Oct 232021
 
 October 23, 2021  Posted by at 7:40 am Finance Tagged with: , , , , , , , , ,  66 Responses »


Vincent van Gogh Autumn landscape 1885

 

Sweden Suspends Moderna Shot Indefinitely (TTC)
Pfizer, BioNTech Announce Their Vaccine Is Useless After 11 Months (Berenson)
CDC Considers Changing Definition Of “Fully Vaccinated” (JTN)
More Americans Getting Boosters Right Now Than First Vaccine Shots (Hill)
Biden Vaccine Mandate Not In Effect, Not Enforceable – Republican AGs (JTN)
Strain Of Delta Variant Causing Panic In UK Has Been Found In US (ZH)
Southwest Airlines Says It Won’t Fire Workers Who Don’t Get COVID Vaccine (ET)
Accountability (Denninger)
“What Am I Doing?” He Asks (Kunstler)
Nunes: ABC News HQ should move to Disney’s Fantasyland (JTN)
NATO Unveils Master Plan To Defeat Russia In Nuclear War (RT)
Magnesium Shortage Threatens To Paralyze Global Car Production (AD)
Chief Justice of England & Wales Joins Bench for Assange Hearing (CN)

 

 

Scary numbers. Among 40-49, infection risk for unvaccinated down some 15%, vaccinated up over 50%.

 

 

“..to anyone under 31..”

Sweden Suspends Moderna Shot Indefinitely (TTC)

New concerns are being raised about side effects from the Moderna vaccine against the coronavirus. Swedish health officials have now decided that a moratorium on giving the Moderna vaccine to anyone under 31 will be extended indefinitely, the U.K. Daily Mail reported. The pause on the Moderna shots had been scheduled to end on Dec. 1. Finland, Iceland and Denmark have taken similar steps. Norway is encouraging men under 30 not to get the Moderna shot, but is not mandating it. For months, the Moderna vaccine has been under scrutiny because of data that shows young men who receive it are at increased risk for myocarditis, an inflammation of the heart muscle, and pericarditis, an inflammation of the sac around the heart.


[..] The decision comes as the U.S. Food and Drug Administration is putting Moderna’s plans for a shot aimed at the population from age 12 to 17 on hold due to concerns over risks of the ailments, according to The Wall Street Journal. Although a federal CDC panel on Thursday approved boosters for the Moderna and Johnson & Johson vaccines, there were some cautions raised, according to CNBC. Dr. Tom Shimabukuro said there is an increased risk of myocarditis and pericarditis with either the Moderna or Pfizer vaccine, in particular after the second dose of the vaccines. According to the Daily Mail, the data indicated the risk was 13 times greater for those getting the Moderna vaccine than for those who got the Pfizer vaccine. Sweden’s Public Health Agency said the unpublished data linking the Moderna vaccine with the two conditions means there is “an increased risk of side effects such as inflammation of the heart muscle or the pericardium.”

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Not sure where he gets the 11 months. I think it might be 6.

Pfizer, BioNTech Announce Their Vaccine Is Useless After 11 Months (Berenson)

Well, that’s not how they phrased it. But it is the only reasonable way to read their press release claiming that the booster is 95% effective. Remember. The booster is given to people who have RECEIVED the vaccine. (That’s why it’s a booster, right?) And when they tested a booster against a placebo in those people, they found a 95% reduction in disease in people who received the booster (for a total of 11 weeks after they received the booster, excluding the first week, because science – by which I mean because including that week would not help their results). 95%! Where have you heard that figure before? Oh yeah, it is EXACTLY the same relative risk reduction they claimed in the pivotal trial last year, when they tested the INITIAL dose against placebo.


The only reasonable read is that the booster is providing (temporary) protection similar to the first two-dose series (temporarily) did AGAINST PLACEBO. But these are VACCINATED people. So where’s the protection from the initial two doses? There is ONE difference, though. The ABSOLUTE risk appeared at least two to three times higher in the vaccinated people in this trial than in UNVACCINATED people in the initial trial – 110 infections in 5,000 people in 10 weeks, compared to 162 infections in 20,000 people in about the same period. Because vaccines work. If you are vaccinated, get ready to take boosters forever. By the way, the press release includes NO specific safety data. Yay Pfizer!

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Worst kept secret.

CDC Considers Changing Definition Of “Fully Vaccinated” (JTN)

The U.S. could change the definition of being fully vaccinated against COVID-19, the director of the Centers for Disease Control and Prevention (CDC) said Friday. The definition might be changed as booster shots become more prevalent, the CDC Director Rochelle Walensky told reporters in a briefing. “We have not yet changed the definition of ‘fully vaccinated.’ We will continue to look at this,” Walensky said. “We may need to update our definition of ‘fully vaccinated’ in the future. If you’re eligible for a booster, go ahead and get your booster and we will continue to follow up.”


According to The Hill, the term “fully vaccinated” applies to people who have received the one-shot Johnson and Johnson vaccine, or both doses of the Pfizer or Moderna vaccines. According to the White House, more than 70 million Americans qualify for a booster shot, while predicting another 120 million Americans should become eligible in the coming months. Currently, the CDC estimates about 58% of the U.S. population is fully vaccinated against the virus, while nearly 68% is only partially vaccinated.

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All under informed consent, we may presume?

More Americans Getting Boosters Right Now Than First Vaccine Shots (Hill)

The number of Americans getting their booster shots is outpacing those who are getting their first vaccine dose, according to new data released by the Centers for Disease Control and Prevention (CDC). According to the latest data, 190 million people are fully vaccinated in the U.S. and 12 million people have received their booster dose since it was authorized in August. An average of roughly 340,000 people are getting a booster shot on a daily basis, compared to a daily average of 157,605 who received their first vaccine shot for the week ending Tuesday, government data shows, according to The Washington Post. The disparity isn’t particularly surprising given the demand for booster shots among the vaccinated population, and the fact that the unvaccinated population has had months to get a shot but has not so far.

But it points to how even with boosters available, a stubborn minority of Americans are likely to not take initial vaccinations or boosters. It is much easier for the coronavirus to spread the larger that population is. An Axios-Ipsos poll published in August found that 20 percent of Americans said they either are not very likely or not likely at all to receive a vaccine. There are now booster recommendations for all three available COVID-19 vaccines in the United States, after the CDC on Thursday approved both the Moderna and Johnson & Johnson boosters. “These recommendations are another example of our fundamental commitment to protect as many people as possible from COVID-19,” CDC Director Rochelle Walensky said in a statement on Thursday.

“The evidence shows that all three COVID-19 vaccines authorized in the United States are safe – as demonstrated by the over 400 million vaccine doses already given. And, they are all highly effective in reducing the risk of severe disease, hospitalization, and death, even in the midst of the widely circulating delta variant,” Walensky said.

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A superbly weird game is being played. As long as it’s not in effect, the White House can’t be sued. There are dozes of court cases pending.

Biden Vaccine Mandate Not In Effect, Not Enforceable – Republican AGs (JTN)

President Joe Biden’s executive order requiring private employees to get the COVID-19 shots hasn’t gone into effect and therefore isn’t enforceable, argue several Republican attorneys general — and if and when the regulation does go into effect, they vow, they will immediately sue to stop it. “No such rule or regulation is currently in effect,” Montana Attorney General Austin Knudsen wrote in an open letter to all Montanans, and “there has been a great deal of confusion” since Biden announced his mandate Sept. 9. The letter was released the same day as an announcement made by Biden, who said, “The Labor Department is going to soon be issuing an emergency rule for companies with 100 or more employees to implement vaccination requirements.”

The Department of Labor’s Occupational Health and Safety Administration only last week submitted the initial text of the mandate’s regulatory language to the Office of Management and Budget for review. This is the first of several steps in the regulatory process. OSHA will implement, oversee and enforce the Biden mandate, which it has yet to do. It plans to do so under an obscure authority known as “emergency temporary standards” that has been used only a handful of times. [..] The mandate was a reversal of policy advocated by the White House just five months earlier. On April 6, White House Press Secretary Jen Psaki told reporters: “The government is not now, nor will we be supporting a system that requires Americans to carry a credential. There will be no federal vaccinations database and no federal mandate requiring everyone to obtain a single vaccination credential.”

However, after Biden’s Sept. 9, mandate, numerous companies issued vaccine mandates requiring employees to provide proof of vaccination status in order to remain employed. Some companies issued fines for employees who chose to not get the shots. Some rejected religious exemption requests, others rejected exemption requests from those who could prove they have natural immunity after they got the coronavirus. Texas Attorney General Ken Paxton argues the mandate is unconstitutional, and in response to pushback throughout the state, Texas Gov. Greg Abbott issued his own mandate prohibiting all entities in Texas from issuing vaccine mandates as a condition of employment. Knudsen says his office is “preparing to immediately challenge and enjoin this federal overreach on a variety of grounds when the Biden administration issues its announced rule.”

Oklahoma Attorney General John O’Connor also announced that no federal rule mandating employers to require their workers to get the shots exists. He’s instructed employers — and Oklahomans — to ignore Biden’s order. “I urge Oklahoma employers to disregard the Biden Administration’s wishes to the contrary,” O’Connor said in a statement. “In the event federal emergency rules are issued that place such an unlawful demand upon employers, our office will be joined by other state Attorneys General across the country to quickly sue and seek an injunction against any implementation or enforcement.”

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Let me guess: mostly found among the vaccinated?

Strain Of Delta Variant Causing Panic In UK Has Been Found In US (ZH)

A mutated version of the delta variant that has caused panic in the UK has been detected in several states in the US, the CDC revealed this week. AY.4.2, a subtype of the highly transmissible delta variant which has become informally known as “delta plus”, accounted for 6% of all sequenced samples of the virus. Its emergence has coincided with a rebound in COVID cases in the UK. To be sure, right now, the strain is still rare in the US and accounts for “well below 0.05%” of cases sequenced, the CDC says. So there’s no reason to panic. “At this time, there is no evidence that the sublineage AY.4.2 impacts the effectiveness of our current vaccines or therapeutics,” the CDC said. “Vaccination remains the best public health measure to slow the spread of the virus and reduce the likelihood of new variants to emerge.”


Around 16,830 AY.4.2 cases have been detected around the world across at least 28 countries, according to data from Outbreak.Info. Jeffrey Barrett, director of the COVID-19 Genomics Initiative at the Wellcome Sanger Institute in the U.K., told Newsweek on Thursday that it’s still unclear whether the subtype is helping drive rising case numbers in the UK. “We are one of the groups that has observed a [roughy] 10 percent growth advantage compared to other Delta.” “I’d say we can’t say for sure yet that that is a true biological advantage, as opposed to a bit of epidemiological ‘luck’ for this lineage, but the data are now accumulating week-by-week in favor of a small growth advantage.”

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Still trying to hide the reason why. Still the weather.

Southwest Airlines Says It Won’t Fire Workers Who Don’t Get COVID Vaccine (ET)

Southwest Airlines’ CEO said the company will not fire employees who do not get the COVID-19 vaccine by Dec. 9 following a Biden administration mandate that was announced last month for federal contractors. In a statement to news outlets Friday, the Dallas-based carrier confirmed to Fox News it does not want to “lose any employee” over President Joe Biden’s mandate, adding that firing a worker over the vaccine “makes no sense.” It came a day after Southwest CEO Gary Kelly made a similar announcement during an earnings call. “This is an evolving process working with the government in terms of what they expect, and very clearly, we wanted our employees to know that nobody is going to lose their job on December the 9th if we’re not perfectly in compliance,” Kelly said, according to news reports.

“It is a work in progress, and we’re going to continue working in good faith to meet the requirements of the executive order. But I’ve already said, and I’m sure you’ve heard, we’re not going to fire anybody who doesn’t get vaccinated,” he continued. Biden’s mandate will start on Dec. 8, requiring federal contractors to make sure their workers are vaccinated. Employees can be granted a medical or religious exemption. But Kelly’s and Southwest’s announcements this week mark a reversal in the carrier’s vaccination stance. Earlier this month, Southwest stated that workers would have to be fully vaccinated or receive an exemption to “continue employment with the airline” after it conducted a “thorough review of President Biden’s COVID Action Plan and determined that the carrier’s contracts with the U.S. government require full compliance with the federal vaccination directive.”

Also on Thursday, Southwest said in its quarterly results that it lost some $75 million after thousands of flights were canceled and delayed earlier this month. The firm blamed the weather and unspecified staffing issues, although there was widespread speculation that pilots and other employees walked out over the vaccine requirement.

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Sometimes I suspect Karl is a faster typer than I am.

“Whether said reprogramming is good, bad, effective or not isn’t the question; it is the claim that such constitutes a “vaccine” that is medically and scientifically false..”

Accountability (Denninger)

That the current jabs are not vaccines is not in question; it is truth. The government has changed the definition of a “vaccine” but you cannot change something that is false into something that is true by making a claim that it is so. A vaccine is a preparation that causes or mimics actual infection but is either attenuated or killed so that it will not harm you. The current “clot shots” are genetic programming designed to alter the core processes of your cells. That the intended outcome of this is to produce an immune response protective against a pathogen does not change the fact that they are not vaccines and that we have discovered the direct result of said programming is pathogenic is not in scientific question either; it is, and is almost-certainly responsible for all the adverse effects of same.

A therapy alters the core processes of your cells to combat a disease; every drug in the pharmacy does this in one form or another. Whether said reprogramming is good, bad, effective or not isn’t the question; it is the claim that such constitutes a “vaccine” that is medically and scientifically false, and no matter how many people believe it, whether that number is zero or 100% of the population does not change the falsity of the statement. That there has never been a successful vaccine — an actual vaccine — against a coronavirus in man or beast is also fact. That is not due to the lack of attempt; there have been many attempts. All have ended in failure; either the protection is non-durable and thus becomes a “required subscription” or worse, it turns on the inoculated individual member of the population and potentiates illness, severely injuring or killing them. Attempting to force that model on the human population through lies or worse, mandates, marks every person involved in advocating or attempting to impose same worthy of immediate imprisonment or even execution as they are wild-eyed extortionists at best or even mass-murdering psychotic criminals.

That every respiratory pandemic in history has progressed into an endemic disease is scientific fact. If it was not, even once, every single one of us would not exist because somewhere before our birth humans would have all been dead. Yet here we are, which is scientific proof that any claim that Covid-19 would not follow the same pattern absent our intervention was and is false. That is not to say that certain pathogens haven’t been worse than others; there have, of course. But the trend toward endemicity and immunity from serious outcome via infection or the mimicry of actual infection, not genetic engineering which only now exists as possible, is fact. Thus my commentary, which I have repeated relentlessly: We are all going to get this thing, there’s nothing we can do about that, and we ought to work on personal resistance to serious outcomes which we know we can have positive impact upon. Indeed, were Covid-19 to have occurred prior to our obsession with obesity and “healthy at any size” it is probable that 99% of those who have died from it in the US would have successfully fought it off and it would have been less serious than seasonal influenza.

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“The Obama-led claque behind all the White House fakery wants to cram this down the country’s craw before things go so far south that Americans start to think they’re living in Tierra del Fuego.”

“What Am I Doing?” He Asks (Kunstler)

The Leader of the Free World wandered the stage, sometimes oddly circling his interlocutor, Anderson Cooper of CNN, who had to step in and rescue the maundering “Joe B,” when he lost himself in thickets of talking points that no amount of rehearsal could avail to untangle. “What am I doing?” he asked more than once, but no one on the scene volunteered to remind him. The “president” frequently assumed poses that signified some kind of gross cognitive dysfunction: head turned down to the floor with his eyes shut… strange, mincing steps in the direction of a fugitive thought… fists balled like a two-year-old resisting some simple instruction… There was a robotic quality to the act, too, as “JB” repeated his place-holder phrase “Here’s the deal” to preface each flight into the murky jargon of Build Back Better.

