might not have induced adequate protection—eg, recipients of vaccines with low efficacy or those who are immunocompromised2 (although people who did not respond robustly to the primary vaccination might also not respond well to a booster). It is not known whether such immunocompromised individuals would receive more benefit from an additional dose of the same vaccine or of a different vaccine that might complement the primary immune response.

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With friends like that ….

1 In 7 Vaccinated Americans Have Dumped Friends Over Covid-19 Jabs (RT)

Many Americans have been jettisoning friends from their lives during the Covid-19 pandemic, and for those who have chosen to get vaccinated, views on the jabs are often the relationship-breaker, a new poll has shown. The survey, conducted earlier this month by researcher OnePoll, showed that 16% of respondents have ended at least three friendships in the past year and a half. About 14% of vaccinated Americans said they have severed relationships with friends who chose not to get inoculated against the virus. In fact, vaccinated respondents were nearly four times as likely as those who don’t intend to get the jabs – 66% to 17% – to have ended friendships during the pandemic. The poll showed that 97% of vaccinated people consider their former friends to be “full-blown anti-vaxxers” and said they could never get them to understand the importance of getting the shots.

Covid-19 vaccination is one of the most divisive issues driving a wedge between Americans. The 14% who cited the jabs as the reason for ending friendships compared with 16% who blamed political differences and 15% whose former pal was dating an ex-mate. Other reasons included discovering their friends were liars (7%) and having a friend make up stories about them (12%).Hollywood has apparently blessed the idea of dumping friends who decline to get vaccinated. Actress Jennifer Aniston – ironically, a star of the television series ‘Friends’ – said last month in an InStyle magazine interview that she had ended relationships with people who refused to get jabbed or chose not to tell her their inoculation status. “It’s a real shame,” she said. “I’ve just lost a few people in my weekly routine.”

The level of vaccine vitriol has escalated in recent weeks. Radio host Howard Stern recently blasted “all the s**theads in our country who won’t get vaccinated” and said those who don’t get the jabs should be denied hospital beds if they get sick. “Stay home, die there with your Covid,” he said. OnePoll said 81% of Democrat survey respondents were fully vaccinated, compared with 64% of Republicans and 69% of independents. About 57% of Republicans and 41% of Democrats said society is “too critical” of unvaccinated Americans. Tolerance for vaccine autonomy is waning in America, as President Joe Biden last week ordered all businesses with 100 or more employees to force their workers to get the shots. “We’ve been patient, but our patience is wearing thin, and your refusal has cost all of us,” Biden said of unvaccinated Americans.

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Forbes moves into desperate propaganda.

“The vast majority of hospitalizations and nearly all deaths from Covid-19 are in unvaccinated people. The huge surge in demand for what few medicines are licensed to treat Covid-19 in the U.S. has triggered nationwide shortages and rationing of scarce supplies.”

Unvaccinated US Covid Patients Cost $5.7 Billion To Treat In Last 3 Months (F.)

Preventable costs associated with treating unvaccinated American Covid-19 patients amounted to at least $3.7 billion in August and $5.7 billion since June, according to research by the Kaiser Family Foundation, as the disease rips through people who elected not to get free and highly effective vaccines. Around 187,000 Covid-19 hospitalizations could have been easily prevented by vaccination in August, research by Kaiser found, up from 68,000 in July and 32,000 in June. These preventable hospitalizations over the past three months cost the U.S. healthcare system around $5.7 billion, Kaiser estimates based on the average Covid-19 hospital bill of approximately $20,000.

The “ballpark figure is likely an understatement of the cost burden from preventable treatment of Covid-19 among unvaccinated adults,” according to the report, which noted significant variations in costs across the country, a “conservative” estimate of the proportion of Covid-19 patients who hadn’t been vaccinated and studies indicating a potentially much higher average cost than the $20,000 used (one cited put the figure at around $42,200). There are also “substantial” costs for outpatient Covid-19 treatment, the report said, though this was not factored into the analysis.

Due to laws preventing insurers from charging unvaccinated people higher premiums, the Kaiser report said the bill will fall on everyone as they will pay only “a small share of the cost” directly. This means a greater burden on the taxpayer and the risk of higher insurance premiums for businesses and workers, the report said. The costs of being unvaccinated are on the rise, however, with some employers charging higher insurance premiums to employees foregoing vaccination and others making it a condition of work. They are also facing elevated costs for healthcare as insurance companies walk back the waivers on out-of-pocket costs for Covid-19 hospital care introduced earlier in the pandemic.

The Covid-19 vaccines used in the U.S. are proven to be safe and highly effective at preventing serious illness, hospitalization and death from Covid-19, including against the delta variant. They are also supposed to be free and have no out-of-pocket costs. Despite being readily available for months, some states still have very low vaccination rates and many have still not hit the target of partially vaccinating 70% of adults that President Joe Biden set for early July. While breakthrough infections are rare, they can and do happen, though vaccines slash the risks of long Covid, hospitalization and serious illness. The vast majority of hospitalizations and nearly all deaths from Covid-19 are in unvaccinated people. The huge surge in demand for what few medicines are licensed to treat Covid-19 in the U.S. has triggered nationwide shortages and rationing of scarce supplies.

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“..the distinguished American public servant will live out his last days in exile among the swooping fruit bats and grinning crocodiles, to the music of toucans screeching in the silk-floss trees (Chorisa speciosa).”

Ordeal by Narrative (Kunstler)

Has doctor Anthony Fauci booked passage to Paraguay yet? Like, on a smallish container barge registered in Cote D’Ivoire, conveying a six months backlog of cars stolen out of Essex County, New Jersey, for detailing and re-sale way up that lazy river to Asunción? The captain has a comfortable guest cabin, price negotiable, but better bring your own food. The US Intel Community will not find the good doctor down there because they will not bother looking for him. And so, the distinguished American public servant will live out his last days in exile among the swooping fruit bats and grinning crocodiles, to the music of toucans screeching in the silk-floss trees (Chorisa speciosa).

Anyway, that’s my fantasy du jour. Walt Disney had it right: America’s fate would be a descent into pure fantasy as the final product of our many twentieth century triumphs. It is increasingly difficult, for instance, to sort fact from fantasy in Dr. Fauci’s magnum opus: the Covid-19 pandemic, starting from the premise that it actually exists. There was some kind of rumpus in Wuhan, China, in January of 2020… folks dropping dead in their tracks on the sidewalks (captured on closed circuit TVs)… folks getting the doors to their apartments welded shut… and then what? Not much indication of further freak-outs inside China since back then. Perhaps the virus has been raging over there all the while, but a million here, a million there, do you really notice the attrition in a land of 1.4 billion? Or did they just switch off that groove on their narrative machine? The CCP can do that, I hear.

Back in the USA, where you’d have to subtract a billion and then-some in population, something was surely killing folks, though, overwhelmingly, most of those folks were already sick, and old, pretty much in the check-out zone. In 2020, the death of old and sick people was declared… impermissible! Death suddenly had no place in the exceptional order of things American. (Ask old Uncle Walt, who reportedly had his head and its gelatinous contents cryogenically frozen, in expectation of future re-animation via science magic! Still waiting for him to come back….)

Of course, the new medical rules-of-engagement circa 2020 included the denial of early treatment with known common anti-viral drugs for folks coming down with early symptoms of the mystery illness. So, while pretending to object to the implacable fact of death — a certainty of the human condition, according to science — we killed a whole bunch of people by withholding treatment. And concurrently, we rolled out the vaccines promising to “protect everybody” only to learn that it provided other, even more diabolical, routes to death.

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This is why I don’t believe the CDC has been undercounting Covid deaths.

Nearly Half Of ‘COVID Hospitalizations’ This Year Have Been Mild Or Asymptomatic (ZH)

A brand new study is calling into question how reliable and meaningful of a number of “patients hospitalized with Covid-19” in the U.S. is. Covid hospitalizations – the most common metric heard when discussing the seriousness of the pandemic – may not be nearly as meaningful of a number as many once thought. And don’t take it from us: The Atlantic published a stunning piece on Tuesday citing a new study that suggests “almost half of those hospitalized with COVID-19 have mild or asymptomatic cases”. The Atlantic had formerly called Covid hospitalizations “the most reliable pandemic number,” last winter. Now, after a nationwide study of hospitalization records was release, the publication is walking back its fervor on that statement.

Researchers from Harvard Medical School, Tufts Medical Center, and the Veterans Affairs Healthcare System took on the task of trying to figure out how serious Covid cases were in those hospitalized, and how many people counted as Covid hospitalizations were actually in the hospital for Covid, versus getting a Covid test after being admitted for something else. The study “analyzed the electronic records for nearly 50,000 COVID hospital admissions at the more than 100 VA hospitals across the country,” The Atlantic wrote. It “checked to see whether each patient required supplemental oxygen or had a blood oxygen level below 94 percent” in order to try and determine if cases met the NIH’s threshold for “severe COVID”.

What the study found was that from March 2020 to January 2021, 36% of Covid cases in the hospital were mild or asymptomatic. From January 2021 to June 2021, during the Delta variant’s spread, that number rose all the way to 48%. For vaccinated hospital patients, the number rose to a stunning 57%.

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Safe and effective.

Israel Health Ministry Chief Says Covid Spread Reaching Record Heights (ToI)

Health Ministry Director-General Nachman Ash said Tuesday that the current wave of coronavirus infections is surpassing anything seen in previous outbreaks and that he is disappointed that a recent downward trend appeared to be reversing. Ash’s remarks via video call to the Knesset Constitution, Law, and Justice Committee came as Health Ministry figures showed that over 10,000 new COVID-19 cases were diagnosed the day before and that the positive test rate was climbing. Pointing out that there is an average of 8,000 new infections each day, with occasional peaks over 10,000, he said, “That is a record that did not exist in the previous waves,” including the massive third wave at the end of last year.


Ash expressed some pessimism, though he observed that, belying fears, there wasn’t a large spike in infections following last week’s Rosh Hashanah holiday — the Jewish New Year — or the opening of the school year at the beginning of the month. After bringing daily infections down to little more than a dozen a day in June, Israel has been battling to control a resurgence of COVID-19 in what has been its fourth wave of infections since the start of the global pandemic. “A week ago we were in a clear downward trend; in recent days we’ve been seeing that decline stop, and the virus reproduction number is [again] above 1,” Ash said of the so-called R number, which indicates how many people each virus carrier will infect. Values above 1 show that the outbreak is growing, below 1 that it is shrinking. “I hoped that we would see a clearer drop, but we are still not seeing it,” he said.

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The boosters work.

Israel Increases Hospital Staff to Fight COVID Surge (Haaretz)

Israel’s hospitals learned on Tuesday that they would receive funding to take on an additional 600 doctors and 1,500 nurses if the government’s forecasts are correct and the number of hospitalized coronavirus patients reaches 4,800 in the next month, with half of them being serious cases. But many health care leaders warned that the extra staff won’t have a profound impact anytime soon because it will take time for them to be trained in treating COVID-19 patients in the midst of a crisis. Their contribution will only be felt only weeks, if not months, after they are hired. Even if the new hires can get up to speed quickly, many doctors said the number of new staff that the government is offering isn’t enough to cope with the growing patient overload – and that is going to affect the quality of care.


Dr. Eytan Wirtheim, CEO of the Rabin Medical Center in Petah Tikva and chairman of the Union of Hospital Directors, told an Israel Medical Association conference on Thursday that the staff additions were critical and that “it’s important that we begin today to fill all these jobs and shifts.” He said that in addition to the extra personnel, hospital chiefs had unsuccessfully sought an additional 300 beds for intensive care patients, 800 for internal medicine units and at least 300 for geriatric internal medicine wards. IMA Chairman Prof. Zion Hagai said the extra medical personnel would not help seriously ill patients in the current COVID-19 wave. “If anyone thinks that we have increased our capacity for new patients, the fact is we have changed nothing – we’ve just added beds without the ability to treat patients,” he told the conference. “What are they thinking? That they can just push a button and out comes a trained physician who can begin to work? Experienced nurses also need to be trained before they can enter coronavirus wards.”

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The PM bribes kids with 50 gigs of free data, to take a shot that won’t do them any good but can cause severe damage for the rest of their lives. Criminal.

Suspensions Put Strain On Greek Health System (K.)

The suspension of unvaccinated doctors and other health workers in effect since September 1, meant as a warning and as an incentive to get inoculated, have resulted in personnel shortages across the public health system. According to the Health Ministry, some 5,500 health workers and other personnel at public hospitals have been suspended, with another 1,000 told they can’t work at primary healthcare centers. The problems are more acute in places with few personnel to begin with, such as on several islands, according to the union of state hospital employees. On the island of Naxos, for example, both surgeons, one of two microbiologists, two out of five lab technicians, two out of seven cleaners and five out of 30 nurses have been suspended. On the smaller island of Amorgos, four out of eight employees are not going in to work.

Newly appointed Health Minister Thanos Plevris tried to put a good spin on the situation. “There are certainly some dysfunctions – I want to be upfront – but those are manageable,” he responded Tuesday to a parliamentary inquiry by SYRIZA MP Andreas Xanthos, health minister in the previous leftist-led government. “We consider that, as the days pass and personnel that get vaccinated resume their duties, and with the activation of three-month contracts [with private sector healthcare providers], even these dysfunctions will be eliminated,” he added. In fact, officials are worried enough that they are considering relaxing the terms of the suspension, allowing personnel who have taken one of the two required vaccine doses back to work. No final decisions have been made about this.

The problem with health workers points to a more general issue concerning the reluctance of people to get vaccinated. Despite all sorts of enticements, incentives and ceaseless messaging, just 56% of the population is fully vaccinated. This drops to 49% for people aged 18-24, who are increasingly getting sick from the Delta variant of the coronavirus. And at schools, which opened Monday and are feared to become new bases for the spread of the disease, less than one in four 12- to 17-year-olds are vaccinated. It remains to be seen whether Prime Minister Kyriakos Mitsotakis’ promise over the weekend of 50 gigabytes of free data for the smartphones of 15- to 17-year-olds will provide any kind of inducement.

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This is going to be fun to watch.

France Health Worker Vaccine Mandate Comes Into Effect (G.)

The French government faces a stand-off with tens of thousands of health workers and carers Wednesday over a new rule requiring them to receive a Covid-19 vaccine or face suspension without pay, AFP reports. Starting Wednesday, hospital staff, ambulance drivers, retirement home workers, private doctors, fire service members and people caring for the elderly or infirm in their homes – some 2.7 million people in total – must be able to prove they have had at least one shot of a vaccine. President Emmanuel Macron issued the ultimatum two months ago, but tens of thousands of carers remain unvaccinated.


One of France’s biggest public sector unions, the hardline CGT, has warned of a “health catastrophe” if the government suspends large numbers of health workers and bars private-sector doctors from practising. Defiant health workers have joined opponents of a new coronavirus “health pass” required for entry to restaurants, cafes and museums at weekly protests held across France in the past two months. On Tuesday, a few hundred people attended a union-led demonstration outside the health ministry in Paris.

Read more …

Where are the boosters?

Bring In Measures Soon Or Risk 7,000 Daily Covid Hospitalisations – Sage (G.)

Between 2,000 and 7,000 people a day could be hospitalised with Covid in England next month unless the government urgently implements a “basket of measures”, government scientific advisers have warned as Boris Johnson made clear he hopes to avoid fresh restrictions. The prime minister confirmed on Tuesday that Covid passports, the return of mandatory mask-wearing and advice to work from home would be kept in reserve as the government’s “plan B”, to be introduced if the NHS is at risk of being overwhelmed. But newly published modelling from experts on the Sage advisory committee warn the government not to wait too long, with cases, hospitalisations and deaths all higher than a year ago despite the success of the vaccination programme.

Speaking alongside Johnson at a Downing Street press conference, the government’s chief scientific adviser, Sir Patrick Vallance, also said experience of battling the virus showed “you have to go earlier than you think you want to, you have to go harder than you think you want to”. He said the UK was now at a “pivot point” where, if the situation worsens, it could do so rapidly. Modellers on the Sage committee expect cases to rise in the coming months after almost all restrictions were lifted this summer, documents show. Daily hospitalisations could plausibly peak at 7,000 in England next month, far surpassing the winter peak, which reached 4,500 UK-wide, according to the updated modelling. Currently about 1,000 people with Covid are being admitted to UK hospital wards each day.


But if enacted early enough, before a rise in cases becomes sustained, even light-touch measures could be sufficient to keep infections flat and prevent a damaging fresh wave of hospitalisations, the Sage documents say. “With the current levels of high prevalence combined with unknown behaviours, the burden on health and care settings could rise very quickly,” the scientists warn. They say “it could be a very difficult winter ahead” if acute Covid combines with other pressures such as long Covid, other infections like flu, or co-infection causes more serious illness. Even though 81% of UK adults are double-jabbed, nearly 6 million are unvaccinated and vulnerable to the highly-transmissible Delta variant now most Covid restrictions have been lifted.

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There’s a dark world down under. Good thing they banned IVM.

Harrowing Account Of NSW ‘Hospital At Home’ Program (News.au)

The wife of a Sydney man stricken with Covid-19 has given a harrowing account of how the “hospital at home” program is operating revealing her husband was told to remain at home even when he was coughing up blood. The family, who spoke to news.com.au on the condition of anonymity, have raised serious concerns over the “call centre” approach to caring for patients which often involves call centre operators, not doctors or nurses, running through checklists of symptoms with patients. Doctors have raised concerns about the “hospital in the home” Covid treatment system after more than 15 people died at home since August 1. NSW has been left with little choice other than to rely on the hospital at home program after the number of Covid infected patients ballooned and the number of people in hospital and ICU continues to rise.

There are currently over 14,000 people with “active” Covid infection in NSW and the vast majority are being left alone at home to battle the illness. In the case of the 37-year-old man whose family spoke to news.com.au, he was “fit and healthy” and had no underlying conditions. “He is incredibly fit and healthy, a rugby player, he’s very into his health and his diet and fitness and doesn’t have any pre-existing health issues,’’ his wife said. “My husband was diagnosed on September 2. He had really mild symptoms at that point. He received a text. He was told to isolate. And they told him to stay home. They said they would call him every day,’’ she said. “But he didn’t have a GP contacting him. We just had NSW Health Unit contact which was like a call centre. He never really saw a doctor at all. He did have one phone call with a doctor.”

In the first week, she said she was given a list of things that would require her husband’s case to be escalated or taken to hospital. The woman is trapped in Victoria where she was trying to help him over the phone. “If you’ve got freezing cold skin and you can’t warm up no matter what you do. If you’ve got shortness of breath, chest pain, infrequent urination, and if you’re coughing up blood. So those are the things. We felt in good hands at that point. Then, he started to deteriorate,’’ she said. A week ago on Sunday, he started “coughing up blood and having respiratory distress”. “We monitored that overnight and on September 6, we called NSW Health to tell them that he was presenting with one of those symptoms, requiring hospitalisation along with shortness of breath,’’ the man’s wife said.

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And that’s where the fun starts.

White House: 75% Of Adults Have At Least One Covid-19 Vaccine Dose

Three-fourths of U.S. adults have been vaccinated with at least one dose of the COVID-19 vaccine, a White House official announced on Tuesday. White House COVID-19 Data Director Cyrus Shahpar marked the milestone in a tweet, saying the country “just hit” 75 percent of adults with at least one shot. He said that from Sunday through Tuesday, 1.51 million doses have been administered, with 681,000 newly vaccinated and 105,000 additional doses, while noting that there is “as usual, lower reporting over the holiday weekend,” referring to Labor Day. The U.S. reached the 75 percent threshold about a month after hitting 70 percent. Previously, President Biden had hoped to achieve the 70 percent mark by July 4.


The Centers for Disease Control and Prevention’s online tracker, last updated Saturday, showed that 74.8 percent of U.S. adults received at least one dose and 64 percent were fully vaccinated. The rate of vaccinations has picked up in recent weeks as the highly transmissible delta variant spreads throughout the country, leading to increased case counts, hospitalizations and deaths. The U.S. administered more than 939,000 vaccine doses on Saturday after a steady rise since mid-July, when the pace was closer to 500,000 a day, according to Our World in Data. Still, only slightly more than half of the overall U.S. population is fully vaccinated: 53 percent are fully vaccinated and 62 percent have received at least one dose.

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Are the Japanese the only ones looking?

Contaminated Pfizer Vaccines Reported In Several Japanese Cities (ZH)

Several cities in Japan have reported ‘white-colored floating substances’ in Vials of Pfizer’s Covid-19 vaccine, according to Bloomberg. The vials came from lot FF5357, where white contaminants were first reported by Kamakura City in Kanagawa prefecture. On Tuesday, two more cities – neighboring Sagamihara and Sakai City in Osaka prefecture reported contaminated vials, however there were no reports of adverse reactions. In Sagamihara, white substances were reported at three different vaccination sites on Sept. 11, 12 and 14. The cities told Bloomberg that they will ask Pfizer for an analysis. Last month Moderna came under fire after black contaminants were found in multiple vials of their Covid-19 vaccine in Japan, causing the Japanese Ministry of Health to pull 1.6 million doses of the vaccine. According to NHK, “black substances” were found in syringes and a vial, while pink substances were spotted in a different syringe.

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“According to Pelosi, she spoke with Milley that day about “available precautions” to prevent Trump from engaging in military action.”

Milley Secretly Called Chinese Officials Out Of Fear Trump Would ‘Attack’ (Fox)

During the final months of former President Donald Trump’s term, Chairman of the Joint Chiefs of Staff Gen. Mark Milley made two phone calls to Chinese officials in fear that Trump would create conflict with the communist nation, a new book has claimed. In the book, authored by Washington Post associate editor Bob Woodward and national political reporter Robert Costa, it is alleged that Milley made two secret phone calls, both to his Chinese counterpart, Gen. Li Zuocheng of the People’s Liberation Army. The book alleges that the phone calls took place prior to the 2020 presidential election on Oct. 30, 2020, and two days after the Jan. 6 Capitol riot, on Jan. 8, 2021.

According to the book, Milley contacted Li after he had reviewed intelligence that suggested Chinese officials believed the United States was planning an attack on China amid military exercises in the South China Sea. “General Li, I want to assure you that the American government is stable and everything is going to be OK,” Milley told him during the first call, the book said. “We are not going to attack or conduct any kinetic operations against you.” The book, excerpted in the Washington Post, also stated that Milley told Li that he would warn him in advance should America decide to “attack.” “Gen. Li, you and I have known each other for now five years. If we’re going to attack, I’m going to call you ahead of time,” Milley added, as reported by the book, “Peril,” which is set to be released next week. “It’s not going to be a surprise.”

The authors of the book also claim Milley contacted Li a second time to reassure him that the U.S. would not make any type of advances or attack China in any form, as Milley promised, “We are 100% steady. Everything’s fine. But democracy can be sloppy sometimes.” Those phone calls, according to the book, were never mentioned to Trump, as Milley believed his mental state had declined following the election, something about which he shared his thoughts in a phone call with House Speaker Nancy Pelosi, D-Calif., on Jan. 8, the same day he called Li the second time. According to Pelosi, she spoke with Milley that day about “available precautions” to prevent Trump from engaging in military action.

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“They are using the opportunity of this book by Woodward and Costa to hit Milley, place the blame for Afghanistan in his lap, and make him the scapegoat so that Joe Biden and the other participants can avoid further scrutiny. ”

CNN and WaPo Finger Milley as Leader of Military Coup Against Trump (CTH)

Today CNN, via Bob Woodward and The Washingon Post, via Robert Costa collaborate on a designed hit against one of the key corrupt actors on Team Two, Joint Chiefs of Staff General Mark Milley. CTH previously said this was coming: “Look for Joint Chief’s Chairman Mark Milley to be the guy who gets canned to protect Joe Biden. Mark Milley knows this is likely.” The framework of the CNN article is that General Milley: …”called a secret meeting in his Pentagon office on January 8 to review the process for military action, including launching nuclear weapons. Speaking to senior military officials in charge of the National Military Command Center, the Pentagon’s war room, Milley instructed them not to take orders from anyone unless he was involved.

“No matter what you are told, you do the procedure. You do the process. And I’m part of that procedure,” Milley told the officers, according to the book. He then went around the room, looked each officer in the eye, and asked them to verbally confirm they understood. “Got it?” Milley asked, according to the book. “Yes, sir.” ‘Milley considered it an oath,’ the authors write. The framework of the Washington Post article paints Milley as even more rogue. A power hungry operator of the industrial military complex, defying civilian oversight:

[…] In a pair of secret phone calls, Gen. Mark A. Milley, the chairman of the Joint Chiefs of Staff, assured his Chinese counterpart, Gen. Li Zuocheng of the People’s Liberation Army, that the United States would not strike, according to a new book by Washington Post associate editor Bob Woodward and national political reporter Robert Costa. One call took place on Oct. 30, 2020, four days before the election that unseated President Trump, and the other on Jan. 8, 2021, two days after the Capitol siege carried out by his supporters in a quest to cancel the vote. The first call was prompted by Milley’s review of intelligence suggesting the Chinese believed the United States was preparing to attack.

That belief, the authors write, was based on tensions over military exercises in the South China Sea, and deepened by Trump’s belligerent rhetoric toward China. “General Li, I want to assure you that the American government is stable and everything is going to be okay,” Milley told him. “We are not going to attack or conduct any kinetic operations against you.” In the book’s account, Milley went so far as to pledge he would alert his counterpart in the event of a U.S. attack, stressing the rapport they’d established through a backchannel. “General Li, you and I have known each other for now five years. If we’re going to attack, I’m going to call you ahead of time. It’s not going to be a surprise.”

[..] You think CNN and the Washington Post only recently came to the understanding that General Mark Milley was a corrupt, politically motivated actor, working on behalf of the interests of the Deep State [4th Branch]? Of course not. They are using the opportunity of this book by Woodward and Costa to hit Milley, place the blame for Afghanistan in his lap, and make him the scapegoat so that Joe Biden and the other participants can avoid further scrutiny. Their play is transparent.

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Moth
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Sep 012021
 
 September 1, 2021  Posted by at 9:05 am Finance Tagged with: , , , , , ,  88 Responses »


Vincent van Gogh Ward in the hospital in Arles 1889

 

Who’s Really Being Hospitalized? (Margulis)
60% of Those Older Than 50 Who Die From Covid Are Double Vaxxed (Mercola)
‘Get Sicker’: Anatomy Of A Failed Policy (Pfeiffer)
There’s An Off Ramp – But It Has A Price (Denninger)
The Case For Covid Vaccine Passports Was Just Demolished (Fee)
Key Vaccine Leaders Departing FDA As Covid-19 Booster Questions Linger (FPhar)
Greek Health Ministry Bracing For ‘Great Exodus’ (K.)
Pharmacy Customers Refuse To Say What Ivermectin Prescription Is For (G.)
Zero Covid, A Once Wildly Popular Ideology, Quietly Faces Extinction (Subs)
Singapore Gives Up Goal of Zero Covid Despite High Vaccination Rate (Gizmodo)
Obama Officials’ Lies About Edward Snowden and Russia (Greenwald)

 

 

 

 

 

 

 

 

The stories are collapsing.

Who’s Really Being Hospitalized? (Margulis)

After a battery of testing, my friend was diagnosed with pancreatitis. But it was easier for the hospital bureaucracy to register the admission as a COVID case. Let me explain. This patient had none of the classic symptoms of COVID: No shortness of breath, no fever, no chills, no congestion, no loss of sense of smell or taste, no neurological issues. The only COVID symptoms my friend had were nausea and fatigue, which could also be explained by the surgery. However, nearly three weeks earlier, a COVID test had come back positive. The mainstream media is reporting that severe COVID cases are mainly among unvaccinated people.

An AP headline from June 29 reads: “Nearly all COVID deaths in US are now among unvaccinated.” Another, from the same date: “Vast majority of ICU patients with COVID-19 are unvaccinated, ABC News survey finds.” Is that what’s really going on? It’s certainly not the case in Israel, the first country to fully vaccinate a majority of its citizens against the virus. Now it has one of the highest daily infection rates and the majority of people catching the virus (77% to 83%, depending on age) are already vaccinated, according to data collected by the Israeli government. After carefully reviewing the available data, including the safety and efficacy profiles of the mRNA vaccines, my friend had taken a cautious approach. Though a medical doctor who gives vaccines in the office every day, my friend opted to wait and see.