It fell short of convincing anyone about who was in charge of the nation’s affairs at a very sketchy moment in history, and at the end Ol “Joe” just ran down like a three-dollar gyroscope. In his most lost moments, such as when AC inaptly tried to prompt him on the border crisis — “I guess I should go down,” he admitted dolefully — the “POTUS” directed the cameras to his wife in the audience, saying, “Jill’s been down there!” We were supposed to conclude that she’d fixed all that for us.

The exercise was also obviously designed to turn up the heat on the two renegade senators, Joe Manchin (WVA) and Kyrsten Sinema (AZ) who are disinclined to vote for the trillions of dollars in pending proposed legislation to drop money from helicopters all over the land and save the economy — and impose all manner of janky surveillance measures and vote-rigging scams on the country. The Obama-led claque behind all the White House fakery wants to cram this down the country’s craw before things go so far south that Americans start to think they’re living in Tierra del Fuego.

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“[T]hey’re not falling for this,” he replied. “There’s something more nefarious going on — ABC News to put something out like that is just bizarre.”

Nunes: ABC News HQ should move to Disney’s Fantasyland (JTN)

Following an ABC News interview with Christopher Steele, author of the discredited Steele dossier used in the Trump-Russia collusion hoax, Rep. Devin Nunes (R-Calif.) said the media outlet’s headquarters should move to Fantasyland at its parent company’s Walt Disney World. “[I]t’s a little bit of an embarrassment for ABC News and Disney Corporation,” said Nunes, who as chairman of the House Intelligence Committee was instrumental in exposing the Trump-Russia narrative as a political dirty trick funded by the Hillary Clinton campaign and DNC in 2016. “I’ve been kind of half joking, but really half not, because you wonder if ABC News is gonna move their headquarters to Fantasyland at Disney World,” Nunes quipped. “It’s such a joke.”

Nunes alleged that the network’s hour-long documentary “Out of the Shadows: The Man Behind the Steele Dossier,” released Monday on Hulu, is “entirely fiction.” “[I]t’s really about what was left out,” he said. “And then the lack of clarity on the folks who are … kind of posing as actors in this — you know, they’re supposedly journalists.” Steele was the one “peddling Russian disinformation and the whole hoax early on,” but in his interview with ABC’s George Stephanopoulos “he’s sitting there going, ‘Oh, we just don’t know if this is true or not,'” observed Nunes. “[I]t’s basically misinformation or disinformation by omission,” he said. Nunes was asked if he was surprised the media is still falling for the Russia collusion narrative five years later.

“[T]hey’re not falling for this,” he replied. “There’s something more nefarious going on — ABC News to put something out like that is just bizarre. “So I have no idea, you know, what’s behind this — the timing, the release of this. That anybody would be defending Steele or those dossiers … at this point is an absolute joke.” While Nunes believes that Special Counsel John Durham is “doing a real investigation” of the Russia collusion hoax, he is concerned about the prosecutor’s ability “to continue this investigation, because we know DOJ is completely politicized.”

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NATO is done. And not a minute too soon. They can’t even win a game of backgammon. But then again that’s been true for the US for many decades too. Just because they can’t win at anything doesn’t mean they can’t be a major nuisance.

NATO Unveils Master Plan To Defeat Russia In Nuclear War (RT)

Top defense chiefs from NATO member states have given a green light to a new grand strategy on how to beat Russia in any potential all-out conflict, as Moscow says the move proves the US-led bloc isn’t open to improving relations. On Thursday, ministers met in Brussels to sign off the scheme, named the “Concept for Deterrence and Defense in the Euro-Atlantic Area.” According to NATO’s General Secretary, Jens Stoltenberg, it is part of efforts to “continue to strengthen our alliance with better and modernized plans.” The bloc’s officials insist they don’t believe an attack is imminent, but that it is worthwhile being prepared in any case.As part of the plan, NATO troops would fight against Russia’s forces in both the Baltic Region and across the Black Sea.


The battle plans also focus on non-conventional warfare, including the use of nuclear weapons, cyber-attacks and even conflict in space. However, Kremlin Press Secretary Dmitry Peskov hit out at the adoption of the strategy on Friday, saying that it shows there is no prospect for turning around rock-bottom relations with the bloc. “There is no need for dialogue under these conditions,” he argued, saying that the adoption “of such a concept by NATO confirms it once again.” According to him, “this alliance was not created for peace, it was conceived, designed and created for confrontation.”

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Google translate from Dutch.

“If the supply of magnesium stops, the entire auto industry may be forced to shut down.”

Magnesium Shortage Threatens To Paralyze Global Car Production (AD)

The automotive industry is already having a hard time due to the shortage of chips and semiconductors, causing many factories to shut down. There is now a threat of a new crisis in Europe due to a magnesium shortage. Magnesium is essential for aluminum production. That material is needed on a large scale for building cars. It is used in gearboxes, steering columns and brakes, seat frames, at fuel tanks, in the bodywork and for many other parts. About 85 percent of global magnesium production comes from China and much of that comes from Yulin City in Shaanxi Province. But due to an energy crisis, production restrictions have been imposed on many factories there. Of the fifty magnesium factories, only fifteen are still active.


They also run at half power to meet the energy requirements. It will remain that way at least until the end of the year. Analysts warn in The Financial Times that stocks of magnesium in the rest of the world are dwindling rapidly. The German and European car industry, almost entirely dependent on China for magnesium, threatens to get nothing in November. “There are no alternatives to aluminum production,” said Barclays analyst Amos Fletcher. “If the supply of magnesium stops, the entire auto industry may be forced to shut down.” In that case, consumers will have to wait even longer for their new car, while the shortage of semiconductors has already doubled or even tripled delivery times.

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He blocked the Lauri Love extradition.

Chief Justice of England & Wales Joins Bench for Assange Hearing (CN)

Ian Duncan Burnett, the most powerful judge in England and Wales, will join Lord Justice Timothy Holroyde on the bench next week for the two-day U.S. appeal in the extradition case of WikiLeaks publisher Julian Assange at the High Court in London, according to a spokesman at the Royal Courts of Justice. Burnett, known as Baron Burnett of Maldon, was the High Court justice who on humanitarian grounds overturned a lower court ruling that British activist Lauri Love should be extradited to the United States. Burnett ruled in February 2018 that Love’s extradition would be “oppressive by reason of his physical and mental condition.” Burnett and Mr. Justice Duncan Ouseley said in their decision that, “We accept that the evidence shows that the fact of extradition would bring on severe depression, and that Mr. Love would probably be determined to commit suicide, here or in America.”


Instead they recommended that Love be tried in the United Kingdom on charges of hacking into U.S. government computers. Unlike Love, Assange is accused of no crimes in Britain. But like Love, he has been deemed (by the magistrate’s court) at high risk of suicide if he were to be extradited to the United States. The U.S. is appealing the lower court’s decision not to extradite Assange to the U.S. based on his propensity for suicide. The U.S. is arguing that Assange is not too sick to be sent to the U.S. and that he is a malingerer. Holroyde is the High Court judge who on Aug. 11 reversed an earlier High Court order limiting the U.S. from appealing Assange’s medical issues.

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Snowden

 

 

 

 

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Oct 212021
 
 October 21, 2021  Posted by at 8:11 am Finance Tagged with: , , , , , , , , ,  71 Responses »


Pablo Picasso Man with arms crossed 1909

 

Child Deaths Are 52% Higher Since They Were Offered The Covid-19 Vaccine (TE)
White House Details Plan To “Quickly” Vaccinate 28M Children Age 5-11 (ZH)
Pfizer, Moderna to Rake in $93 Billion in 2022 COVID Vaccine Sales (CHD)
Adenovirus Covid-19 Vaccine Shows Lower But ‘Stable’ Immunity (RT)
Repositioning Ivermectin For Covid-19 Treatment (SD)
The FDA’s War Against The Truth On Ivermectin (AIER)
Washington State Patrol Staff Shortage, Officers Quit Over Vaccine Mandate (RT)
Why Are Thousands Of Postal Workers Still Unvaxxed? (WND)
Djokovic Claims It Would Be ‘Inappropriate’ To Say If He Is Vaccinated (RT)
Dewey, Cheat’em And Howe (Denninger)
“The Bidens”: Is the First Family Corrupt, or Merely Crazy? (Taibbi)
Hillary’s Secretive, Russiagate-Flogging Pair of Super-Lawyers (Maté)
The Killing Of Gaddafi 10 Years Ago Led To The Death Of The Nation Of Libya (RT)

 

 

 

 

Sign at Chick-Fil-A

 

 

Just

 

 

The Exposé feels a little chaotic at times, but they do the work.

Child Deaths Are 52% Higher Since They Were Offered The Covid-19 Vaccine (TE)

Chris Whitty advised the UK Government to roll-out the Pfizer Covid-19 vaccine to all children over the age of 12 in week 37 of 2021. Thanks to preparations already being made by the NHS to intrude on education in schools and administer the jab to children the programme got underway the following week (week 38). Official Office for National Statistics (ONS) data shows that between week 38 and week 40, the five-year-average number of deaths occurring among children aged between 10 and 14 was 17. However, the latest data available from the ONS shows that between week 38 and week 40, the number of deaths occurring among children aged between 10 and 14 was 26. This represents a 52% increase on the five-year average.

Sixteen of those deaths were among boys, representing a 60% increase on the five-year-average in which there had been 10 deaths among boys between week 38 and week 40. Whilst 10 of those deaths were among girls, representing a 43% increase on the five-year-average in which there had been 7 deaths among girls between week 38 and week 40. What’s even more concerning about the above numbers though is that deaths among children aged between 10 and 14 were significantly lower than the five-year-average up to the point Chris Whitty advised the Government to offer all children over the age of 12 a Covid-19 vaccine.

Official Office for National Statistics (ONS) data shows that between week 1 and week 37, the five-year-average number of deaths occurring among children aged between 10 and 14 was 207. However, the 2021 dataset from the ONS shows that between week 1 and week 37 of 2021 there were just 178 deaths among children aged between 10 and 14. This means deaths among children aged week 10 and 14 were 14% down on the five-year-average prior to being offered the Covid-19 injection.

However, it is known that children deemed to be vulnerable to Covid-19 due to certain underlying conditions were already being offered a Covid-19 injection prior to Chris Whitty’s decision to overrule the JCVI and offer the jab to all healthy children. [..] we assessed the numbers from the ONS five-year-average dataset on deaths (found here) and the ONS 2021 dataset on deaths and discovered that there had also been a notable increase in deaths among children since vulnerable kids had first been given the Covid-19 vaccine. We’ve compiled the following table on the ONS data:

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Child Deaths Are 52% Higher?! Let’s jab all the kids.

White House Details Plan To “Quickly” Vaccinate 28M Children Age 5-11 (ZH)

The Biden administration on Wednesday unveiled its plan to ‘quickly’ vaccinate roughly 28 million children age 5-11, pending authorization from the Food and Drug Administration (FDA). The jab – which doesn’t prevent transmission of Covid-19 will be available at pediatricians, local pharmacies, and possibly even at schools, according to the White House, which expects FDA authorization of the Pfizer shot for children – the least likely to fall seriously ill or die from the virus, in a matter of weeks, according to the Associated Press. “Federal regulators will meet over the next two weeks to weigh the benefits of giving shots to kids, after lengthy studies meant to ensure the safety of the vaccines. Within hours of formal approval, expected after the Centers for Disease Control and Prevention advisory meeting scheduled for Nov. 2-3, doses will begin shipping to providers across the country, along with smaller needles necessary for injecting young kids, and within days will be ready to go into the arms of kids on a wide scale”. -AP


According to the announcement, the White House has secured enough to supply more than 25,000 doses for pediatricians and primary care physicians who have already signed up to deliver the vaccine, while the country now has enough Pfizer vaccine to jab roughly 28 million kids who will soon be eligible, meaning this won’t be a slow roll-out like we saw 10 months ago when doses and capacity issues meant adults had to wait. Meanwhile, the White House is rolling out an ‘advertising’ campaign to convince parents and kids that the vaccine is safe and effective. According to the report, “the administration believes trusted messengers — educators, doctors, and community leaders — will be vital to encouraging vaccinations.” “COVID has also disrupted our kids lives. It’s made school harder, it’s disrupted their ability to see friends and family, it’s made youth sports more challenging,” said surgeon general Dr. Vivek Murthy in a Wednesday statement to NBC. “Getting our kids vaccinated, we have the prospect of protecting them, but also getting all of those activities back that are so important to our children.”

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Why jab the kids? Well…

Pfizer, Moderna to Rake in $93 Billion in 2022 COVID Vaccine Sales (CHD)

Vaccine makers Pfizer and Moderna are projected to generate combined sales of $93.2 billion in 2022 nearly twice the amount they’re expected to rake in this year, said Airfinity, a health data analytics group. Airfinity put total market sales for COVID vaccines in 2022 at $124 billion, according to the Financial Times. Pfizer vaccine sales are predicted to reach $54.5 billion in 2022, and Moderna’s will hit $38.7 billion. The estimates blow the earlier figures — $23.6 billion for Pfizer and $20 billion for Moderna — out of the water. “The numbers are unprecedented,” Rasmus Beck Hansen, CEO of Airfinity, told the Financial Times. Sales of the mRNA shots will continue to rise in 2022 due to boosters and countries stockpiling to ward off variants, Airfinity said.

Pfizer will generate 64% of its sales, and Moderna 75% of its sales, from high-income countries in 2022, the analysts predicted. In April, Pfizer predicted 2021 COVID vaccine sales of $26 billion. After second-quarter results were reported, Pfizer upped the figure to $33.5 billion. Bernstein analyst Ronny Gal said the company could ring up an additional $10 billion in vaccine sales in 2021. Gal wrote: “The numbers are going to be much higher. The guidance of $33.5B reflects contracts signed to today which reflect total commitment to sell 2.1 million doses (at average price of $15.95). Pfizer notes they expect to manufacture 3 million doses. Presumably much of those will be sold as well, albeit at lower average price as consumption shifts to emerging markets. This is probably another $10 billion.”

“The second quarter was remarkable in a number of ways,” Pfizer CEO Albert Bourla said. “Most visibly, the speed and efficiency of our efforts with BioNTech to help vaccinate the world against COVID-19 have been unprecedented, with now more than a billion doses of BNT162b2 having been delivered globally.” On a conference call, Bourla said that while “it’s very early to speak” about the company’s sales expectations for next year, he put Pfizer’s 2022 production capacity at 4 billion doses.

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“..mRNA jabs’ initially higher number of antibodies “declines sharply” over the same period..”

Adenovirus Covid-19 Vaccine Shows Lower But ‘Stable’ Immunity (RT)

Different effects of the world’s Covid injection types are revealed in new study that shines light on ‘Adenovirus v mRNA’ debate The one-shot adenovirus J&J Covid-19 vaccine provides stable but low-level immunity that stays for months, a new study has found, while mRNA jabs’ initially higher number of antibodies “declines sharply” over the same period. An immune response induced by Johnson & Johnson’s Janssen adenovirus vaccine appears to show “minimal-to-no evidence of decline” over eight months, the fresh study in the US reports, detailing the dynamics of the antibody response in the “follow-up period” after immunizations with each of the three American vaccines.

Apparently, Pfizer and Moderna cannot boast a similar durability in their mRNA vaccines’ efficacy, the study shows. Antibody titer levels (a term of measurement) elicited by both of them tend to decline “sharply by six months after vaccination” and fall even further by eight months, according to the data collected by the specialists from the Beth Israel Deaconess Medical Center in Boston, Massachusetts, and the University of North Carolina at Chapel Hill. The two mRNA vaccines apparently still greatly outperform the one-shot Johnson & Johnson jab during the “peak immunity” period, between two and four weeks after full immunization, the study admits. In the long run, however, they quickly lose their sizeable lead in efficacy and eventually land at the same antibody response level as that of the Johnson & Johnson jab based on the adenovirus vector principle – the same as the ones used by the UK’s AstraZeneca and by Russia’s Sputnik V.

The study also demonstrated that the Johnson & Johnson jab supposedly even somewhat outperforms both mRNA vaccines when it comes to antibody responses eight months after full immunization. Its live-virus neutralizing antibody response and a certain type of T-cell response appeared to be higher than those of Pfizer and Moderna jabs at that time. Whether it is indeed better in the long run is difficult to ascertain, though, since the data obtained from just over 60 participants, including only eight immunized with a Johnson & Johnson jab, appear to be somewhat “lacking,” Maxim Skulachev, a leading research associate at the Belozersky Institute at Moscow State University (MSU), believes.

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“..a marked reduction of 93% of released virion and 99.98% unreleased virion levels upon administration of IVM..”

Repositioning Ivermectin For Covid-19 Treatment (SD)

Drug repositioning is a useful and effective idea for Covid-19 antiviral discovery. • Ivermectin has proven effective for HIV-1, Adenovirus, Influenza virus, SARS-CoV, and many more, in the past.• Due to genomic similarity between SARS-CoV-2 and the SARS-CoV, the role of the IMPα/β1 complex for viral protein (NSP12-RdRp) shuttling between the nucleus and cytoplasm holds great potential. • Ivermectin also exhibits great potential in reducing SARS-CoV-2 viral replication via numerous modes of action, such as the disruption of the Importin heterodimer complex (IMPα/β1)

Ivermectin (IVM) is an FDA approved macrocyclic lactone compound traditionally used to treat parasitic infestations and has shown to have antiviral potential from previous in-vitro studies. Currently, IVM is commercially available as a veterinary drug but have also been applied in humans to treat onchocerciasis (river blindness – a parasitic worm infection) and strongyloidiasis (a roundworm/nematode infection). In light of the recent pandemic, the repurposing of IVM to combat SARS-CoV-2 has acquired significant attention. Recently, IVM has been proven effective in numerous in-silico and molecular biology experiments against the infection in mammalian cells and human cohort studies. One promising study had reported a marked reduction of 93% of released virion and 99.98% unreleased virion levels upon administration of IVM to Vero-hSLAM cells.

IVM’s mode of action centres around the inhibition of the cytoplasmic-nuclear shuttling of viral proteins by disrupting the Importin heterodimer complex (IMPα/β1) and downregulating STAT3, thereby effectively reducing the cytokine storm. Furthermore, the ability of IVM to block the active sites of viral 3CLpro and S protein, disrupts important machinery such as viral replication and attachment. This review compiles all the molecular evidence to date, in review of the antiviral characteristics exhibited by IVM. Thereafter, we discuss IVM’s mechanism and highlight the clinical advantages that could potentially contribute towards disabling the viral replication of SARS-CoV-2. In summary, the collective review of recent efforts suggests that IVM has a prophylactic effect and would be a strong candidate for clinical trials to treat SARS-CoV-2.

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“The FDA waits for a deep-pocketed sponsor to present a comprehensive package that justifies the approval of a new drug or a new use of an existing drug.”

The FDA’s War Against The Truth On Ivermectin (AIER)

The FDA judges all drugs as guilty until proven, to the FDA’s satisfaction, both safe and efficacious. By what process does this happen? The FDA waits for a deep-pocketed sponsor to present a comprehensive package that justifies the approval of a new drug or a new use of an existing drug. For a drug like ivermectin, long since generic, a sponsor may never show up. The reason is not that the drug is ineffective; rather, the reason is that any expenditures used to secure approval for that new use will help other generic manufacturers that haven’t invested a dime. Due to generic drug substitution rules at pharmacies, Merck could spend millions of dollars to get a Covid-19 indication for ivermectin and then effectively get zero return. What company would ever make that investment?

With no sponsor, there is no new FDA-approved indication and, therefore, no official recognition of ivermectin’s value. Was the FDA’s warning against ivermectin based on science? No. It was based on process. Like a typical bureaucrat, the FDA won’t recommend the use of ivermectin because, while it might help patients, such a recommendation would violate its processes. The FDA needs boxes checked off in the right order. If a sponsor never shows up and the boxes aren’t checked off, the FDA’s standard approach is to tell Americans to stay away from the drug because it might be dangerous or ineffective. Sometimes the FDA is too enthusiastic and these warnings are, frankly, alarming. Guilty until proven innocent.

There are two reasons that Merck would warn against ivermectin usage, essentially throwing its own drug under the bus. Once they are marketed, doctors can prescribe drugs for uses not specifically approved by the FDA. Such usage is called off-label. Using ivermectin for Covid-19 is considered off-label because that use is not specifically listed on ivermectin’s FDA-approved label. While off-label prescribing is widespread and completely legal, it is illegal for a pharmaceutical company to promote that use. Doctors can use drugs for off-label uses and drug companies can supply them with product. But heaven forbid that companies encourage, support, or promote off-label prescribing. The fines for doing so are outrageous.

During a particularly vigorous two-year period, the Justice Department collected over $6 billion from drug companies for off-label promotion cases. Merck’s lawyers haven’t forgotten that lesson. Another reason for Merck to discount ivermectin’s efficacy is a result of marketing strategy. Ivermectin is an old, cheap, off-patent drug. Merck will never make much money from ivermectin sales. Drug companies aren’t looking to spruce up last year’s winners; they want new winners with long patent lives. Not coincidentally, Merck recently released the clinical results for its new Covid-19 fighter, molnupiravir, which has shown a 50% reduction in the risk of hospitalization and death among high-risk, unvaccinated adults. Analysts are predicting multi-billion-dollar sales for molnupiravir.

While we can all be happy that Merck has developed a new therapeutic that can keep us safe from the ravages of Covid-19, we should realize that the FDA’s rules give companies an incentive to focus on newer drugs while ignoring older ones. Ivermectin may or may not be a miracle drug for Covid-19. The FDA doesn’t want us to learn the truth. The FDA spreads lies and alarms Americans while preventing drug companies from providing us with scientific explorations of existing, promising, generic drugs.

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“..The former officers laid their boots and hats on the steps of the Capitol building in a stunt meant to represent “what the state’s lost..“

Washington State Patrol Staff Shortage, Officers Quit Over Vaccine Mandate (RT)

Some 127 Washington State Patrol employees, more than half of them officers, were terminated after a vaccination deadline passed this week, with the force now bracing for staff shortage in critical areas and major costs. 74 commissioned officers – including 67 troopers, six sergeants and a captain – as well as 53 civil servants were “separated from employment” as they missed the October 18 deadline to provide proof of vaccination, the Washington State Patrol (WSP) reported earlier this week. The WSP stated that the employees quit the force “for varying reasons and in varying ways,” with chief John R. Batiste declaring that “we will miss every one of them.” “I extend a hardy thanks to those who are leaving the agency. I truly wish that you were staying with us,” he said.

The mass exodus from the 2,200-strong force is set to put a strain on the depleted ranks. Speaking to the Oregonian, WSP spokesman Chris Loftis said that in some cases, such as vehicle collisions that result in no casualties or obstruction to traffic, the affected drivers might be told to figure out the incident on their own and “clear the area rather than wait for a trooper to show up,” as would happen under normal circumstances Some employees fired over the vaccine requirement successfully received exemptions from the order, but that did not prevent them from being terminated. Loftis said that over 400 people were granted such exemptions, but not all of them were offered alternative employment due to the nature of the agency’s work. Still, he stressed that the 74 troopers that were effectively forced out “were people that we knew and cared about.”

This wasn’t a situation where 74 troopers left one day because they did something bad – they left in standing opposition to the vaccine mandate, based on their personal principles and convictions. Some of the terminated troopers turned out at the state Capitol on Tuesday in a symbolic protest against the mandate. The former officers laid their boots and hats on the steps of the Capitol building in a stunt meant to represent “what the state’s lost,” one of the participants, ex-trooper Bill Jordan, told local media. Jordan claimed that he received a religious exemption from the mandate, but WSP failed to accommodate him regardless. While Loftis said that the agency would step up its recruitment efforts by filling up new academy classes, the training of would-be troopers will come with a hefty price tag.

It is estimated that the mass exodus could cost taxpayers some $12.4 million, as about $168,000 per year is needed to train just a single cadet – the WSP has lost 67. The Washington State Patrol has not been the only agency to see resistance from state employees to compulsory vaccination orders. More than 1,800 workers in Washington state have been fired, resigned or retired due to the mandate, according to official data released on Tuesday. This amounts to about 3% of the state’s workforce that falls under the mandate, and those numbers could yet rise, as the cases of some 2,887 state employees are still pending.

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“They don’t have to. They have friends in the White House.”

Why Are Thousands Of Postal Workers Still Unvaxxed? (WND)

After spending several futile hours rummaging through media accounts and the United States Postal Service (USPS) website, I still had no answer to the question I set out to address: Are postal workers subject to a vaccine mandate? Wanting the straight skinny, I decided not to call USPS headquarters but to visit a facility and talk to the workers loading and unloading mail. To my good fortune I found a well-spoken, straightforward supervisor who told me, through his mask, what I wanted to know. “We are encouraged to get vaccinated, but we do not face a vaccine mandate like the military does,” he volunteered. “But,” he added helpfully, “we do have an indoor mask mandate.”

Two questions emerge from this encounter. The first is: Why are postal workers exempt from a mandate that is stripping other public service entities, including the military, of thousands of needed personnel? The second, why did I have to ask a postal worker to get the truth? The answer to the second question is the easier of the two – the media don’t want you to know. In mid-September there was a flurry of questions around the status of the USPS. On Sept. 16, the USA Today fact checker put those questions to rest. On that same day, the USPS put out an impressively ambiguous statement on COVID-19 vaccines. After much self-serving blather about the hard work of its 650,000 employees, management concluded:

“We are working closely with our union leadership so that once OSHA’s COVID-19 Vaccination Emergency Temporary Standard (ETS) is issued we can move quickly to determine its applicability to our employees and how best to implement.” Translation: “We are in no big hurry.” The ETS represents the fulfillment of President Joe Biden’s COVID-19 Action Plan announced on Sept. 9. The OSHA ETS runs a perversely long 44 pages and includes any number of useless admonitions, such as: “An employer with one or more employees working in a physical location controlled by another employer must notify the controlling employer when those employees are exposed to conditions at that location that do not meet the requirements of this section.”

On Oct. 12, OSHA submitted the ETS to the White House’s Office of Information and Regulatory Affairs for approval, which is where it stands as of this writing. USPS brass might argue that their hands are tied until the OSHA ETS is formalized, but unlike many private and public employers, they are making no obvious efforts to prepare their workers for this eventuality. They don’t have to. They have friends in the White House.

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“People go too far these days in taking the liberty to ask questions and judge a person. “Whatever you say – ‘yes, no, maybe, I am thinking about it’ – they will take advantage.”

Djokovic Claims It Would Be ‘Inappropriate’ To Say If He Is Vaccinated (RT)

Novak Djokovic says people are “taking the liberty” to ask questions about vaccine status and “judge a person”, speaking as an Australian head of government warned that unvaccinated players will face a struggle to receive visas. World number one Djokovic has repeatedly expressed his reservations about players being pressured to take a Covid jab, and the reigning Australian Open champion insists his decision is a “private matter” amid a string of controversies surrounding the likes of NBA star Kyrie Irving, who has been left out by the Brooklyn Nets because he is not vaccinated. Djokovic rival Stefanos Tsitsipas found himself at the center of a political row after he made a wide range of remarks about Covid and vaccines, and the Greek – whose own government seemed to distance themselves from views which appeared to include a suggestion that spreading the virus could have positive effects – now appears to be willing to be vaccinated.


Russian contender Andrey Rublev has become the latest player to drop their apparent reluctance because of the logistical issues not being vaccinated could cause, but Djokovic is yet to openly say he has had the treatment. “Things being as they are, I still don’t know if I will go to Melbourne,” Djokovic told Blic, speaking ahead of a first Grand Slam of the year in January which is likely to take place under tight restrictions. “I will not reveal my status, whether I have been vaccinated or not – it is a private matter and an inappropriate inquiry. “People go too far these days in taking the liberty to ask questions and judge a person. “Whatever you say – ‘yes, no, maybe, I am thinking about it’ – they will take advantage.”

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“If you mandate, as a private employer, “vaccination” against Covid-19 any and all adverse events as a result of said jabs are now chargeable to you..”

Dewey, Cheat’em And Howe (Denninger)

Oh, you’re a woke-poke employer eh? You think hiding behind OSHA — or the threat to issue a mandate by the government — in some way prevents you from being liable for injuries and/or deaths related to the vaccines? Uh, how would you like to defend that position in court given all of the following are true: The PREP act has no provision giving you legal immunity and cannot be amended by executive order as it is law, so you would need both houses of Congress to pass such a thing — and they have not. The producing firms and health care providers are immune from damages under that same PREP Act. Therefore under the general principle of joint and several liability guess who gets all of it: You do. You could have tried to claim that the Federal Government refused liability (and got away with it) for direct employees, and that would have been a pretty decent argument….. except, oops, that just went up in a puff of smoke.

“The Federal Employees’ Compensation Act (FECA) covers injuries that occur in the performance of duty. The FECA does not generally authorize provision of preventive measures such as vaccines and inoculations, and in general, preventive treatment is a responsibility of the employing agency under the provisions of 5 U.S.C. 7901. However, care can be authorized by OWCP for complications of preventive measures which are provided or sponsored by the agency, such as adverse reaction to prophylactic immunization. See PM 3-0400.7(a). Further, deleterious effects of medical services furnished by the employing establishment are generally considered to fall within the performance of duty. These services include preventive programs relating to health. See PM 2-0804.19. However, this executive order now makes COVID-19 vaccination a requirement of most Federal employment. As such, employees impacted by this mandate who receive required COVID-19 vaccinations on or after the date of the executive order may be afforded coverage under the FECA for any adverse reactions to the vaccine itself, and for any injuries sustained while obtaining the vaccination.”

Oops. If you mandate, as a private employer, “vaccination” against Covid-19 any and all adverse events as a result of said jabs are now chargeable to you, as the Federal Government itself has deemed that “mandated” vaccinations are indeed injuries that occurred while performing the job in question, irrespective of where the jab took place. Oh by the way your insurance firm has likely inserted a “pandemic exemption” into your liability coverage. That’s shown up in a whole lot of those policies over the last year or so, and it’s odds-on that’s the case for you as well. Incidentally there is plenty of evidence that these jabs will be eventually found to be responsible for a whole host of serious problems, and those do not end within a couple of weeks of the jab itself.

Indeed, the evidence is mounting rapidly (see the all-cause “excess death” rates for various age groups, particularly cardiac and circulatory related, among young people now showing up in places like Scotland and England for examples) that there is a causal link between both strokes and heart attacks. I remind you that the FDA and pharmaceutical industry claimed, not all that long ago, that no such link existed for Vioxx. It was only after about 60,000 Americans had heart attacks and died, and several hundred thousand had non-fatal heart problems caused by it, that it was withdrawn from the market — five years later. Moderna and Pfizer may be immune from lawsuit but you are not, and further, the precedent by the Federal Government itself now exists based on their own public statement that if an employee gets screwed by the jab you demanded they take you’re on the hook whether that injury is evident five minutes afterward or five years later. Good luck *******s; you just got ****ed and it couldn’t happen to a nicer bunch.