According to WebMD, a “huge number” of frontline hospital workers have also chosen not to get the vaccine. Indeed, various news reports, from California to New York, confirm that up to 40% of health care workers have decided the risks of the vaccines do not outweigh the benefits. After admission, I spoke to the nurse on the COVID ward. She was suited up in a plastic yellow disposable gown, teal gloves, and two masks underneath a recirculating personal respiratory system that buzzed so loudly she could barely hear. The nurse told me that she had gotten both vaccines but she was feeling worried: “Two thirds of my patients are fully vaccinated,” she said. How can there be such a disconnect between what the COVID ward nurse told me and the mainstream media reports?

For one thing, it is very hard to get any kind of accuracy when it comes to actual numbers. In fact, the Centers for Disease Control and Prevention (CDC) have publicly acknowledged that they do not have accurate data. As reported by the Associated Press, “The CDC itself has not estimated what percentage of hospitalizations and deaths are in fully vaccinated people, citing limitations in the data.” At the same time, data collection is done on a state by state basis. In most states, a person is only considered fully vaccinated fourteen days after they have had the full series of the vaccine. This means that anyone coming into an American hospital who has only had one dose, or who has had both vaccines but had the second one less than two weeks prior, will likely be counted as “unvaccinated.”

So when the South Carolina’s Department of Health and Environmental Control released a report about COVID severity on July 23, 2021, they reported higher morbidity and mortality rates in the “not fully vaccinated.” Are these people who have had one vaccine and gotten sick, two vaccines and gotten sick, or no vaccines at all? Without more details, it is impossible to know what is really going on. “We don’t have accurate numbers,” insists Dr. James Neuenschwander, an expert on vaccine safety based in Ann Arbor, Michigan. But what we do know, Neuenschwander says, is that the vaccines are not as effective as public health officials told us they would be. “This is a product that’s not doing what it’s supposed to do. It’s supposed to stop transmission of this virus and it’s not doing that.”

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“…breakthrough cases are now multiplying at breakneck speed. “There are so many breakthrough infections that they dominate..”

60% of Those Older Than 50 Who Die From Covid Are Double Vaxxed (Mercola)

The oft-repeated refrain right now is that we’re in a “pandemic of the unvaccinated,” meaning those who have not received the COVID jab make up the bulk of those hospitalized and dying from the Delta variant. For example, August 20, 2021, England’s chief medical officer professor Chris Whitty tweeted: “Four weeks working on a COVID ward makes stark the reality that the majority of our hospitalized COVID patients are unvaccinated and regret delaying. Some are very sick including young adults. Please don’t delay your vaccine.” Curiously, if you take the time to actually look at the data, you’ll find that this blanket statement is rather deceptive. Here’s a graphic published in the Evening Standard, sourced from Public Health England:

As you can see, as of August 15, 2021, 58% of COVID patients admitted to hospital who were over the age of 50 had actually received two doses of COVID injections and 10% had received one dose. So, partially or fully “vaccinated” individuals made up 68% of hospitalizations. Only in the 50 and younger category were a majority, 74%, of hospitalizations among the unvaccinated. Whitty, however, completely neglected to differentiate between the age groups. The same applies to deaths. Unvaccinated only make up the majority of COVID deaths in the under-50 age group. In the over-50 group, the clear majority, 70%, are either partially or fully “vaccinated.” It’s also unclear whether hospitals in the U.K. (and elsewhere) are still designating anyone who is admitted and tests positive with a PCR test as a “COVID patient.” If so, people with broken bones or any number of other health problems who have no symptoms of COVID-19 at all might be unfairly lumped into the “unvaccinated COVID patient” total.


In Israel, where vaccine uptake has been very high due to restrictions on freedom for those who don’t comply,4 data show those who have received the COVID jab are 6.72 times more likely to get infected than people with natural immunity. The fully “vaccinated” also made up the bulk of serious cases and COVID-related deaths in July 2021, as illustrated in the graphs below.8 The red is unvaccinated, yellow refers to partially “vaccinated” and green fully “vaccinated” with two doses. By mid-August, 59% of serious cases were among those who had received two COVID injections,9 mirroring the data coming out of the U.K.

In an August 16, 2021, Science article,10 Israeli Minister of Health Nitzan Horowitz is quoted saying the nation has entered a “critical time” in the race against the pandemic. Horowitz allegedly was given a third booster shot August 13, 2021, the day they began offering a third dose to people over the age of 50. From Public Health England’s data, it seems clear that the COVID shots are failing to protect people over the age of 50 in the U.K. as well, so it’s probably only a matter of time before booster shots are rolled out there too. And, provided the COVID injections are the same irrespective of country, there’s every reason to assume the same trends will emerge in other countries, including the U.S.


According to Science magazine, breakthrough cases are now multiplying at breakneck speed. “There are so many breakthrough infections that they dominate and most of the hospitalized patients are actually vaccinated,” Uri Shalit, a bioinformatician at the Israel Institute of Technology told Science. Nearly 1 million Israelis over the age of 50 have now received a third booster of Pfizer’s mRNA shot. Time will tell whether this will worsen the rate of breakthrough cases or tame it. Dvir Aran, a biomedical data scientist at the Israel Institute of Technology doesn’t seem very hopeful, telling Science the surge is already so steep, “even if you get two-thirds of those 60-plus [boosted], it’s just gonna give us another week, maybe two weeks until our hospitals are flooded” again.

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“Existing drugs could have relegated COVID to a manageable outpatient disease by the first half of 2021.”

‘Get Sicker’: Anatomy Of A Failed Policy (Pfeiffer)

Throughout COVID, the media has stepped into line like good soldiers in a war on disease, failing, in the process, to do its job. It gave government a pass on the dearth of outpatient care. It fostered the fiction that aggressively treating COVID is a right-wing construct. It dismissed vaccine side effects as rare. It enabled vast censorship. News outlets might be excused for initially minimizing falling vaccine efficacy in this dynamic situation. But it cannot be excused for its politicization of and disdain for generic early treatments. As a mainstream community journalist for decades, with two books and many awards, I am appalled at what this profession has become.

Existing drugs could have relegated COVID to a manageable outpatient disease by the first half of 2021. We have promising generics: ivermectin primarily but also fluvoxamine, hydroxychloroquine, budesonide and protocols that employ them with zinc, Vitamin D and the like. They have been suppressed around the globe, as countries – mainly, but not all, in the first world — have caved under pressure to conform to the U.S.-hatched strategy. In the white-hot frenzy of pack journalism, doctors’ licenses have been threatened, and reputations imperiled, including of a prison doctor who used ivermectin and kept inmates out of hospitals. Will nursing home practitioners, who told me of their own ivermectin success, be next in this witch hunt? Indeed, somehad used it to control scabies and found a remarkable drop in COVID.

As the globe is buttressed by new variants, vaccine efficacy is being tested and so is that of ivermectin. Leading proponents are adjusting doses and adding to treatment cocktails as part of a logical ongoing effort: Use emerging science and clinical experience to learn what works. Although off-label use of approved drugs is well established — accounting for 21 percent of office prescriptions and half of oncology drugs – doctors have instead been told to follow only a few, patented, government-sanctioned treatments, available only in hospitals. Who could blame them, in this heated environment, for not practicing medicine but following orders? Nonetheless, the forces of commerce and incompetence that have pushed a false narrative and demonized treatment for COVID must be held to account.

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“The fifth jab would put the risk of getting screwed at ten percent, which is approximately the rate of death from the original SARS and the sixth would be odds-on as literal suicide.”

There’s An Off Ramp – But It Has A Price (Denninger)

[..] all of the current vaccines deliberately produce that spike protein, which by itself causes disease, specifically clotting-related disease, in your body. Deliberately causing your body to produce that pathogen (which then elicits the antibody response) is how all of them work. This means there is no safe way to vaccinate against this disease because introducing the spike into your body, no matter how you do it, inherently runs the risk of serious clotting-based disorders. You might or might not get nailed but there is no avoiding the risk. That same risk is what kills you, most of the time, if you actually get Covid-19 and die but the premise that you avoid that risk when taking a jab is a lie.

You cannot; the risk is inherent in introducing the spike into your circulation and there is no way around that with an IM injection because the muscles of the body are very well-perfused (that is, there’s a lot of blood flow in them) even if the person who performs the injection does not hit a blood vessel, and they might. These facts are not up for debate on a scientific basis any longer. They also fully explain the myocarditis, pericarditis and myriad other so-called “rare” events that occur with these jabs such as strokes, heart attacks and other clotting-based disorders. In addition the data is that the 2nd shot in the 2-shot series is much more dangerous than the first, which implies an exponential expansion of risk. Whether that expansion of risk bleeds back off over a couple of months or so is entirely unknown as it has not been studied.

Without a data set of hundreds of thousands (so as to get statistical significance) and both baseline and follow-up d-Dimer testing, at minimum, we will never be able to put numbers on this, nor get a decay rate on the risk if it decays, and nobody is doing those studies. That’s the bad news; if you take repeated shots and the risk does not bleed off then eventually you will kill yourself. If, for example, the risk on the first shot is 1/100,000 (extremely rare), on the second 1/10,000 (that’s a bad pattern) and the risk does not bleed off over the space of three or four months then the risk from the third is 1/1,000 (that’s 0.1% and quite nasty) while the risk from a fourth jab rises to 1% at which point you’re in the ballpark for a severely morbid person when it comes to Covid-19 infection itself killing them.

The fifth jab would put the risk of getting screwed at ten percent, which is approximately the rate of death from the original SARS and the sixth would be odds-on as literal suicide. How many jabs did you say you’re willing to risk taking again? You cannot get your health back if you ruin it by being stupid. The younger you are the worse the risk is in terms of years of enjoyable life lost. To take that sort of risk when you’re 85, fat, diabetic, you have an almost-10% risk of death in the next year from all causes and the Coof is 10% likely to kill you is very different than to take that same risk to your health when you’re 17, male, have a BMI under 25, there’s not a damn thing wrong with you medically, your all-cause risk of death (most of it by violence) is 7/10,000 and your risk, by the CDC’s numbers, of Covid-19 killing you if infected is approximately 1/100,000.

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Never was one.

The Case For Covid Vaccine Passports Was Just Demolished (Fee)

A newly published medical study found that infection from COVID-19 confers considerably longer-lasting and stronger protection against the Delta variant of the virus than vaccines. “The natural immune protection that develops after a SARS-CoV-2 infection offers considerably more of a shield against the Delta variant of the pandemic coronavirus than two doses of the Pfizer-BioNTech vaccine, according to a large Israeli study that some scientists wish came with a ‘Don’t try this at home’ label,” the Scientific American reported Thursday. “The newly released data show people who once had a SARS-CoV-2 infection were much less likely than vaccinated people to get Delta, develop symptoms from it, or become hospitalized with serious COVID-19.” Put another way, vaccinated individuals were 27 times more likely to get a symptomatic COVID infection than those with natural immunity from COVID.

The findings come as many governments around the world are demanding citizens acquire “vaccine passports” to travel. New York City, France, and the Canadian provinces of Quebec and British Columbia are among those who have recently embraced vaccine passports. Meanwhile, Australia has floated the idea of making higher vaccination rates a condition of lifting its lockdown in jurisdictions, while President Joe Biden is considering making interstate travel unlawful for people who have not been vaccinated for COVID-19. Vaccine passports are morally dubious for many reasons, not the least of which is that freedom of movement is a basic human right. However, vaccine passports become even more senseless in light of the new findings out of Israel and revelations from the CDC, some say.

Harvard Medical School professor Martin Kulldorff said research showing that natural immunity offers exponentially more protection than vaccines means vaccine passports are both unscientific and discriminatory, since they disproportionately affect working class individuals. “Prior COVID disease (many working class) provides better immunity than vaccines (many professionals), so vaccine mandates are not only scientific nonsense, they are also discriminatory and unethical,” Kulldorff, a biostatistician and epidemiologist, observed on Twitter.

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Very odd moment: boosters.

Key Vaccine Leaders Departing FDA As Covid-19 Booster Questions Linger (FPhar)

Two key vaccine leaders will leave the FDA this fall, just as the agency faces key decisions over COVID-19 booster shots and as variants take a bite out of the shots’ efficacy. FDA Office of Vaccines Research and Review Director Marion Gruber, Ph.D. and Deputy Director Phillip Krause, M.D. will depart the agency. Both have been with the agency for decades and have been pivotal in the United States’ effort to authorize COVID-19 vaccines to fight the pandemic. The news was first reported by Biocentury. Gruber will leave the agency on Oct. 31 and Krause’s last day will be sometime in November, according to a letter shared by the FDA with Fierce Pharma. The letter was signed by Peter Marks, M.D., Ph.D., director of the Center for Biologics Evaluation and Research, under which the vaccine research office sits.

Marks will serve as acting director of the OVRR for now as a search begins for a new chief. An acting director will be announced later. “[Gruber’s] contributions throughout her career have been immeasurable, but never more so than during the COVID-19 pandemic,” Marks said. “Her leadership in the center’s efforts to authorize three COVID-19 vaccines, and more recently to approve one of those vaccines, ensured that the vaccines met the high standards the public has come to expect from FDA, and has positively impacted the public health in the U.S. and across the globe.” [..] For his part, Krause was responsible for liaising with public health officials around the world to “address critical vaccine-related issues,” according to Marks. “His keen insight and experience in addressing a wide variety of challenges will truly be missed,” the letter said.

The departures are the latest high-profile officials to leave the key federal agency that still lacks a permanent leader. Janet Woodcock is leading the agency on an acting basis and will not be considered for the commissioner job permanently. Nevertheless, the FDA expressed confidence that the vaccine work would go on. “We are confident in the expertise and ability of our staff to continue our critical public health work, including evaluating COVID-19 vaccines,” an FDA spokesperson said. Gruber and Krause are leaving the agency following criticism of the White House’s decision to leap frog over the agency to recommend COVID-19 booster shots. The move to start boosters next month has been blasted by the World Health Organization, which questions the data to support the need for a third shot—especially as poorer nations continue to struggle with getting first shots to people.

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Note: in the top article, WebMD is cited as saying in the US, up to 40% of health care workers have chosen not to get the vaccine. But Greece claims “more than 90% of the doctors and 80% of the nurses had been vaccinated”.

Greek Health Ministry Bracing For ‘Great Exodus’ (K.)

With the deadline for the mandatory vaccination of health workers expiring on Wednesday, the Heath Ministry is preparing for an imminent “great exodus” of staff due to the suspensions that will ensue with a wide array of preemptive measures to fill the gaps and to ensure that services are fully operational. These measures include a reshuffle of healthcare workers within hospitals, mergers of clinics and departments, the replacement of those suspended with auxiliary staff and partnerships with the private sector for support services such as catering, care etc. Wednesday is the last day for staff to get at least the first dose of vaccine against Covid-19 so as to avoid suspension as of tomorrow. The government has insisted the relevant legislation for mandatory vaccinations will be strictly implemented.


Those who are exempt from the precepts of the legislation are obviously those that have already been vaccinated and workers who have been infected with the coronavirus within the last six months. Those who do not fall into these categories and have not received approval for exemption due to health issues by the competent committees will be suspended. Moreover, as clarified by the former deputy minister of health, Vassilis Kontozamanis, based on the payroll system in the public sector, which provides advance payment of earnings every two weeks, the government will request that they return this amount of salary as unduly paid. Speaking on the radio station 9.84 on Tuesday, Secretary General of Health Services Yiannis Kotsiopoulos estimated that about 10,000 health workers will not continue working in the National Health System. According to the most recent data, more than 90% of the doctors and 80% of the nurses had been vaccinated against Covid-19, while the percentages are lower for the rest of the staff.

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The Guardian campaign vs ivermectin. Check the picture they use.

Pharmacy Customers Refuse To Say What Ivermectin Prescription Is For (G.)

Australian pharmacists have reported an increasing number of people arriving with prescriptions for the drug ivermectin, but refusing to say what it will be used for. The Pharmaceutical Society of Australia said its members were encountering resistance from some customers when asked why they were seeking ivermectin. “PSA is aware that some pharmacists have experienced an increase in presentations of prescriptions for ivermectin, including where the patient is unwilling or unable to discuss what they are being used for,” a PSA spokesperson said. The Therapeutic Goods Administration on Monday said there had been a shortage of Stromectol 3mg ivermectin tablets in August.


The drug is typically used in humans for treating river blindness, scabies and roundworm infections, but has increasingly been sought as a treatment for Covid-19, despite not being approved for that use in Australia. The TGA also noted there had been a tenfold increase in detections of the drug being imported into Australia, prompting the regulator to warn against using the drug for Covid-19 treatment, stating there is “insufficient evidence” that it works and it may be dangerous to health. The university behind the initial lab trial for ivermectin used to treat Covid-19 has also warned against people self-medicating with the drug or buying drugs meant for livestock. Much of the initial focus on the drug as a Covid-19 treatment stemmed from an April 2020 lab trial at Monash University in Melbourne, where ivermectin was found to have killed the Covid-19 virus in a cell culture within 48 hours.

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“New Zealand is fully trapped in the Zero COVID death spiral, and it has no way out of it for the foreseeable future.”

Zero Covid, A Once Wildly Popular Ideology, Quietly Faces Extinction (Subs)

The Zero COVID ideology began with a Chinese government lie. Zero COVID once recruited almost unanimous advocates in world governments, “global health” organizations, and “public health experts” far and wide. Yet today, just 18 months after its first implementation, the Zero COVID ideology is so rare and so unpopular that you have to travel to remote parts of Oceania or within the confines of an elite American liberal arts university in order to find it. Zero COVID, the idea that demands the total elimination of a virus from a nation state, was spawned as part of a disinformation operation by the Chinese Communist Party in Wuhan, China. In early 2020, Chinese authorities declared the virus that causes COVID-19 had been successfully eliminated from the population through brute force restrictions such as lockdowns, masks, and using the power of a Police State to force people to stay inside their homes for an indefinite period of time.

When COVID-19 spread far and wide, almost every nation in the world (other than rare holdouts such as Sweden and Belarus) implemented the aforementioned draconian policies in an attempt to “stop the spread” and eliminate the virus from the world. In the beginning, even questioning these baseless, pseudoscientific ideas was tantamount to being something of a bioterrorist. Through much of 2020, yours truly was constantly castigated by actors across the political spectrum for asking about the wisdom of using the power of government to wage an elimination war against a submicroscopic infectious particle. Zero COVID was science. Zero COVID was truth. Zero COVID superseded every constitutional protection out there, because no right was too important when a virus was out there.

In 2020, COVID Zero’s membership roster was probably in the billions. Now, the adherents of the COVID Zero ideology are facing imminent extinction. The 18 month effort to contain COVID-19 was not only unsuccessful, it brought unprecedented economic and societal disaster in addition to the unconstrained virus problem. Today, few, if any governments have fully owned up to their failures. Most have taken the scapegoat approach, and without evidence, have blamed “the unvaccinated,” the “highly contagious” Delta variant, or some combination of the two to justify their catastrophic blunders. Over the past few months, the remains of the Zero COVID damn broke in the few nation state holdouts where rulers still adhered to the Zero COVID ideology.

In Australia, Vietnam, South Korea, Singapore, and elsewhere around the world, the lid on the pressure cooker came flying off, and local populations saw skyrocketing COVID numbers. Now, every country in the world but one has quietly, through their own policies, accepted the failure of the “global elites’” Zero COVID virus elimination strategy. Read some of the media stories that lauded Zero COVID “success story” nations, and you’ll find that they’ve come to age like months-old milk. New Zealand, the one Zero COVID country that remains, is currently under another hard lockdown, which has recently been extended until at least mid September. The country is now almost 2 years into its self siege, in which the government has decreed that the vast majority of citizens cannot enter or exit the country. As for a reopening timeline, Auckland no longer has one. New Zealand is fully trapped in the Zero COVID death spiral, and it has no way out of it for the foreseeable future.

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Bit late.

Singapore Gives Up Goal of Zero Covid Despite High Vaccination Rate (Gizmodo)

Singapore has decided to give up on the dream of covid-zero and will instead learn to “live with the virus,” according to the country’s Prime Minister, Lee Hsien Loong on Sunday. The decision comes despite the fact that Singapore has one of the highest covid-19 vaccination rates in the world, with 80% of the adult population fully vaccinated—second only to the country of Malta’s 82%. Singapore, a country of roughly 5.7 million people, has been among a handful of countries that have pursued a strategy of completely eliminating covid-19, rather than just suppressing the virus. Other covid-zero countries over the past year have included New Zealand, Taiwan, China, Vietnam, and Australia.

“It is no longer possible to bring covid-19 cases down to zero, even if we lock down for a long time. Therefore, we must prepare for covid-19 to become endemic, like the flu or chicken pox,” Lee said on Sunday during a speech to commemorate the country’s National Day, according to a transcript from the Strait Times. “Fortunately, with vaccination and added precautions, we can live with the virus and become ‘Covid resilient’,” Lee continued. Singapore has done exceptionally well during our global health crisis, reporting roughly 67,000 cases of covid-19 since the start of the pandemic, and just 55 deaths. And Singapore was reporting fewer than 30 cases per day for much of 2021 until a surge of cases in July that saw the country averaging 150 cases per day.

But Loong promises his government isn’t giving up on suppressing the virus, they’re just abandoning the covid-zero model. “We may have to tap on the brakes from time to time, but we want to avoid having to slam on the brakes hard. So in the next phase, we will move step by step. Not in one big bang like in some countries but cautiously and progressively, feeling our way forward,” Lee said. That “big bang” is likely a veiled reference to countries like the UK, which celebrated a “freedom day” in July where all covid-19 restrictions were lifted, only to see a surge in cases and deaths. Case numbers in the UK have started to plateau again, thanks largely to the vast majority of people in the region having covid-19 antibodies either through vaccination or previous infection, but cases are still very high at roughly 25,000 per day. The U.S. has also seen a surge of infections recently, with a seven-day average of about 157,000 new cases each day.

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“It is hard to overstate how dispositively Rhodes’ own book proves that Obama officials generally, and Rhodes specifically, lied blatantly and cavalierly to the public about what happened..”

Obama Officials’ Lies About Edward Snowden and Russia (Greenwald)

Ever since Edward Snowden received asylum from Russia in 2013, Obama officials have repeatedly maligned his motives and patriotism by citing his “choice” to take up residence there. It has long been clear that this narrative was a lie: Snowden, after meeting with journalists in Hong Kong, intended only to transit through Moscow and then Havana on his way to seek asylum in Latin America. He was purposely prevented from leaving Russia — trapped in the Moscow airport — by the very Obama officials who then cynically weaponized his presence there to imply he was a civil-liberties hypocrite for “choosing” to live in such a repressive country or, even worse, a Kremlin agent or Russian spy.

But now we have absolute, definitive proof that Snowden never intended to stay in Russia but was deliberately prevented from leaving by the same Obama officials who exploited the predicament which they created. The proof was supplied unintentionally in the memoir of one of Obama’s senior national security advisers, Ben Rhodes, entitled The World as It Is: A Memoir of the Obama White House. It is hard to overstate how dispositively Rhodes’ own book proves that Obama officials generally, and Rhodes specifically, lied blatantly and cavalierly to the public about what happened: a level of sustained and conscious lying that can be explained only by sociopathy.

The memoir of Rhodes, now appropriately an MSNBC contributor, is an incredibly self-serving homage to himself that repeatedly attempts to demonstrate his own importance and accomplishments. The passage about Rhodes’ conduct regarding Snowden is very much aligned with those goals. While repeatedly emphasizing how traumatic the Snowden revelations were for the Obama administrations, Rhodes boasts of the crucial role he played in preventing Snowden from leaving Russia as the NSA whistleblower was desperately attempting to do so — exactly the opposite of what people like Rhodes and Hillary Clinton were telling the public about Snowden.

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Aug 282021
 
 August 28, 2021  Posted by at 8:30 am Finance Tagged with: , , , , , , , , ,  107 Responses »


Vincent van Gogh The yellow house (The Street), Arles 1888

 

Former Pfizer Employee: “Checkmate. Game Over. We WIN” (Peters)
CDC Counts People Dying Within 14 Days of Jab as “Unvaccinated” (GR)
Israel Cracks The Code: Jabs Don’t Work (Denninger)
Natural Immunity 13x More Effective Than Vaccines At Stopping Delta (ZH)
Denmark To Scrap All Covid-19 Restrictions (ZH)
Judge Strips Mother Of Parental Rights Over Vaccination Status (Fox32)
US Mandates Vaccinations For Marines (PPundit)
US Special Forces Vets Launch Mission To Get Afghan Allies Out (DM)
Low and Dark (Kunstler)
Marine Commander Fired For Blasting ‘Inept’ Military Leadership (WND)

 

 

Update from the CDC:

 

 

 

 

 

 

 

“FDA approval is checkmate for Pfizer.”

Don’t miss this. Start at about 3:40min. Watch to the end.

If only half of what she says is true, Pfizer is in enormous trouble. And so is the FDA; they knew too.

Pfizer has two weeks to list all ingredients in its vaccine. Graphene oxide makes its comeback.

Former Pfizer Employee: “Checkmate. Game Over. We WIN” (Peters)

Karen Kingston is a former Pfizer employee, a pharmaceutical marketing expert and biotech analyst. Kingston joins Stew Peters, and brings the receipts! Kingston reveals how the FDA “approval” is sure to be the “checkmate” move to end the shots that have caused unprecedented injury and death, worldwide. Kingston shared slides and brought the receipts, which are available at StewPeters.tv, and document everything she states in her BOMBSHELL claims during her exclusive and revealing deliver of damnation to big pharma, and those responsible for pushing these injections onto a global population.

Read more …

“Unvaccinated L.A. County residents [are] 5 times more likely to get COVID, 29 times more likely to be hospitalized.”

Here’s where those numbers come from.

CDC Counts People Dying Within 14 Days of Jab as “Unvaccinated” (GR)

Citing the Los Angeles County Morbidity and Mortality Weekly Report released on Tuesday, even local news promoted the claim that “Unvaccinated L.A. County residents [are] 5 times more likely to get COVID, 29 times more likely to be hospitalized.” Looking at a screenshot of the CDC release, one can observe the definitions for what they consider “fully vaccinated,” “partially vaccinated,” or “unvaccinated.” According to the chart, “unvaccinated <14 days receipt of the first dose of a 2-dose series or 1 dose of the single-dose vaccine or if no vaccination registry data were available. This means if someone was hospitalized, admitted to ICU, required mechanical ventilation or died within two weeks of getting the jab they are being counted as “unvaccinated.”

Unfortunately, because the data is not specific enough, we don’t know how many truly unvaccinated people were hospitalized or died of Covid in Los Angeles County from May to late July. The entire report can basically be tossed into the trash thanks to the inclusion of the recently vaccinated in the unvaccinated category. This intentionally misleading data is now being used to infringe on the rights of the people of California and across the entire United States as vaccine mandates and passports are being rolled out nationwide.

Read more …

“.. the dosing they used, and the original titers, concealed the decay below effective levels which was not being tested for..”

Israel Cracks The Code: Jabs Don’t Work (Denninger)

If you recall early on before the jabs were “released” under EUA I pointed out that some of the early study work had odd results that I could not reasonably explain a purpose to, and they bothered me a lot. One of the most-glaring was the wildly higher antibody titers produced by them as opposed to natural infection. I mused at the time that this could easily be explained by the truncation (or simply ignorance of) the usual dose-ranging studies that are done on all drugs; those require time, of course, and when you’re after Warp Speed time is something you don’t have. But now it appears that Pfizer may have known there was a problem — they may not have known how serious it was, but they may well have known it existed and may have deliberately set the dosing to try to hide it. And, as it turns out, that wasn’t the only problem.


“In vaccinated subjects, antibody titers decreased by up to 40% each subsequent month while in convalescents they decreased by less than 5% per month. Six months after BNT162b2 vaccination 16.1% subjects had antibody levels below the seropositivity threshold of <50 AU/mL, while only 10.8% of convalescent patients were below <50 AU/mL threshold after 9 months from SARS-CoV-2 infection.” In other words the dosing they used, and the original titers, concealed the decay below effective levels which was not being tested for but would have shown up in infections among vaccinated people had the original level been lower. That’s bad; the question now becomes did Pfizer know this and do it deliberately, and if not, what is the logical explanation for the dosing used? Why not set dosing roughly identical to natural infection? Simple: If they did that before the four months of the study ran a crap-ton of people would have gotten infected since the antibody titer would have worn off.