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“..one somehow feels bad for Hunter Biden. He’s not just a wreck, but a wreck with spectacularly bad luck.”

“The Bidens”: Is the First Family Corrupt, or Merely Crazy? (Taibbi)

Schreckinger is young, and The Bidens was clearly written in a bit of a hurry, but he’s a skilled storyteller. The initial framing is clever, with a first first chapter titled, “Chekhov’s Laptop,” a reference to Russian playwright’s famous dictum that “if in the first act you have hung a pistol on the wall, then in the following one it should be fired.” Having primed the reader to look for that metaphorical gun on the wall, he opens with a scene that’s bananas even by the outré standards of first son Hunter Biden’s “tumultuous” life. Hunter in October of 2018 had gotten in an argument with his then-girlfriend, Hallie, who according to the funhouse physics of the first family was of course the widow of his late brother Beau.

In the course of that dispute, Hallie had taken his .38 revolver and thrown it out of Hunter’s pickup truck (a pickup truck?) into a trash can outside “Janssen’s, a high-end grocery store near Wilmington the family had long frequented.” When Hunter found out the gun was gone, he chivalrously sent Hallie back into the trash to get it. This turns out to be the first of many moments in The Bidens where despite a seemingly tireless instinct for indulgent selfishness, and a maximally unattractive profile as the coddled scion of political privilege, one somehow feels bad for Hunter Biden. He’s not just a wreck, but a wreck with spectacularly bad luck. In this case, not only has his dead brother’s widow taken advantage of his trusting nature and thrown away his pistol (the one a person with his recreational leanings probably shouldn’t have anyway, but does, and moreover has left unattended), she picked the one bin that’s both across the street from a high school and in a spot where an old man hunting for recyclables somehow finds it.

Now the thing is missing and poor Hunter, who if nothing else has a keen sense of his own potential for disaster, must be imagining the worst, which in his family is likely a headline: Boy, 13, Uses Gun Registered to Dickhead Senator’s Son to Kill Parents, Neighbor, Dog, Self. The Delaware State Police are called, the FBI for some instantly suspicious reason also shows up, the Secret Service also reportedly appears at the store where Hunter bought the gun (I say reportedly because the Secret Service denies this, the first of many details in The Bidens that ends up receding in a fog of conflicting accounts), and the ATF even makes an appearance. The gun was eventually found after a few days, when the old man turned it in. By that point Hunter had already skipped town and begun setting in motion a preposterous chain of events that have ramifications in national politics to the present day.

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If a country is not capable of digging up the truth in matters like this (and the Bidens), it is a failed nation.

Hillary’s Secretive, Russiagate-Flogging Pair of Super-Lawyers (Maté)

The indictment of Hillary Clinton lawyer Michael Sussmann for allegedly lying to the FBI sheds new light on the pivotal role of Democratic operatives in the Russiagate affair. The emerging picture shows Sussmann and his Perkins Coie colleague Marc Elias, the chief counsel for Clinton’s 2016 campaign, proceeding on parallel, coordinated tracks to solicit and spread disinformation tying Donald Trump to the Kremlin. In a detailed charging document last month, Special Counsel John Durham accused Sussmann of concealing his work for the Clinton campaign while trying to sell the FBI on the false claim of a secret Trump backchannel to Russia’s Alfa Bank. But Sussmann’s alleged false statement to the FBI in September 2016 wasn’t all. Just months before, he helped generate an even more consequential Russia allegation that he also brought to the FBI.

In April of that year, Sussmann hired CrowdStrike, the cybersecurity firm that publicly triggered the Russiagate saga by lodging the still unproven claim that Russia was behind the hack of Democratic National Committee emails released by WikiLeaks. At the time, CrowdStrike was not the only Clinton campaign contractor focusing on Russia. Just days before Sussmann hired CrowdStrike in April, his partner Elias retained the opposition research firm Fusion GPS to dig up dirt on Trump and the Kremlin. These two Clinton campaign contractors, working directly for two Clinton campaign attorneys, would go on to play highly consequential roles in the ensuing multi-year Russia investigation. Working secretly for the Clinton campaign, Fusion GPS planted Trump-Russia conspiracy theories in the FBI and US media via its subcontractor, former British spy Christopher Steele.

The FBI used the Fusion GPS’s now debunked “Steele dossier” for investigative leads and multiple surveillance applications putatively targeting Trump campaign volunteer Carter Page. CrowdStrike, reporting to Sussmann, also proved critical to the FBI’s work. Rather than examine the DNC servers for itself, the FBI relied on CrowdStrike’s forensics as mediated by Sussmann. The FBI’s odd relationship with the two Democratic Party contractors gave Sussmann and Elias unprecedented influence over a high-stakes national security scandal that upended U.S. politics and ensnared their political opponents. By hiring CrowdStrike and Fusion GPS, the Perkins Coie lawyers helped define the Trump-Russia narrative and impact the flow of information to the highest reaches of U.S. intelligence agencies.

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“Libyans enjoyed free healthcare, free education, and a high standard of living.”

“We came, we saw, he died,” she said.

The Killing Of Gaddafi 10 Years Ago Led To The Death Of The Nation Of Libya (RT)

During his 42 years in power, he increased the country’s literacy rate from 25% to 88%. Libyans enjoyed free healthcare, free education, and a high standard of living. Basic necessities such as electricity and gas were cheap, and the country was guaranteed a strong social safety net and welfare programs. Libya is 90% desert. Gaddafi sought to provide fresh water to all Libyans for consumption and agriculture – an endeavor in which he succeeded. He built the world’s largest irrigation project, the ‘Great Man-Made River’ in the 1980s. Boasting the world’s largest pipe network, it provides 70% of all the fresh water in Libya. Gaddafi called it the “Eighth Wonder of the World”. Costing over $25 billion, the project was entirely self-financed, without any loans or credits from foreign banks. Libya had grown to be a very wealthy country and had no external debt. NATO bombed the Great Man-Made River in July 2011, destroying key civilian infrastructure: a war crime.

[..] Instead of an abundance of water, gold and oil in a thriving country with great infrastructure, Libya now has open slave-trade markets. Smugglers and human traffickers take advantage of migrants and refugees passing through to Europe, selling them off into bondage. Rival tribes and political factions fight over oil and other precious resources, determined to seize power for themselves. Meanwhile, pockets of Islamic State (IS, formerly ISIS), Al-Qaeda and other jihadist fighters lurk in the shadows, plaguing the war-torn country and its neighbors – groups who wouldn’t have dared establish a presence in Gaddafi’s Libya. Once a prosperous nation, since his fall, it has been taken over by terrorists, opportunists and thieves, and has plunged into chaos. This is what has become of Libya these last 10 years. This is what NATO created.

[..] In the 1970s, he tried to merge Libya with Egypt and Syria to form a unified Arab state. In 2009, he proposed that African nations adopt a single currency: the gold dinar. The Libyan Central Bank, which was 100% state-owned, had reserves of 144 tons of gold that he intended to use for this purpose. Gaddafi proposed that African countries buy and sell their resources exclusively in this new pan-African currency. This would enable them to transition away from the US dollar and the Central Africa (CFA) franc – a colonial currency used in 14 countries and controlled entirely by France. This was Gaddafi’s biggest sin. In wanting African nations to adopt a single currency, to control their own resources and have true independence, he posed a threat to Western monetary hegemony, so he had to go.

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Oct 122021
 


Pablo Picasso Two naked figures 1908

 

Covid Response ‘One Of UK’s Worst Ever Public Health Failures’ (G.)
Down To Only One Question Now.. (Denninger)
The Waiting Is The Hardest Part (Kunstler)
Seattle PD May Lose 40% Of Officers Over Covid-19 Vaccine Mandate (ZH)
Southwest Says Staffing Shortages Contributed To Flight Snarls (Y!)
Texas Gov. Abbott Issues Order Banning Covid Vaccination Mandates (NBC)
Ivermectin as Covid Pre-Exposure Prophylaxis Method in Healthcare Workers (NIH)
Russian Drug To Calm Cytokine Storm (RT)
FDA Responds To Nordic Countries Suspending Moderna COVID Vaccine Usage (ET)
Thousands More People Than Usual Are Dying … But It’s Not From Covid (Tel.)
Live Free Or Die: Why Medical Autonomy Matters (Miele)
Is Durham Circling Jake Sullivan? (Turley)
Southwest Offers Free Flights To Anyone Vaccinated Who Can Fly A Plane (BBee)

 

 

 

 

The report itself is as big a failure. What went wrong? Lockdowns came too late.. But the vaccines are a resounding success. Yeah, sure. Just look at all the new cases. Oh, and in the 2nd graph, what are all those recent excess deaths? Where do they come from? Couldn’t be the vaccines, could it?

Not one word on early treatment or prophylaxis. Not one.

Covid Response ‘One Of UK’s Worst Ever Public Health Failures’ (G.)

Britain’s early handling of the coronavirus pandemic was one of the worst public health failures in UK history, with ministers and scientists taking a “fatalistic” approach that exacerbated the death toll, a landmark inquiry has found. “Groupthink”, evidence of British exceptionalism and a deliberately “slow and gradualist” approach meant the UK fared “significantly worse” than other countries, according to the 151-page “Coronavirus: lessons learned to date” report led by two former Conservative ministers. The crisis exposed “major deficiencies in the machinery of government”, with public bodies unable to share vital information and scientific advice impaired by a lack of transparency, input from international experts and meaningful challenge.

Despite being one of the first countries to develop a test for Covid in January 2020, the UK “squandered” its lead and “converted it into one of permanent crisis”. The consequences were profound, the report says. “For a country with a world-class expertise in data analysis, to face the biggest health crisis in 100 years with virtually no data to analyse was an almost unimaginable setback.” Boris Johnson did not order a complete lockdown until 23 March 2020, two months after the government’s Sage committee of scientific advisers first met to discuss the crisis. “This slow and gradualist approach was not inadvertent, nor did it reflect bureaucratic delay or disagreement between ministers and their advisers. It was a deliberate policy – proposed by official scientific advisers and adopted by the governments of all of the nations of the UK,” the report says.


“It is now clear that this was the wrong policy, and that it led to a higher initial death toll than would have resulted from a more emphatic early policy. In a pandemic spreading rapidly and exponentially, every week counted.”

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“.. that the vaccine makes you more likely to both get and give to others the virus is now established.”

Down To Only One Question Now.. (Denninger)

Unfortunately what this means is that now for anyone over 30 you are more likely to get infected, yes, adjusted for the population that is vaccinated, if you are vaccinated. Indeed in the 40-49 age group you’re close to double as probable on a per-population basis. This means that if your employer mandates the jabs he or she can be sued for putting those who can’t get vaccinated at double the risk, on purpose, by enforcing the mandate. Since there are people who can’t (due to immune compromise, such as cancer patients) be vaccinated this is now intentional risk. In other words this is hard, scientific evidence that these mandates by employers have increased the risk of customers (and other employees) contracting Covid-19. This isn’t a natural risk, it’s a man-made one created by the employer.

That’s actionable. So far this is not translating into higher risk of Covid hospitalization and death on a per-100,000 basis. But that the vaccine makes you more likely to both get and give to others the virus is now established. It is fact. It is in fact true for everyone who is over 30. I have pointed out that preventing infection was never in the cards; it was not part of the EUA, it was not part of the studies, it was never demonstrated. But this is much worse because now we are talking about a direct threat to others The CDC, NIH and Biden almost-certainly know this. This is why the mad rush to demand you get jabbed; they know damn well what this means and that while the manufacturer is immune the employers are not and in fact any such mandate leaves them wide open legally as soon as an unvaccinated person gets infected after being at said firm either as an employee or customer and sues the company on the basis of intentionally and maliciously increasing their risk by forcing their employees to get the jab, which is exactly what they did.

The data from England is conclusive in that regard. I bet that they’ve known this was happening right here in the US for months now. I expected no effective protection. What I did not expect was negative protection, but that’s what we got. This portends the potential for very, very bad things. Specifically, if the impairment is only toward Covid-19; that is, this is some sort of VEI specific to Covid, then the issue ends there. For those with natural (recovered) immunity they don’t care and absolutely should not get the jab; indeed, if you’re recovered and take them you may destroy your protection in part or whole and wind up susceptible to repeat infection you would otherwise not be hit with! If you do that you’re stupid and may well win a stupid prize.

But the 900lb Gorilla is that the impairment may not Covid-19 specific. In other words the impairment may be immune system generalized, in which case those who took the jabs are screwed because that immune damage could be long-lasting or even permanent, yet the protection against serious outcomes is specific to Covid. So yes, you’re “safer” against a serious outcome even while screwing everyone else, but at the same time you are wildly more-susceptible to a severe or fatal outcome due to, for example, influenza.

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“If you were paranoid, you might suspect that something was up in this attempt to roadblock cheap, safe, and effective treatments..”

The Waiting Is The Hardest Part (Kunstler)

Meanwhile, we have the arrival on-the-scene of another joker: Merck’s new anti-Covid-19 drug molnupiravir, said to reduce the risk of hospitalization and death from Covid by 50 percent. Merck and its partner, Ridgeback Biotherapeutics, have applied for an emergency use authorization (EUA) from the FDC for this new drug, the same legal loophole that Pfizer and Moderna got for their mRNA vaxes. “Joe Biden” promised to spend $1.2 billion procuring a big batch of the new drug, so bringing it on must be a done deal. The catch is, molnupiravir is in the same order of nucleoside analogue drugs as remdesivir, a clinically-proven failure in the treatment of Covid 19. The stuff killed patients left and right. Molnupiravir’s mutagenic mechanism is supposed to mess with the DNA of Covid-19 viruses, incrementally disabling them and killing them off.


The trouble is, mutagenic drugs are notorious for broad spectrum action, so Molnupiravir might do the same thing to the various cells in your body, too: instant cancer. I guess we’ll have to stand-by and see how that works out. It pays to remember, though, that the EUA didn’t work out so well for the Covid-19 vaccines, did it? The waiting is the hardest part. Molnupiravir was shoved out onstage after two years of the public health authorities (Drs. Fauci, Collins, et al.) and the corporate news media casting curses on the existing suite of cheap drugs that proved clinically effective in the early treatment of Covid-19, namely ivermectin (a.k.a. “horse paste”), hydroxychloroquine, fluvoxamine, prednisone, etc. If you were paranoid, you might suspect that something was up in this attempt to roadblock cheap, safe, and effective treatments in favor of untested novelties that would just happen to be another multibillion-dollar boon for drug companies.

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How many of these “leaders” will give in before Christmas?

Seattle PD May Lose 40% Of Officers Over Covid-19 Vaccine Mandate (ZH)

It was inevitable – as vaccine mandates across the country approach their deadlines, vast swaths of American workers, service members and atheletes face termination or disciplinary action for refusing to take the Covid-19 jab. In Los Angeles, nearly 1,000 firefighters are about to sue the city over the mandate. Southwest Airlines’ pilot union sued the company last week, before staffing shortages led to the cancellation of more than 2,000 flights over the weekend (and more on Monday). Meanwhile, doctors and nurses across the country have begun suing their employers. Interestingly, after a group of officers from the Los Angeles Police Department sued over the mandate, Sheriff Alex Villanueva announced that he would not ‘force anyone’ to take the jab.


But not Seattle – which stands to lose 40% of its 1,000 person force for failing to get vaccinated as an Oct. 18 deadline approaches. “The environment has been pretty toxic and negative,” one officer anonymously told Fox 13. “Not just from this whole mandate, but prior to that as well. I’m not sure this would be a good place for me to work long-term for my mental health. It has been very stressful.” Recall that this is on the heels of the city losing around 300 officers amid Black Lives Matter riots and the “defund the police” movement. By the numbers, as of Oct. 6, 292 sworn personnel had yet to provide proof of a COVID-19 vaccination per the report, down from 354 on Tuesday. An additional 111 officers are awaiting the results of exemption requests, meaning the total number of potentially fired Seattle cops is as high as 403.

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The hide and seek game continues.

Southwest Says Staffing Shortages Contributed To Flight Snarls (Y!)

After initially blaming air traffic control issues and weather for thousands of flight cancelations, Southwest Airlines on Monday acknowledged that staffing shortages also played a role in the service disruption. The carrier cancelled 1,124 flights on Sunday — by far the highest rate of any airline — 800 the day before and another 326 on Monday, according to airline tracker FlightAware. “On Friday evening, the airline ended the day with numerous cancellations, primarily created by weather and other external constraints, which left aircraft and crews out of pre-planned positions to operate our schedule on Saturday,” the low-cost carrier said in a statement. “Unfortunately, the out-of-place aircraft and continued strain on our crew resources created additional cancelations across our point-to-point network that cascaded throughout the weekend and into Monday.”


CNBC reported Southwest Chief Operating Officer Mike Van de Ven acknowledged to employees that the company “is still not where we need to be on staffing, and in particular with flight crews.” Like most airlines, Southwest let employees go when air traffic collapsed as the Covid-19 pandemic began, but has seen business surge this year as vaccinations spur people to travel again. The weekend’s snarls caused speculation that some pilots or other Southwest staff were participating in a work slowdown as a way to express opposition to the company’s decision to require its employees to be vaccinated against Covid-19. In their statement, Southwest said “the operational challenges were not a result of Southwest employee demonstrations” and they hope to restore normal operations “as soon as possible.”

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The value of freedom.

Texas Gov. Abbott Issues Order Banning Covid Vaccination Mandates (NBC)

Texas Gov. Greg Abbott issued an executive order Monday prohibiting any entity, including private businesses, from imposing Covid-19 vaccination requirements on employees or customers. “The COVID-19 vaccine is safe, effective, and our best defense against the virus, but should remain voluntary and never forced,” Abbott said in a statement. Abbott, a Republican, said in his order that it was prompted by the Biden administration’s vaccination mandate, which he said was federal overreach. President Joe Biden announced a mandate last month requiring companies with 100 or more employees to ensure that their workforces are vaccinated or regularly tested. The Labor Department has yet to release details of the emergency rule, but Biden last week called on companies to act now and not to wait for the requirement to go into effect.


Abbott, who tested positive for Covid in August, has also resisted mask mandates and requiring proof of vaccination. Texas has continued to experience a rise in cases and crowded hospitals, prompting Abbott to invest in monoclonal antibody infusion centers. Abbott issued executive orders over the summer banning local governments and school districts from requiring either masks or vaccinations, issuing $1,000 fines to those who failed to comply. School districts in San Antonio and Dallas have challenged the order in court. The Legislature also passed a bill in June banning private businesses from requiring proof of vaccination from customers.

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From the NIH: ” Ivermectin is a drug that has been shown to be active against coronavirus disease 19 (COVID-19) in previous studies”.

Any further questions?

Ivermectin as Covid Pre-Exposure Prophylaxis Method in Healthcare Workers (NIH)

Background: Ivermectin is a drug that has been shown to be active against coronavirus disease 19 (COVID-19) in previous studies. Healthcare personnel are highly exposed to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Therefore, we decided to offer them ivermectin as a pre-exposure prophylaxis (PrEP) method.

Purpose: Primary outcome was to measure the number of healthcare workers with symptomatic SARS-CoV-2 infection and a positive reverse transcription polymerase chain reaction (RT-PCR) COVID-19 test in the ivermectin group and in the control group. Secondary outcome was to measure the number of sick healthcare workers with a positive RT-PCR COVID-19 test whose condition deteriorated and required hospitalization and/or an Intensive Care Unit (ICU), or who died, in the ivermectin group and in the control group.

Material and methods: This observational and retrospective cohort study was carried out in two medical centers, Centro Medico Bournigal (CMBO) in Puerto Plata and Centro Medico Punta Cana (CMPC) in Punta Cana, Dominican Republic. The study began on June 29, 2020, and ended on July 26, 2020. A Statistical Package for Social Sciences (SPSS) Propensity Score Matching procedure was applied in a 1:1 ratio to homogeneously evaluate 271 healthcare personnel that adhered to a PrEP program with ivermectin at a weekly oral (PO) dose of 0.2 mg/kg, and 271 healthcare personnel who did not adhere to the program were assigned as a control group.

Results: In 28 days of follow-up, significant protection of ivermectin preventing the infection from SARS-CoV-2 was observed: 1.8% compared to those who did not take it (6.6%; p-value = 0.006), with a risk reduction of 74% (HR 0.26, 95% CI [0.10,0.71]). Conclusions: These results suggest that compassionate use of weekly ivermectin could be an option as a preventive method in healthcare workers and as an adjunct to immunizations, while further well-designed randomized controlled trials are developed to facilitate scientific consensus.

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Promising, but…

Russian Drug To Calm Cytokine Storm (RT)

A group of Russian scientists have created a drug that may potentially revolutionize the treatment of Covid-19 by defusing the most catastrophic reaction the disease causes in patients, while not destroying their immune response. The drug, called Leitragin, was developed by the Biomedical Technology Research Center of the Russian Federal Medical and Biology Agency (FMBA), and is currently undergoing clinical trials in Russia. Although its base substance was previously known and used in ulcer treatment medicine by Soviet and Russian doctors, it was the FMBA team that discovered how to apply it for the treatment of severe cases of Covid-19 and, potentially, other deadly diseases that cause life-threatening lung inflammation.


The Russian scientists had tasked themselves with finding a substance that would act as an ‘off switch’ for the chain reaction that, after being triggered by the invading SARS-CoV-2 virus, actually causes potential organ failure and death. This reaction of the immune system, dubbed the “cytokine storm,” has been variously described as our body’s overreaction to the virus or a “suicide attack” against the invading pathogen, and even as an evolutionary mechanism to stop the spread of deadly infections with the death of the host. Trying to stop this uncontrolled immune response while still preserving the body’s ability to fight the virus without causing more damage is what scientists and medics in intensive care units across the world have been wrestling with during the Covid-19 pandemic. In that regard, Leitragin is being touted as a game-changer, since its novel mechanism acts in a targeted way, and is said to be completely safe for one’s health.

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Wait, so Iceland ditches Moderna because it has enough Pfizer… which it says has the same effects as Moderna.

FDA Responds To Nordic Countries Suspending Moderna COVID Vaccine Usage (ET)

The Food and Drug Administration (FDA) responded to Nordic countries limiting the use of Moderna’s COVID-19 vaccine last week, saying the shot’s benefits outweigh the risks. Health officials in Finland, Norway, Sweden, and Iceland suspended the use of the Moderna vaccine for younger people due to a risk of side effects including myocarditis. Sweden said it would pause the vaccine for people under the age of 30, and Denmark did the same for those under 18. Finland said that males under the age 30 shouldn’t receive the jab, while Icelandic officials added over the weekend that they would suspend use of the shot.

“The FDA is aware of these data. At this time, FDA continues to find that the known and potential benefits of vaccination outweigh the known and potential risks for the Moderna COVID-19 Vaccine,” an FDA official said in a statement to news outlets over the weekend in response to the Nordic nations’ decision to suspend the vaccine for certain age groups. Moderna, meanwhile, said in a statement after the countries’ decision that it was “aware of the very rare occurrence of myocarditis and/or pericarditis following administration of mRNA vaccines against COVID-19.” “These are typically mild cases and individuals tend to recover within a short time following standard treatment and rest. The risk of myocarditis is substantially increased for those who contract COVID-19, and vaccination is the best way to protect against this,” the company’s statement continued.

Moderna’s vaccine is still being administered under the Food and Drug Administration’s emergency use authorization. The company’s application for full approval is still pending. On Oct. 10, Iceland’s Health Directorate said the Moderna vaccine would be entirely suspended due to the risk of cardiac inflammation. “As the supply of Pfizer vaccine is sufficient in the territory … the chief epidemiologist has decided not to use the Moderna vaccine in Iceland,” according to a statement published on the Health Directorate website. The move was handed down due to “the increased incidence of myocarditis and pericarditis after vaccination with the Moderna vaccine, as well as with vaccination using Pfizer/BioNTech,” its statement continued.

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Sep 24. yeah, we have no idea what kills all those people…

Thousands More People Than Usual Are Dying … But It’s Not From Covid (Tel.)

While focus remains firmly fixed on Covid-19, a second health crisis is quietly emerging in Britain. Since the beginning of July, there have been thousands of excess deaths that were not caused by coronavirus. According to health experts, this is highly unusual for the summer. Although excess deaths are expected during the winter months, when cold weather and seasonal infections combine to place pressure on the NHS, summer generally sees a lull. This year is a worrying outlier. According to the Office for National Statistics (ONS), since July 2 there have been 9,619 excess deaths in England and Wales, of which 48 per cent (4,635) were not caused by Covid-19. So if all these extra people are not dying from coronavirus, what is killing them?

Data from Public Health England (PHE) shows that during that period there were 2,103 extra death registrations with ischemic heart disease, 1,552 with heart failure, as well as an extra 760 deaths with cerebrovascular diseases such as stroke and aneurysm and 3,915 with other circulatory diseases. Acute and chronic respiratory infections were also up with 3,416 more mentions on death certificates than expected since the start of July, while there have been 1,234 extra urinary system disease deaths, 324 with cirrhosis and liver disease and 1,905 with diabetes. Alarmingly, many of these conditions saw the biggest drops in diagnosis in 2020, as the NHS struggled to cope with the pandemic.

A report released last week by the Government detailing the direct and indirect health impacts of the pandemic reported that there were an estimated 23 million fewer GP consultations – both in-person and online, in 2020 compared with 2019. Diagnosis of Chronic Obstructive Pulmonary Disease (COPD) fell by 51 per cent, atrial fibrillation 26 per cent, heart failure 20 per cent, diabetes 19 per cent, coronary heart disease, 17 per cent and stroke and transient ischemic attack by 16 per cent.

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“I make my choices, and you make yours. Except with COVID. Then Joe Biden makes my choices, trying to protect me from myself.”

Live Free Or Die: Why Medical Autonomy Matters (Miele)

I think vaccines have done the world a world of good. I remember getting my smallpox vaccine and waiting eagerly to get the scar on my arm that my mother’s arm showed off like a badge of courage, but it never appeared for me. Then when the oral polio vaccine was developed, I remember lining up in the gym at North Garnerville Elementary School in New York to get my first dose on a sugar cube. Yum. So yes, I’m pro-vaccine. I also generally get the flu vaccine every year. I even got a shot last year, although for some peculiar reason, influenza vanished last winter while COVID was enjoying its greatest reign of terror. And naturally, my three children have all been vaccinated against the usual childhood diseases and taken whatever was recommended to keep them safe.

But one thing I never thought of doing was forcing my neighbors to get vaccinated against the flu. Did you know that influenza kills as many as 50,000 Americans a year? That’s approaching the number of U.S. soldiers killed in the entire length of the Vietnam War. On average, flu kills as many Americans every year as car crashes. Yet did anyone — even St. Anthony Fauci — ever dare to suggest that vaccination for flu should be mandatory because it would save lives? Hell, no, and even though many vaccinations are required of school children for good reasons, we also have allowed religious and medical exemptions for families that needed them. Because we aren’t supposed to be a nation of slaves, but a nation of citizens. If someone had a personal reason why they rejected vaccines, we didn’t put them through an inquisition or try to burn them at the stake of public opinion. This was America — land of the free.

I also never thought of celebrating when a person who opted not to get the flu vaccine died of influenza. But vaccine mandate supporters seem to get giddy when a vaccine refusenik falls ill from COVID and dies on a ventilator or worse. This isn’t science; it’s scientific imperialism — and the CDC centurions are ruthless in their application of power to the masses. Obey or die. So why might a reasonable person decide not to be vaccinated against COVID-19 in such a hysterical climate? Maybe because it’s an experimental and untested drug using a technology (mRNA) that has the power to tamper with the very genetic makeup of the cells in my body. Maybe because I’m more worried about herd instinct than herd immunity. Maybe because I’ve heard wonky scientists gloating about the power they wield over everyday Americans.

Maybe because Big Pharma’s getting rich by inventing reasons why you just might need to get a new shot every year. Maybe because I want to decide for myself what’s best for me. Think of it this way. You are afraid of dying of COVID-19. So am I. But that doesn’t mean I am going to die from COVID. In fact, there is what I would characterize as an acceptably small chance I will die of COVID, and I’m 66 years old, right smack in the realm of the supposedly at-risk elderly population. According to data from the CDC reported at RationalGround.com, from Jan. 1, 2020 until Sept. 11, 2021, there were 12,702 U.S. deaths from COVID for my age cohort out of an estimated population of 3,618,069. That’s a death rate of 0.365%.

Meanwhile, 100,449 people my age died during the same period of all causes, suggesting I have about a 12% chance of dying of something this year, a much scarier possibility than dying of COVID-19. Think of it! If I’m going to die this year, I’m 33 times more likely to die of anything else besides COVID. Based on the propaganda we are inundated with every day about the virus, I should be terrified! There are way worse things out there trying to kill me than COVID. But I’m not terrified, not even slightly, because life is always a risk. I can temper my risks by avoiding downhill skiing, ATVs, booze, surfing, and motorsports. Those are my choices, but heaven forbid I should dictate that you have to avoid those activities because they are not 100% safe. Your behavior is none of my business. I make my choices, and you make yours. Except with COVID. Then Joe Biden makes my choices, trying to protect me from myself.

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Wouldn’t he be circling Biden then?

Is Durham Circling Jake Sullivan? (Turley)

As soon as the conspiracy theory was packaged and delivered the FBI and the media by Sussman, the indictment recounts an exchange between some of those “VIPs”: “… on or about September 15, 2016, Campaign Lawyer-1 exchanged emails with the Clinton Campaign’s campaign manager, communications director, and foreign policy advisor concerning the Russian Bank-1 allegations that SUSSMANN had recently shared with Reporter-1.” The campaign lawyer reportedly was Elias, and the “foreign policy advisor” reportedly was Sullivan. Sullivan was quoted in an official campaign press statement as stating that the Alfa Bank allegation “could be the most direct link yet between Donald Trump and Moscow.”

In the statement, Sullivan said: “Computer scientists have apparently uncovered a covert server linking the Trump Organization to a Russian-based bank. This secret hotline may be the key to unlocking the mystery of Trump’s ties to Russia … This line of communication may help explain Trump’s bizarre adoration of Vladimir Putin.” The U.S. intelligence community ultimately rejected the Alfa Bank conspiracy. It also concluded that the Steele dossier not only relied on a suspected Russian agent but likely was used by Russian intelligence to spread disinformation through the Clinton campaign. Yet, when Sullivan was later questioned by Congress, he went full Sergeant Schultz, claiming he basically did not have a clue about the basis or origins of the Alfa Bank controversy or other campaign-orchestrated scandals.

Sullivan was adept at laying qualifiers upon qualifiers to render statements useless: “broadly speaking, at some point in the summer, and I don’t remember exactly when it was, around the convention, I learned that there was an effort to do some research into the ties between Trump and Russia.” That will make any false statement claim difficult absent direct involvement in the planning of these “campaign efforts.” Sullivan denied knowing that Elias or Sussman were working for the Clinton campaign, despite numerous news articles identifying Elias as the campaign’s general counsel. Sullivan just shrugged and said: “To be honest with you, Marc wears a tremendous number of hats, so I wasn’t sure who he was representing. I sort of thought he was, you know, just talking to us as, you know, a fellow traveler in this — in this campaign effort.”