It gets worse: “In our study, we show that following vaccination, the levels of anti-SARS-CoV-2 antibodies decrease rapidly, indicating that BMPCs may not be created adequately and therefore anti-SARS-CoV-2 humoral immunity might be transient (Ibarrondo et al., 2020; Seow et al., 2020).” If there is little or no B-cell recall then the vaccine is a failure as it cannot stimulate durable immunity at all. That is, the jabs are basically the same (via a different mechanism) to receiving monoclonal antibodies if you get infected; yes, you have an antibody titer but the jabs fail to train your immune system to recognize the infection in the future. As that titer wanes the protection becomes increasingly worthless and, since we know mutational binding changes are occurring the potential for vaccine-caused harm by potentiating infections remains a distinct possibility as that occurs.

Read more …

Funny we’ve been talking about this all week, and now this gets 1 million views at Zero Hedge.

Natural Immunity 13x More Effective Than Vaccines At Stopping Delta (ZH)

Dr. Anthony Fauci and the rest of President Biden’s COVID advisors have been proven wrong about “the science” of COVID vaccines yet again. After telling Americans that vaccines offer better protection than natural infection, a new study out of Israel suggests the opposite is true: natural infection offers a much better shield against the delta variant than vaccines. The study was described by Bloomberg as “the largest real-world analysis comparing natural immunity – gained from an earlier infection – to the protection provided by one of the most potent vaccines currently in use.” A few days ago, we noted how remarkable it was that the mainstream press was finally giving voice to scientists to criticize President Biden’s push to start doling out booster jabs. Well, this study further questions the credibility of relying on vaccines, given that the study showed that the vaccinated were ultimately 13x as likely to be infected as those who were infected previously, and 27x more likely to be symptomatic.

Alex Berenson, a science journalist who has repeatedly questioned the efficacy of vaccines and masks at preventing COVID, touted the study as enough to “end any debate over vaccines v natural immunity.” Here’s an excerpt from a report by Science Magazine: “The new analysis relies on the database of Maccabi Healthcare Services, which enrolls about 2.5 million Israelis. The study, led by Tal Patalon and Sivan Gazit at KSM, the system’s research and innovation arm, found in two analyses that people who were vaccinated in January and February were, in June, July, and the first half of August, six to 13 times more likely to get infected than unvaccinated people who were previously infected with the coronavirus. In one analysis, comparing more than 32,000 people in the health system, the risk of developing symptomatic COVID-19 was 27 times higher among the vaccinated, and the risk of hospitalization eight times higher.”

This time, the data leave little doubt that natural infection truly is the better option for protection against the delta variant, despite the fact that the US won’t acknowledge the already infected as having antibodies protecting them from the virus. As the first country to achieve widepsread coverage by the vaccine, Israel is now in an unthinkable situation: daily case numbers have reached new record levels as the delta variant penetrates the vaccines’ protection like a hot knife slicing through butter.

Read more …

Because of “record high vaccination rates”. Oh boy…

Denmark To Scrap All Covid-19 Restrictions (ZH)

Denmark will on September 10th stop classifying Covid-19 as an “illness which is a critical threat to society”, meaning all remaining special pandemic restrictions will expire, The Local reported. In a press release issued on Friday morning, the country’s health minister Magnus Heunicke said that the high level of vaccination in Denmark, particularly among the vulnerable, had radically altered the risks posed by the virus. “The epidemic is under control, we have record high vaccination rates,” he said in a statement. “As a result, on September 10th, we can drop some of the special rules we have had to introduce in the fight against Covid-19.”


September 10th marks the expiry date for that the executive order classifying Covid-19 as a “socially critical illness”, which was passed by the Danish parliament’s Epidemic Committee on March 10th last year. The parties in the centre-right blue bloc, led by the Liberal Party, have already said that they believe that Covid-19 should no longer be classed as a serious threat to society, and the health ministry’s announcement came less than an hour before the ruling Social Democrats were due to discuss the issue with the other parties in the Epidemic Committee. “When it sinks in for the Social Democrat government that they are in a minority, they then come up with better ideas just 45 minutes before the meeting in the Epidemic Committee is starting,” said Sophie Løhde, a member of the committee for the Liberal Party.

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Crazy, that’s the only word.

Judge Strips Mother Of Parental Rights Over Vaccination Status (Fox32)

A Chicago mother says a Cook County judge has taken away her parental rights after learning that she is not vaccinated against COVID-19. In what all parties agree is a very unusual and perhaps unprecedented step, a judge at Chicago’s Daley Center has stripped Rebecca Firlit of custody because she refuses to get a vaccination shot. “I miss my son more than anything. It’s been very difficult. I haven’t seen him since August 10th,” Firlit told FOX 32 News in an exclusive interview. That’s the day Firlit appeared in court via Zoom along with her ex-husband for a child support hearing involving their 11-year-old son. The two have been divorced for seven years and share custody and parenting time.

She says out of the blue, Cook County Judge James Shapiro asked her whether she had been vaccinated. Firlit told Shapiro she had not because she has had bad reactions to vaccines in the past. Shapiro then ordered that Firlit be stripped of all parenting time with her son until she gets vaccinated. Over the past two weeks, Firlit has been able to talk to her son on the phone and through video calls, but has not seen him in person. “I think that it’s wrong. I think that it’s dividing families. And I think it’s not in my son’s best interest to be away from his mother,” Firlit said.

Firlit is now appealing the court order, saying the judge has no business taking away her parenting rights simply because she’s not vaccinated. “It had nothing to do with what we were talking about. He was placing his views on me. And taking my son away from me,” Firlit said. Annette Fernholz, Firlit’s attorney, says the judge has overstepped his authority. “In this case you have a judge, without any matter before him regarding the parenting time with the child deciding ‘Oh, you’re not vaccinated. You don’t get to see your child until you are vaccinated.’ That kind of exceeds his jurisdiction,” Fernholz said.

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Twitter thread. Highly ironic given what soldiers are being put through in Kabul. It’s like the mandates for healthcare workers. Blind.

US Mandates Vaccinations For Marines (PPundit)

1. SCOOP: Biden Admin is not done putting members of U.S. armed services at risk, mandating U.S. Marines receive first dose vaccinations before WTI (Weapons Tactics Instructions) in a week, ignoring apps for exemptions that include religious and history of Myocarditis. 2. Further, the second dose will be administered during WTI, in a remote location with only field medic attention available to them. Again, this is ordered for those who have known medical conditions that were considered viable causes for exemptions only a week ago. These are all people who had no problem getting vaccinated for scores of other diseases. They were told they would have the ability to obtain waivers and are now facing the choice between risk to personal harm and/or violation of conscience, or professional ruination.

Reading the documents provided to us (of course it’s documented), service members who refuse to take the vaccination will be “dealt with via administrative or disciplinary measures, i.e., AdSep, NJP or court-martial.” There is not enough time for waivers to be issued. Again, the main issue here, which is expected given how these things play out in real life, is that the Biden Admin is claiming there is an accommodation for religious exemption and exemption for certain medical conditions, but in reality is not afforded to them. It’s a Catch 22. If you have a religious exemption, then DoD tells them to apply for it, claims they were allowed. Except, they won’t actually have time for the “Chaplain Interview Checklist” (sound familiar @DeptofDefense?) because they just got orders and the deadline is here.

And honestly, this is what many of them are concerned about. Not for themselves, but for their Battles who they know are seeking waivers for legitimate conditions linked to Pfizer. They are NOT “anti-vaccine”. For those seeking religious exemptions, there is no time for them to get a “Chaplain Interview Checklist” before the “Religious Accommodation Review Board”. Again, sound familiar @DeptofDefense? These service members have been scammed. I thought we had enough of that, this week “And the worse part is, you dont get the vaccine, you don’t go on exercises, you get no job training, you’re kicked out.” I realize most Americans have never served, don’t understand what it means to be in this situation. We lie to them about wars. We lie to them about waivers.

Read more …

‘I just want to get my people out,’ said one of the retired troops..”

US Special Forces Vets Launch Mission To Get Afghan Allies Out (DM)

A group of American war veterans in Kabul are secretly saving hundreds of Afghan Special Forces troops and their families who helped them in the war but have now been left for dead as the US withdraws from Afghanistan. The group of special op soldiers includes retired Green Berets and SEAL Team commanders who launched the mission, which they are calling Pineapple Express, after one of the Afghan commandos they served with contacted them to say he was on the run from the Taliban. His visa had not been approved when the Taliban took over on August 14 and thousands ran for the airport.

The special ops soldiers first devised a system with US troops at the airport where they sent their comrades to a gate and told them to identify themselves with the password ‘pineapple’ to be put on a plane by the Marines on the ground. Some also showed the troops pictures of pineapples on their phones. After successfully getting hundreds through that way, the special ops teams started going into Kabul, behind enemy lines, to rescue more of their comrades and their families in the cover of darkness. It’s unclear how long they have been in Afghanistan and how they got there but some of those involved spoke to ABC News about the mission on Friday, explaining they simply could not leave their comrades behind.

‘I just want to get my people out,’ said one of the retired troops involved while another said the Afghan allies they were saving had a prouder sense of Democracy than some Americans. Their astonishingly courageous efforts have saved hundreds while Biden and his team have bungled the evacuation mission by haphazardly telling some US citizens and allies to go to the airport while rejecting visas for others and leaving any Americans to fend for themselves. They are one of several ad-hoc volunteer groups on the ground that are frantically trying to save people before time runs out.

The disastrous government rescue mission became even more tragic on Thursday when ISIS bombers targeted the crowds at the airport, slaughtering 170 people with a suicide bomb that also killed 13 US troops. It has since emerged that Biden’s administration also gave a list of Afghan allies’ names to the Taliban in the naïve hope they would then help get them out. Former President Donald Trump called it a ‘kill list’ that all but guaranteed their deaths. The US now one of the only nations still evacuating from Kabul amid increasing threats of another ISIS attack.

Read more …

“Some of said bigwigs, including the managing parties behind “Joe Biden,” might be cooking up a neat operation in which “Joe Biden” resigns, Ms. Harris gets elevated to POTUS… Ms. Harris appoints Barack Obama vice-president… and then Ms. Harris resigns, making the popular ex-president president again.”

Low and Dark (Kunstler)

His managers installed a “poison pill” named Kamala Harris as his vice-president, and even members of her own party get the vapors at mere fugitive thoughts of her trying to run the country, giggling from one crisis to another. Meanwhile, the veep cut short her tour of Southeast Asia, rushing to aid beleaguered California Governor Gavin Newsom at a rally to fight his recall vote… but then cut short her Newsom rescue mission to fly on to Washington. Electioneering during the greatest hostage crisis in US history probably equals more poor optics. She will presumably spend the days ahead “standing by” on developments, within reach of the Xanax vial — while a claque of party bigwigs importunes her to get rolling on the 25th amendment.

Some of said bigwigs, including the managing parties behind “Joe Biden,” might be cooking up a neat operation in which “Joe Biden” resigns, Ms. Harris gets elevated to POTUS… Ms. Harris appoints Barack Obama vice-president… and then Ms. Harris resigns, making the popular ex-president president again. The 22nd Amendment only prevents presidents from being elected more than twice, not from being appointed by happenstance. Would they dare? Well, why not? They dared to engineer some pretty audacious election hijinks in 2020.

One thing you can count on, the situation has the potential to get a whole lot worse, both for the nation and for “Joe Biden”. Our new Taliban “partners,” assigned to provide security in-and-around Kabul, may prove to be less than steadfast in their duties as hoped. Thursday’s bloodbath hints at their inadequacies. The number of Americans stranded in Afghanistan remains hypothetical, a thousand… six thousand…nobody seems to know. Plus, Gawd knows how many NATO-ally civilian personnel, international NGO workers, and other people of, shall we say, the Western persuasion, remain trapped.

The ISIS suicide bombings made a pretty bold statement, too. If one ventured to say that our new Taliban partners are something less than gentlemen, how would you describe the cadres of Al Qaeda and ISIS? Poor sports? Ruffians? Misogynists? They have the run of Kabul now, the ability to go from door-to-door, rooting Westerners out, something they probably regard as fun. Do you remember from just a few years ago what kinds of things they like to do to their captives? Cut their heads off. (Notice I didn’t say chop.) Roast them in cages. That could start any minute. What then, “Joe Biden”?

Read more …

When the military turns against politics, throwing away entire careers to do it, you’re in trouble.

Marine Commander Fired For Blasting ‘Inept’ Military Leadership (WND)

A sitting Marine battalion commander was fired Friday after he slammed the “ineptitude” of U.S. military leadership over the disastrous Afghanistan withdrawal. Lt. Col. Stuart Scheller said in a video posted on YouTube after the deadly suicide attack Thursday that he was willing to risk his career and his pension — only three years from retirement — to “demand accountability” from top military brass, the Washington Free Beacon reported. “I want to say this very strongly. I have been fighting for 17 years. I am willing to throw it all away to say to my senior leaders: I demand accountability,” said Scheller. In a Facebook post Friday, he announced he had been “relieved for caused based on a lack of trust and confidence.”

In his video, he said he had a close relationship with one of the 13 service members who were killed Thursday in a suicide bombing at a gate at the Hamid Karzai International Airport. He said he is not the only service member who is upset about how the withdrawal has been handled. “The reason people are so upset on social media right now is not because the Marine on the battlefield let someone down. That service member always rose to the occasion and done extraordinary things,” Scheller said. “People are upset because their senior leaders let them down and none of them are raising their hands and accepting accountability or saying, ‘We messed this up.'”

Scheller, the Free Beacon reported, reacted to an Aug. 18 public letter by Gen. David Berger, commandant of the Marine Corps. Berger attempted to reassure Marines who were expressing their frustration on social media that their service was “meaningful, powerful, and important.” Scheller said the letter missed the point, arguing the withdrawal was a major policy failure from the highest levels of military leadership. He called out Secretary of Defense Lloyd Austin and the joint chiefs of staff. “I’m not saying we’ve got to be in Afghanistan forever. But I am saying, did any of you throw your rank on the table and say, ‘Hey, it’s a bad idea to evacuate Bagram Airfield, a strategic airbase, before we evacuate everyone’? Did anyone do that? And when you didn’t think to do that, did anyone raise their hand and say, ‘We completely messed this up’?” asked Scheller.

Read more …

 

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 August 27, 2021  Posted by at 9:30 am Finance Tagged with: , , , , , , , , , ,  64 Responses »


Claude Monet Hollowed Cliff near Étretat 1883

 

Coroner Confirms 44-Year-old BBC Presenter Died From Vaccine Side Effect (RT)
New Zealand Police Break Up One-Person Anti-lockdown Protest In Auckland (G.)
‘Bombshell’ Study Finds Natural Immunity Superior To Vaccination (Unherd)
The Suspicious FDA “Approval” Of The Pfizer Vaccine (Techno Fog)
******nit, Stop The FRAUD (Denninger)
What Can We Learn About COVID Tyranny From Australia And Afghanistan? (Smith)
The Weaponization Of Medicine (FMP)
Health Workers Protest Against Introduction Of Mandatory Covid Jabs (K.)
Arkansas Jail Dosing Inmates With Ivermectin, In Spite Of FDA Warnings (AP)
The Cost-Benefit Analysis of COVID (Greenwald)
Biden Does Surreal Press Conference, Vows To Hunt Down Isis, Blames Trump (ZH)
US Provided Taliban With Names Of Americans, Afghan Allies To Evacuate (Pol.)
Taliban Opens Chain Of U.S. Army Surplus Stores (BBee)

 

 

 

 

 

 

Who ordered this autopsy? Where are the reports on all the other autopsies?

Coroner Confirms 44-Year-old BBC Presenter Died From Vaccine Side Effect (RT)

A coroner’s report has confirmed that late BBC Radio presenter Lisa Shaw died from “complications” related to AstraZeneca’s Covid-19 vaccine. Shaw died on May 21 at the age of 44 roughly three weeks after she received her first dose of AstraZeneca’s vaccine. She did not have any known underlying health problems but developed blood clots after receiving the jab. On Thursday – over three months after her death – a coroner finally confirmed that Shaw died from complications that were suffered as a result of vaccination. Coroner Karen Dilks declared that Shaw “died due to complications of an AstraZeneca Covid vaccination,” or specifically, “vaccine-induced thrombotic thrombocytopenia” which caused the blood clots in her brain.


In the weeks after the vaccine, Shaw had complained about severe headaches. Some 332 similar cases and 58 deaths have been recorded in relation to the AstraZeneca vaccine. Many countries have suspended or completely stopped the use of AstraZeneca’s vaccine, with some limiting its use for those over the age of 60. In the UK, however, the age restriction is significantly lower. On May 7, just over a week after Shaw received her dose, the UK government announced that those under the age of 40 should be offered an alternative to AstraZeneca “if available and if it does not cause delays in having the vaccine.” The government currently warns that AstraZeneca’s side effects can include rare blood clots, capillary leak syndrome and Guillain-Barre Syndrome, and that those who experience “a severe headache that is not relieved with simple painkillers or is getting worse or feels worse” should “seek medical advice urgently.”

Read more …

How do you “break up” one person?

New Zealand Police Break Up One-Person Anti-lockdown Protest In Auckland (G.)

A one-person anti-lockdown protest in central Auckland has been shut down, after the police were alerted to discussions of a potential gathering on social media. New Zealand police said officers were on Queen Street on Friday after hearing a protest was being planned, but only one person arrived with the intention of protesting, Newshub reported. “Police have been in the area and have spoken to one person who arrived intending to attend the protest. Police spoke to the individual who was encouraged to comply with alert level four restrictions and chose to leave,” a spokesman said. They said they are continuing to monitor the situation. An Instagram account had called on people “who see the bigger picture” to get involved in the protest, Newshub reported, despite also saying it wasn’t involved in the demonstration and had no idea who was behind it.


The post criticised prime minister Jacinda Ardern and the government for “destroying the economy” and “destroying jobs”, despite the unemployment rate dropping to 4 percent in the June 2021 quarter and the economy weathering the pandemic better than expected. Last week, around 100 anti-lockdown protesters gathered on Queen Street, and four people were arrested. Four people were also arrested at a protest of about 20 people in the city of Tauranga outside the local police station. Another group gathered outside a police station in the South Island city of Nelson the same day, but dispersed after officers issued 20 verbal warnings.

Read more …

We’ve known this all along. Where’s the bombshell?

‘Bombshell’ Study Finds Natural Immunity Superior To Vaccination (Unherd)

A major study conducted by Israeli researchers into natural immunity has found that immunity acquired via infection from Covid-19 is superior to immunity from the Pfizer vaccine. Researchers at Maccabi Healthcare and Tel Aviv University compared the outcomes of over 76,000 Israelis in three groups: the doubly vaccinated (with the Pfizer vaccine), the previously infected but unvaccinated, and the previously infected with a single dose. They found that fully vaccinated people were significantly more likely to have a “breakthrough” Covid infection than people who had previously been infected and recovered from the disease. “This study demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease and hospitalisation caused by the Delta variant,” the authors conclude.


The study is only published as a preprint at this stage and has not been peer reviewed. Critics including British immunologist Andrew Croxford have pointed out potential limitations, but it has been described by infectious diseases expert Professor Francois Balloux as a “bombshell” development. If the findings are confirmed, the implications for global Covid policy will be profound. It would not undermine the importance of vaccination for more vulnerable groups in society. However it would weaken the case for vaccinating children, despite the programme being confirmed in the UK today, as they (and the people around them) would get superior future protection from contracting the disease. And it would pose a fundamental challenge to the singular emphasis on vaccine passports for travel and large events, if unvaccinated people who have already had Covid actually pose less of a risk.

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“For those who received two doses of the Pfizer Vaccine in January 2021, the vaccine is “only 16% effective against symptomatic infection.”

The Suspicious FDA “Approval” Of The Pfizer Vaccine (Techno Fog)

The FDA says COMIRNATY is “safe and effective in preventing COVID-19 in individuals 16 years of age and older.” How effective? They state (~6 months after dose 2) that it is “91% effective in preventing COVID-19 disease,” citing to a study where Pfizer observed “77 cases of COVID-19 occurring in the vaccine group.” This leaves us with an important question. The Pfizer study is from a “follow-up through March 13, 2021.” That is over 5 months ago. Is the FDA using outdated data in support of the COMIRNATY approval? In other words, how long does the effectiveness really last? Pfizer has an answer for us. According to its August 23, 2021 fact sheet, “The duration of protection against COVID-19 is currently unknown.”

If you’re looking for data on the waning effectiveness of the Pfizer Vaccine against COVID-19, you have to search for yourself. You won’t find it with the FDA or Pfizer, underscoring an apparent effort to cherry-pick the data for the “approval.” According to one UK study of over 400,000 people (a study that is, by the way, much more rigorous than the one cited in the FDA approval), the “effectiveness fell to 74% five or sixth months after receiving both doses of the Pfizer vaccine.”

The news out of Israel is worse. For those who received two doses of the Pfizer Vaccine in January 2021, the vaccine is “only 16% effective against symptomatic infection.”

As we have observed, the CDC has promoted a misleading message on the risks the vaccines present to pregnant mothers. They used self-reporting studies that were racially skewed studies (~79% white and 1.4% black) and limited to looking at miscarriages from weeks 6-20. (This caused them to omit from the study 35 self-reported pregnancy losses at less than 6 weeks.) The new approval mentions a study on the Pfizer Vaccine exposure during pregnancy to be completed in 2025. Four years from now pregnant women will know whether this vaccine is safe. As for the current data? Here’s what the COMIRNATY package insert says about there being “insufficient” information on the vaccine risks to pregnancy.

Ok Techno, I’m with you so far… but did Pfizer do any studies on whether the vaccine was safe for pregnant women? YES! They did toxicology studies on female rats.

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“..if being vaccinated makes the person who gets it more-infectious then being jabbed is not only personally dangerous it is dangerous to public health..”

******nit, Stop The FRAUD (Denninger)

in the best case you must repeatedly take the risk of strokes and heart attacks, along with other serious adverse effects, in order to maintain protection. If the risk is 1/10,000 to do it once then the risk is 1/5,000 to do it twice, assuming the risk is linear which we do not know. If its exponential, and there is a strong suggestion that is the case because most of these events occurred after the second jab in the series, then the risk from taking three jabs may be 1/1,000 instead of 1/10,000 which is ridiculously higher and makes the decision to risk infection rather than vaccination simple for most people since only the quite-morbid are at higher risk from infection than 1/1,000 (0.1%) even if we assume the risk of eventual infection, if you do nothing, is 100%.

Note that if there is no end to these jabs then eventually even the most-morbid are stupid to take them since the risk of the jab killing them will rapidly exceed that of the virus doing so and this assumes that vaccine-induced enhancement does not show up and wildly multiply the risk of serious disease and death from the virus itself. There is no way to know whether these risks will converge either naturally or by forced action of a malevolent party but that they exist and are independently present is now known with scientific certainty as all of those mutations have now been found in the gene banks from sampled patients. If that “next mutation” winds up being of benefit to “being first” in an uninfected, non-recovered host and worse, if being vaccinated makes the person who gets it more-infectious then being jabbed is not only personally dangerous it is dangerous to public health and will cause a wave of serious illness and death to tear through the vaccinated population and if that happens there is nothing that can be done to stop it.

The FDA knows all of this as they have the same access to the published scientific work I do. They didn’t hold a hearing or take public comment, as they are supposed to, because then people like myself could submit into the formal, government record papers like the one I cited above. In addition the FDA cut off the data far enough back to deliberately ignore the most-recent few weeks, which show crazy deterioration in the percentage of people who die of Covid-19 and are vaccinated. In some counties (e.g. Clark, NV) the vaccinated are now the majority of the deaths. Does this prove vaccine-induced enhancement is here and raging? No; the data is too thin. But what it does prove is that being jabbed doesn’t stop you from getting sick nor does it stop you from giving the virus to others and that by itself reduces the decision to be vaccinated to one of personal choice at best.

And finally even Pfizer admits that they can’t get ahead of such a mutational event whether it occurs naturally or is forced and released by a malevolent actor. They say they can turn around a new version of the jab within 95 days but then you have to get it into the hundreds of millions of Americans and that can’t happen any faster the second time than the first. Assuming you immediately can ramp up production and distribution expecting that you can get effective coverage within less than another three to six months is fantasy-level bull**** as we didn’t manage that the first time and the virus mutates faster than you can accomplish it, making the attempt a game of whack-a-mole which you will inevitably lose. Never mind the risk that the reformulated version may produce immediate and extremely dangerous adverse events at a wildly-elevated rate: Without trials, which again will add months or years to the time required to deploy, there is no way to know! It is sheer arrogance to presume none of this will happen when we now have hard proof that least some of it did with the first go-around.

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“..these measures cannot be fast tracked in the same way in the US because Americans are heavily armed and have the ability to bury the establishment six feet under if we organized to do so..”

What Can We Learn About COVID Tyranny From Australia And Afghanistan? (Smith)

I have warned consistently that all governments around the world would eventually try to adopt proof of vaccination requirements in order for people to participate in everyday activities such as going to public venues, going to school, shopping in stores or even getting a job. The mainstream media and governments consistently claimed last year that vaccine passports were “not going to happen”, and that the very notion was a conspiracy theory. Now, the vaccines passports are being implemented in numerous countries including some parts of the US and anyone who stands against them is called a “conspiracy theorists”. You see how that works? If you expose the truth of an authoritarian plot the establishment lies and calls you a “conspiracy theorist”.

Once the establishment admits to the plot and you refuse to comply with it those same liars call you a conspiracy theorist AGAIN, as well as a “terrorist.” Yes, this was also predicted by myself and others at the beginning of the pandemic. We said that the people that fight against vaccine passport tyranny would be quickly labeled as traitors and terrorists “putting others at risk” because we are too “selfish” to bow down and take the experimental jab or submit to the lockdowns. This is exactly what has happened, with the DHS recently announcing that one of the warning signs of a potential terrorist includes opposition to covid mandates and vaccines.

I also predicted that the ultimate goal of the covid agenda will be to create domestic travel restrictions and state and city checkpoints, not to mention covid “camps” or prisons for the unvaccinated. In the US the DHS is admitting that they are entertaining the concept of interstate travel limits and a “papers please” system to prevent Americans from moving around freely. The state of New York hinted at covid camps many months ago, but the real plan is being revealed overseas in other Western nations like Australia and New Zealand.

And here is where we find the telegraphed punches… I have specifically examined Australia and New Zealand’s fast track covid tyranny plans a year ago in my article ‘The Totalitarian Future Globalists Want For The Entire World Is Being Revealed’ and I noted that whatever happens in these countries along with certain countries in Europe is going to be tried in the US in the near term. The main difference being that these measures cannot be fast tracked in the same way in the US because Americans are heavily armed and have the ability to bury the establishment six feet under if we organized to do so.

Read more …

“Once “medicine” and “science” are mixed with social pressure, they are no longer science or medicine. At that point they are instruments of thuggery, and nothing more.”

The Weaponization Of Medicine (FMP)

#1: Science is not consensus. Ten, one hundred, or a million people, all draped in lab coats and saying the same thing, does NOT make it so. In fact, it matters not at all. It’s nothing but theater, and it’s anti-science. All science is, really, is a process of testing ideas; it is not an organization, it is not based upon authority (it’s inherently anti-authority), and it is very certainly not allied with power. All that matters in science are verifiable results.

#2: Medicine stands apart from, and above, politics. Medicine is the application of science to the furtherance of human health. Politics is the use of persuasion and power to rule masses of humans. These are fully separate disciplines. To place politics over medicine is to subjugate and degrade medicine: it’s a path backwards into darkness. I’ll leave details on this point to working medical practitioners, who can provide them with far greater specificity than I can… provided they’re not too frightened to do so.

#3: Peer review no longer means much. Again I won’t go into great detail, but peer review has been captured by academic hierarchies and almost fully separated from science proper. It has become a tool of institutional power, wielded by academics who have sold out science for the favors of power and politics. At one time, “peer review” referred to the honest replication of experiments. That time is past.

#4: Medicine and science have nothing to do with social pressure. Once “medicine” and “science” are mixed with social pressure, they are no longer science or medicine. At that point they are instruments of thuggery, and nothing more.

#5: If you don’t read multiple scientific papers, especially from rebels and cast-outs, you simply don’t know. You can pretend you know, of course, and you can be sure that agents of the status quo will provide you with passable reasons to repeat their slogans, but you won’t actually know. What you see on TV is propaganda. What you see on Facebook, Twitter and YouTube is pre-censored. If you want to really know, you’ll have to find the scientific papers that address your question… and you’ll need papers that are rejected by televised authorities. If you don’t, all you’ll have are pre-censored conclusions, the underlying facts of which may or may not be reliable. At this point, if you don’t include “conspiracy theory” research, you’re more or less stuck with Orwell’s Ministry of Truth. Sad but mostly true.

Read more …

Working their asses off for 20 months and getting a mandate as their reward.