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“..other skills that were not required, but beneficial: Experience calming herds of rabid, sleepless passengers, expertise in flying through mysterious, invisible weather events, and the ability to land the plane.”

Southwest Offers Free Flights To Anyone Vaccinated Who Can Fly A Plane (BBee)

A spokesperson for Southwest Airlines has announced delays in flights due to strange weather that seems to pass over competitors’ planes, only affecting their own signature blue and orange aircraft. The airline has stated these delays have no connection to their pilots protesting vaccine mandates. The spokesperson then announced a new Southwest Airlines incentive program for potential passengers: All flights, domestic or international, are free to any passenger who is vaccinated and can also fly a plane.


“The requirements to take advantage of these incredible savings are simple,” said Southwest CEO Bob Southwest to a crowd of customers who have been stuck at the airport all weekend and were frothing at the mouth in anger. “Show us proof of vaccination against COVID-19 and promise us you know how fly commercial airliners, and your flight is on us.” The CEO then mentioned other skills that were not required, but beneficial: Experience calming herds of rabid, sleepless passengers, expertise in flying through mysterious, invisible weather events, and the ability to land the plane.

Read more …

 

 

 

 

 

 

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Oct 082021
 


René Magritte Pandora’s box 1951

 

 

Pfizer Covid Jab ‘90% Effective Against Hospitalisation For At Least 6 Months’, says a recent Guardian headline. Do you remember 1 year ago or so, when these things were first reported on? We were told things like 95% effective against infection, nobody talked about hospitalization, and nobody ever mentioned a time limit.

I’m not sure if they are just moving goalposts or if maybe a whole new and different game has been started, but those changes in wording are stark. Effectively, we’ve been sold one narrative for a year and are now finding out that it was never true. It’s just that the propagandists, like the Guardian, are not yet ready to catch up with the changes. Here’s thinking that will change.

Meanwhile, a few billion people have been injected with substances that essentially don’t do what we were told they would. As for the effectiveness against hospitalization, that’s murky at best. For instance because in the US, as of August 7th 60% of hospitalizations were among fully-vaccinated individuals. But protection vs severe disease is the last leg the vaccine fanatics have to stand on, and they will protect that leg with all they got. Until they no longer can.

And even this article admits “Effectiveness against all Covid infections fell from 88% within a month of having two doses to 47% after six months..” OK, so after 6 months they’re useless. You wouldn’t get a EUA for 47%. But what do things look like after 3 months?

 


https://www.humetrix.com/powerpoint-vaccine.html

 

As you can see, things already get worse after a few weeks. Let’s be generous and say the substances are “effective” for 3 months. Of course, minus the first two weeks, when they are known to increase infection risk. That leaves 10 weeks of “effectiveness”. And after 6 months there’s nothing left. Says even Reuters.

Covid Vaccine Antibody Levels Drop ‘Nearly 10-Fold’ After About Six Months

A preliminary study this week claimed to have found a steep reduction in the number of coronavirus-fighting antibodies in patients roughly half a year after they received the COVID-19 vaccine. Researchers “analyzed blood samples from 46 healthy, mostly young or middle-aged adults after receipt of the two doses and again six months after the second dose,” Reuters reported this week. The study indicated that “vaccination with the Pfizer-BioNtech vaccine induces high levels of neutralizing antibodies against the original vaccine strain, but these levels drop by nearly 10-fold by seven months,” two of the researchers told the news wire.


The study, which has not yet been certified by peer review, comes amid growing talk of the possible need for a booster shot of the COVID-19 vaccine to ensure a robust immune response. The study determined that “administering a booster dose at around 6 to 7 months following the initial immunization will likely enhance protection against SARS-CoV-2 and its variants.”

Enhance protection? Or kill it? You be the judge. The Exposé looked at the latest report available from the UK Health Security Agency, which has recently replaced Public Health England. Its conclusion:

Covid-19 Vaccine Negative Effectiveness As Low As Minus 86%

The efficacy of all available vaccines combined is as low as – 85.71% within the 40-49 age group, and as high as – 3.4% in the 30-39 age group. This shows that the Covid-19 vaccines are making people more susceptible to catching Covid-19, rather than preventing cases of Covid-19 by the claimed 95%. By combining the numbers provided for all age groups over the age of 30, we have been able to calculate an average vaccine effectiveness of – 47.69%, and we’re definitely seeing this in the number of confirmed cases by vaccination status.


Between week 36 and week 39 of 2021 there were 41,149 confirmed Covid-19 cases in the unvaccinated over 30’s, 14,649 confirmed cases in the partly vaccinated over 30’s, and a frightening 243,373 confirmed cases in the fully vaccinated over 30’s. The new UK Health Security Agency report proves without a shadow of a doubt that the Covid-19 vaccines do not work, and actually make the recipients worse.

 

 

So, as I asked, now what? For the moment, the push for the vaccines is only getting stronger. People are being fired left right and center, including long term and dedicated health care professionals. Freedoms and rights continue to be taken away, and increasingly so. But people will start to see some of the real numbers, no matter how hard you try to hide them.

So as a politician or media person, you better try and stay ahead of the game. A huge number of people have died because, in order to get the authorizations for the vaccines, all prophylactics and early treatments had to be banned. And now the vaccines begin to actively kill many more. There is no way you can keep that hidden. And there’s no way you can keep pushing the vaccines when they kill those who are inoculated.

 

 

In many countries, the campaigns for booster shots are getting fired up. They will only make things worse, and fast. Ever more people will become spike protein factories, as their immune systems are no longer capable of dealing with the increasing amounts of spikes their own bodies produce. While the time the boosters provide “protection” will shorten. If you get a booster today, you’re likely to need another one around Christmas.

If I were a politician, I would be getting very worried about this. And I would probably look for someone to blame it all on, so I don’t get blamed myself. Maybe I would say Pfizer and Moderna have misled me, or my own experts. But I wouldn’t wait till fingers inevitably begin to point in my direction. Just saying.

 

 

 

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


Pablo Picasso Swimming 1908

 

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

 

 

 

 

Biden speech

 

 

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

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

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

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

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

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

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

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

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

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


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

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

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

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

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

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

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

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Yup, it’s a horse drug. Priceless.

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

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

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

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

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

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

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Exhaustive study by Jessica Rose and Peter McCullough.

Myocarditis Adverse Events in VAERS (SD)

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


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

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Karl’s take on that study.

Stop This NOW (Denninger)

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

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

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

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

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It’s a sales job. Always has been.

The Cult of the Vaccine Neurotic (Taibbi)

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

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

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

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

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

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

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

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

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

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

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

Biden Keeps Pushing Nonexistent Worker Vaccine Mandate (CTH)

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

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

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

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

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

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

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

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

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

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Scapegoat?

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

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

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

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

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

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

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Veritas Pfizer fetal tissue

 

 

 

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

 

Oct 072021
 


M. C. Escher Order and chaos 1950

 

Covid-19 Response and the Tyranny of Evidence-Based Medicine (Amerling)
Reverse-transcribed SARS-CoV-2 RNA Can Integrate Into The Genome (Pnas)
New Lancet Study Confirms Plummeting Vaccine Effectiveness (DS)
GOP Senators Demand More Early Treatment Options For Covid-19 (JTN)
Sweden Halts Use Of Moderna’s Covid Vaccine For Younger Adults (RT)
And… Here We Go (Denninger)
Covid Commissars Financially Squeezing, Blackballing Dissenting Doctors (JTN)
Ontario Doctor Resigns Over Forced Vaccines And Falsehoods (LSN)
Mandatory Vaccination Is A Human Rights Violation (Spec.au)
Colorado Hospital Set To Deny Kidney Transplant For Unvaxxed Woman (ZH)
That Untraversed Land (Greer)
The Anonymous Executioners of the Corporate State (Hedges)
Key US Witness Against Assange Arrested in Iceland (Lauria)

 

 

 

 

The protected
https://twitter.com/i/status/1445681587547299851

 

 

Yellow badges

 

 

“If hundreds of thousands of patients die unnecessarily, their doctors will not be held responsible. “I was just following the guidelines” has replaced “I was just following orders.”

Covid-19 Response and the Tyranny of Evidence-Based Medicine (Amerling)

When the first wave of what was then known as the Wuhan virus hit in March-April 2020, medical attention was almost completely focused on management of the acutely ill patient. This was notable for its very high failure rate, particularly post-intubation. A handful of intrepid doctors, including Zev Zelenko in upstate NY and Didier Raoult in Marseille, France, addressed early outpatient treatment using repurposed existing drugs such as hydroxychloroquine (HCQ). These physicians achieved remarkable clinical results, but instead of being embraced and emulated, they were censored and harassed. As should now be obvious to even the most naïve, Pharma and other stakeholders had to suppress successful, cheap remedies to pave the way for the rollout of the “vaccines” that were already developed.

How was this accomplished? By using the tyranny of Evidence-Based Medicine (EBM). “These treatments are not evidence-based!” they screamed. “Where are the randomized controlled trials (RCTs)?” they demanded. Kind of hard to have RCT data on a brand new disease, but so what. The authorities had spoken. In their excellent book, Tarnished Gold: The Sickness of Evidence-Based Medicine, Steve Hickey and Hillary Roberts write: “EBM encourages totalitarian medicine. It is displacing the doctor-patient unit as the ultimate decision-making authority. Peer review is used as censorship. EBM is a self-referential closed system, where critical appraisal means checking whether a study conforms to its rules. So-called evidence-based medicine wrongly claims the authority of medical and scientific gold-standards. EBM repackages and uses concepts from legal proof, in an attempt to impose a medical dictatorship.”

EBM is a movement that began in the early 1990s with the noble intention of incorporating high quality research into clinical practice. Over the last 20 years, EBM has steadily replaced traditional medicine, which depended on understanding pathophysiology and pathology (i.e. basic science), along with careful patient management including following response to treatments. EBM was quickly hijacked by industry to promote the use of their products through clinical practice guidelines, which are based on little more than a consensus of “experts,” the majority of whom receive financial support from industry. Ironically, many guideline recommendations are based on low quality, or no evidence.

EBM arrogantly claims for itself the mantle of “science,” but is actually pseudoscientific. It relies heavily on studies of large populations and therefore statistics, which are inherently unreliable and easy to manipulate. The conceit of EBM is that the results of large population studies can and should be used to dictate treatment of individual patients. It exalts metanalyses, statistical compilations of many studies, that can be created to support almost any pre-conceived idea. The vast majority of physicians are unable to understand, let alone deconstruct, the statistics used in most studies. “Evidence” is not science. Evidence can always be found to support any hypothesis, no matter how absurd. Remember that according to the “evidence,” Paul McCartney has been dead since 1966!

Whoever controls the “evidence” controls “the science” and through the bogus and corrupt guideline process, controls clinical practice. EBM creates an arbitrary hierarchy of evidence, with RCTs and metanalyses at the top and clinical experience, insultingly called ‘anecdotes,’ at the bottom. This is absurd on its face. The logical conclusion is that clinical experience is not needed to practice medicine! Just buy a guideline cookbook and go out there and heal! Perhaps that’s where things are headed. Or perhaps we are already there. If hundreds of thousands of patients die unnecessarily, their doctors will not be held responsible. “I was just following the guidelines” has replaced “I was just following orders.”

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Yes, scary. Very.

Reverse-transcribed SARS-CoV-2 RNA Can Integrate Into The Genome (Pnas)

Continuous or recurrent positive severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) PCR tests have been reported in samples taken from patients weeks or months after recovery from an initial infection. Although bona fide reinfection with SARS-CoV-2 after recovery has recently been reported, cohort-based studies with subjects held in strict quarantine after they recovered from COVID-19 suggested that at least some “re-positive” cases were not caused by reinfection. Furthermore, no replication-competent virus was isolated or spread from these PCR-positive patients, and the cause for the prolonged and recurrent production of viral RNA remains unknown. SARS-CoV-2 is a positive-stranded RNA virus.

Like other beta-coronaviruses (SARS-CoV-1 and Middle East respiratory syndrome-related coronavirus), SARS-CoV-2 employs an RNA-dependent RNA polymerase to replicate its genomic RNA and transcribe subgenomic RNAs. One possible explanation for the continued detection of SARS-CoV-2 viral RNA in the absence of virus reproduction is that, in some cases, DNA copies of viral subgenomic RNAs may integrate into the DNA of the host cell by a reverse transcription mechanism. Transcription of the integrated DNA copies could be responsible for positive PCR tests long after the initial infection was cleared. Indeed, nonretroviral RNA virus sequences have been detected in the genomes of many vertebrate species with several integrations exhibiting signals consistent with the integration of DNA copies of viral mRNAs into the germline via ancient long interspersed nuclear element (LINE) retrotransposons.

Furthermore, nonretroviral RNA viruses such as vesicular stomatitis virus or lymphocytic choriomeningitis virus (LCMV) can be reverse transcribed into DNA copies by an endogenous reverse transcriptase (RT), and DNA copies of the viral sequences have been shown to integrate into the DNA of host cells.

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47% after five months. Better get back in that jab line.

New Lancet Study Confirms Plummeting Vaccine Effectiveness (DS)

A study appeared in the Lancet this week confirming that vaccine effectiveness against infection is fading fast. The study involved 3,436,957 people over the age of 12 who are members of the healthcare organisation Kaiser Permanente Southern California. It sought to assess the effectiveness of the Pfizer vaccine against SARS-CoV-2 infections and COVID-19-related hospital admissions for up to six months, with a study period covering December 14th 2020 to August 8th 2021. Comparing fully vaccinated to unvaccinated, and controlling for confounders such as prior infection, the researchers found that effectiveness against infection plummeted from 88% (95% confidence interval 86-89%) during the first month after double-vaccination to 47% (43-51%) after five months. The variation by age (depicted above) was largely within the margins of error.

Among sequenced infections, the researchers found vaccine effectiveness against Delta infection was 93% (85-97%) during the first month after double-vaccination but dropped to 53% (39-65%) after four months. Effectiveness against infection from other variants the first month after double-vaccination was 97% (95-99%), but declined to 67% (45-80%) at 4-5 months. Vaccine effectiveness against hospital admissions for Delta infection held up at around 93% (84-96%) for the six months across all ages. However, the researchers note that the latest data from Israel “suggests that some reduction in effectiveness against hospital admissions has been observed among older people (65 years and over) roughly six months after receiving the second dose of [Pfizer]”.

One question that’s arisen recently is to what extent vaccine effectiveness estimates are affected by whether more people who have been previously infected decide not to be vaccinated. According to this study the answer is: not very much at all. Among the unvaccinated, 2.3% had one or more previous positive PCR tests, only slightly more than the 2% of the double-vaccinated who did.

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“..NIH’s ongoing compassionless guideline of doing virtually nothing until COVID-19 patients are so sick they require hospitalization..”

GOP Senators Demand More Early Treatment Options For Covid-19 (JTN)

Senator Ron Johnson of Wisconsin and 21 other Republicans are pressuring the Biden Administration to offer more early treatment options for COVID-19 to the American Public. “Throughout the COVID-19 pandemic, public health officials have not only ignored potential early treatments, but at times seem to have participated in an aggressive campaign against the use of specific early treatment options,” the group’s letter to officials stated. The letter was addressed to Xavier Becerra, Secretary of Health and Human Services; Dr. Anthony Fauci, Director of National Institute of Allergy and Infectious Diseases; Dr. Rochelle Walensky, Director of Centers for Disease Control and Prevention; and Dr. Janet Woodcock, Acting Commissioner of Food and Drug Administration.

“Even though a basic tenet of medicine is: early detection allows for early treatment which produces better results; your agencies have overtly discouraged the use of cheap and widely-available early treatments like ivermectin in favor of expensive new drugs like Remdesivir (which costs more than $3,000 per treatment),” the letter said. The group charged that the Administration a “strong bias” against ivermectin and “other potential early treatment drugs.” The letter from the Republican senators comes as the Biden administration started capping how many doses of antibody treatments it would be giving to states.

“We strongly believe you should explain to the American people why your agencies have failed to sufficiently examine and ensure access to a growing list of drugs being used by doctors who have had the courage to ignore NIH’s ongoing compassionless guideline of doing virtually nothing until COVID-19 patients are so sick they require hospitalization,” the group wrote. Sen. Johnson previously held two hearings on early treatment of COVID-19.

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Sweden: people under 30. Denmark: people under 18.

Do they really think no-one will notice?

Sweden Halts Use Of Moderna’s Covid Vaccine For Younger Adults (RT)

The Swedish Public Health Agency has decided to suspend offering Moderna’s Covid vaccine to anyone born in 1991 and later for precautionary reasons, citing the slightly increased risk of heart inflammation following inoculation. On Wednesday, the agency issued a statement announcing that it will pause dishing out Moderna’s jab, marketed as Spikevax, to people under 30. Instead, the Comirnaty vaccine manufactured by Pfizer-BioNTech will be offered to this age group. Announcing the suspension, the agency said data pointed to an “increased incidence” of heart inflammation diseases myocarditis and pericarditis – mainly in younger men and adolescent boys – “in connection with vaccination against Covid-19.”


The notice stated that “new preliminary analysis from Swedish and Nordic data sources indicate that the connection is especially clear when it comes to Moderna’s vaccine Spikevax, especially after the second dose.” Younger Swedes who have already received their first dose of the paused jab, estimated to be around 81,000 people, will now be unable to receive the second shot of that vaccine as per its usual delivery regimen. The health agency said it was looking for the best alternative to offer this group. Anders Tegnell, Sweden’s chief epidemiologist, said that those who have been vaccinated recently, either with their first or second jab, should not worry about the risk, noting that it is very small. He added though that Swedes should be vigilant for symptoms of the two inflammatory conditions. Nordic neighbor Denmark also stopped the use of Spikevax on Wednesday, although only for minors under 18, citing similar concerns of rare side effects such as myocarditis.

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So you take that difference between 18 and 30 years above, and then ask: what age are most people in the army?

And… Here We Go (Denninger)

Ah, the rumor is real. “STOCKHOLM, Oct 6 (Reuters) – Sweden will pause the use of Moderna’s (MRNA.O) COVID-19 vaccine for people born 1991 and later after reports of possible rare side effects, such as myocarditis, the Swedish health agency said on Wednesday. The health agency said data pointed to an increase of myocarditis and pericarditis among youths and young adults that had been vaccinated.” That’s anyone under 30 years old. Ok folks, how many people did we screw here in the US with mandates, with “strong recommendations” and similar?


How many businesses, along with all of their directors and officers need to be completely destroyed as a consequence of mandates? Oh, and what percentage of the MILITARY active duty are under 30? Threatened with a dishonorable discharge for refusal to put your cardiac health at risk of permanent harm eh? Note that Sweden previously approved the Moderna shot for anyone over 12. That turns out to be wrong. They claim the risk of being affected is “very small.” Would you quantify “very small” please? No? Gee, why not? Incidentally on the data that we have available the Pfizer jab, which Sweden is still willing to use in young people, also has the same potential adverse effect.

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“[M]erely drawing different conclusions based on consideration of scientific evidence does not render the Vaccine Policy arbitrary and irrational..”

It should make it subject of discussion. And that’s what’s being suppressed.

Covid Commissars Financially Squeezing, Blackballing Dissenting Doctors (JTN)

Medical professionals are facing threats to their careers and livelihoods for challenging COVID-19 orthodoxy, while an oft-censored Harvard Medical School professor is facing his latest Big Tech kerfuffle. The University of California put psychiatrist and bioethics professor Aaron Kheriaty on “investigatory leave” after he sued the university system for refusing to recognize natural immunity such as his among exemptions to its COVID vaccine mandate. Writing in the Wall Street Journal, Kheriaty had previously invoked the post-Nazi Nuremberg code in urging universities to abandon their mandates. In his personal newsletter Wednesday, Kheriaty said he’ll lose half his income while on so-called paid leave, because he’s banned from “seeing my patients, supervising resident clinics, and engaging in weekend and holiday on-call duties.”

His contract also bans him from working as a physician outside the UC system to recoup his revenue loss. “The University may be hoping this pressure will lead me to resign ‘voluntarily,’ which would remove grounds for my lawsuit,” Kheriaty wrote. UC’s action came a day after a court refused to issue a preliminary injunction, functionally declaring a draw between each party’s scientific arguments about different forms of immunity and what risk vaccination poses for the recovered. “[M]erely drawing different conclusions based on consideration of scientific evidence does not render the Vaccine Policy arbitrary and irrational,” U.S. District Judge James Selna wrote. Protecting “a campus community of more than half a million students, faculty, and staff from a deadly infectious disease … far outweighs any harm Kheriaty may face” from choosing between vaccination or his job.

The only remaining defendant now is UC President Michael Drake, after Kheriaty agreed to drop the regents this week. The professor disclosed he filed another natural immunity federal lawsuit last week, this time against California’s vaccine mandate for health professionals. Just the News couldn’t find that lawsuit in the docket, and Kheriaty didn’t respond to a request to share it or explain how his investigatory leave may affect his UC lawsuit, such as a new retaliation claim. Canadian physician Charles Hoffe has also lost half his income while under investigation for sharing government data on the COVID recovery rate with patients, who are mostly First Nations members, according to his lawyers at the Justice Centre for Constitutional Freedoms (JCCF).

British Columbia’s Interior Health Authority had already warned Hoffe to stop promoting “vaccine hesitancy” after it learned he had been telling colleagues about his patients’ adverse reactions to the Moderna vaccine — one death and nine “disabling long-term side-effects.” A dozen European countries had pulled the AstraZeneca vaccine around that time for its association with blood clots, and Hoffe’s own investigation found “strong evidence” his patients had the same problems. A provincial health official referred Hoffe to a vaccine safety specialist who dismissed his concerns as “coincidences,” according to JCCF.

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How does this improve health care? 1000s of professionals are being thrown out.

Ontario Doctor Resigns Over Forced Vaccines And Falsehoods (LSN)

Dr. Rochagné Kilian recently resigned as an emergency room and family practice physician due to her concerns that the Ontario health system and Grey Bruce Health Services (GBHS) crossed ethical lines throughout the pandemic. In a virtual meeting that included GBHS CEO Gary Sims and other staff members, Dr. Kilian asked Sims a series of questions about what she believes is unethical behaviour on behalf of the Ontario health system at all levels. Sims appeared to be unprepared for difficult questions pertaining to the ongoing rollout of vaccination mandates and vaccine segregation restrictions the Ontario heath system is championing. Kilian estimated that 80 percent of the patients she saw in the ER during the past month who had inexplicable symptoms were “double vaxxed.”

Dr. Kilian relocated to Owen Sound – a small city in Grey County, Ontario – from South Africa after previously working in British Columbia. When she resettled in Owen Sound with her family, she expressed to a local paper how happy she was to live there: “Our recruitment to Owen Sound might have been by chance, but our choice to settle here was definitely not. Our four months in Owen Sound have been blessed. A little town with lots of soul, surrounded by beautiful landscapes, filled with welcoming residents and businesses, and exciting festivals, programs and activities. We truly feel fortunate to raise a family here.”

The first issue that Dr. Kilian brought up during the meeting was informed consent regarding the COVID jab and what she considered to be a coercive mentality of pressuring people to accept medications that she pointed out are still in “clinical trials.” An GBHS administrator did not answer her question directly, but instead passed the buck to the provincial government and stated they do not have “oversight or input” regarding consent mechanisms presented to patients. Kilian added that having more input into what patients are consenting to is something that GBHS “should consider,” especially in light of enacting the government-recommended vaccination mandates with their own staff. Referring to informed consent and mandating experimental vaccines that been linked to thousands of deaths and injuries, Sims explained that because of the “pandemic,” certain procedural normalities will not take place.

[..] Dr. Kilian pressed Sims about claims that protocols of informed consent can be skirted due to an emergency, and clarified that the Tri-Council Policy Statement stipulates that an emergency situation does not warrant skirting protocols that protect the population from being put at risk due to medical experimentation. The Tri-Council Policy Statement is a Canadian guideline for the ethical conduct of research involving humans and/or human biological materials. As the vaccinations are still technically under experimental trial, they are being implemented under a research-based framework on the population.

It was Kilian’s opinion that the ethical framework is being ignored, thus health workers and citizens are being forced to take something against their will that is not proven to be safe or effective in the long term, as a result of vaccination mandates. Sims reacted sharply to Kilian and said, “Nobody is forcing you to do this, you have a right to say no, but the reality is the government has the right to say that you’re not employed.” “When the law looks at it, the law is saying you have the right to do it [enforcing vaccine mandates],” he added.

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“Conscription didn’t end because it was a breach of human rights, it ended because the public pressure was just too much.”

Mandatory Vaccination Is A Human Rights Violation (Spec.au)

Mandating or coercing COVID vaccination is one of the most important civil liberties issues of my lifetime. It’s a fundamental breach of human rights allegedly guaranteed by a number of international conventions and Australian law, as well as our long tradition of liberal democracy. Nowhere is the legal case against put more clearly than in a judgment of the Fair Work Commission published on Monday. It says, in a dissenting judgment, that because the vaccines are part of a clinical trial, coercing someone to take them breaches The Nuremburg Code, the Universal Declaration of Human Rights, the Declaration of Helsinki, and the Siracusa Principles.

The judgement also holds that vaccine mandates also breach Australian law as the Australian Human Right Commission Act 1986 (Cth) gives effect to Australia’s obligations under the International Covenant on Civil and Political Rights Article 7 which provides “…no one shall be subjected without his free consent to medical or scientific experimentation”. So the issue isn’t whether it is a breach, but how great a breach, and whether that will have any practical consequences. In my view, it is in the top tier of breaches – much worse than infringements on free speech, but not as bad as conscripting someone to war (the most serious breach I have seen). Unlike many abuses of human rights, in this case there are physical risks and benefits to taking the vaccines, some of which are “known unknowns”, or perhaps even “unknown unknowns” to borrow Donald Rumsfeld’s taxonomy of knowledge.

However, on “known knowns”, the US CDC estimates, using the VAERS database that the risk of death is .021 per thousand. That would be 525 deaths from the vaccine if everyone in Australia was vaccinated. And for what? We also know that a percentage of those vaccinated will also die from COVID. Another way of measuring the severity is to ask what individual Australians will put at risk to avoid the vax. The answer to that is that thousands have protested on the streets, risking fines in the thousands, and others are about to protest silently by losing their jobs and livelihoods, a price greater than any of the current fines.

What that adds up to one can only guess, but it will be significant, not only to the individuals but to the country as well as expertise is taken out of the system, perhaps never to return. Of particular concern must be that a significant proportion of these are health professionals. This will increase the stress on our hospitals at the moment when they are likely to be hit by a wave of illness from the Delta wave. In the end, the individual will is more important than the legalities. Conscription didn’t end because it was a breach of human rights, it ended because the public pressure was just too much.

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The sheer insanity. Move to a red state?!

Colorado Hospital Set To Deny Kidney Transplant For Unvaxxed Woman (ZH)

Now that vaccines are widely available and 56% of the US population is vaccinated (significantly missing President Biden’s Jul. 4 target of 70%), a little less than half of the country is unvaxxed and subjected to shocking and dehumanizing discrimination, making life very stressful. Across the country, the hot-button subject entering the fall is COVID vaccination passes for restaurants and football stadiums in certain cities, counties, and or even states. This has made life painful for the unvaxxed (as planned by the administration) who can’t go to their favorite eatery or cheer on their favorite sports team. However, the latest discrimination story of an unvaxxed person is terrifying.

A Colorado woman with stage 5 kidney failure is scrambling to find a new hospital because she and her donor are unvaxxed, and the hospital system has given them 30 days to get vaccinated or be taken off the transplant list. UCHealth, a healthcare system headquartered in Aurora, Colorado, adopted new transplant rules requiring patients to be fully vaccinated. “Here I am, willing to be a direct donor to her. It does not affect any other patient on the transplant list,” Jaimee Fougner, Leilani Lutali’s kidney donor, told Colorado-based news station CBS4. “How can I sit here and allow them to murder my friend when I’ve got a perfect kidney and can save her life?” Fougner said.

Lutali received a letter from UCHealth last week explaining she and Fougner had until the end of October to begin the vaccine process, or they would be removed from the transplant list. “I said I’ll sign a medical waiver. I have to sign a waiver anyway for the transplant itself, releasing them from anything that could possibly go wrong,” said Lutali. “It’s surgery, it’s invasive. I sign a waiver for my life. I’m not sure why I can’t sign a waiver for the COVID shot.” In August, UCHealth told Lutali that being vaxxed wouldn’t be a requirement for the surgery. “At the end of August, they confirmed that there was no COVID shot needed at that time,” she said. “Fast forward to Sept. 28. That’s when I found out. Jamie learned they have this policy around the COVID shot for both for the donor and the recipient.”

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“If you want people to put up patiently with long hours of drudgery at miserably low wages, subject to wretched conditions and humiliating policies, so that their self-proclaimed betters can enjoy lifestyles they will never be able to share, it’s a really bad idea to make them stop work and give them a good long period of solitude..”

That Untraversed Land (Greer)

I think that in retrospect, the decision to lock down entire societies to stop the coronavirus will end up in the history books as one of the most spectacular blunders ever committed by a ruling class. Partly, of course, the lockdowns didn’t work—look at graphs of case numbers over time from places that locked down vs. places that didn’t, and you’ll find that locking down societies and putting millions of people out of work didn’t do a thing to change the size and duration of the outbreak. Partly, the economic damage inflicted by the lockdowns would have taken years to heal even if the global industrial economy wasn’t already choking on excessive debt and running short of a galaxy of crucial raw materials. But there’s more to it than that.

If you want people to put up patiently with long hours of drudgery at miserably low wages, subject to wretched conditions and humiliating policies, so that their self-proclaimed betters can enjoy lifestyles they will never be able to share, it’s a really bad idea to make them stop work and give them a good long period of solitude, in which they can think about what they want out of life and how little of it they’re getting from the role you want them to play. It’s an especially bad idea to do it so that they have no way of knowing when, or if, they will ever be allowed to return to their former lives, thus forcing them to look for other options in order to stay fed, clothed, housed, and the like. (We can set aside the question of vaccine mandates for now—that’s another kettle of fish—but of course those feed into this same effect.)

So there’s a labor shortage, and it’s concentrated in exactly those jobs that are most essential to keeping the economy running. These are also the jobs most likely to have lousy pay and worse conditions. This isn’t accidental. It unfolds from one of the most pervasive and least discussed features of contemporary economic life: the metastatic growth of intermediation. Let’s unpack that phrase a bit. The simplest of all economic exchanges takes place between two people, each of whom has something the other wants. They make an exchange, and both go off happy. If what one of the people brings to the exchange is labor, and the other person brings something the first person wants or needs in exchange for labor, we call that “employment,” and the first person is an employee and the second an employer, but it’s still a simple exchange.

So long as there’s no overt or covert coercion involved on either side, it’s a fair trade. What happens as a society becomes more complex, however, is that people insert themselves into that transaction and demand a cut. Governments—national, local, and everything in between—tax income, sales, and everything else they can think of. Banks charge interest and fees on every scrap of money that passes through their hands. Real estate owners drive up the cost of land so that they can take an ever larger share of the proceeds in rent and mortgage payments. Then you have a long line of other industries lobbying government for their share of the take.