Health Workers Protest Against Introduction Of Mandatory Covid Jabs (K.)

Hundreds of Greek frontline health workers protested on Thursday against a plan to make Covid-19 vaccinations mandatory for the care sector as infection rates remained high. Healthcare workers observed a four-hour work stoppage against new rules obliging medical staff to vaccinate against the coronavirus, and to call for more resources to public health. The mandatory jab comes into effect for healthcare workers on Sept. 1. Those who do not comply and have not had at least one shot of a vaccine will be suspended from their jobs. According to the POEDIN labor union, about 10 percent of healthcare workers have not had a first vaccine jab. Protesters said that while the call for vaccination was widely acknowledged and complied with by healthcare workers, the view of a dissenting few should to be respected.


“I’m here today because I want to support the constitutional right of every Greek citizen to say ‘yes’ or ‘no’ to vaccination. I personally am vaccinated, but I believe it is my colleagues’ right to not get vaccinated if they don’t want to,” said Evangelia Karatzouli, a nurse at a public hospital. Greece on Thursday reported 3,538 new coronavirus cases in a single day, with 28 deaths. It reported a record daily rate of 4,608 infections on Tuesday. read more The Greek public hospital workers union will support unvaccinated colleagues, said its president, Michalis Yiannakos. “They consist of a tiny number, and have for the last 18-19 months been on the frontlines, caring for patients in the Covid wards, and have not ever gotten infected, and now they are being thrown out on the streets,” he said.

Read more …

“Whatever a doctor prescribes, that is not in my bailiwick..”

Arkansas Jail Dosing Inmates With Ivermectin, In Spite Of FDA Warnings (AP)

Inmates at a north-west Arkansas jail have been prescribed a medicine for treating coronavirus that is normally used to deworm livestock, despite federal health warnings to the public in exasperated tones. Washington county’s sheriff confirmed this week that the jail’s health provider had been prescribing the drug. The US Food and Drug Administration (FDA), the federal drugs regulator, issued a warning via Twitter last weekend. “You are not a horse,” it said. “You are not a cow. Seriously, y’all. Stop it.” Sheriff Tim Helder did not say how many inmates at the 710-bed facility had been given ivermectin and defended the health provider that has been prescribing the medication. “Whatever a doctor prescribes, that is not in my bailiwick,” Helder told members of the Washington county quorum court, the county’s governing body.


[..] It is not clear what information inmates who were prescribed the drug have been given about it, including warnings that it is not approved to treat Covid. The US FDA has approved ivermectin in both people and animals for some parasitic worms and for head lice and skin conditions. The FDA has not approved its use in treating or preventing Covid-19 in humans. “Using any treatment for Covid-19 that’s not approved or authorized by the FDA, unless part of a clinical trial, can cause serious harm,” the FDA said in a warning about the drug. Prominent rightwingers have been promoting the drug for Covid and public health officials have come under attack from some Republicans for urging Americans to get vaccinated against coronavirus.

Read more …

Zero.

The Cost-Benefit Analysis of COVID (Greenwald)

[..] we employ a rational framework of cost-benefit analysis, whereby, when making public policy choices, we do not examine only one side of the ledger (number of people who will die if cars are permitted) but also consider the immense costs generated by policies that would prevent those deaths (massive limits on our ability to travel, vastly increased times to get from one place to another, restrictions on what we can experience in our lives, enormous financial costs from returning to the pre-automobile days). So foundational is the use of this cost-benefit analysis that it is embraced and touted by everyone from right-wing economists to the left-wing European environmental policy group CIVITAS, which defines it this way:

“Social Cost Benefit Analysis [is] a decision support tool that measures and weighs various impacts of a project or policy. It compares project costs (capital and operating expenses) with a broad range of (social) impacts, e.g. travel time savings, travel costs, impacts on other modes, climate, safety, and the environment.” This framework, above all else, precludes an absolutist approach to rational policy-making. We never opt for a society-altering policy on the ground that “any lives saved make it imperative to embrace” precisely because such a primitive mindset ignores all the countervailing costs which this life-saving policy would generate (including, oftentimes, loss of life as well: banning planes, for instance, would save lives by preventing deaths from airplane crashes, but would also create its own new deaths by causing more people to drive cars).

While arguments are common about how this framework should be applied and which specific policies are ideal, the use of cost-benefit analysis as the primary formula we use is uncontroversial — at least it was until the COVID pandemic began. It is now extremely common in Western democracies for large factions of citizens to demand that any measures undertaken to prevent COVID deaths are vital, regardless of the costs imposed by those policies. Thus, this mentality insists, we must keep schools closed to avoid the contracting by children of COVID regardless of the horrific costs which eighteen months or two years of school closures impose on all children.

It is impossible to overstate the costs imposed on children of all ages from the sustained, enduring and severe disruptions to their lives justified in the name of COVID. Entire books could be written, and almost certainly will be, on the multiple levels of damage children are sustaining, some of which — particularly the longer-term ones — are unknowable (long-term harms from virtually every aspect of COVID policies — including COVID itself, the vaccines, and isolation measures, are, by definition, unknown). But what we know for certain is that the harms to children from anti-COVID measures are severe and multi-pronged.

Read more …

This is far from over.

Biden Does Surreal Press Conference, Vows To Hunt Down Isis, Blames Trump (ZH)

President Biden on Thursday vowed to “hunt down” the terrorists responsible for a spate of deadly bombings at the Kabul airport which left 12 US servicemembers dead and 15 wounded. “Know this; We will not forgive. We will not forget. We. will hunt you down and make you pay,” he said. In a surreal press conference that included bible quotes, a moment of silence, and blaming President Trump, Biden said he was open to sending US forces back into Afghanistan to assist with the withdrawal. “Whatever they need, if they need additional force, I will grant it,” he said, adding that the US military can target ISIS-K without “large scale military operations.”


Biden said he was in near ‘constant’ communication with military commanders via letter, and that he’d asked them to draw up plans to retaliate against the terrorist group (via carrier pigeon?). Of note, after reading his speech on the teleprompter, Biden said out loud “The first person I was instructed to call upon…” before taking questions. Trump also said he ‘bears responsibility for all that’s happened,’ before turning around and blaming Trump for the deal he ‘inherited.’ He then gave Trump credit for the only reason there was relative peace in Afghanistan until now. Then, towards the end of the presser, Biden said “I have another meeting, for real” – implying other ‘meetings’ haven’t been?

Read more …

“It’s just appalling and shocking and makes you feel unclean.”

US Provided Taliban With Names Of Americans, Afghan Allies To Evacuate (Pol.)

U.S. officials in Kabul gave the Taliban a list of names of American citizens, green card holders and Afghan allies to grant entry into the militant-controlled outer perimeter of the city’s airport, a choice that’s prompted outrage behind the scenes from lawmakers and military officials. The move, detailed to POLITICO by three U.S. and congressional officials, was designed to expedite the evacuation of tens of thousands of people from Afghanistan as chaos erupted in Afghanistan’s capital city last week after the Taliban seized control of the country. It also came as the Biden administration has been relying on the Taliban for security outside the airport.

Since the fall of Kabul in mid-August, nearly 100,000 people have been evacuated, most of whom had to pass through the Taliban’s many checkpoints. But the decision to provide specific names to the Taliban, which has a history of brutally murdering Afghans who collaborated with the U.S. and other coalition forces during the conflict, has angered lawmakers and military officials. “Basically, they just put all those Afghans on a kill list,” said one defense official, who like others spoke on condition of anonymity to discuss a sensitive topic. “It’s just appalling and shocking and makes you feel unclean.” Asked about POLITICO’s reporting during a Thursday news conference, President Joe Biden said he wasn’t sure there were such lists, but also didn’t deny that sometimes the U.S. hands over names to the Taliban.

“There have been occasions when our military has contacted their military counterparts in the Taliban and said this, for example, this bus is coming through with X number of people on it, made up of the following group of people. We want you to let that bus or that group through,” he said. “So, yes there have been occasions like that. To the best of my knowledge, in those cases, the bulk of that has occurred and they have been let through. “I can’t tell you with any certitude that there’s actually been a list of names,” he added. “There may have been. But I know of no circumstance. It doesn’t mean that it doesn’t exist, that here’s the names of 12 people, they’re coming, let them through. It could very well have happened.”

[..] After the fall of Kabul, in the earliest days of the evacuation, the joint U.S. military and diplomatic coordination team at the airport provided the Taliban with a list of people the U.S. aimed to evacuate. Those names included Afghans who served alongside the U.S. during the 20-year war and sought special immigrant visas to America. U.S. citizens, dual nationals and lawful permanent residents were also listed. “They had to do that because of the security situation the White House created by allowing the Taliban to control everything outside the airport,” one U.S. official said. But after thousands of visa applicants arrived at the airport, overwhelming the capacity of the U.S. to process them, the State Department changed course — asking the applicants not to come to the airport and instead requesting they wait until they were cleared for entry. From then on, the list fed to the Taliban didn’t include those Afghan names. As of Aug. 25, only U.S. passport and green card holders were being accepted as eligible for evacuation, the defense official said.

Read more …

“The U.S. Government has taken note as new store locations open up for future drone pilot target practice.”

Taliban Opens Chain Of U.S. Army Surplus Stores (BBee)

Now that Allah has seen fit to bless the Taliban with bountiful weapons and equipment from the U.S. Military, terrorists around Afghanistan have built an already thriving chain of U.S. Army Surplus stores. “We need weapons to kill and subjugate the Afghan people under Sharia Law, but there’s just too much gear here!” said local Taliban leader Bob Muhammed. “There’s, like, billions of dollars and 20 years worth of weaponry around here, and now I can build a thriving business out of selling my wares to other terrorist folk who happen to pass through! Allah be praised!”


Although the merchandise will not be available to the general public (for obvious reasons), Muhammed’s Army Surplus will feature a full selection of deadly weaponry, ammunition, combat boots, MREs, helmets, hashish, and whatever else a soldier of Allah may need. If successful, Bob Muhammed hopes to open more stores in Iraq and Syria. The U.S. Government has taken note as new store locations open up for future drone pilot target practice.

Read more …

 

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Aug 252021
 


Vincent van Gogh The red tree house 1890

 

 

The FDA. the U.S. Food and Drug Administration, announced on Monday that it gave full approval to a vaccine. But it didn’t. Or rather, it did, but the approval is for a vaccine that doesn’t exist. Or rather, it exists, but it’s not being produced. Or rather, it’s being produced, but under different names and with different legal statuses.

The FDA is playing a game with Americans, in order to get them to submit to being vaccinated. And this has to stop. No more. The role of the FDA is to protect people, not cajole them into politically desired but illegal actions. Below are 3 -bullet points of- articles about the (non-) approval. One from Peter Doshi, senior editor at The BMJ, and a powerful foe to the FDA, one from Robert Kennedy jr, and one from Jill Malone, wife of Dr. Robert Malone.

But first, yet another lie -BIG, not noble- from Anthony Fauci, as told to Anderson Cooper. There is no approval for “the Pfizer product”, and Fauci knows that very well. Or rather, there is approval for a Pfizer product that is not available to anyone. And that should never have been approved the way it was in the first place, but that’s another story. Still, Fauci said it.

In theory, if he were called on it (but of course he won’t be by any reporter he talks to), he could say that the products are the same anyway. But he won’t say that, because he realizes full well that they have different legal statuses; they are “legally distinct” in the words of the FDA. So Fauci can’t say they are the same. Even if it’s just a matter of a different label on a vial.

Yes, it sounds crazy, but that’s the legal labyrinth the FDA and Pfizer have negotiated themselves into. Why? Kennedy says it best: Pfizer is unlikely to allow any American to take a Comirnaty vaccine until it can somehow arrange immunity for this product..

And: “If it says “Comirnaty,” it’s a licensed product. If it says “Pfizer-BioNTech,” it’s an experimental product, and under 21 U.S. Code 360bbb, you have the right to refuse. If it comes from Moderna or Johnson & Johnson (marketed as Janssen), you have the right to refuse. [..] If it doesn’t say Comirnaty, you have not been offered an approved vaccine.”

Jill Malone: The vaccine that is likely to be supplied for some time, WILL BE THE Pfizer – EUA vaccine. So any mandates based on full approval are meaningless.

 

Fauci Dismisses “Freedom” In Call For Vaccine Mandates: “The Time Has Come. Enough Is Enough.”

“There was some poll that showed about 30% of people who are not anti-vax, they were just waiting to get what they felt was the real final stamp of approval, which we just got today with the Pfizer product.” He continued, “And those 30% are saying when that occurs, they will feel very, very comfortable about getting vaccinated. So right away, you’re talking about 30%. I hope they come through with what the survey said.”

[..] “They’re going to give a lot of incentive and backing for a lot of institutions and organizations and places of employment to mandate, and that could be colleges, university, the military, organizations that employ a lot of people, some of the big corporations are going to say if you want to work for us in person, you’ve got to be there and get vaccinated.”


[..] “I know I respect people’s freedom, but when you’re talking about a public health crisis that we’ve been going through for well over a year and a half, the time has come. Enough is enough. We’ve just got to get people vaccinated.” “If we keep lingering without getting those people vaccinated that should be vaccinated, this thing could linger on, leading to the development of another variant which could complicate things.”

Here’s Peter Doshi, senior editor at The BMJ.

Does The FDA Think These Data Justify The First Full Approval Of A Covid-19 Vaccine?

On 28 July 2021, Pfizer and BioNTech posted updated results for their ongoing phase 3 covid-19 vaccine trial. The preprint came almost a year to the day after the historical trial commenced, and nearly four months since the companies announced vaccine efficacy estimates “up to six months.” But you won’t find 10 month follow-up data here.

While the preprint is new, the results it contains aren’t particularly up to date. In fact, the paper is based on the same data cut-off date (13 March 2021) as the 1 April press release, and its topline efficacy result is identical: 91.3% (95% CI 89.0 to 93.2) vaccine efficacy against symptomatic covid-19 through “up to six months of follow-up.”

[..] the recent reports from Israel’s Ministry of Health caught my eye. In early July, they reported that efficacy against infection and symptomatic disease “fell to 64%.” By late July it had fallen to 39% where Delta is the dominant strain. This is very low. For context, the FDA’s expectation is of “at least 50%” efficacy for any approvable vaccine.

[..] evidence of waning immunity was already visible in the data by the 13 March 2021 data cut-off… And it’s hard to imagine how the Delta variant could play a real role here, for 77% of trial participants were from the United States, where Delta was not established until months after data cut-off.

[..] Despite the reference to “six month safety and efficacy” in the preprint’s title, the paper only reports on vaccine efficacy “up to six months,” but not from six months. This is not semantics, as it turns out only 7% of trial participants actually reached six months of blinded follow-up (“8% of BNT162b2 recipients and 6% of placebo recipients had ≥6 months follow-up post-dose 2.”) So despite this preprint appearing a year after the trial began, it provides no data on vaccine efficacy past six months, which is the period Israel says vaccine efficacy has dropped to 39%.

[..] —a total of three covid-19 related deaths (one on vaccine, two on placebo). There were 29 total deaths during blinded follow-up (15 in the vaccine arm; 14 in placebo). The crucial question, however, is whether the waning efficacy seen in the primary endpoint data also applies to the vaccine’s efficacy against severe disease.

[..] here we are, with FDA reportedly on the verge of granting a marketing license 13 months into the still ongoing, two year pivotal trial, with no reported data past 13 March 2021, unclear efficacy after six months due to unblinding, evidence of waning protection irrespective of the Delta variant, and limited reporting of safety data.

Robert F. Kennedy, Jr. and Meryl Nass, M.D. at childrenshealthdefense.org.

2 Things Mainstream Media Didn’t Tell You About FDA’s Approval of Pfizer Vaccine

Monday, the U.S. Food and Drug Administration (FDA) approved a biologics license application for the Pfizer Comirnaty vaccine. The press reported that vaccine mandates are now legal for military, healthcare workers, college students and employees in many industries. New York City Mayor Bill de Blasio has now required the vaccine for all teachers and school staff. The Pentagon is proceeding with its mandate for all military service members.

[..] First, the FDA acknowledges that while Pfizer has “insufficient stocks” of the newly licensed Comirnaty vaccine available, there is “a significant amount” of the Pfizer-BioNTech COVID vaccine — produced under Emergency Use Authorization (EUA) — still available for use. The FDA decrees that the Pfizer-BioNTech vaccine under the EUA should remain unlicensed but can be used “interchangeably” (page 2, footnote 8) with the newly licensed Comirnaty product. Second, the FDA pointed out that the licensed Pfizer Comirnaty vaccine and the existing, EUA Pfizer vaccine are “legally distinct,” but proclaims that their differences do not “impact safety or effectiveness.”

[..] EUA products are experimental under U.S. law. Both the Nuremberg Code and federal regulations provide that no one can force a human being to participate in this experiment. Under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), “authorization for medical products for use in emergencies,” it is unlawful to deny someone a job or an education because they refuse to be an experimental subject. Instead, potential recipients have an absolute right to refuse EUA vaccines.

U.S. laws, however, permit employers and schools to require students and workers to take licensed vaccines. EUA-approved COVID vaccines have an extraordinary liability shield under the 2005 Public Readiness and Preparedness Act. [..] At least for the moment, the Pfizer Comirnaty vaccine has no liability shield. Vials of the branded product, which say “Comirnaty” on the label, are subject to the same product liability laws as other U.S. products.

When the Centers for Disease Control and Prevention’s (CDC) Advisory Committee for Immunization Practices places a vaccine on the mandatory schedule, a childhood vaccine benefits from a generous retinue of liability protections. But licensed adult vaccines, including the new Comirnaty, do not enjoy any liability shield. Just as with Ford’s exploding Pinto, or Monsanto’s herbicide Roundup, people injured by the Comirnaty vaccine could potentially sue for damages. And because adults injured by the vaccine will be able to show that the manufacturer knew of the problems with the product, jury awards could be astronomical.

Pfizer is therefore unlikely to allow any American to take a Comirnaty vaccine until it can somehow arrange immunity for this product.

[..] the FDA’s acknowledgement in its approval letter that there are insufficient stocks of the licensed Comirnaty, but an abundant supply of the EUA Pfizer BioNTech jab, exposes the “approval” as a cynical scheme to encourage businesses and schools to impose illegal jab mandates. The FDA’s clear motivation is to enable Pfizer to quickly unload inventories of a vaccine that science and the Vaccine Adverse Events Reporting System have exposed as unreasonably dangerous, and that the Delta variant has rendered obsolete.

Americans, told that the Pfizer COVID vaccine is now licensed, will understandably assume COVID vaccine mandates are lawful. But only EUA-authorized vaccines, for which no one has any real liability, will be available during the next few weeks when many school mandate deadlines occur. [..] While the media has trumpeted that the FDA has approved COVID vaccines, the FDA has not approved the Pfizer BioNTech vaccines, nor any COVID vaccines for the 12- to 15-year age group, nor any booster doses for anyone.

And the FDA has not licensed any Moderna vaccine, nor any vaccine from Johnson & Johnson — so the vast majority, if not all, of vaccines available in the U.S. remain unlicensed EUA products.

Here’s what you need to know when somebody orders you to get the vaccine: Ask to see the vial. If it says “Comirnaty,” it’s a licensed product. If it says “Pfizer-BioNTech,” it’s an experimental product, and under 21 U.S. Code 360bbb, you have the right to refuse. If it comes from Moderna or Johnson & Johnson (marketed as Janssen), you have the right to refuse. The FDA is playing bait and switch with the American public — but we don’t have to play along. If it doesn’t say Comirnaty, you have not been offered an approved vaccine..

And Jill Malone.

FDA Pfizer Authorization (Comirnaty): Key Points To Consider And Discuss

FDA Pfizer authorization (Comirnaty): Key points to consider and discuss.
These points are an aggregate of many minds, including Dr. Robert Malone. 23 Aug 2021
General talking points
• Why mandates if herd immunity isn’t possible?
• What happens 8 months after boosters?
• What’s the plan for the next variant?
• Why we’re messing with vaccine injury liability if the vaccines are safe and effective?

There are now TWO LEGALLY distinct (Pfizer vs. BionTech), but otherwise identical products, based on two FDA letters, as well as a press release. The analysis of these FDA products below is preliminary and subject to change.

Letter to Pfizer
https://www.fda.gov/media/150386/download
DOES NOT GIVE FULL APPROVAL
• Extends EUA to allow supply of current Pfizer under EUA because limited supply of BioNTech version.
• “The products are legally distinct with certain differences that do not impact safety or effectiveness. (page 2, Pfizer letter) [..] here FDA quietly admits that the licensed Pfizer vaccine and the authorized Pfizer vaccine are identical with regard to safety/efficacy, but they are “legally distinct.” That’s code for one has manufacturer liability, while the other doesn’t. It is also code for “we don’t want to impose a mandate on the EUA product cause it is illegal, but we can probably get away with a mandate on the licensed product.”

[..] yes, we licensed the vaccine, but…there is a lot of the old vaccine out there, actually “a significant amount” and this amount will be considered an EUA and will continue to be used. Now, why would they do that? Why specify that identical versions of the product will be legally different? Because they need the license to impose the mandates. But they need the EUA to evade liability.

Along with the license comes liability for the manufacturer. (While all EUA products were given a liability shield.) the feds want us to THINK the vaccine we are receiving is licensed, which will make people submit because they think it can now be mandated , but instead we are almost certain to receive the EUA vials instead, to save Pfizer’s behind.

Press release
https://www.fda.gov/news-events/press-announcements/fda-approves-first-covid-19-vaccine

“On August 23, 2021, FDA approved the biologics license application (BLA) submitted by BioNTech Manufacturing GmbH for COMIRNATY (COVID-19 Vaccine, mRNA) for active immunization to prevent COVID-19 caused by SARS-CoV-2 in individuals 16 years of age and older.” The efficacy claims are based on outdated data. The press release indicates that the basis of the efficacy claims was as quoted below. However, those data are outdated, and captured with strains of virus (Alpha, Beta) that are no longer predominant. The efficacy claims are therefore invalid – it is quite clear that the vaccine is much less effective in preventing infection by the currently circulating strain (Delta)

In its letter to BioNTech, the FDA states “” We have determined that an analysis of spontaneous postmarketing adverse events reported under section 505(k)(1) of the FDCA will not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis. Furthermore, the pharmacovigilance system that FDA is required to maintain under section 505(k)(3) of the FDCA is not sufficient to assess these serious risks.” The first sentence says that VAERS will be incapable of assessing known serious risk The second sentence says that the other pharmacovigilance systems that by law FDA employs (supposedly about 20 different databases when they were bragging about them last October) are similarly incapable of assessing known serious risk.

• The risks in pregnancy remain unknown. “although not FDA requirements, the company has committed to additional post-marketing safety studies, including conducting a pregnancy registry study to evaluate pregnancy and infant outcomes after receipt of Comirnaty during pregnancy.” The prescribing info says: “There is a pregnancy exposure registry for COMIRNATY. Encourage individuals exposed to COMIRNATY around the time of conception or during pregnancy to register by visiting https://mothertobaby.org/ongoingstudy/covid19-vaccines/ .” WHY ARE THEY DOING A PREGNANCY STUDY?

FDA has licensed the BioNTech vaccine for 16 and up
• All of the authorized vaccine on shelves and in freezers will remain only authorized, until the new product with Cominaty labelling arrives.
• 3d or booster doses and vaccine for 12-15 year olds remains under EUA
• Why not also approve the Pfizer version? Why leave it under EUA?
• When the press says the “Pfizer vaccine is fully approved.” It is not. The vaccine that is likely to be supplied for some time, WILL BE THE Pfizer – EUA vaccine. So any mandates based on full approval are meaningless.

THE BLA acknowledges LONG term myocardial issues with a 5 year follow up consistent with the lower range for LTFU for Gene Therapy Products. Is FDA quietly acknowledging the Gene Therapy classification? These products have been classified by FDA as Gene Therapy Products which require UP to 15 years long term follow up in studies. This was acknowledged by Moderna in their 2Q 2020 filing.

Using superior CDC published methods, normalizing for people vaccinated, Children’s Health Defense estimates 176x reports of VAERS deaths associated with C19 vaccines compared with flu vaccines. 35x the number for H1N1 (where stimulated reporting is speculated) Using CDC published methods we estimate under-reporting of VAERS deaths to be 5- 15x. for a total of 30,000-90,000 deaths, mostly non-C19. Underreporting for lifethreatening events may be 24-64x. IN ADDITION – (Israel MOH, combined with Dagan study), we have estimated between 35-86,000 EXCESS USA deaths due to Covid in those vaccinated (>=1 dose)

 

 

 

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Aug 252021
 


Salvador Dali The Madonna of Port Lligat 1950

 

Vaccine Effectiveness 15% in the Over-50s, 37% in the Under-50s (DS)
Fauci Dismisses “Freedom”: “The Time Has Come. Enough Is Enough.” (SN)
FDA Pfizer Authorization (Comirnaty): Key Points (Jill Malone)
Pfizer CEO Predicts A Vaccine-Resistant Covid-19 Variant (JTN)
Don’t Use Pfizer’s COVID Vax Off-Label in Kids, Experts Warn (MPT)
A Most Unusual Thing in Australia, Alice (CTH)
New Zealand Won’t ‘Throw In Towel’ On Covid-zero Strategy (G.)
Unvaccinated Removed From Transplant Waiting Lists (JTN)
Ivermectin: Enigmatic Multifaceted ‘Wonder’ Drug Continues To Surprise (Nature)
Supreme Court Orders ‘Remain in Mexico’ Policy Reinstated (AP)
Biden’s Approval Rating Down To Lowest Levels Yet (PM)
Largest US Food Distributor Having Trouble Keeping Shelves Stocked (ZH)

 

 

Yesterday I posted this on mandates:

On Twitter, this was doubted, and a Verify thingy added.

But Snopes of all places confirms the first suggestion. After someone went through the trouble to write on Twitter that he used to love reading the Automatic Earth, but now that guy does nothing but spread misinformation on Covid. Who said the interwebs can’t be fun?

 

 

A New York Post tweet:

“Twitter cheers when an unvaxxed conservative dies and uses that fact against the right. When three Broward County, Fla., teachers died on the same day, their deaths were cited to attack Gov. Ron DeSantis (R) for refusing to mandate masks in schools. Rarely mentioned in news stories is that the school had not yet opened.”

 

 

You can read anywhere that vaccine effectiveness is down to 60% or so. The Daily Sceptic goes further.

“Calculating the vaccine effectiveness against Delta infection in the over-50s [..] gives a figure of just 15%..”

Vaccine Effectiveness 15% in the Over-50s, 37% in the Under-50s (DS)

Public Health England (PHE) has released a new technical briefing on the variants of concern, number 21, and this allows us to update our estimate of (unadjusted) vaccine effectiveness against the Delta variant using the data it provides on confirmed Delta cases. We subtract the figures in briefing 21 from those in briefing 17 to give the figures for the period June 22nd to August 15th. We also use figures for proportions of the population vaccinated by age derived from the PHE Covid surveillance reports. Starting with the over-50s, for the period June 22nd to August 15th, PHE reports 29,282 Delta infections in the double vaccinated and 3,915 in the unvaccinated. PHE figures show that in this period the proportion of the over-50s double vaccinated was stable at 88% and the proportion unvaccinated was 10%.

Calculating the vaccine effectiveness against Delta infection in the over-50s (1-(29,282/88%)/(3,915/10%)) gives a figure of just 15%, down from 17% using data from the briefing two weeks ago. This is very different to the estimate in the recent Oxford University study using ONS survey data, a study which I criticised for numerous implausible findings. With regard to deaths with Covid (within 28 days of a positive test), PHE reports 602 in the double vaccinated and 280 in the unvaccinated in the over-50s in this period. This works out (1-(602/88%)/(280/10%)) at a vaccine effectiveness against death of 76%, down slightly from 77% using data from the previous briefing. This is a 76% reduction in mortality including any reduced risk of infection, not in addition to it. It’s an encouraging figure, albeit lower than earlier studies have suggested.

For the under-50s, for the period June 22nd to August 15th, PHE reports 36,855 Delta infections in the double vaccinated and 125,394 in the unvaccinated. PHE figures show that on June 20th 61% of under-50s were unvaccinated while 18% were double vaccinated. On August 15th those figures were 52% unvaccinated and 35% double vaccinated. Taking the average of these gives 56% unvaccinated and 26% double vaccinated for the period. Using this to calculate the vaccine effectiveness against Delta infection in the under-50s (1-(36,855/26%)/(125,394/56%)) gives a figure of 37%. This is higher than in the over-50s, but still very low and much lower than earlier studies (including the trial) indicated.

For deaths, PHE reports 27 in the double vaccinated and 66 in the unvaccinated in the under-50s in this period. This works out (1-(27/26%)/(66/56%)) at a vaccine effectiveness against death of just 12%. Why this would be so much lower than in the over-50s is unclear, but it’s worth bearing in mind that these are small numbers of deaths which may make the estimate unreliable. These figures are much lower than those commonly quoted and used in modelling, and if they are closer to the truth then they mean the official, self-congratulatory estimates of “100,000 deaths” and “24.4 million infections” prevented by the vaccines are huge overestimates.

Read more …

“..they were just waiting to get what they felt was the real final stamp of approval, which we just got today with the Pfizer product.”

No, you did not. Pfizer was not approved. And people should be told that. Enough is enough, alright, of the lies.

Fauci Dismisses “Freedom”: “The Time Has Come. Enough Is Enough.” (SN)

After the FDA fully approved the Pfizer COVID vaccine, Anthony Fauci immediately issued a decree via his permanent CNN propaganda platform that it is time for nationwide vaccine mandates. Fauci declared that “There was some poll that showed about 30% of people who are not anti-vax, they were just waiting to get what they felt was the real final stamp of approval, which we just got today with the Pfizer product.” He continued, “And those 30% are saying when that occurs, they will feel very, very comfortable about getting vaccinated. So right away, you’re talking about 30%. I hope they come through with what the survey said.”


Fauci added “They’re going to give a lot of incentive and backing for a lot of institutions and organizations and places of employment to mandate, and that could be colleges, university, the military, organizations that employ a lot of people, some of the big corporations are going to say if you want to work for us in person, you’ve got to be there and get vaccinated.” Fauci then dismissed freedom as an after thought, noting “I know I respect people’s freedom, but when you’re talking about a public health crisis that we’ve been going through for well over a year and a half, the time has come. Enough is enough. We’ve just got to get people vaccinated.” “If we keep lingering without getting those people vaccinated that should be vaccinated, this thing could linger on, leading to the development of another variant which could complicate things.” Fauci further proclaimed.

Read more …

What Fauci doesn’t say is that the FDA approval is not straightforward, at all. The approval is for BioNTech only, but there are no supplies of that. So the Pfizer shot you’ll get has not been approved.

This is part of a document by Jill Malone, Robert Malone’s wife. Do read the whole pdf, it’s excellent.

FDA Pfizer Authorization (Comirnaty): Key Points (Jill Malone)

FDA Pfizer authorization (Comirnaty): Key points to consider and discuss.
These points are an aggregate of many minds, including Dr. Robert Malone. 23 Aug 2021
General talking points
• Why mandates if herd immunity isn’t possible?
• What happens 8 months after boosters?
• What’s the plan for the next variant?
• Why we’re messing with vaccine injury liability if the vaccines are safe and effective?

There are now TWO LEGALLY distinct (Pfizer vs. BionTech), but otherwise identical products, based on two FDA letters, as well as a press release. The analysis of these FDA products below is preliminary and subject to change.

Letter to Pfizer
https://www.fda.gov/media/150386/download
DOES NOT GIVE FULL APPROVAL
• Extends EUA to allow supply of current Pfizer under EUA because limited supply of BioNTech version.
• “The products are legally distinct with certain differences that do not impact safety or effectiveness. (page 2, Pfizer letter)
o here FDA quietly admits that the licensed Pfizer vaccine and the authorized Pfizer vaccine are identical with regard to safety/efficacy, but they are “legally distinct.” That’s code for one has manufacturer liability, while the other doesn’t. It is also code for “we don’t want to impose a mandate on the EUA product cause it is illegal, but we can probably get away with a mandate on the licensed product.”
o page 12 AA (Conditions with Respect to Use of Licensed Product). This tells you that yes, we licensed the vaccine, but…there is a lot of the old vaccine out there, actually “a significant amount” and this amount will be considered an EUA and will continue to be used.
o Now, why would they do that? Why specify that identical versions of the product will be legally different? Because they need the license to impose the mandates. But they need the EUA to evade liability.
o Along with the license comes liability for the manufacturer. (While all EUA products were given a liability shield.)
o Unfortunately, our federal governments would prefer us to be without recourse if we are injured, rather than have Pfizer defend its product in court. So, the feds want us to THINK the vaccine we are receiving is licensed, which will make people submit because they think it can now be mandated, but instead we are almost certain to receive the EUA vials instead, to save Pfizer’s behind. Yes, a stingy CICP injury program exists, but it has not paid out for a single COVID vaccine injury yet.
• Warning about myocarditis and pericarditis

Letter to BioNTech (COMIRNATY): (signed by Mary Malarkey) – MARKET AUTHORIZES BLA (APPROVAL)
https://www.fda.gov/media/151710/download
• For “active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 16 years of age and older.”
• Analysis of […] adverse events reported […] not be sufficient to assess known serious risks of myocarditis and pericarditis and identify an unexpected serious risk of subclinical myocarditis.
• 13 Post marketing studies required
o Pediatric (3 studies) < 6m to <15 y
o Myocarditis and pericarditis (6 studies), with UP TO 5 years follow up
o Pregnancy – teratology (1 study)
o Dose levels, VA, effectiveness in Kaiser system (3 studies)
• The FDA bypassed/disregarded the normal advisory committee and public comment process for this license. See p2 “We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your BLA, including the clinical study design and trial results, did not raise concerns or controversial issues that would have benefited from an advisory committee discussion.”

[..] • FDA has licensed the BioNTech vaccine for 16 and up
• All of the authorized vaccine on shelves and in freezers will remain only authorized, until the new product with Cominaty labelling arrives.
• 3d or booster doses and vaccine for 12-15 year olds remains under EUA
• Why not also approve the Pfizer version? Why leave it under EUA?
• When the press says the “Pfizer vaccine is fully approved.” It is not. The vaccine that is likely to be supplied for some time, WILL BE THE Pfizer – EUA vaccine. So any mandates based on full approval are meaningless.

Read more …

“Every time that the variant appears in the world, our scientists are getting their hands around it..”

Pfizer CEO Predicts A Vaccine-Resistant Covid-19 Variant (JTN)

Pfizer CEO Albert Bourla said on Tuesday that there will likely be a COVID-19 variant that is resistant to the vaccine, but that his company would be able to get a variant-specific shot out in about three months. “Every time that the variant appears in the world, our scientists are getting their hands around it,” Bourla said on Fox News’ America’s Newsroom. “They are researching to see if this variant can escape the protection of our vaccine. We haven’t identified any yet but we believe that it is likely that one day, one of them will emerge.” Pfizer has a process that would take 95 days to develop a variant-specific vaccine from the identification of the variant, Bourla said. In February, Bourla told Fortune that a vaccine-resistant variant was possible.


“Theoretically, it’s a very possible scenario. If you protect a very big part of the population, and if there is a strain that emerges that can use this pool of population to replicate while the current strains cannot, obviously this will overtake the original. So it’s not a certainty, but it is now, I believe, a likely scenario,” he said. The day of Bourla’s interview with Fox News, the Centers for Disease Control and Prevention (CDC) released a report that found COVID-19 vaccines dropped from 91% effectiveness before the Delta variant to 66% effectiveness during the peak of the variant. The study included 4,217 participants who were fully vaccinated, with 65% having received the Pfizer vaccine, 33% Moderna, and 2% Johnson&Johnson.

Read more …

“..For kids under 5, the dose being studied is only 3 mcg. “We can’t have physicians writing for the approved 30 mcg dose to be used in someone under 12..”

Don’t Use Pfizer’s COVID Vax Off-Label in Kids, Experts Warn (MPT)

Pediatric infectious disease experts are warning that Pfizer’s COVID-19 vaccine, now fully approved and marketed as Comirnaty, should not be used off-label in children under 12. While full approval gives physicians the legal grounds to administer the vaccine off-label, experts noted that the doses being studied in younger children are much lower than those used in adults. There also have been no data published about use of the vaccine in children under 12. David Kimberlin, MD, a pediatric infectious disease expert at the University of Alabama at Birmingham, told MedPage Today that the dose authorized for individuals 12 and up is 30 mcg — but the dose being evaluated in kids ages 5 to 11 “is a third of that,” at 10 mcg.


For kids under 5, the dose being studied is only 3 mcg. “We can’t have physicians writing for the approved 30 mcg dose to be used in someone under 12,” Kimberlin said. “It’s a much higher dose than what’s being studied.” The lower dose “was chosen because of immunogenicity and reactogenicity,” he added. “We are going to have to get the word out that we should not be simply taking the Pfizer vaccine approved for adults and putting it in the arms of those under 12.” FDA Acting Commissioner Janet Woodcock, MD, warned against off-label use of the Pfizer vaccine in younger children during a press briefing Monday, warning that they’re “not just small adults.”

Read more …

Pretty good!

A Most Unusual Thing in Australia, Alice (CTH)

“Contrariwise,’ continued Tweedledee, ‘if it was so, it might be; and if it were so, it would be; but as it isn’t, it ain’t. That’s logic.” So goes the wonderful words of Lewis Carroll from Alice’s Adventures in Wonderland…. Which is the only appropriate frame of reference for what you are about to discover. You see… …The COVID madness has created a most unusual dynamic for the resident’s down-under and the painfully monitored Australian media who have to be careful not to run afoul of the government COVID compliance watchers. Once a nation creates an alternate reality of itself, in this case a totalitarian reality based on government needing to create an irrational illusion of fear that becomes part of the accepted national identity, how can a media outlet call attention to the outcomes without finding themselves in front of the governmental board of inquisition?


Put another way,… if the pod under your bed malfunctioned, but the pods under all the other beds in the city worked, what happens when you awaken and realize you are not one of them, but you must engage in the world of them while looking for others -like yourself- whose pods hopefully malfunctioned? That is the current challenge for media in Australia trying to report on their reality and yet avoid the ire from the national board of COVID compliance who have successfully brainwashed the audience. One Australian media outlet seems to have found a way. In this report from Sky News Australia, they avoid the censors by reporting on how the world is viewing Australian news, by sharing American news clips of Australian news. It is weird and the perfect example of how bizarre the world has become over COVID. WATCH:

Sky News host Rita Panahi says “to us, a bunch of teenagers being handcuffed in the middle of the night and fined $1,000 each for the crime of meeting at a Sydney beach has become normal,” she said. “But the rest of the world looks in abject horror.” Ms Panahi then shares how people around the world are “marveling” at what’s happening in Australia, noting Fox News anchor Tucker Carlson has taken aim at how Australian police are treating protesters. “There is similar commentary and discussions I’ve seen from the UK,” Ms Panahi said. “Is this how we want to be perceived as a country?” As a rather prescient Lewis Carroll continued to share in his novel of Alice, Through The Looking Glass: “If I had a world of my own, everything would be nonsense. Nothing would be what it is, because everything would be what it isn’t. And contrary wise, what is, it wouldn’t be. And what it wouldn’t be, it would. You see?”


So here we are. Cheers !

Read more …

Wonder how many questions are asked on the TV news down there.

New Zealand Won’t ‘Throw In Towel’ On Covid-zero Strategy (G.)

New Zealand’s Covid response minister says the country will not “throw in the towel” with its elimination strategy, as cases continue to rise. New Zealand announced 63 new cases of Covid-19 on Wednesday, bringing the total to 210 cases. It is the largest single-day jump since the outbreak began last week, and 12 people are hospitalised with the virus. Some commentators and media overseas have questioned whether the country should continue its elimination strategy, but Covid-19 response minister Chris Hipkins said the country would be staying its course. “To New Zealanders at home who are saying, ‘is this still the right strategy’, it’s too soon to throw in the towel,” he said. “We’ve come this far, it would be an absolute waste for us to give up on this now. We still want to drive this particular outbreak of Covid-19 out of our community and get back to a sense of normality.”


“Of course we do want to get to the point where lockdowns aren’t the answer to potential outbreaks within the community, but we’re not there yet, and we’re certainly not willing to give up before we get to that point,” Hipkins said. His comments echoed those of the prime minister, Jacinda Ardern, on Monday: “For now, everyone is in agreement: elimination is the strategy. There is no discussion or debate amongst any of us about that, because that is the safest option for us while we vaccinate our people,” she said. Support for the government’s approach to Covid remains sky high in New Zealand. According to polling conducted by The Spinoff and released on Wednesday, just 10% of New Zealanders did not think elimination was the right strategy. Sixty-nine percent still backed the approach, and 21% said they were unsure. An additional poll found 84% of New Zealanders supported the decision to move into lockdown last week.

Read more …

Little dictators. It’s a small step from Hippocrates to hypocrisy.

Unvaccinated Removed From Transplant Waiting Lists (JTN)

The University of Washington Medical Center has reportedly told two patients awaiting organ transplants that they would be placed further down their respective lines over their refusal to receive the COVID-19 vaccine. Sam Allen, 64, told Seattle radio station KTTH that he was informed in June he was being removed from the transplant waitlist over his refusal to be vaccinated. Allen said he has been on the list for more than two years. According to KTTH, Allen said his heart was damaged during a previous surgery and three leaky heart valves lessened the amount of blood reaching his lungs, making it hard to breathe. The problem first arose over Allen’s refusal to wear a face mask during hospital visits, saying it made his breathing problems even worse.

“The cardiologist called me and we had a discussion and he informed me that, ‘well, you’re going to have to get a vaccination to get a transplant,’ and I said that’s news to me,” Allen told KTTH. A letter Allen received from the hospital shortly after states “Your name has been removed from the waitlist at the University of Washington Medical Center. This was done in follow-up to your recent conversation with providers regarding the hear transplant selection committee’s concerns about compliance with COVID-19 related policies and recommendations.” The letter added that Allen would be reconsidered for reinstatement “should the compliance concerns resolve in the future.”

A second patient, Derek Kovic, told KTTH he is awaiting a third liver transplant due to bile duct failure and was also told by the hospital he would have to receive the vaccine to remain high on the active list. Both Kovic and Allen told news outlets that they are hesitant to get vaccinated because of physical side effects. Kovic told Fox News because of his liver problems that he already suffers from high fevers and other problems people have reported after receiving the vaccine. The University of Washington Medical Center responded to their stories, saying immunity suppression becomes an issue shortly after a transplant.

Read more …

The long background story of ivermectin, before Covid.

From Nature, The Journal of Antibiotics, February 2017.

Ivermectin: Enigmatic Multifaceted ‘Wonder’ Drug Continues To Surprise (Nature)

Over the past decade, the global scientific community have begun to recognize the unmatched value of an extraordinary drug, ivermectin, that originates from a single microbe unearthed from soil in Japan. Work on ivermectin has seen its discoverer, Satoshi Omura , of Tokyo’s prestigious Kitasato Institute, receive the 2014 Gairdner Global Health Award and the 2015 Nobel Prize in Physiology or Medicine, which he shared with a collaborating partner in the discovery and development of the drug, William Campbell of Merck & Co. Incorporated. Today, ivermectin is continuing to surprise and excite scientists, offering more and more promise to help improve global public health by treating a diverse range of diseases, with its unexpected potential as an antibacterial, antiviral and anti-cancer agent being particularly extraordinary.

The unique and extraordinary microorganism that produces the avermectins (from which ivermectin is derived) was discovered by Omura in 1973. It was sent to Merck laboratories to be run through a specialized screen for anthelmintics in 1974 and the avermectins were found and named in 1975. The safer and more effective derivative, ivermectin, was subsequently commercialized, entering the veterinary, agricultural and aquaculture markets in 1981. The drug’s potential in human health was confirmed a few years later and it was registered in 1987 and immediately provided free of charge (branded as Mectizan)—‘as much as needed for as long as needed’—with the goal of helping to control Onchocerciasis (also known as River Blindness) among poverty-stricken populations throughout the tropics. Uses of donated ivermectin to tackle other so-called ‘neglected tropical diseases’ soon followed, while commercially available products were introduced for the treatment of other human diseases.

[..] Today, ivermectin remains a relatively unknown drug, although few, if any, other drugs can rival ivermectin for its beneficial impact on human health and welfare. Ivermectin is a broad-spectrum anti-parasitic agent, primarily deployed to combat parasitic worms in veterinary and human medicine. This unprecedented compound has mainly been used in humans as an oral medication for treating filarial diseases but is also effective against other worm-related infections and diseases, plus several parasite-induced epidermal parasitic skin diseases, as well as insect infestations. It is approved for human use in several countries, ostensibly to treat Onchocerciasis, lymphatic filariasis (also known as Elephantiasis), strongyloidiasis and/or scabies and, very recently, to combat head lice. However, health workers are increasingly utilizing it in an unsanctioned manner to treat a diverse range of other diseases

And ivermectin today:

Read more …

The exact same argument that upheld DACA against Trump’s policies. Ironic.

Supreme Court Orders ‘Remain in Mexico’ Policy Reinstated (AP)

The Supreme Court on Tuesday said the Biden administration likely violated federal law in trying to end a Trump-era program that forces people to wait in Mexico while seeking asylum in the U.S. With three liberal justices in dissent, the high court refused to block a lower court ruling ordering the administration to reinstate the program informally known as Remain in Mexico. It’s not clear how many people will be affected and how quickly. Under the lower court ruling, the administration must make a “good faith effort” to restart the program. There also is nothing preventing the administration from trying again to end the program, formally called Migrant Protection Protocols.

A federal judge in Texas had previously ordered that the program be reinstated last week. Both he and the 5th U.S. Circuit Court of Appeals refused the administration’s request to put the ruling on hold. Justice Samuel Alito ordered a brief delay to allow the full court time to consider the administration’s appeal to keep the ruling on hold while the case continues to make its way through the courts. The 5th Circuit ordered expedited consideration of the administration’s appeal. The court offered little explanation for its action, although it cited its opinion from last year rejecting the Trump administration’s effort to end another immigration program, Deferred Action for Childhood Arrivals.

In that case, the court held that the decision to end DACA was “arbitrary and capricious,” in violation of federal law. The administration has “failed to show a likelihood of success on the claim that the memorandum rescinding the Migrant Protection Protocols was not arbitrary and capricious,” the court wrote Tuesday in an unsigned order. The three dissenting justices, Stephen Breyer, Elena Kagan and Sonia Sotomayor, did not write an opinion expressing their views of the case. In a statement, the Department of Homeland Security said it regrets that the high court declined to issue a stay. The department said it would continue to challenge the district court’s order.

Read more …

The Dems have sleepless nights over Kamala stepping up.

Biden’s Approval Rating Down To Lowest Levels Yet (PM)

President Biden is facing severe backlash due to the failed exit from Afghanistan. According to USA Today, Biden’s approval rating has sunk to 41 percent. Up until last week, most polls showed the President sitting above 50 percent. Biden has also taken a hit beyond overall approval ratings. While he still has 87 percent of Democrats supporting him, only 32 percent of Independents say he is doing a good job. This poll was taken Thursday through Monday, as the nation and the world witnessed the shocking images of the Taliban taking Kabul, Afghanistan. Only 26 percent of Americans approve of Biden’s handling of Afghanistan and his numbers on domestic issues are not much better, with 39 percent saying he’s handling the economy well.


“Today, President Biden’s overall approval has taken a turn for the worse due to his awful job performance rating on Afghanistan,” said David Paleologos, director of the Suffolk Political Research Center. “His approval on immigration and the economy are also upside down. The only issue keeping him remotely in the game is his handling of the COVID-19 pandemic, where he is barely at 50%.” Biden’s initial call to exit Afghanistan was approved by 53 percent of Americans, but a whopping 62 percent disapproved of how his administration handled the departure. “He basically handed the Taliban all these weapons, and he’s inspired a resurgent ISIS now,” said fifty-one-year-old Aubrey Schlumbrecht of Lakewood, Colorado. The home healthcare nurse and political independent was among those polled and said, “He is not even taking any responsibility. He says he owns it, but he’s blaming other people and he’s blaming the Afghan people themselves.”

Read more …

No workers. But please don’t say “food inflation”. It is meaningless because from there it’s just one small step to “cookie inflation”.

Largest US Food Distributor Having Trouble Keeping Shelves Stocked (ZH)

One of the defining features of the early phases of the covid pandemic, when public fear was rampant and when few wanted to take chances that supply chains would remain viable, is that for a brief period US supermarkets resembled those of the USSR circa the late 1980s: many items were in short supply, and some – notably toilet paper, clorox, and perishables such as milk – were out of stock for weeks. Fast forward to today when fears about the Delta strain are being fanned by the liberal media, the US may be facing a similar shortage of key products… only this time for a very different reason: not a surge in demand, but rather a drop in supply. According to Bloomberg, some of the largest U.S. food distributors are “reporting difficulties in fulfilling orders as a lack of workers weighs on the supply chain.”

Take distribution giant Sysco, North America’s largest wholesale food distributor, which is turning away customers in some areas where demand is exceeding capacity. Worse, food inflation is about to soar: the company said prices for key goods such as chicken, pork and paper products for takeout packaging are climbing amid tight supplies. In particular, production has slowed for high-demand, labor-intensive cuts like bacon, ribs, wings and tenders, Sysco said. And if intermediate and final wholesale prices are “rising”, just wait until they emerge on the consumer side. The culprit for the coming price shock? Biden’s catastrophic stimmies and universal basic income which has unleashed havoc on the US job market and led to historic labor shortages.

“There are certain areas across the country that are more challenged by the labor shortage and our volume of orders is regularly exceeding our capacity,” Sysco Chief Executive Officer Kevin Hourican said in a letter to clients earlier this month. “This has, unfortunately, led to service disruptions for some of our customers.” Hourican’s troubling observations were confirmed by an analysis from DecaData, which tracks retailer transactions with shoppers and manufacturers; it showed that retailers are bumping up against manufacturer capacity as they stockpile ahead of the holiday season. In July, the incidence of suppliers limiting or putting a cap on orders from customers was more than double what it was in January, its data show.

Read more …

 

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Aug 242021
 


George Caleb Bingham The verdict of the people 1854

 

Pfizer-BioNTech Vaccine Becomes First To Win FDA’s Full Approval (USAT)
Does The FDA Think These Data Justify Approval Of A Covid-19 Vaccine? (BMJ)
Fully Vaccinated Healthcare Workers Carry 251 Times Viral Load (McCullough)
FDA Ignores Both Science and Law (Denninger)
Pfizer and Moderna Lost The Clinical Trial Control Group (CTH)
Everything You Need to Know About Informed Consent (21CW)
Statistical Fraud in the FDA Vaccine Approval Process (JoshM)
The More Masks Fail, The More We Need Them (Ian)
Pentagon To Mandate Covid-19 Vaccinations For All Military Personnel (RT)
NYC Orders 150,000 Teachers & School Staff To Get Vaccinated (ZH)
Truckers Threaten To Shut Down Australia Due to Covid Insanity (OI)
Keeping Fear Alive (Tierney)
Throwdowns and Showdowns (Kunstler)

 

 

It’s been an insane 24 hours. You’d think a full approval of a vaccine would be a straightforward event, but the FDA just made things more, and extremely, complicated. First, a few bits and pieces from what they issued:

 

 

“COMIRNATY is the first COVID-19 vaccine to be granted FDA approval ”
also:
“These may not be all the possible side effects of the vaccine. Serious and unexpected side effects may occur. THE VACCINE IS STILL BEING STUDIED IN CLINICAL TRIALS.”

 

 

On August 23, 2021, FDA approved the biologics license application (BLA) submitted by BioNTech Manufacturing GmbH for COMIRNATY (COVID-19 Vaccine, mRNA) for active immunization to prevent COVID-19 caused by SARS-CoV-2 in individuals 16 years of age and older…

…the EUA will remain in place for the Pfizer-BioNTech COVID-19 vaccine for the previously-authorized indication and uses, and to authorize use of COMIRNATY (COVID-19 Vaccine, mRNA) under this EUA for certain uses that are not included in the approved BLA…

COMIRNATY (COVID-19 Vaccine, mRNA) is the same formulation as the PfizerBioNTech COVID-19 Vaccine and can be used interchangeably with the Pfizer-BioNTech COVID-19 Vaccine to provide the COVID-19 vaccination series…

 

 

C. There is no adequate, approved, and available [see Note 9] alternative to the emergency use of Pfizer-BioNTech COVID 19 Vaccine to prevent COVID-19.

[Note 9:] Although COMIRNATY (COVID-19 Vaccine, mRNA) is approved to prevent COVID-19 in individuals 16 years of age and older, there is not sufficient approved vaccine available for distribution to this population in its entirety at the time of reissuance of this EUA. Additionally, there are no products that are approved to prevent COVID-19 in individuals age 12 through 15, or that are approved to provide an additional dose to the immunocompromised population described in this EUA.

 

 

Conditions Related to Printed Matter, Advertising, and Promotion

X. All descriptive printed matter, advertising, and promotional material, relating to the use of the Pfizer-BioNTech COVID 19 Vaccine shall be consistent with the authorized labeling, as well as the terms set forth in this EUA, and meet the requirements set forth in section 502(a) and (n) of the FD&C Act and FDA implementing regulations.

Y. All descriptive printed matter, advertising, and promotional material relating to the use of the Pfizer-BioNTech COVID 19 Vaccine clearly and conspicuously shall state that:

” This product has not been approved or licensed by FDA, but has been authorized for emergency use by FDA, under an EUA to prevent Coronavirus Disease 2019 (COVID-19) for use in individuals 12 years of age and older; and

” The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of the medical product under Section 564(b)(1) of the FD&C Act unless the declaration is terminated or authorization revoked sooner.

 

 

The original documents. Just check the dates. What happened to those?

 

 

Two high vaccination rates: Iceland Full Vaxxed 74%, Israel 62%

 

 

“The Pfizer-BioNTech emergency use authorization was based on clinical trials involving about 37,000 people.”

Well, not really, because they stopped those trials.

Pfizer-BioNTech Vaccine Becomes First To Win FDA’s Full Approval (USAT)

Eight months after authorizing the Pfizer-BioNTech COVID-19 vaccine for emergency use in the USA, the Food and Drug Administration issued its full stamp of approval. Now that the companies’ detailed, so-called biologics license application has been granted, it’s likely that vaccination will be required by many companies, schools and other entities. The FDA decision clears the way for the companies to market their vaccine, which is not permitted without full licensure. And it may launch a race for booster shots, allowing doctors to prescribe extra Pfizer-BioNTech shots “off label” to anyone they think should get one. The FDA confirmed late last year through a more streamlined evaluation process that the vaccine, from pharmaceutical giant Pfizer and its partner, German startup BioNTech, was safe, effective and could be reliably produced.

The review of the 340,000-page license application was completed in just 97 days by FDA staff working “night and day,” said Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, which approves vaccines “We completed this in about 40% of the normal clock time for a submission of this magnitude,” he said. The license application was three times the size of the emergency use authorization submission, which weighed in at 110,000 pages. The companies have manufactured more than 2 billion doses, more than 200 million of which were administered in the USA, the most of any of the three vaccines allowed for use in the country. The full license includes four more months of efficacy and safety data, confirming trial results and detailing manufacturing processes.

The Pfizer-BioNTech emergency use authorization was based on clinical trials involving about 37,000 people. The full approval was based on study results involving more than 44,000 people followed for six months. The license applies only to those 16 and over, but the vaccine is allowed for those 12 to 15 under the previous authorization. “Based on the longer-term follow-up data that we submitted, today’s approval for those aged 16 and over affirms the efficacy and safety profile of our vaccine at a time when it is urgently needed,” Pfizer chairman and CEO Albert Bourla said in a statement. “I am hopeful this approval will help increase confidence in our vaccine, as vaccination remains the best tool we have to help protect lives and achieve herd immunity.”

Read more …

Not sure it’s a great idea for the FDA to have pissed off Peter Doshi, senior editor at The BMJ, one of the most reputable magazines around. Much more at the original (link).

Does The FDA Think These Data Justify Approval Of A Covid-19 Vaccine? (BMJ)

On 28 July 2021, Pfizer and BioNTech posted updated results for their ongoing phase 3 covid-19 vaccine trial. The preprint came almost a year to the day after the historical trial commenced, and nearly four months since the companies announced vaccine efficacy estimates “up to six months.” But you won’t find 10 month follow-up data here. While the preprint is new, the results it contains aren’t particularly up to date. In fact, the paper is based on the same data cut-off date (13 March 2021) as the 1 April press release, and its topline efficacy result is identical: 91.3% (95% CI 89.0 to 93.2) vaccine efficacy against symptomatic covid-19 through “up to six months of follow-up.” The 20 page preprint matters because it represents the most detailed public account of the pivotal trial data Pfizer submitted in pursuit of the world’s first “full approval” of a coronavirus vaccine from the Food and Drug Administration. It deserves careful scrutiny.

[..] The elephant named “waning immunity”…“Waning immunity” is a known problem for influenza vaccines, with some studies showing near zero effectiveness after just three months, meaning a vaccine taken early may ultimately provide no protection by the time “flu season” arrives some months later. If vaccine efficacy wanes over time, the crucial question becomes what level of effectiveness will the vaccine provide when a person is actually exposed to the virus? Unlike covid vaccines, influenza vaccine performance has always been judged over a full season, not a couple months. And so the recent reports from Israel’s Ministry of Health caught my eye. In early July, they reported that efficacy against infection and symptomatic disease “fell to 64%.” By late July it had fallen to 39% where Delta is the dominant strain. This is very low. For context, the FDA’s expectation is of “at least 50%” efficacy for any approvable vaccine.

Delta may not be responsible Enter Pfizer’s preprint. As an RCT reporting “up to six months of follow-up,” it is notable that evidence of waning immunity was already visible in the data by the 13 March 2021 data cut-off… And it’s hard to imagine how the Delta variant could play a real role here, for 77% of trial participants were from the United States, where Delta was not established until months after data cut-off. Waning efficacy has the potential to be far more than a minor inconvenience; it can dramatically change the risk-benefit calculus.

The “six month” preprint based on the 7% of trial participants who remained blinded at six months Despite the reference to “six month safety and efficacy” in the preprint’s title, the paper only reports on vaccine efficacy “up to six months,” but not from six months. This is not semantics, as it turns out only 7% of trial participants actually reached six months of blinded follow-up (“8% of BNT162b2 recipients and 6% of placebo recipients had ≥6 months follow-up post-dose 2.”) So despite this preprint appearing a year after the trial began, it provides no data on vaccine efficacy past six months, which is the period Israel says vaccine efficacy has dropped to 39%. It is hard to imagine that the <10% of trial participants who remained blinded at six months (which presumably further dwindled after 13 March 2021) could constitute a reliable or valid sample to produce further findings.

Severe disease And on preventing death from covid-19, there are too few data to draw conclusions—a total of three covid-19 related deaths (one on vaccine, two on placebo). There were 29 total deaths during blinded follow-up (15 in the vaccine arm; 14 in placebo). The crucial question, however, is whether the waning efficacy seen in the primary endpoint data also applies to the vaccine’s efficacy against severe disease. Unfortunately, Pfizer’s new preprint does not report the results in a way that allows for evaluating this question.

Approval imminent without data transparency, or even an advisory committee meeting? …But here we are, with FDA reportedly on the verge of granting a marketing license 13 months into the still ongoing, two year pivotal trial, with no reported data past 13 March 2021, unclear efficacy after six months due to unblinding, evidence of waning protection irrespective of the Delta variant, and limited reporting of safety data. (The preprint reports “decreased appetite, lethargy, asthenia, malaise, night sweats, and hyperhidrosis were new adverse events attributable to BNT162b2 not previously identified in earlier reports,” but provides no data tables showing the frequency of these, or other, adverse events.) It’s not helping matters that FDA now says it won’t convene its advisory committee to discuss the data ahead of approving Pfizer’s vaccine. (Last August, to address vaccine hesitancy, the agency had “committed to use an advisory committee composed of independent experts to ensure deliberations about authorization or licensure are transparent for the public.”)

Read more …

“..the jab allows vaccinated individuals to carry unusually high viral loads without becoming ill at first, potentially transforming them into presymptomatic superspreaders.”

Fully Vaccinated Healthcare Workers Carry 251 Times Viral Load (McCullough)

A groundbreaking preprint paper by the prestigious Oxford University Clinical Research Group, published Aug. 10 in The Lancet, includes alarming findings devastating to the COVID vaccine rollout. The study found vaccinated individuals carry 251 times the load of COVID-19 viruses in their nostrils compared to the unvaccinated. While moderating the symptoms of infection, the jab allows vaccinated individuals to carry unusually high viral loads without becoming ill at first, potentially transforming them into presymptomatic superspreaders. This phenomenon may be the source of the shocking post-vaccination surges in heavily vaccinated populations globally. The paper’s authors, Chau et al, demonstrated widespread vaccine failure and transmission under tightly controlled circumstances in a hospital lockdown in Ho Chi Minh City, Viet Nam.

The scientists studied healthcare workers who were unable to leave the hospital for two weeks. The data showed that fully vaccinated workers — about two months after injection with the Oxford/AstraZeneca COVID-19 vaccine (AZD1222) — acquired, carried and presumably transmitted the Delta variant to their vaccinated colleagues. They almost certainly also passed the Delta infection to susceptible unvaccinated people, including their patients. Sequencing of strains confirmed the workers transmitted SARS-CoV-2 to one another. = This is consistent with the observations in the U.S. from Farinholt and colleagues, and congruent with comments by the director of the Centers for Disease Control and Prevention conceding COVID-19 vaccines have failed to stop transmission of SARS-CoV-2.

On Feb. 11, the World Health Organization indicated the AZD1222 vaccine efficacy of 63.09% against the development of symptomatic SARS-CoV-2 infection. The conclusions of the Chau paper support the warnings by leading medical experts that the partial, non-sterilizing immunity from the three notoriously “leaky” COVID-19 vaccines allow carriage of 251 times the viral load of SARS-CoV-2 as compared to samples from the pre-vaccination era in 2020. Thus, we have a key piece to the puzzle explaining why the Delta outbreak is so formidable — fully vaccinated are participating as COVID-19 patients and acting as powerful Typhoid Mary-style super-spreaders of the infection.

Vaccinated individuals are blasting out concentrated viral explosions into their communities and fueling new COVID surges. Vaccinated healthcare workers are almost certainly infecting their coworkers and patients, causing horrendous collateral damage. Continued vaccination will only make this problem worse, particularly among frontline doctors and nurses workers who are caring for vulnerable patients. Health systems should drop vaccine mandates immediately, take stock of COVID-19 recovered workers who are robustly immune to Delta and consider the ramifications of their current vaccinated healthcare workers as potential threats to high risk patients and coworkers.

Read more …

“..prior infection and recovery produces durable and stable immunity in essentially everyone who has a competent immune system..”

FDA Ignores Both Science and Law (Denninger)

So the FDA has “fully approved” the Pfizer jab for Covid. In doing so standing alone they have broken the law and thus have irrevocably destroyed their authority and any reason for anyone to ever do anything based on them ever again. Let me explain. Under black letter law an EUA is illegal if there is an alternative that is considered safe, effective and available. This was the reason the FDA did not (for 18 months!) run the studies and evaluate them on other early-intervention drugs for Covid-19. We all know what they are. I’m living proof they work too, as are millions of others worldwide. But, more-importantly, this “full approval” voids all other vaccine EUAs for Covid-19. That is, under the law the Moderna and J&J instantly became illegal to offer or use within the United States.

The makers can apply for full authorization, of course, but the EUAs are void as of this morning and under black letter law cannot be administered to anyone in the United States as they are now unlicensed and unlawful products in human beings until and unless they are given full approval themselves. No medical provider can offer or administer any other than the Pfizer Covid-19 shot in the United States as of the moment of that approval. You can bet the law will be ignored; note MRNAs stock price this morning. It should have instantly been cut in half. In addition the FDA broke the law itself when it issued the “approval.” The law requires a full hearing and the data from the full set of trials; the trials are not capable of being completed until early 2022 by the original submissions and they deliberately did not hold the hearing. This is a black letter violation of the law as well, but nobody cares.

As for me, I don’t give a crap. I’ve been infected, 98% certain it was Delta (because that’s all that’s circulating right now in the US where the index case I got infected by came from, and I know who it was) and am recovered. I hit it with meds immediately and I’m fine. I know, scientifically, it was Covid-19 and not some other virus as I now have IgG antibodies and did not for the previous 18 months which I know factually as I repeatedly tested myself. There is thus exactly zero medical benefit I can derive from the jabs. I will walk without fear into a Covid-19 ICU unit right now without any PPE on whatsoever.

I have no fear of this virus because as with every other viral infection of note including those that are much more-dangerous than Covid, such as measles, prior infection and recovery produces durable and stable immunity in essentially everyone who has a competent immune system, and I do. Those of you who trust the jabs to be equally effective to an active infection and recovery are free to come with me. I will bet my life that I’m sterile immune to the virus as a result of said infection and recovery. Are you willing to place the same bet, given the many known failures to protect by the shot, including Jesse Jackson and his wife, both of whom are in the hospital with Covid-19 despite being vaccinated in a very public spectacle in January of this year? There you have it.

Read more …

“..the FDA will grant approval on results that were intentionally constructed to produce only one outcome.”

Pfizer and Moderna Lost The Clinical Trial Control Group (CTH)

According to the New York Times and multiple media outlets, Pfizer is expected to get full FDA approval today. “The move would make it the first Covid vaccine to go from emergency use authorization to full FDA approval.” With that in mind, it is worth a reminder that both Pfizer and Moderna stopped the clinical trials the FDA was using in their review: The Moderna and Pfizer vaccine tests were conducted, as customary, with a control group; a group within the trial who were given a placebo and not the test vaccine. However, during the trial -and after the untested vaccines were given emergency use authorization- the vaccine companies conducting the trial decided to break protocol and notify the control group they were not vaccinated. Almost all the control group were then given the vaccine.

Purposefully dissolving the placebo group violates the scientific purpose to test whether the vaccine has any efficacy; any actual benefit and/or safety issues. Without a control group there is nothing to compare the vaccinated group against. According to NPR, the doctors lost the control group in the Johnson County Clinicial Trial (Lexena, Kansas) on purpose: “(Via NPR) […] “Dr. Carlos Fierro, who runs the study there, says every participant was called back after the Food and Drug Administration authorized the vaccine. “During that visit we discussed the options, which included staying in the study without the vaccine,” he says, “and amazingly there were people — a couple of people — who chose that.” He suspects those individuals got spooked by rumors about the vaccine. But everybody else who had the placebo shot went ahead and got the actual vaccine. So now Fierro has essentially no comparison group left for the ongoing study. “It’s a loss from a scientific standpoint, but given the circumstances I think it’s the right thing to do,” he says.

People signing up for these studies were not promised special treatment, but once the FDA authorized the vaccines, their developers decided to offer the shots. Just so we are clear, the final FDA authorization and approval for the vaccines are based on the outcome of these trials. As noted in the example above, the control group was intentionally lost under the auspices of “the right thing to do”, so there is no way for the efficacy, effectiveness or safety of the vaccine itself to be measured. There’s no one left within the control group, of a statistically valid value, to give an adequate comparison of outcomes for vaxxed -vs- non-vaxxed. This is nuts. That NPR article is one to bookmark when people start claiming the vaccination is effective. How can the vaccine not be considered effective when there is no group of non-vaccinated people to compare the results to?

Good grief, the entire healthcare system is operating on a massive hive mindset where science, and the scientific method, is thrown out the window in favor of ideological outcomes and self-fulfilling prophecies. The fact that the researchers and doctors, apparently under the payroll of the pharmaceutical companies that have a vested financial interest in the vaccine outcome, lost the control group on purpose is alarming. Of course, Big Pharma will promote the vaccine as beneficial, and the controlled media will promote that message with a complete disconnect from the clinical trial details, and the FDA will grant approval on results that were intentionally constructed to produce only one outcome.

Read more …

Another video on informed consent is way below. Also from Canada.

Everything You Need to Know About Informed Consent (21CW)

In Canada, informed consent to medical interventions – including vaccines – is the law. The same is true in the US, UK, EU, Australia, and New Zealand. But these governments, along with corrupt drug regulators, are now running roughshod over what were once sacrosanct laws prohibiting misleading and coercive medical procedures, and instead have unleashed a multibillion dollar media campaign of fear and mass-panic designed to pave-over the right to informed consent.

Read more …

“Vaccine A is quite safe, and vaccine B is extremely dangerous. And yet the formula for PRR will produce the same result for vaccine A and B!”

Statistical Fraud in the FDA Vaccine Approval Process (JoshM)

There are several systems for reporting vaccine reactions, including deaths, but the only one available to the public is VAERS. It is incomplete, because it relies on voluntary reporting, there is no incentive to report to VAERS, and it is a cumbersome process. We may compare reports of the COVID vaccines to past years, when there were also hundreds of millions of vaccinations, including annual flu shots and childhood vaccine schedules. The comparison is dramatic. There were more than twice as many deaths related to the COVID vaccines this year as the sum total of all vaccine deaths in the 30-year history of VAERS. Given this safety record, how is there any possibility of approval? Here is where the statistical fraud comes in. [I am grateful to have been alerted to this situation by Matthew Crawford]

The safety criterion they have chosen is an obscure computation called PRR for Proportional Reporting Ratio. As the name implies, it is based on RATIOS of different event types and is utterly blind to the ABSOLUTE RATE of such events. PRR measures the distribution of different kinds of adverse events, e.g. blood clots, heart attacks, and deaths. If those ratios are severely out of line with the great variety of vaccine reactions in the past, PRR would detect that. For example, if the new vaccines caused an extraordinary risk of myocarditis, but everything else was low, then PRR would flag that. But if myocarditis was just one risk among many that have been reported from past vaccines, then PRR would not pick that up.

The real scandal is that PRR is blind to the absolute risk numbers. PRR is defined in such a way as to look for unusual PATTERNS of adverse events, but it is completely insensitive to unusual RATES of adverse events. Of course, it is the rates and not the patterns that are of primary concern, and the PRR is designed NOT to reflect that.

For example, suppose we have 2 vaccines:

Vaccine A has 1 reported death per million vaccinations, 3 reported heart attacks per million, and 20 reported headaches per million.

Vaccine B has 1 reported death per hundred vaccinations, 3 reported heart attacks per hundred, and 20 reported headaches per hundred.

Vaccine A is quite safe, and vaccine B is extremely dangerous. And yet the formula for PRR will produce the same result for vaccine A and B!

Clearly, PRR is not an appropriate criterion for evaluating safety of any particular vaccine. Someone has arranged to cook the books.

Read more …

“Regardless of the anti-science, despicable pieces regularly appearing in those outlets, such as suggesting that actually, masking kids is good for their learning ability.”

The More Masks Fail, The More We Need Them (Ian)

The push for masking, as always, boils down to a combination of incompetence, cowardice, fear, and political pressure. Experts enjoy the ability to be seen as “doing something,” and must never appear to be “anti-mask,” since it would immediately discredit them in the eyes of their peers, the greater scientific community and their ideological compatriots. Politicians want the “get out of jail free” card that masking provides; the opportunity to blame others for poor results. The “it would have worked if you’d all just listened to me” line of defense. The media simply outsources all critical thinking to like-minded ideologues and refuses to acknowledge or take seriously the few brave experts willing to tell the truth.

And as a result, corporations, whose decision makers are exclusively influenced by the same media sources, like The New York Times, follow right along. Regardless of the anti-science, despicable pieces regularly appearing in those outlets, such as suggesting that actually, masking kids is good for their learning ability. But everywhere you look, the cultural groupthink is dramatically failing. Counties and states following the CDC’s new guidance are not succeeding, and those ignoring it are faring no worse. Locations that never removed masks, such as Hawaii and Japan, are seeing their highest numbers of the pandemic, but manage to escape the vitriol and hatred leveled at Ron DeSantis because they’re following orders and implementing what the hive mind of acceptable opinion mandates.


The dramatic, predictable failure resulting from the CDC’s science-ending reversal would, in a sane world, be cause for intellectually honest experts to revisit their guidance and accept that their efforts to “control” infections is always doomed to fail. But naturally, we’re seeing the exact opposite. The more masks fail, the more we need them.

Read more …

One third has said they won’t comply. Maybe this is where the real fight will happen.

Pentagon To Mandate Covid-19 Vaccinations For All Military Personnel (RT)

The Pentagon has said it will update its own guidance on Covid-19 vaccinations, mandating the jab for all military personnel, following the US drug regulator’s decision to fully approve the Pfizer vaccine. Speaking on Monday, US Department of Defense spokesman John Kirby said the military was aware of the Food and Drug Administration’s (FDA) decision to fully approve the Pfizer vaccine for use in people over 16, and was preparing to issue updated guidance to all service personnel. “We’re going to move forward making that vaccine mandatory,” Kirby told reporters. “We’re preparing the guidance to the force right now,” he stated, adding that the exact timetable for mandating the jab was still being worked out. Earlier on Monday, the FDA announced that the Pfizer jab had been fully approved for use in the US.


The shot has been administered under emergency-use authorization since mid-December 2020. The FDA added that the Pfizer vaccine will retain its emergency-use authorization for use in adolescents and for those requiring a third dose due to other health conditions. Earlier in August, the Washington Post reported that around 65% of active-duty military personnel were fully vaccinated, compared to around 59% of eligible Americans. Defense Secretary Lloyd Austin has previously encouraged all military personnel to get vaccinated against Covid. “To defend this nation, we need a healthy and ready force. I strongly encourage all DoD military and civilian personnel – as well as contractor personnel – to get vaccinated now and for military service members to not wait for the mandate,” Austin stated earlier in August.

Read more …

“I do not expect a staffing shortage,” Porter said.”

NYC Orders 150,000 Teachers & School Staff To Get Vaccinated (ZH)

As the NYT explained, education staffers are the first group of city workers to face a full vaccine mandate. The announcement also opens the door to a broader vaccine mandate of city workers, which the mayor said Monday the city was considering. Last month, Mayor Bill de Blasio issued a mandate for city workers that allowed for those unvaccinated to submit for weekly coronavirus testing. “We know this is going to help ensure that everyone is safe,” Mr. de Blasio said during a news conference on Monday, adding that city schools had extremely low virus transmission last year. The mandate, the mayor said, will help the city “build on that success.”

While the mayor’s push is likely to prove unpopular with many rank-and-file members; the city’s teacher’s unions, and unions representing other DoE staff, have signed off on the new mandate (though they’re still negotiating about what might happen to workers who continue to refuse). UFT President Michael Mulgrew acknowledged that the city had the legal right to impose the mandate, but he told reporters details were still being hashed out. The city announced last month that any teacher who failed to comply with both the vaccination requirement, and the required weekly testing for those who didn’t get the jab, would be suspended without pay.

“While the city is asserting its legal authority to establish this mandate, there are many implementation details, including provisions for medical exceptions, that by law must be negotiated with the U.F.T. and other unions, and if necessary, resolved by arbitration,” Mr. Mulgrew said in a statement. Mayor de Blasio has insisted that even if negotiations stall, the mandate will still be implemented. Meisha Porter, the chancellor of NYC’s schools, said she expects a high level of compliance from school staff on the mandate. “I do not expect a staffing shortage,” Porter said.

Read more …

No clue how serious this is, but it’s a good idea.

Truckers Threaten To Shut Down Australia Due to Covid Insanity (OI)

Australia seems to be in the grips of COVID-induced insanity as people across the country are vigorously protesting against the lockdown measures imposed to curb the spread of the renewed bout of coronavirus outbreak. After violent ruckus witnessed on the streets of major Australian cities, including Brisbane, Sydney and Melbourne, and dogs shot dead by a rural council in New South Wales to prevent volunteers from travelling during Covid restrictions, Australian truck drivers have threatened to shut down major highways across the country as a mark of protest against Covid lockdowns. Social media websites are awash with a video of a truck driver who said in his video that truck drivers are ‘planning to shut down the country’ to ‘remove the s*** government’.


He further warned the Aussies that their demonstration could end up choking supply chains and urged them to stock up on groceries to get them through the next couple of weeks. “It’s on. The truckies are doing it. The truckies are going to shut down the country,’ the man says in the video. What that means is you need to go shopping now, get what you can for the next week or two, load your fridge, freezers,” the truck driver could be seen saying in the video.

Read more …

“The same progressives who regularly denounce “systemic racism” and “Western imperialism” are now enforcing policies that disproportionately punish minorities and the poor..”

Keeping Fear Alive (Tierney)

Throughout the pandemic, American political and public-health leaders have been following Rahm Emanuel’s classic dictum for power-seeking officials: “You never want a serious crisis to go to waste.” Now they’ve adopted a corollary: you never want a crisis to end. So they are prolonging the national misery instead of easing it, which could be done with a few simple strategies. Explain to the public that the virus will never disappear but is no longer a mortal threat to the vast majority of Americans. Encourage the minority still at risk to get vaccinated by honestly discussing who is in jeopardy and what scientists have learned about infections. Promote treatments proven to prevent infection and speed recovery while avoiding unproven treatments and mandates that cause collateral damage and generate mistrust.

Above all, make it clear to Americans that we finally have reason to celebrate: what once seemed an unprecedented danger is now just one of many pathogens that we know how to live with. But the nation’s crisismongers aren’t about to relinquish their hold over the public, so they’ve set new goals that are as unachievable as they are unnecessary and harmful. Making vaccines available to every American adult is no longer sufficient; now the crisis cannot end until the entire population has been vaccinated. Instead of focusing efforts on vaccinating the vulnerable, officials obsess on compelling universal obedience, even if that means squandering vaccines on people who already have acquired natural immunity or are at minimal risk of serious illness.

The same progressives who regularly denounce “systemic racism” and “Western imperialism” are now enforcing policies that disproportionately punish minorities and the poor, both in the United States (the majority of black teenagers and young adults in New York have been banished from much of public life by the city’s new vaccine-passport policy) and in the rest of the world. The hypocrisy was deftly captured in a tweet by Martin Kulldorff, the Harvard epidemiologist: “If you favor university vaccine mandates for low-risk American and European students, when there is not enough vaccine for older high-risk people in Asia, Africa and Latin America, please remove your #BLM tags from your Twitter/Facebook profiles.”

Children are being sentenced to another round of unnecessary mask mandates and probably more school closures based on evidence-free warnings from Anthony Fauci and others that the Delta variant will be more deadly to them than the original virus. While the variant is more infectious, the evidence does not show it to be any more lethal. In fact, the current mortality rate among American children with Covid is lower than it was last year—and last year many more children died of the flu than of Covid. One of the most thorough studies, in England, shows that the survival rate for those under 18 with Covid is 99.995 percent. But instead of emphasizing these reassuring statistics, public-health officials like Jerome Adams, the surgeon general, keep looking for new ways to scare parents and children.

“I’m an anesthesiologist,” he tweeted last weekend. “And a dad. And I can assure you in both capacities that your child will be far more comfortable if they’re in a face mask, than on a ventilator. If you’re making a choice on behalf of a child, please choose based on their comfort, vs yours.” He offered no new evidence that children are at heightened risk from the virus, much less any evidence that a mask would make any difference, but he did make sure to include a gruesome photograph of a child on a ventilator. It was a new low in public-health demagoguery, but unfortunately not so different from the fearmongering of other officials, the press, and social-media platforms. They lament that a minority of the public remains reluctant to get vaccinated without recognizing that their own tactics are a likely a chief cause of this reluctance. They have been misleading people for so long—and censoring challenges to their misinformation—that it’s no wonder polls show that an overwhelming majority of unvaccinated Americans say they don’t trust Fauci or the CDC.

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“Britain and France managed to get their nationals out last week, only to be rebuked by American brass for “making us look bad.” That helped, I’m sure.”

Throwdowns and Showdowns (Kunstler)

Notice, there are two sets of hostages in this phase of what looks like an engineered US collapse: the thousands of stranded Americans who can’t get out of Afghanistan thanks to the history-rockin’ ineptitude of “Joe Biden,” Tony Blinken, and General Mark Milley, and the millions of We-the-People back home whose minds are hostage to the narratives concocted in a shadowland of sinister governance. Welcome to a week of throwdowns and showdowns, a force majeure of mind change. A strange paralysis in the Pentagon has prevented the use of US power to clear an escape corridor to Kabul’s airport and establish order in the facility — this, after the tactically mystifying decision to abandon the US Bagram military airfield, a good twenty miles outside of festering Kabul, and surrounded by more easily-securable empty desert.

Britain and France managed to get their nationals out last week, only to be rebuked by American brass for “making us look bad.” That helped, I’m sure. And then how long can the stranded Americans even stay hidden and alive? They have to eat. Either they come out of their hidey-holes and get to some market, or they would (theoretically) have to send some Afghani servants to fetch them supplies, But, what Afghani in his right mind would want to be caught in service to the Americans by the Taliban? That quandary must have a pretty short time-horizon on it. Standing by to see how it works out….

Next in this week’s throwdown parade is the FDA’s imminent approval of Pfizer’s Covid-19 vaccine, without any of the usual extensive trials. How does that even happen, with an efficacy rate of 39 percent maximum and a runaway train of vicious side effects ranging from brain and heart damage to infertility? The so-called mRNA “vaccines” are also implicated in the ongoing mutation of the disease, producing a cavalcade of variants. Is that, perhaps, on-purpose, to keep the pandemic going, preventing it from burning-out?

Read more …

 

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Aug 232021
 


Vasily Polenov Moscow courtyard 1878

 

The FDA Is Begging You Not to Take Horse Dewormer for Covid-19 (RS)
How Does Covid-19 Affect The Brain? (NatGeo)
Potential Use Of Ivermectin For Treatment And Prophylaxis Of SARS-CoV-2 (SD) /span>
Ivermectin for Prevention and Treatment of COVID-19 Infection (AJT)
Stop The Mandates Or People Die (Denninger)
Molecular Determinants of SARS-CoV-2 Variants (Cell)
Biden Team’s Misguided And Deadly Covid-19 Vaccine Strategy (WT)
100s Of Doctors Sign Open Letter: Need Debate On ‘Flawed Covid Guesses’ (Exp.)
Rescue Dogs Shot Dead By NSW Council Due To Covid-19 Restrictions (SMH)
Afghan Staff At US Embassy Losing Faith In Evacuation Efforts (NBC)
White House Announces They’ve Lost Kamala Harris (BBee)

 

 

 

 

A drug safely used by an estimated 3 billion people has been relabeled a horse dewormer. This is a dangerous campaign. Lives are being lost.

The FDA Is Begging You Not to Take Horse Dewormer for Covid-19 (RS)

“You are not a horse. You are not a cow,” the Food and Drug Administration tweeted on Saturday alongside a link to a page on their website explaining “Why you should not use Ivermectin to treat or prevent Covid-19.” Why? Because Ivermectin, a medication usually reserved for deworming livestock, is responsible for a spike in poison control calls in Mississippi as people duped by conspiracy theories have purchased the drug and ingested it, hoping it will treat or prevent Covid-19 — something the drug is not proven to do. According to an alert issued by the Mississippi Department of Health on Friday, 70 percent of all recent calls to poison control in the state “have been related to ingestion of livestock or animal formulations of ivermectin purchased at livestock supply centers.”

Although most callers (85 percent) only reported mild symptoms, one person was advised to seek additional treatment. “Animal drugs are highly concentrated for large animals and can be highly toxic in humans,” the alert said. Ivermectin is sometimes used in humans to treat parasites or scabies, but in much smaller doses than are given to livestock. The calls have clearly baffled health officials in the state. “I think some people are trying to use it as a preventative which is really kind of crazy,” Dr. Thomas Dobbs, Mississippi’s state health officer, said. “So please don’t do that.”

“You wouldn’t get your chemotherapy at a feed store,” Dobbs added. “You wouldn’t treat your pneumonia with your animal’s medication. It can be dangerous to get the wrong doses of medication, especially with something meant for a horse or a cow.” But the obvious risks of humans ingesting Ivermectin haven’t stopped people at Fox News — including hosts Laura Ingraham, Sean Hannity, and Tucker Carlson — from dangerously suggesting that it is a safe and effective treatment for Covid-19, as Rachel Maddow pointed out on her Friday night show where she showed clips of Fox personalities pushing the drug consistently over the last six months.

Read more …

Very little is clear. Only thing to do is keep people from being infected. And the vaccines don’t do that:

..an internal document from the C.D.C. states that some 35,000 vaccinated people experience symptomatic coronavirus infections each week..

How Does Covid-19 Affect The Brain? (NatGeo)

If SARS-CoV-2 doesn’t infect brain cells, how is so destructive to cognition? There are two leading hypotheses. The first is that the infection somehow triggers inflammation in the brain. Some COVID-19 patients have suffered encephalitis, or swelling of the brain, which can cause confusion and double vision, and in serious cases, speech, hearing, or vision problems. If left untreated, patients can develop cognitive problems. Viruses like West Nile and Zika can cause encephalitis by directly infecting the brain cells, but how COVID-19 may lead to brain inflammation is less clear. An immune response run amok, known as autoimmunity, might be to blame for some instances of inflammation throughout the body, including the brain.

When the immune system is fighting a disease like COVID-19, it unleashes antibodies to do battle against the infection. But sometimes a person’s immune system becomes hyperactive and instead starts making self-attacking antibodies, known as autoantibodies, which can contribute to inflammation and blood clots. These autoantibodies have been found in the cerebrospinal fluid of COVID-19 patients with neurological symptoms. In the Columbia study, researchers found clusters of microglia—special immune cells in the brain whose job is to clear out damaged neurons—that appeared to be attacking healthy neurons. The phenomenon is called neuronophagia. Most of these rogue microglia were in the brain stem, which regulates heartbeat, breathing, and sleeping.

The researchers think these microglia may get activated by signaling molecules called inflammatory cytokines found in patients with severe COVID-19. These molecules are supposed to help regulate the immune system, but some people’s bodies release too many inflammatory cytokines in response to a viral infection. When researchers at Stanford looked at brain tissue from eight patients who died of COVID-19, they also observed signs of inflammation compared to 14 control brains. Using a technique called single-cell RNA sequencing, they found that hundreds of genes associated with inflammation were activated in brain cells from COVID-19 patients compared to controls.

They also noted molecular changes in the cerebral cortex, the part of the brain involved in decision-making and memory that suggested signaling imbalances in neurons. Similar imbalances have been seen in patients with Alzheimer’s disease. The results were published in Nature in June. A second explanation for cognitive issues is that COVID-19 may restrict blood flow to the brain and deprive it of oxygen. In patients who have died of COVID-19, researchers have found evidence of brain tissue damagecaused by hypoxia, or the lack of oxygen.

Read more …

Slow but sure take-up by serious medical journals.

Science Direct (Elsevier). Current Research in Translational Medicine
Volume 69, Issue 4, October 2021, 103309

Potential Use Of Ivermectin For Treatment And Prophylaxis Of SARS-CoV-2 (SD)

Ivermectin performs its function mainly through inhibition of nuclear transport mediated by the imported heterodimer a/b1 , which is responsible for the translocation of proteins of several viral species (Human Immunodeficiency Virus, type 1- HIV1, and Simian Virus 40 – SV40; a known oncogenic DNA), and such translocation is, in turn, essential for viral replication [7,8]. This inhibition appears to affect a considerable number of RNA viruses. It has recently been shown that ivermectin inhibits the replication of the SARS-CoV-2 virus in vitro [8, 9], although it is not clear how this occurs. However, since the causal agent of COVID-19 is an RNA virus, the interference with the same proteins and molecular processes described above can reasonably be expected.

However, these studies were conducted at concentrations substantially higher than expected in the plasma and lungs of humans who receive the approved dose of ivermectin. Pharmacokinetic and pharmacodynamic studies suggest that in order to achieve the plasma concentrations required for in vitro antiviral efficacy, it would be necessary to administer doses up to 100 times higher than approved for human use. However, increasing the dose/kg of body weight may be a strategy to increase efficacy, the increase of the risk of toxicity is not conclusive. Currently, there is a noteworthy absence of efficacious treatments for patients with early infection. Although most patients present mild or moderate symptoms, up to 5-10% may have a bad disease progression, so there is a pressing need for effective drugs to be administered early in the course of infection, even before the appearance of severe symptoms, i.e. when the course of the disease is more modifiable to prevent disease progression and longer-term complications.

In fact, it is known that the earlier the antiviral therapies are started, the greater the benefits for patients, in both influenza [15] and SARS infections [16], as well as, more generally, for all infections. Given the need to find an effective drug that can mitigate the harmful consequences of COVID-19, a large number of studies are being carried out in order to assess the effectiveness of different existing drugs, including ivermectin, with promising results. This narrative review summarizes and outlines the evidence-based effectiveness and safety of ivermectin in patients with SARS-CoV-2 infection, recommending the drug for the treatment of COVID-19 especially in the early stages of the disease.

Read more …

American Journal of Therapeutics: July/August 2021

Ivermectin for Prevention and Treatment of COVID-19 Infection (AJT)

Ivermectin is a well-known medicine that is approved as an antiparasitic by the World Health Organization and the US Food and Drug Administration. It is widely used in low- and middle-income countries (LMICs) to treat worm infections. Also used for the treatment of scabies and lice, it is one of the World Health Organization’s Essential Medicines. With total doses of ivermectin distributed apparently equaling one-third of the present world population, ivermectin at the usual doses (0.2–0.4 mg/kg) is considered extremely safe for use in humans. In addition to its antiparasitic activity, it has been noted to have antiviral and anti-inflammatory properties, leading to an increasing list of therapeutic indications.8

Since the start of the SARS-CoV-2 pandemic, both observational and randomized studies have evaluated ivermectin as a treatment for, and as prophylaxis against, COVID-19 infection. A review by the Front Line COVID-19 Critical Care Alliance summarized findings from 27 studies on the effects of ivermectin for the prevention and treatment of COVID-19 infection, concluding that ivermectin “demonstrates a strong signal of therapeutic efficacy” against COVID-19.9 Another recent review found that ivermectin reduced deaths by 75%. Despite these findings, the National Institutes of Health in the United States recently stated that “there are insufficient data to recommend either for or against the use of ivermectin for the treatment of COVID-19,”and the World Health Organization recommends against its use outside of clinical trials.

Ivermectin has exhibited antiviral activity against a wide range of RNA and some DNA viruses, for example, Zika, dengue, yellow fever, and others.13 Caly et al14 demonstrated specific action against SARS-CoV-2 in vitro with a suggested host-directed mechanism of action being the blocking of the nuclear import of viral proteins that suppress normal immune responses. However, the necessary cell culture EC50 may not be achievable in vivo.16 Other conjectured mechanisms include inhibition of SARS-CoV-2 3CLPro activity(a protease essential for viral replication), a variety of anti-inflammatory effects,19 and competitive binding of ivermectin with the viral S protein as shown in multiple in silico studies. The latter would inhibit viral binding to ACE-2 receptors suppressing infection. Hemagglutination via viral binding to sialic acid receptors on erythrocytes is a recently proposed pathologic mechanism that would be similarly disrupted. Both host-directed and virus-directed mechanisms have thus been proposed, the clinical mechanism may be multimodal, possibly dependent on disease stage, and a comprehensive review of mechanisms of action is warranted.

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You can’t force people. And you shouldn’t be trying.

Stop The Mandates Or People Die (Denninger)

Better watch this one folks and let it sink in.

“If I don’t show up for my job, as I just explained to you, people die. On Saturday night at 10 p.m. I got a page. I did not want to go to work. Somebody was having a very critical problem, they were dying. I worked until 6 a.m. the next day. If I had not of showed up, there would have been nobody to do my job. These guys can’t show up to their job, and I’m sorry, your jobs are not as important as mine.” There are tens if not hundreds of thousands of people just like him They’re everywhere in the health care system. They have unique skills without which the system does not function, and when you need those skills you need them now, not later. There is no “later”; there is either now or death. Take someone on dialysis. This is not a “robotic procedure”; each patient has specific levels of various drugs and their specific metabolic reactions to them that must be individually managed.

The people who do that job are not replaceable on short notice, if at all. If you need dialysis and do not get it, you die. This is not a “maybe” or “might die” you WILL die with absolute, 100% certainty. Things happen at odd hours of the day and night. Most real medical emergencies are not scheduled — heart attacks, strokes, car wrecks, gunshots and similar. They happen when they happen and either someone is there to respond to it and deal with it or the person in question dies. Those hundreds of thousands of people who are utterly essential to people not dying every single day — hundreds if not thousands who will otherwise die if those employees refuse to show up — and exactly zero of those people can be compelled to work. This is America. It is not the Soviet Union. It is not North Korea.

NOBODY is a slave and EVERYONE has the right to say “**** you” and walk out. EVERYONE. ALL THE TIME. Then there are of course both cops and firefighters. You want someone to put your house out if its on fire, right? What if the firefighters say “**** you” to a jab mandate and quit? Who’s going to put the fire out? Do you even have a wrench to get the hydrant open, say much less the correct fittings and hose? What happens when your child is in that burning house and there is no firefighter to put it out? He or she dies. You cannot arrest and jail someone for quitting their job or refusing a mandate and being fired. All employment is voluntary, no matter how “essential” the position. THERE ARE NO EXCEPTIONS and there is no way to replace the people who do these jobs without which hundreds of people per day WILL DIE.

Therefore you have a choice to make America and you have to make it NOW. You will stand up and stop these mandates. You will do it now. You will do it or every single person who dies as a result of your failure to do so, and the refusal of others to consent, is YOUR responsibility. Not their person who quits — YOURS. THEY are not slaves. THEY cannot be compelled to consent. THEY have NO obligation to put up with your bull****. You’d better get this through your thick ******n skull RIGHT NOW. YOU are why that person who needs dialysis will be dead. YOU are why the person who is in critical trouble in a hospital and there is no perfusionist available right now will die. YOU either stop this madness, right now, by whatever means are necessary, without exception from top to bottom or YOU are responsible for those deaths and those deaths WILL come.

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“While replication-associated mutations generate small changes in the viral genome, recombination may introduce more important modifications, leading to dramatic changes in the phenotype of SARS-CoV-2..”

Molecular Determinants of SARS-CoV-2 Variants (Cell)

Accumulation of genomes with replication-associated random mutations within the same cell has the potential to generate a heterogeneous mix of viral proteins, including spike protein, which brings into question the true diversity of the spike on the surface of individual virions and subsequent tissue-level spread of SARS-CoV-2 and its variants. If a more orderly molecular process to regulate the homogeneous distribution of spike protein variants on individual virions exists, it remains to be identified. Regular RNA sequencing analyses are unable to identify these differences since they can only be captured by ultra-high-resolution single-virion protein sequencing, the technology for which is in its infancy.


The SARS-CoV-2 genomic mutation rate in humans is estimated at 0.8-2.38 x 10-3 nucleotide substitutions per site per year largely based on analysis of sequencing data archived in public repositories. Emerging studies are attempting to confirm this mutation rate using experimental investigations. By comparison, mutations rates for influenza A virus and Middle East respiratory syndrome CoV (MERS-CoV) are 2.3 x 10-3 and 1.12 x 10-3 nucleotide substitutions per site per year, respectively. Human CoVs (HCoV)-OC43 and HCoV-229E have an average mutation rate of 3-6 x 10-4 nucleotide substitutions per site per year. Emerging experimental data suggest that SARS-CoV-2 is capable of mutating and accumulating changes when facing a new cell type, albeit in the absence of immune surveillance in a single-cell-type infection model. A clinical study also reported the rapid evolution of SARS-CoV-2 variants in the presence of antibodies from convalescent plasma therapy. While random errors during replication may induce genetic mutations in SARS-CoV-2, multiple extrinsic factors, such as individual and population-level immunity, play a vital role in the selection of these variants. More research is warranted to fully understand the cellular and molecular drivers of genomic mutation and selection in SARS-CoV-2. As SARS-CoV-2 accumulates new genetic changes, we shall need to reassess the mutation rate to better understand the contribution of replication-associated random mutations and its impact on SARS-CoV-2 transmission and emergence of new variants.


Figure 1 Replication-Associated Generation of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Variants.

While replication-associated mutations generate small changes in the viral genome, recombination may introduce more important modifications, leading to dramatic changes in the phenotype of SARS-CoV-2 (Figure 2). Discontinuous transcription of CoV genomes enables recombination in a cell coinfected with more than one CoV species or variant via ‘strand switching’ by the viral RdRp (Figure 2A). This process leads to the production of chimeric subgenomic RNA and proteins. Chimeric proteins may have consequences for the fate of infected cells and for cellular and tissue tropism of progeny virions. As technology evolves, we might be able to track the spread of individual virions, along with deciphering the heterogeneity of their composition.


Figure 2 Recombination-Induced Variants.

Read more …

Dr. Robert Malone and Peter Navarro.

Biden Team’s Misguided And Deadly Covid-19 Vaccine Strategy (WT)

The Biden administration’s strategy to universally vaccinate in the middle of the pandemic is bad science and badly needs a reboot. This strategy will likely prolong the most dangerous phase of the worst pandemic since 1918 and almost assuredly cause more harm than good – even as it undermines faith in the entire public health system. Four flawed assumptions drive the Biden strategy. The first is that universal vaccination can eradicate the virus and secure economic recovery by achieving herd immunity throughout the country (and the world). However, the virus is now so deeply embedded in the world population that, unlike polio and smallpox, eradication is unachievable. SARS-CoV-2 and its myriad mutations will likely continually circulate, much like the common cold and influenza.

The second assumption is that the vaccines are (near) perfectly effective. However, our currently available vaccines are quite “leaky.” While good at preventing severe disease and death, they only reduce, not eliminate, the risk of infection, replication, and transmission. As a slide deck from the Centers for Disease Control has revealed, even 100% acceptance of the current leaky vaccines combined with strict mask compliance will not stop the highly contagious Delta variant from spreading. The third assumption is that the vaccines are safe. Yet scientists, physicians, and public health officials now recognize risks that are rare but by no means trivial. Known side effects include serious cardiac and thrombotic conditions, menstrual cycle disruptions, Bell’s Palsy, Guillain Barre syndrome, and anaphylaxis.

Unknown side effects which virologists fear may emerge include existential reproductive risks, additional autoimmune conditions, and various forms of disease enhancement, i.e., the vaccines can make people more vulnerable to reinfection by SARS-CoV-2 or reactivation of latent viral infections and associated diseases such as shingles. With good reason, the FDA has yet to approve the vaccines now administered under Emergency Use Authorization. The failure of the fourth “durability” assumption is the most alarming and perplexing. It now appears our current vaccines are likely to offer a mere 180-day window of protection – a decided lack of durability underscored by scientific evidence from Israel and confirmed by Pfizer, the Department of Health and Human Services, and other countries.

Here, we are already being warned of the need for universal “booster” shots at six-month intervals for the foreseeable future. The obvious broader point that militates for individual vaccine choice is that repeated vaccinations, each with a small risk, can add up to a big risk. It’s an arms race with the virus.

Read more …

Still not sure what they’re mad about, other than lockdowns.

100s Of Doctors Sign Open Letter: Need Debate On ‘Flawed Covid Guesses’ (Exp.)

A hundred and thirty three doctors, nurses, psychiatrists paramedics and midwives signed the letter released today which states that despite a “complete lack of widespread approval among health professionals,” of the pandemic policies, “no attempt” has been made to measure the harms of lockdown policies. The letter, also addressed to the Health Secretary and First Ministers for Scotland, Wales and Northern Ireland states: “You have failed to engage in dialogue and show no signs of doing so. You have removed from people fundamental rights and altered the fabric of society with little debate in Parliament.” The signatories, from a broad range of specialities, came forward despite the risk of doing so to both their jobs and reputations.

Founding signatory Dr Ros Jones, a retired paediatric consultant said: “We wrote the letter as a group of healthcare professionals, connected only by our deep concern and shared commitment to “first do no harm.” We can no longer stand by in silence. We are not the first group of medically and scientifically qualified professionals to write in such terms to the Government. In March, 22 eminent scientists publicly called for drastic policy change. We sincerely hope we will be the last who feel the need to write such a letter.” Dr Alan Mordue, another founding signatory said: “To move forward now our governments urgently need to facilitate a wider and open debate within the medical and scientific community, for the short term as we lift restrictions, and the longer term to improve how we manage winter respiratory viruses and pandemics in the future.”

Concerns voiced in the letter include accusations that no Minister responsible for policy “has engaged in an open and full discussion of alternative ways of managing the pandemic,” despite being aware of other medical and scientific viewpoints. It adds the pandemic response policies have caused “significant, permanent and unnecessary harm” to the UK and “must never be repeated.” The letter focuses on 10 areas where the UK’s approach to COVID failed. It argues the nature of the covid threat has been exaggerated, it claims the use of behavioural science to generate fear was “inappropriate and unethical” and it argues the role of asymptomatic spread has been overplayed and used to promote public compliance with restrictions.

Finally it states that restrictions have been imposed with an overreliance on modelling data whilst ignoring real world data. The signatories called for a “sea change within the Government “which must now pay proper attention to those esteemed experts outside its inner circle who are sounding these alarms.”

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New normal. I see videos every day from Australia that make me want to vomit.

Rescue Dogs Shot Dead By NSW Council Due To Covid-19 Restrictions (SMH)

Several impounded dogs due to be rescued by a shelter have instead been shot dead by a rural council in NSW under its interpretation of COVID-19 restrictions, alarming animal activists and prompting a government probe. Bourke Shire Council, in the state’s north-west, killed the dogs to prevent volunteers at a Cobar-based animal shelter from travelling to pick up the animals last week, according to council’s watchdog, the Office of Local Government. “OLG has been informed that the council decided to take this course of action to protect its employees and community, including vulnerable Aboriginal populations, from the risk of COVID-19 transmission,” a spokesman from the government agency said.

The spokesman said the agency was examining the circumstances of the incident to find out whether companion animal and cruelty prevention laws had been broken. The Herald attempted to contact the council administration multiple times, but received no response, and a member of Rural Outback Respite/Rescue – the shelter that was supposed to receive the dogs – declined to comment. A source who is familiar with the arrangement said the shelter volunteers are distressed and had COVID-safe measures in place to handle the dogs, one of which was a new mother. According to NSW Health, there have been no recent locally acquired COVID-19 cases in Cobar, although fragments of the virus have been found in the area’s sewerage system.

The Office of Local Government Minister Shelley Hancock, who has previously faced questions in Parliament over the shooting of animals in council pounds, did not comment. However, animal liberation campaigner Lisa Ryan called for an urgent investigation. “We are deeply distressed and completely appalled by this callous dog shooting and we totally reject council’s unacceptable justifications that this killing was apparently undertaken as part of a COVID- safe plan,” Ms Ryan, Animal Liberation’s regional campaign manager, said.

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“It would be better to die under the Taliban’s bullet” than face the crowds again..”

Afghan Staff At US Embassy Losing Faith In Evacuation Efforts (NBC)

Local staff members at the U.S. Embassy in Kabul are “deeply disheartened” by U.S. evacuation efforts and have expressed a sense of betrayal and distrust in the U.S. government, according to a State Department diplomatic cable obtained by NBC News. The cable, which was sent Saturday, said memos were sent Wednesday inviting Afghan staff members at the embassy to head to Hamid Karzai International Airport in Kabul. It told them to take food and to prepare for difficult conditions. “However, no one anticipated the brutal experience that occurred,” the cable said.

Staffers reported being jostled, hit, spat on and cursed at by Taliban fighters at checkpoints near the airport, it said, adding that criminals were taking advantage of the chaos while the U.S. military tried to maintain order “in an extremely physical situation.” Some staff members reported that they were almost separated from their children, while others collapsed in a crush of people and had to be taken to hospitals with injuries, the cable said. Others said they had collapsed on the road because of heat exhaustion, it said. “It would be better to die under the Taliban’s bullet” than face the crowds again, a staff member was quoted as saying in the cable.

“Happy to die here, but with dignity and pride,” another said, while a third accused the U.S. of prioritizing Afghan government elites with contacts in the U.S., who already had the correct paperwork and other ways to flee the country. A local embassy staff member reported that his home had been tagged with spray paint — a tactic the Taliban have used in the past to identify homes’ occupants for further questioning, the cable said, adding that the family had been forced to flee their home but was unable to get to the airport. Others shared concerns about conditions in Qatar, where many refugees have been flown before they make their way to other locations.

The U.S. began evacuating its citizens, diplomatic staff members and Afghans who aided its mission in the country last week after the Taliban seized control of much of Afghanistan before they finally walked into Kabul last Sunday without firing a shot. A State Department spokesperson said the U.S. has a “special commitment” to local embassy staff members who “have suffered hardship, pain and loss because of their dedication to working with us to build a better future for all Afghans.”

Read more …

… But They’re Also Not Looking For Her Very Hard

White House Announces They’ve Lost Kamala Harris (BBee)

In an interview with Morning Joe, White House communications director Kate Bedingfield revealed they have lost Kamala Harris and have no idea where she’s gone, although she admitted nobody is really looking for her all that hard. “Yeah, I dunno. She’s somewhere, I guess. I mean, she didn’t just disappear,” said Bedingfield. “We have some people looking for her I think, but we’re not too worried, honestly. I’m sure she’ll turn up sooner or later.” “Wait, wait, wait,” said the show’s host. “You mean to tell me that in this time of crisis, you have literally no idea where the Vice President of the United States is?”

“Well, it sounds bad when you put it that way,” replied the Communications Director. “I don’t really see how this is a big deal. It’s been kind of nice and quiet around here since she left… we’re not even quite sure what she does, anyway,” she said with a shrug. Anonymous sources have suggested Kamala may be somewhere around Camp David, as locals reported the sound of cackling through the night.

Read more …

 

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 August 21, 2021  Posted by at 6:04 pm Finance Tagged with: , , , , , ,  21 Responses »


René Magritte The false mirror 1928

 

 

Look, we get it. The people working at institutions such as the FDA and CDC were anonymous nobodies with science degrees for as long as they can remember, just following protocols written by others, and getting relatively well paid. And then Covid came, and everyone looked at them to save the nation. Especially the government and the pharmaceutical industry. And they exert a lot of pressure.

Pressure to ditch established protocols in particular. Because those stand between them and enormous amounts of profits and political power. So, yeah, we get that part. But these little clerks and their little managers are the last bastion to keep Americans safe from dangerous abuses from the nation’s chemical giants, so there can be huge amounts of American lives at stake. So ditching protocols and good practice is never really an option. You would think. Until now.

On August 5 (last update) this was still up on clinicaltrials.gov (U.S. National Library of Medicine) for the Pfizer trials:

 

 

May 2 2023. But the trial will be finished around August 25 2021 (just as Dr. Fauci has been “predicting“ for weeks now). Which leads to the somewhat bizarre paradoxical conclusion that as the FDA declares the vaccine “Safe”, at the same time it declares the opposite. Because there has been no time for the study of medium- to long term effects of the substance; they just skipped over those entirely.

Which in turn, given the questions raised by many medical professionals about such issues as antibody-dependent enhancement (ADE) and OAS (immune priming), is equally bizarre. At the very least, the forces in the government and the pharmaceutical industry, and now the regulatory agencies too, know there are very realistic risk factors related to the “vaccine”. And they just turn a blind eye.

We see people all the time discussing the credibility of these agencies, and that discussion is now over. That credibility will be reduced to zero around August 25. Is it really worth it? Guess that discussion is now obsolete as well.

And it’s not just the medium- to long term effects that are worrying. The same FDA has displayed no reaction whatsoever to the short term either. Here’s the US VAERS system on adverse reactions, August 13:

 

 

And its European sister, EudraVigilance, on August 14:

 

 

Both these systems are estimated to report 1 in 10 to 1 in 100 cases. They’re poorly set up on purpose, difficult to use etc. A Hawaii court care mentions 45,000 deaths. US statistician Mathew Crawford, whom I’ve cited a few times now, puts the number at 276,300. But even if we would limit ourselves to the “official”numbers, some 35,000 people in the EU and US have died from the vaccine (not all Pfizer, we know). And that’s just official numbers, that’s not the potenntially 10-100 times larger ones. I know, you might say: no way 350,000 died, someone would have told us! Okay, who told you about the 35,000, then?

Crawford also says: “At some point, when the potential for conflicts of interest are high and the point of failure is fundamental to the task of those doing the job, incompetence should no longer be differentiated from criminal intent.”

The FDA has strayed so far from its protocols and practices it’s hard to believe. A vaccine that killed more than 25-50 people in a trial would always be cut short. Now, at 35,000+ deaths, its crickets. And not just crickets, but an upcoming full approval. Someone should seriously look at taking the little clerks and their little managers to court for murder. Pfizer may have gotten full immunity, but perhaps they have not. And as of August 25, they will be just as guilty.

 

 

Let’s go to how the news today reported the approval.

No, we haven’t seen ADE (where your antibodies help the spike proteins enter your cells, to replicate and then kill them) take off on a large scale. But that was never expected, that would always take 6-24 months after inoculation. And even then, there’s nothing saying that what is now labeled Delta is not often already ADE. In the same vein, some are claiming that the rise in Covid in children is in reality RSV, not Covid. If the FDA and CDC are capable of what I’m describing in this article, who’s to say what they are not capable of?

But yeah, full approval would mean more pressure instruments, that’s the whole idea. Now everyone can take your Nuremberg and “Universal Declaration on Bioethics and Human Rights” rights away, because the little clerks and managers at the FDA said so. And when did all this happen? Just a year ago, none of those who now clamor to declare you a leper would have even dreamed of doing that. Then they saw the light.

Let me put this in simple terms: there is no chance in hell that they will ever get more than two-thirds of people “vaccinated”. None. And that means the entire vaccination scheme is moot from day one. One third of people will remain unvaccinated. And society, the economy, cannot afford to lose them. All it can do is threaten. And do you really think an approval without proper protocol will make another 10% “give in”? I don’t see it.

And besides, we already know the vaccines don’t work. All this talk about rare and one-in-a million events, humbug. It’s one every hour. No protection from infection, and very little from severe disease. You’re caught in a propaganda treadmill and it’s time to get out.

 

FDA ‘Finalizing Paperwork’ With Pfizer Aiming To Give Full Approval To Covid-19 Vaccine Next Week

The FDA will give full authorization to Pfizer’s Covid jab sometime next week, according to multiple reports, putting it on track to be the first in the US to get approval and likely paving the way for additional vaccine mandates. The US regulator is expected to give the greenlight for Pfizer’s immunization in the coming days, the New York Times and Politico reported on Friday, citing several “people familiar” with the agency’s planning. Though the FDA still has a “substantial amount of paperwork and negotiation with the company” to get through, it could give full approval as soon as Monday, the Times added. It was previously reported that the FDA hoped to grant authorization before Labor Day on September 6, and now appears set to meet that informal deadline.

With a number of hospital systems and universities around the US signaling plans to mandate vaccinations against Covid-19 upon full approval, the move is likely to trigger a spate of new requirements around the country. The US military, moreover, has also said it would compel immunizations for its 1.3 million active-duty troops by the middle of next month, but could do so sooner should the FDA give its blessing to Pfizer. While the Joe Biden administration previously suggested the president would issue a waiver to allow vaccine mandates for soldiers, it decided to hold off until regulators signed off.

Reports of the FDA’s plans come soon after the White House began promoting booster shots for all fully vaccinated adults, citing US health agencies, which noted the immunizations are losing effectiveness over time, particularly against more infectious Delta mutation. While the FDA hasn’t yet approved third doses for all healthy Americans, the agency did give the go-ahead for those with compromised immune systems, while Pfizer recently submitted its initial trial data for universal boosters. Health officials have voiced hopes that full approval for the Covid jabs could improve vaccination numbers in the US, which have been losing pace since hitting a peak in April. Recent polling by the Kaiser Family Foundation showed that more than 30% of respondents would be “more likely” to be vaccinated if the FDA authorized the shots, suggesting the move could indeed spur immunizations.

From the British Medical Journal. This simply stinks so badly, hell and high water got nothing. They don’t want a discussion, even if the protocol demands one. They don’t want Malone, McCullough or Yeadon, or you and me, to speak. And perhaps more importantly, they don’t want anyone to see the paperwork (re: “FDA ‘Finalizing Paperwork’ With Pfizer ..”) that the decision is based on. “The Science” has become awfully small.

 

FDA Set To Grant Full Approval To Pfizer Vaccine Without Public Discussion Of Data

Transparency advocates have criticised the US Food and Drug Administration’s (FDA) decision not to hold a formal advisory committee meeting to discuss Pfizer’s application for full approval of its covid-19 vaccine. Last year the FDA said it was “committed to use an advisory committee composed of independent experts to ensure deliberations about authorisation or licensure are transparent for the public.”1 But in a statement, the FDA told The BMJ that it did not believe a meeting was necessary ahead of the expected granting of full approval. “The FDA has held numerous meetings of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) related to covid-19 vaccines, including a 22 October 2020 meeting to discuss, in general, the development, authorisation, and licensure of covid-19 vaccines,” an FDA spokesperson said.

“The FDA also has held meetings of the VRBPAC on all three covid-19 vaccines authorised for emergency use and does not believe a meeting is needed related to this biologics license application.” The spokesperson added, “The Pfizer BioNTech covid-19 vaccine was discussed at the VRBPAC meeting on 10 December 2020.3 If the agency had any questions or concerns that required input from the advisory committee members we would have scheduled a meeting to discuss.” The vaccine has already been rolled out to millions of Americans through an emergency use authorisation. Companies typically apply for full approval after a longer period has elapsed so that more data are available for review.

But with the US government indicating this week that it plans to start making booster shots widely available next month, experts said the decision not to meet to discuss the data was politically driven. Kim Witczak, a drug safety advocate who serves as a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee,4 said the decision removed an important mechanism for scrutinising the data. “These public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightning speed under emergency use authorisation,” she said. “The public deserves a transparent process, especially as the call for boosters and mandates are rapidly increasing. These meetings offer a platform where questions can be raised, problems tackled, and data scrutinised in advance of an approval.”

Witczak is one of the more than 30 signatories of a citizen petition5 calling on the FDA to refrain from fully approving any covid-19 vaccine this year to gather more data. She warned that without a meeting “we have no idea what the data looks like.” “It is already concerning that full approval is being based on 6 months’ worth of data despite the clinical trials designed for two years,” she said. “There is no control group after Pfizer offered the product to placebo participants before the trials were completed. “Full approval of covid-19 vaccines must be done in an open public forum for all to see. It could set a precedent of lowered standards for future vaccine approvals.”

 

 

Finally, from a Google Doc I can’t trace the origins of, other than Steve Kirsch is involved. It saves me some time from stating the obvious.

7 Reasons Why The Covid Vaccines And Vaccine Mandates Should Not Be Approved

1/ The vaccines kill more people than they save. Although the vaccines reduce the number of COVID deaths, that benefit comes at a steep price: death from other causes. Pfizer’s own Phase 3 study (6 month) showed that more people died who got the vaccine than who got the placebo. Today, there is no risk-benefit analysis showing that the vaccines have saved more lives than they’ve taken. The VAERS data shows that the vaccines are extremely unsafe and for those under 50 years old will kill more people than they save. The vaccines elevate dozens of serious adverse cardiovascular and neurological events, reactivate latent viruses, and can make cancers worse. Healthy young people have died shortly and unexpectedly after vaccination.

2/ Multiple studies show that the vaccines have killed 150,000 Americans so far. More than 10 different analyses show that approximately 150,000 Americans have been killed by the vaccines. These analyses have not been disproven despite a $1M reward for any scientist who does so.

3/ There are safer, more effective options available. Early treatments are faster, safer, cheaper, and more effective (over 99% for all variants). VIrtually no one hospitalized for COVID today was treated with a proven early treatment protocol. Unlike the vaccine, nobody dies from these treatments.

4/ The required safety testing still has not been done. The proper testing still hasn’t been done. We don’t know if the vaccine will make people more susceptible to COVID infections through antibody dependent enhancement (ADE) and/or linked-epitope suppression (“original antigenic sin”). No study to date has covered the span of a single human gestation cycle. We know the spike protein is associated with Lewy bodies which are associated with prion diseases like dementia.

5/ No open forum to resolve the concerns of qualified scientists who have safety concerns. The CDC and FDA refuse to engage in discussions with top scientists, such as Robert Malone, inventor of the mRNA vaccine, to discuss the fatality and VAERS analysis in a public forum. The CDC and FDA refuse to see the evidence that is contrary to the “safe and effective narrative.”

6/ No autopsies. There have been no autopsies of anyone dying after getting the COVID vaccine. This is troubling since one of the world’s top pathologists did such a study on 40 patients who died within 2 weeks after vaccination and found that at least 30% to 40% were killed by the vaccine. Despite the availability of robots that perform autopsies that include blood analysis, either none have been performed, or else they have been withheld from the public.

7/Clinical trial fraud. There was clear fraud in the Phase 3 Pfizer trial where at least one participant, 12-year old Maddie de Garay, was paralyzed less than 24 hours after receiving the vaccine. The FDA promised to investigate and did nothing. Today, Maddie cannot feel below her waist, cannot walk unassisted, cannot hold her head up, and must eat through a feeding tube. There were only 1,131 children in the treatment arm. One child in 1,131 being paralyzed is unacceptable to mitigate a potential risk that is close to zero.

 

Comments:

Unfortunately, it looks like full licensure of the Pfizer vaccine could be just around the corner. This breaks promises the FDA made, including accelerating the time to considering approval. So much data and associated concerns have accumulated in the past eight months, including recently learning that duration of immunity (DOI) is only ~4.5-6 months, which necessitates rapid boosting, which exacerbates safety issues (especially if damage is cumulative). And yet the FDA claims they have no questions beyond what they had in Dec. 2020. Narrowly focused immunity, ridiculously short DOI, largely ineffective against the delta variant, and the dangers associated with it have been underestimated by an unknown but substantial degree and there remain many questions about potential long-term harms. Unbelievable. Buckle your seatbelts. This is a runaway train that needs to be stopped immediately.

Dr. Byram W. Bridle,
Associate Professor of Viral Immunology,
University of Guelph, Ontario, Canada

 

It’s incredibly depressing to know that what was once the worlds most-respected medicines regulator is going full-on corrupt. They not only do not have anything enough duration after dosing to have a clue what’s going to happen, but the product has picked up enough baggage to warrant being pulled from the market, permanently. Anyone remember how the FDA handled thalidomide? Now look. I despise them.

Dr Mike Yeadon

 

PS: And the little clerks and mass murderers? Yes, I was very much thinking about the “decent” Germans in the 1940’s.

 

 

 

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Aug 212021
 


Salvador Dali Swans reflecting elephants 1937

 

FDA Aiming To Give Full Approval To Pfizer Covid-19 Vaccine Next Week (RT)
FDA To Grant Full Approval To Pfizer Vaccine Without Public Discussion (BMJ)
Development Of Safe And Effective Covid-19 Vaccines (Nature)
Vaccinated Man Dies In Florida, Daughters Urge People To Get Vaccinated (Hill)
World First Plasmid DNA Covid-19 Vaccine Gets Emergency Approval In India (RT)
Director Of Yale University Research Center About Ivermectin (CdS)
French Businesses Are Refusing to Enforce Vaccine Passport (SN)
Almost 9 In 10 Britons Likely Or Very Likely To Go For Covid Booster Shot (RT)
The Heebie-Jeebies of August (Kunstler)
2020: A Propaganda Masterpiece 2: Divide and Conquer (Perspectives on the Pandemic)
Dr. Peter McCullough (1 of 2) | Episode #19 (Perspectives on the Pandemic)

 

 

Quite the paradox. That not even everybody recognizes.

 

 

 

 

In Canada, 15 people <19 have died with Covid. So 10 million must be jabbed.

And remember what Yeadon said:

 

 

 

 

How little managers become mass murderers.

FDA Aiming To Give Full Approval To Pfizer Covid-19 Vaccine Next Week (RT)

The FDA will give full authorization to Pfizer’s Covid jab sometime next week, according to multiple reports, putting it on track to be the first in the US to get approval and likely paving the way for additional vaccine mandates. The US regulator is expected to give the greenlight for Pfizer’s immunization in the coming days, the New York Times and Politico reported on Friday, citing several “people familiar” with the agency’s planning. Though the FDA still has a “substantial amount of paperwork and negotiation with the company” to get through, it could give full approval as soon as Monday, the Times added. It was previously reported that the FDA hoped to grant authorization before Labor Day on September 6, and now appears set to meet that informal deadline.

With a number of hospital systems and universities around the US signaling plans to mandate vaccinations against Covid-19 upon full approval, the move is likely to trigger a spate of new requirements around the country. The US military, moreover, has also said it would compel immunizations for its 1.3 million active-duty troops by the middle of next month, but could do so sooner should the FDA give its blessing to Pfizer. While the Joe Biden administration previously suggested the president would issue a waiver to allow vaccine mandates for soldiers, it decided to hold off until regulators signed off.

Reports of the FDA’s plans come soon after the White House began promoting booster shots for all fully vaccinated adults, citing US health agencies, which noted the immunizations are losing effectiveness over time, particularly against more infectious Delta mutation. While the FDA hasn’t yet approved third doses for all healthy Americans, the agency did give the go-ahead for those with compromised immune systems, while Pfizer recently submitted its initial trial data for universal boosters. Health officials have voiced hopes that full approval for the Covid jabs could improve vaccination numbers in the US, which have been losing pace since hitting a peak in April. Recent polling by the Kaiser Family Foundation showed that more than 30% of respondents would be “more likely” to be vaccinated if the FDA authorized the shots, suggesting the move could indeed spur immunizations.

On August 5 (last update), this was still up on clinicaltrials.gov for the Pfizer trials:

Read more …

They don’t want anyone to see the paperwork.

FDA To Grant Full Approval To Pfizer Vaccine Without Public Discussion (BMJ)

Transparency advocates have criticised the US Food and Drug Administration’s (FDA) decision not to hold a formal advisory committee meeting to discuss Pfizer’s application for full approval of its covid-19 vaccine. Last year the FDA said it was “committed to use an advisory committee composed of independent experts to ensure deliberations about authorisation or licensure are transparent for the public.”1 But in a statement, the FDA told The BMJ that it did not believe a meeting was necessary ahead of the expected granting of full approval. “The FDA has held numerous meetings of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) related to covid-19 vaccines, including a 22 October 2020 meeting to discuss, in general, the development, authorisation, and licensure of covid-19 vaccines,” an FDA spokesperson said.

“The FDA also has held meetings of the VRBPAC on all three covid-19 vaccines authorised for emergency use and does not believe a meeting is needed related to this biologics license application.” The spokesperson added, “The Pfizer BioNTech covid-19 vaccine was discussed at the VRBPAC meeting on 10 December 2020.3 If the agency had any questions or concerns that required input from the advisory committee members we would have scheduled a meeting to discuss.” The vaccine has already been rolled out to millions of Americans through an emergency use authorisation. Companies typically apply for full approval after a longer period has elapsed so that more data are available for review.

But with the US government indicating this week that it plans to start making booster shots widely available next month, experts said the decision not to meet to discuss the data was politically driven. Kim Witczak, a drug safety advocate who serves as a consumer representative on the FDA’s Psychopharmacologic Drugs Advisory Committee,4 said the decision removed an important mechanism for scrutinising the data. “These public meetings are imperative in building trust and confidence especially when the vaccines came to market at lightning speed under emergency use authorisation,” she said. “The public deserves a transparent process, especially as the call for boosters and mandates are rapidly increasing. These meetings offer a platform where questions can be raised, problems tackled, and data scrutinised in advance of an approval.”

Witczak is one of the more than 30 signatories of a citizen petition5 calling on the FDA to refrain from fully approving any covid-19 vaccine this year to gather more data. She warned that without a meeting “we have no idea what the data looks like.” “It is already concerning that full approval is being based on 6 months’ worth of data despite the clinical trials designed for two years,” she said. “There is no control group after Pfizer offered the product to placebo participants before the trials were completed. “Full approval of covid-19 vaccines must be done in an open public forum for all to see. It could set a precedent of lowered standards for future vaccine approvals.”

Read more …

October 2020.

Development Of Safe And Effective Covid-19 Vaccines (Nature)

In the 1960s, scientists found that antiviral antisera might result in an exceptional increase in viral infectivity of animal viruses. This phenomenon that viral infection can be enhanced by internalization associated with antibody Fc receptors (FcRs), denoted as ‘antibody-dependent enhancement’ (ADE; Box 1), was then widely reported in infections with flaviviruses and other viruses. Later, more antibody FcR-mediated effects, such as complement activation and release of inflammatory cytokines, were reported to be involved in severer disease. ADE has also been observed in vaccinated animals after viral challenge with the corresponding virus.

For example, cats immunized with a vaccine expressing the feline infectious peritonitis virus (FIPV) S protein on a recombinant pox virus vector died earlier than control animals when challenged with FIPV25. Given that passive immunization with feline serum containing high-titre antibodies reactive with feline FIPV also resulted in a more rapid disease after FIPV challenge, the vaccine-induced disease exacerbation may be attributed to ADE. Apart from ADE, type 2 T helper cell (TH2 cell)-based immunopathologic responses induced by homologous viral challenge after vaccination could also result in disease exacerbation.

In this Perspective, we use the term ‘vaccine-associated disease enhancement’ (VADE; Box 1) to describe both antibody-dependent and TH2 cell-dependent disease exacerbation (Fig. 1). We summarize examples of VADE in the history of the development of vaccines against respiratory syncytial virus (RSV), dengue virus (DENV), SARS-CoV and Middle East respiratory syndrome coronavirus (MERS-CoV), each of which provides clues for safe COVID-19 vaccine development and highlights the need for rigorous preclinical and clinical safety testing.

There have been warnings that ADE should be fully evaluated for coronavirus vaccines to avoid repeating the tragic failure of the RSV vaccine. The first RSV vaccine, based on formalin-inactivated RSV (FI-RSV), entered a clinical trial in 1965, a time when several other inactivated or attenuated virus-based vaccines had already been successfully developed, such as vaccines against smallpox and polio. The FI-RSV vaccine was well tolerated and appeared to be moderately immunogenic at first. However, instead of protecting study participants, the FI-RSV vaccine exhibited a paradoxical disease-strengthening effect (enhanced respiratory disease (ERD); Box 1) during subsequent natural RSV infection. Among the 20 infants who received the FI-RSV vaccine, 16 required hospitalization, including two who subsequently died, whereas only one of the 21 participants in the control group was hospitalized. The FDA then urgently suspended all clinical studies of RSV vaccines.

Vaccination induces humoral and cellular immune response in immunized individuals. In the normal condition, when the homologous virus enters an immunized body, it will be neutralized or cleared by vaccine-induced neutralizing antibodies (Abs) or specific T cells, respectively. In the context of vaccine-associated disease enhancement, vaccines mainly induce non-neutralizing Abs or low titres of neutralizing Abs (suboptimal concentration) or type 2 T helper cell (TH2 cell)-biased T cell responses. When these vaccinated individuals are challenged by homotypic or heterotypic serotype viruses, the antibodies will immediately recognize the viruses and mediate antibody-dependent disease exacerbation in two ways. First, virus–antibody complexes might enter Fc receptor (FcR)-bearing cells, such as dendritic cells and monocytes, by FcR-mediated internalization, which is termed ‘antibody-dependent enhancement’ (ADE). For viruses with innate tropism for FcR-bearing cells, such as dengue virus, ADE will result in higher viral loads than in conditions without antibodies.

a | After entry, the virus, no matter whether it replicates or does not replicate, may activate a harmful immune response, resulting in the release of proinflammatory cytokines. b | Aside from ADE, antibody–antigen complexes can stimulate the complement pathway through activation of the C1q pathway, thus further strengthening the inflammatory responses c | Vaccine-associated disease enhancement can also involve a TH2 cell-biased immune response. The activated TH2 cells contribute to the activation of antibody production. However, they release interleukin-4 (IL-4), IL-13 and IL-5, as well as eosinophil chemoattractant, thus resulting in eosinophil infiltration and proinflammatory cytokine production in the lung. d | Natural killer (NK) cells and CD8+ cytotoxic T lymphocytes (CTLs) are poorly stimulated in TH2 cell-skewed immune responses. The exaggerated cytokine release (part b), activation of the complement pathway (part c) and the excessive mobilization of eosinophils all contribute to the infiltration of the lung by eosinophils, neutrophils and lymphocytes, and production of inflammatory cytokines (part d), leading to acute lung injury or acute respiratory distress syndrome.

Read more …

Tragic, of course it is. But:

Blame unvaccinated people, blame Florida all you want. The vaccine still didn’t work. How do you not reach that conclusion?

And his doctor is a doofus who says there’s a “one-in-a-million” chance of a “breaktrough” infection. He should get informed. There’s an every hour, if not more.

Vaccinated Man Dies In Florida, Daughters Urge People To Get Vaccinated (Hill)

A fully vaccinated man who resided in a Florida retirement home died from COVID-19. His daughters wrote an obituary urging people to get vaccinated and blame the state for his life ending. Clark Allen died on July 22 after contracting a breakthrough case of COVID-19, a “one-in-a-million” chance, according to the man’s doctor. The surviving daughters of Clark Allen, Danielle and Nicole Allen-Gentile, expressed their anger in an obituary about how their father could have been infected and said his death was preventable, The Washington Post reported. America is changing faster than ever! Add Changing America to your Facebook or Twitter feed to stay on top of the news.

“He was infected by someone who chose to not get vaccinated and his death was preventable,” the obituary reads. “It is the wish of his family that everyone get vaccinated in order to prevent further death, sickness and heartbreak.” The daughters also told The Washington Post that if their father were in a different state, they believe he wouldn’t have died. During the pandemic, Clark Allen’s two daughters — along with their five siblings — debated whether their father should be in an assisted living home in Florida or Connecticut. The daughters received a blunt message from a Connecticut home: “You need to get him out of Florida. He will die in Florida,” The Washington Post reports. The daughters speculate that he contracted the virus from an unvaccinated person at Carlisle Palm Beach, an assisted living facility in Lantana, Fla.

Allen reportedly took the virus very seriously, paying close attention to public health measures as he had chronic obstructive pulmonary disease that could make a possible infection more severe, according to the Tampa Bay Times, which first shared the story. “It was a relief when he got vaccinated, but the reality was he was around a lot of unvaccinated people,” Danielle Allen, who lives in Portland, Ore., told The Post. “I’m attempting to not be very angry at unvaccinated people and it’s become extremely difficult. We’re all really angry and struggling.” In response to the claim, a spokesperson for Senior Lifestyle, the company that operates Carlisle Palm Beach, told The Post that its facility implements safety measures provided by Centers for Disease Control and Prevention (CDC) and “other expert sources and health authorities.”

Read more …

“The system delivers medicine to intramuscular and subcutaneous tissue depths without needles, which may prove particularly useful in a world competing for needles and syringes.”

World First Plasmid DNA Covid-19 Vaccine Gets Emergency Approval In India (RT)

India’s drug regulator has approved a three-dose Covid-19 vaccine which uses plasmid DNA technology developed by indigenous drugmaker Zydus Cadila, after trials indicated it was 66.6% effective. On Friday, the Drug Controller General of India gave the green light to Zydus Cadila’s Covid-19 vaccine. The inoculation, now the sixth such to be approved in India, has received Emergency Use Authorization (EUA) for use in adults and children aged 12 and above. The generic drugmaker, which applied for authorization of its three-dose vaccine in July, enlisted 28,000 volunteers into its trial. Data from the late-stage trial suggested the jab was 66.6% effective at preventing symptomatic Covid-19.

The vaccine, known as ZyCoV-D, is the world’s first vaccine against Covid-19 that uses plasmid DNA technology. It works by injecting genetically-engineered plasmid containing the DNA sequence of the pathogen. Cadila’s vaccine was developed in partnership with India’s Department of Biotechnology and is the second home-grown shot to be approved for use against Covid-19; the first being Bharat Biotech’s Covaxin jab. Instead of traditional syringes, the vaccine is administered using a needle-free applicator. The system delivers medicine to intramuscular and subcutaneous tissue depths without needles, which may prove particularly useful in a world competing for needles and syringes.

Cadila has already started stockpiling its vaccine and hopes to make 100 million to 120 million doses every year, enough for 40 million people, the company’s managing director told Reuters in April. Despite being one of the world’s largest vaccine manufacturers, India’s Covid-19 inoculation program has fallen flat amid a shortage of shots. Delhi has been pushing for ‘Atmanirbhar Bharat’, a Hindi phrase roughly translating as ‘self-reliant India’, in a number of fields, including defense technology and medical products. The vaccination program was meant to reflect India’s self-reliance and burgeoning manufacturing capacity in the medical and pharmaceutical industry.

Read more …

Google translate. Like his description of the “mechanisms” of both the virus and IVM.

Director Of Yale University Research Center About Ivermectin (CdS)

Ivermectin has more than one potentially effective mechanism of action against Covid 19. A major one is its ability to adhere to the Coronavirus Spike1 protein at various strategic points used by the virus to bind and enter our cells. For this reason, unlike monoclonal antibodies, it can act against all variants. By doing so, you prevent the virus from attaching itself to ACE2, which is the main gateway for the virus to enter our cells, and this allows it to reduce the virus’s ability to enter our body. If Covid stays outside of our cells, it becomes easy prey for our immune system, which can get rid of it much more easily. It is important to note that the protein docking region of the virus, the spike spikes, binds not only to our ACE2 receptors, but also to other docking receptors that are very important to the virus, those that depend on sialic acid, Receptor CD147 and on a cholinergic receptor called a7nAChr. I don’t want to get into technicalities, but this premise helps us understand how Covid attacks our body.

Once it has entered our lungs and damaged them, the virus enters the blood and travels through our body carried by red blood cells and platelets that are found in large quantities in our blood. Today we know that the virus attaches itself to red blood cells and platelets because both are coated with sialic acid receptors and CD147 and thanks to this it invades all blood vessels until it is “released” into the endothelium (the inner part of our blood vessels ). ) and then causes systemic vasculitis, which is why most of us are ultimately unable to overcome the infection. When the virus replicates within the endothelial cells of the vessels, it inflames them and creates sticky aggregates of red blood cells and platelets – dense masses,Small clots that initially hamper cause circulation in small vessels (capillaries), but then progressively swell and block larger and larger vessels. When this happens in the lungs, it causes a lack of oxygen that therefore damages all our organs such as the brain, liver, kidneys and heart, especially in the elderly, diabetics and people with previous diseases.

The mechanism by which the virus moves in the blood also explains why Covid is more lethal in people with high glucose levels, such as diabetics and prediabetics. The reason is because the receptors made of sialic acid and CD147 are basically zuccheri. In a diabetic, these sialic acids are richer in sugar (glucose) and the virus sticks better and its systemic spread is even easier. This selectivity of the virus for the characteristics of some subjects is also given by blood groups, for example those with blood group A or B have red blood cells with a greater presence of sialic acid / sugars on the surface, while those with a Type 0 blood group, on the other hand, is less susceptible to the virus as it has less sialic acid / receptor that lines red blood cells and,therefore, the virus sticks less. Patients with diabetes or those with these blood groups (A and B) have a statistically more severe course of the disease.

One of the fundamental mechanisms by which ivermectin acts in patients is because it “puts a wall” (a shield) between our body (red blood cells, platelets and vessels) and the virus, and therefore no longer allows it to latch on in our cells. thus facilitating the flow of red blood cells that carry oxygen in the blood vessels. Ivermectin appears to be able to quickly break the link between the virus (Spike’s key) and its receptors (the ACE2 gate, sialic acids, the CD147 receptor, and a7nAChr), so patients miraculously begin to breathe and oxygenate properly again normally within 24- 48 hours. This is also what happens in the rest of the microcirculation of the whole body and leads to the rapid improvement of the functionality of the various organs.

Read more …

The protests will now grow fast. In many countries.

French Businesses Are Refusing to Enforce Vaccine Passport (SN)

Anecdotal evidence detailed by former Google software engineer Mike Hearn strongly suggests that most restaurants, cafes and other businesses in France are not enforcing the country’s controversial vaccine passport system. As we highlighted last week, on the first day the new program was in place, police were visibly patrolling bars and cafes demanding customers show proof they’ve had the jab. However, this seems to have largely been a bluff as just days later, businesses and venues have become very lax at checking people’s papers despite the threat of large fines. “I decided to do a simple experiment to find out: always present an expired test even though I had a valid negative one, and see what happens,” writes Hearn.

“Over a four day stay I was required to show a valid pass exactly zero times; that includes at the airports in both directions. Compliance is absolutely min viable and often lower.” “At small businesses enforcement was non-existent: sometimes the pass requirement was ignored entirely, other times we were asked “do you have a pass” and our answer wasn’t checked. One restaurant had come up with a clever way to detect police stings without requiring customers to actually present a pass. As expected, enforcement was stricter by larger firms, however even there we saw the following:

– Test certificates being checked once and then swapped for a token that doesn’t expire.
– Expired tests being accepted.
– People accepting paper test certificates without scanning them.
– Scanning tests and then not looking at the screen to see the results.
– Accepting QR codes that failed to scan.”

Hearn also reveals how mask mandates in theme parks and other venues are also not being followed, despite signs everywhere ordering people to cover their faces, while social distancing is also a “forgotten memory.” Images showing empty cafes and bars on the first day the system was introduced may have spooked venues into taking a hands off approach. In passing the law but failing to ensure that it is enforced, France is following the same model as Israel, where the point of introducing the system wasn’t really to enforce it, but merely as a means of bullying young people into getting the vaccine. As we highlighted last week, despite the odious and draconian nature of the vaccine passport system, President Macron asserted that the it was actually introduced to protect people’s “freedom,” which is like saying putting you in prison is for your own safety.


French Health Pass has space for 8 shots

Read more …

A country inhabited by spike protein reservoirs.

Almost 9 In 10 Britons Likely Or Very Likely To Go For Covid Booster Shot (RT)

Nearly 90% of people across the UK are “likely or very likely” to accept a third Covid-19 jab if offered, a new survey released by the Office for National Statistics (ONS) has revealed. On Friday, the ONS released the latest data from its ongoing Opinions and Lifestyle Survey project, which found that a whopping 87% of respondents would be in favour of receiving a Covid booster shot. Older members of the population expressed more enthusiasm at the prospect of a third jab, with almost 96% of those aged 70 or over saying they would be “likely or very likely” to do so. The survey figure was lower for younger Britons in the 16 to 29 age-bracket, standing at 78%. Speaking to reporters on Thursday, Britain’s Health Secretary Sajid Javid said that the proposed booster scheme will likely start in September. Javid, however, did not pinpoint an exact date, citing that the government first needs final advice on the matter from the Joint Committee on Vaccination and Inoculation (JCVI).


A handful of countries have already introduced a booster dose as part of their vaccination regimens. Serbia and Hungary began offering its citizens a third Covid shot earlier this month, while Israel continues to lower the eligible age for its booster jabs after rolling out the scheme at the end of July. The head of the WHO Tedros Adhanom Ghebreyesus urged nations to pause or delay issuing third shots in a bid to alleviate vaccine inequity between high and low income states. “WHO is calling for a moratorium on boosters until at least the end of September, to enable at least 10% of the population of every country to be vaccinated,” he implored the governments of richer nations. The JCVI last month recommended that all adults in the UK aged 50 and over, pensioners living in care homes, frontline workers, and anyone aged 16 and higher who is clinically vulnerable or immunocompromised should be offered a vaccine top-up this autumn.

Read more …

“Nobody is at the controls of this outfit as we sail into the fog.”

The Heebie-Jeebies of August (Kunstler)

Jimmy Carter was undone by a mere fifty-two hostages in Iran, 1979, but this fiasco is orders of magnitude greater. The Taliban could easily put an end to the whole question of extracting the thousands of Americans stuck in Af-stan just by firing a few RPG rounds onto the runway of Hamid Karzai International Airport. After that, would they go about the grisly business of beheading any Afghani who so much as took a stick of gum from an American?

“Graveyard of Empires,” indeed. Rome waited a few centuries to collapse but America seems to be demonstrating we can git’er done in just a couple of years. And, beyond these questions of global hegemony, there is the matter of what happens here in the so-called Homeland. The Covid-19 vaccine-and-masking hysteria is coming to a head. The school boards are getting an earful about race-based everything in the curriculum. Certain state governors and mayors seem determined to destroy what remains of small business. A mutiny is brewing against Bill de Blasio’s new semi-lockdown in New York City. Gavin Newsom is about to be tossed into the North Pacific Gyre.

Any moment, the Arizona election audit will issue a preliminary report, said to be shocking. Financial markets are in the wobble-zone. Supply lines are down for many parts of things needed to run daily life in this land. And millions are wondering anxiously now: what really are the latent effects of those jabs? Things are shaking loose all over the place. As Bob Dylan once said, the order is rapidly fading (and he’s even older than “Joe Biden.”) Everyone I know has got the heebie-jeebies. Nobody is at the controls of this outfit as we sail into the fog.

Read more …

Part 1 of this interview is in the August 4 Debt Rattle. Interesting voice.

2020: A Propaganda Masterpiece 2: Divide and Conquer (Perspectives on the Pandemic)

Mark Crispin Miller is Professor of Media, Culture and Communication at New York University. His research interests include modern propaganda, history and tactics of advertising, American film, and media ownership. He is the author of Boxed In: The Culture of TV; Seeing Through Movies; Mad Scientists: The Secret History of Modern Propaganda; Spectacle: Operation Desert Storm and the Triumph of Illusion; and The Bush Dyslexicon.

Read more …

And since we’re with Perspectives on the Pandemic, here’s part 1 of their piece with Peter McCullough.

Dr. Peter McCullough (1 of 2) | Episode #19 (Perspectives on the Pandemic)

Renowned physician and professor of medicine Dr. Peter McCullough describes early treatment protocols for COVID-19 that have saved countless lives… and the forces that have aligned themselves against their widespread adoption.

Read more …

 

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