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“He has ordered me to pay millions to Chevron to cover their legal fees in attacking me, and then he let Chevron go into my bank accounts and take all my life’s savings because I did not have the funds to cover these costs. Chevron still has a pending motion to order me to pay them an additional $32 [million] in legal fees..”

The Anonymous Executioners of the Corporate State (Hedges)

Donziger and his lawyers have two weeks to appeal the judge’s order that Donziger be sent immediately to jail. Preska denied Donziger bail claiming he is a flight risk. If the Federal Court of Appeals turns down Donziger’s appeal he will go to jail for six months. The irony, not lost on Donziger and his lawyers, is that the higher court may overturn Preska’s ruling against him, but by the time that decision is made he will potentially have already spent six months in jail. “What Judge Preska is trying to do is force me to serve the entirety of my sentence before the appellate court can rule,” Donziger told me by phone on Monday. “If the appellate court rules in my favor, I will still have served my sentence, although I am innocent in the eyes of the law.”

Donziger, his lawyers have pointed out, is the first person under U.S. law charged with a “B” misdemeanor to be placed on home confinement, prior to trial, with an ankle monitor. He is the first person charged with any misdemeanor to be held under home confinement for over two years. He is the first attorney ever to be charged with criminal contempt over a discovery dispute in a civil case where the attorney went into voluntary contempt to pursue an appeal. He is the first person to be prosecuted under Rule 42 (criminal contempt) by a private prosecutor with financial ties to the entity and industry that was a litigant in the underlying civil dispute that gave rise to the orders. He is the first person tried by a private prosecutor who had ex parte communications with the charging judge while that judge remained (and remains) unrecused on the criminal case.

“No lawyer in New York for my level of offense ever has served more than 90 days and that was in home confinement,” Donziger told the court. “I have now been in home confinement eight times that period of time. I have been disbarred without a hearing where I have been unable to present factual evidence; thus, I am unable to earn an income in my profession. I have no passport. I can’t travel; can’t do human rights work the normal way which I believe I am reasonably good at; can’t see my clients in Ecuador; can’t visit the affected communities to hear the latest news of cancer deaths or struggles to maintain life in face of constant exposure to oil pollution. In addition, and this is little known, Judge [Lewis A.] Kaplan has imposed millions and millions of dollars of fines and courts costs on me. [Kaplan is the judge for Chevron’s lawsuit against Donziger; Preska is his handpicked judge for the contempt charges.]

He has ordered me to pay millions to Chevron to cover their legal fees in attacking me, and then he let Chevron go into my bank accounts and take all my life’s savings because I did not have the funds to cover these costs. Chevron still has a pending motion to order me to pay them an additional $32 [million] in legal fees. That’s where things stand today. I ask you humbly: might that be enough punishment already for a Class B misdemeanor?”

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“..a “rarely invoked” law that allows police in Iceland to detain someone considered to be in the middle of crime spree..”

Key US Witness Against Assange Arrested in Iceland (Lauria)

A key U.S. witness in the conspiracy to commit computer intrusion charge against imprisoned WikiLeaks publisher Julian Assange, who earlier this year admitted to fabricating evidence he gave to the FBI, has been arrested in Iceland, according to a report in the Icelandic newsmagazine Stundin. Sigurdur “Siggi” Thordarson was arrested in Reykjavík on Sept. 24 after returning from Spain under a “rarely invoked” law that allows police in Iceland to detain someone considered to be in the middle of crime spree, Stundin reported. Thordarson “was brought before a judge after police requested indefinite detention intended to halt an ongoing crime spree. The judge apparently agreed that Thordarson’s repeated, blatant and ongoing offences against the law put him at high risk for continued re-offending,” Stundin said.

Thordarson admitted in an interview with Stundin last month that he was engaged in ongoing criminal activity. Thordarson admitted in an earlier interview with Stundin in June that he lied to the FBI about Assange directly ordering hacking operations — a key element of the U.S. computer charge against the WikiLeaks founder. Thordarson was granted immunity by the FBI against prosecution in exchange for becoming an FBI informant in a sting against WikiLeaks in 2010. It is not clear if Thordarson recanting his testimony is related to his recent arrest. In his September interview Thordarson said the FBI promised not to reveal to Icelandic authorities any crimes he committed in Iceland in exchange for his cooperation.

Stundin reported: “It is not clear to what extent the Icelandic authorities were informed about these arrangements, if at all. Indeed Thordarson claims he was assured by the FBI that no information would be shared with the Icelandic police about crimes he committed in Iceland, particularly the hacking attempts against Icelandic institutions. Siggi: ‘My worry was that if I told them who was hacked and how, like Landsvirkjun and the government’s website and all that, I would become a target of Icelandic authorities.’ Reporter: ‘Why?’ Siggi: “Eventually I asked if they [Icelandic authorities] would get access to the data I talked about and they [the FBI] just said no, that would never happen. That was the only discussion I had with the FBI about Icelandic authorities.’” But Thordarson also said if he lied to the FBI the immunity deal would be off.

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Celente

 

 

 

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

 

Aug 292021
 


Eugène-Louis Boudin Beach at Étretat 1890

 

Covid Cases In England Are 26 Times Higher Than A Year Ago (G.)
Vaccine-Resistant Viruses Are Driving ‘Breakthrough’ Covid Infections (MN)
Antibody-Resistant SARS-CoV-2 Variants In Vaccine Breakthrough Cases (Medrxiv)
Impact Of Daily High Dose Oral Vitamin D Therapy On Covid 19 Patients (Nature)
1 in 4 COVID Patients Hospitalized While Vitamin D Deficient Die – Study (ToI)
Is It Time To Stop Obsessing Over Covid Figures? (DM)
Differentiation of Long-Lived SARS-CoV-2-Specific CD8+ T Cells (JoI)
Contaminant In 1.63m Moderna Vaccine Doses In Japan Believed To Be Metal (R.)
Covid Vaccine Doubter Alex Berenson Permanently Banned From Twitter (NYP)
Escapes From Afghanistan, Coordinated From A Home Office In Connecticut (CTM)

 

 


A full page ad in the Wall Street Journal paid for by the owner of the Tampa Bay Buccaneers.

 

 

Sleepy Joe

 

 

Paris

 

 

So what happened? Well, we vaccinated everyone…

Covid Cases In England Are 26 Times Higher Than A Year Ago (G.)

Coronavirus infections in England are now 26 times the levels that were experienced this time last year, according to the Office for National Statistics. Scientists described the figures as “sobering”. They warned that the reopening of schools in England this week was likely to trigger further rises in Covid cases – with more to follow when students return to universities and colleges. A fresh wave of infections could, in turn, lead to new social restrictions being imposed as winter approaches. As a result, pressure is mounting on the Joint Committee on Vaccination and Immunisation to approve the deployment of booster jabs for vulnerable people and the extension of vaccinations to most 12- to 15-year-olds.

The latter move would bring the UK into line with the US and most large European nations and is backed by most ministers. Simon Clarke, associate professor in cellular microbiology at Reading University, said that in the week ending 20 August, the ONS estimated that 756,900 people in England were infected with Covid-19, which equated to one person in 70. “This time last year, the ONS estimated that 28,200 people in England were infected. That is the equivalent of one person in 1,900 being infected with Covid-19. That means that community infections are 26 times more common now than they were a year ago, when the population was unvaccinated and the country was three months into its reopening.”

The fact that deaths and hospital admissions from Covid-19 are a fraction of their levels in August 2020 demonstrates the protective power of the vaccines – more than 60% of the UK population has had two jabs. “The last time infections were at their current level in England was late January,” said Kevin McConway, emeritus professor of applied statistics at the Open University. “There were around 2,300 daily hospital admissions and 1,100 deaths a day then. By contrast, the most recent daily figures for England are about 770 hospital admissions and about 80 deaths.”

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“People who never develop symptoms during a “breakthrough” infection carry very low levels of virus..”

Vaccine-Resistant Viruses Are Driving ‘Breakthrough’ Covid Infections (MN)

Waning immunity and ferocious contagion are known to be fueling the troubling surge in “breakthrough” COVID-19 cases among vaccinated people. But a new UC San Francisco analysis of 1,373 Bay Area cases reveals a third, and more ominous, problem: The coronavirus is learning to outsmart our immune system. Variants with antibody-resistant mutations are playing an ever-larger role in our highly vaccinated region’s pandemic, according to research by prominent virologist Dr. Charles Chiu. His team found that 78% of infections in fully vaccinated people among the study were caused by variants with these mutations, compared to 48% of the cases among unvaccinated people, who remained an easier target for earlier generations of the virus. Overall, the proportion of cases linked to these variants more than doubled between February and June.

The findings add to a growing list of studies that are unraveling why the vaccinated are still so susceptible to infection — and provide a deeper understanding of what we may encounter in the future. Vaccinated people are still much more protected from serious illness, hospitalization and death than unvaccinated people, the study confirmed. “But I worry that as long as the virus is circulating, it will continue to mutate and evolve, which will, in turn, allow it to continue spreading,” he said. The study suggests that new iterations of the virus will likely become even more resistant, over time, “until, eventually, you’re going to see the vaccine not work, or its efficacy will be reduced significantly,” he said. Our vaccines won’t suddenly become useless, he added. So far, it appears to be a gradual process. The resistant variants will slowly dominate over time, he predicted.

The team’s second major finding was more reassuring: People who never develop symptoms during a “breakthrough” infection carry very low levels of virus – a finding that should ease concerns that vaccinated people are unknowingly fueling the pandemic. However, vaccinated people who do have symptoms had the same levels of virus as infected unvaccinated people – so can spread the virus. This confirms a finding first revealed weeks ago by a CDC study in Provincetown, Massachusetts. “You’re essentially as infectious as someone who was unvaccinated,” he said. [..] Vaccination is not to be blamed for the increase in variants with these mutations, Chiu said. Because we naturally produce antibodies in response to exposure and infection, the virus is constantly changing to survive. “The virus is going to evolve to become antibody resistant, whether or not you deploy a vaccine,” he said. “But because we have a vaccine, there’s a way to prevent the virus from spreading and evolving further.”

Read more …

“Fully vaccinated were more likely than unvaccinated persons to be infected by variants carrying mutations associated with decreased antibody neutralization [..] but not by those associated with increased infectivity..”

Antibody-Resistant SARS-CoV-2 Variants In Vaccine Breakthrough Cases (Medrxiv)

Associations between vaccine breakthrough cases and infection by SARS coronavirus 2 (SARS-CoV-2) variants have remained largely unexplored. Here we analyzed SARS-CoV-2 whole-genome sequences and viral loads from 1,373 persons with COVID-19 from the San Francisco Bay Area from February 1 to June 30, 2021, of which 125 (9.1%) were vaccine breakthrough infections. Fully vaccinated were more likely than unvaccinated persons to be infected by variants carrying mutations associated with decreased antibody neutralization (L452R, L452Q, E484K, and/or F490S) (78% versus 48%, p = 1.96e-08), (L452R and/or N501Y) (85% versus 77%, p = 0.092). Differences in viral loads were non-significant between unvaccinated and fully vaccinated persons overall (p = 0.99) and according to lineage (p = 0.09 – 0.78).


Viral loads were significantly higher in symptomatic as compared to asymptomatic vaccine breakthrough cases (p < 0.0001), and symptomatic vaccine breakthrough infections had similar viral loads to unvaccinated infections (p = 0.64). In 5 cases with available longitudinal samples for serologic analyses, vaccine breakthrough infections were found to be associated with low or undetectable neutralizing antibody levels attributable to immunocompromised state or infection by an antibody-resistant lineage. These findings suggest that vaccine breakthrough cases are preferentially caused by circulating antibody-resistant SARS-CoV-2 variants, and that symptomatic breakthrough infections may potentially transmit COVID-19 as efficiently as unvaccinated infections, regardless of the infecting lineage.

Read more …

May 2021

60,000 IU per day.

Impact Of Daily High Dose Oral Vitamin D Therapy On Covid 19 Patients (Nature)

COVID-19 pandemic caused by SARS-CoV-2 virus has created an unprecedented hardship in the recent times1,2. Serious consequences of COVID-19 were attributed to the immune dysregulation leading to the enhanced production of pro inflammatory mediators (cytokine storm). In the absence of a specific vaccine or a treatment, strategies to minimize the effects of COVID-19 have become extremely important. Recent observational studies have reported that the patients with higher levels of serum vitamin D (vit.D) had less severe symptoms and vice versa and have postulated the usefulness of vit.D in prevention and treatment of COVID-19. The beneficial effects of vit.D in COVID-19 were attributed to be mediated through its multiple actions on the immune system.

Vit.D is known to enhance the production of various anti-microbial peptides by the immune cells and vit.D modulates the immune system according to the internal milieu. It reduces the dysregulated production of self-damaging pro-inflammatory cytokines and promotes the expression of anti-inflammatory cytokines by immune cells. The dynamic role of vit.D can be of immense value in the context of immune dysfunction observed in COVID-19 patients with cytokine storm and acute respiratory distress syndrome. Though the protective immuno-modulatory effects of vit.D were explored in many autoimmune diseases and respiratory tract infections, there is a dearth of information from the randomised clinical trials in COVID-19.

Pulse D therapy is a targeted approach to increase the serum vit.D level by using high dose (60,000 IUs) oral supplementation of vit.D daily for a specific period of time determined by the individual’s BMI, initial level of vit.D and the formulation19. This study aims to objectively investigate the role of vit.D and the impact of Pulse D therapy in reducing the inflammatory biomarkers of COVID-19.

Read more …

June 2021

Anyone seen any vit. D campaigns yet?

1 in 4 COVID Patients Hospitalized While Vitamin D Deficient Die – Study (ToI)

Hospitalized COVID-19 patients are far more likely to die or to end up in severe or critical condition if they are vitamin D-deficient, Israeli researchers have found. In a study conducted in a Galilee hospital, 26 percent of vitamin D-deficient coronavirus patients died, while among other patients the figure was at 3%. “This is a very, very significant discrepancy, which represents a big clue that starting the disease with very low vitamin D leads to increased mortality and more severity,” Dr. Amir Bashkin, endocrinologist and part of the research team, told The Times of Israel. For much of the pandemic, many scientists have suggested that the so-called sunshine vitamin may help people fight the disease. The new study represents one of the most compelling pieces of supporting research yet.

“In short, after conducting this study I would say to people that during this pandemic, you certainly want to make sure that you have adequate vitamin D, because if you contract the coronavirus it will help you,” said Dr. Amiel Dror, who led the research. He analyzed data on 1,176 patients admitted to the Galilee Medical Center, 253 of whom had vitamin D levels on record, for a study that has been published online but not yet been peer-reviewed. Half of those with recorded levels were vitamin D-deficient. “We were very interested to see just what a big difference this made, with these patients some 14 times more likely, on average, to end up in severe or critical condition,” said Dror, who, like Bashkin, is a physician at Galilee Medical Center, as well as a researcher at Bar Ilan University.

Numerous studies have been conducted on the association between vitamin D levels and the SARS-CoV-2 infection, and they have produced mixed results. Most of them measured vitamin D levels once patients were already sick, which can complicate interpretation of the results. Israel’s centralized health record-keeping has allowed Bar Ilan researchers to easily access patient vitamin levels that are on record from before infection. This data led to an important study that lauded vitamin D’s prospects for fighting the disease last year, as well as the new study.

“This study is important because of the results, because of the fact that it uses data from before admission, and also because we were careful to isolate all factors like age and diabetes,” Dror said. “We saw that vitamin D deficiency is an independent factor that significantly influences the status of the patient.” Dror added that the fact that such a large proportion of patients were vitamin D-deficient in Israel, despite the abundance of sunshine, highlights the value of people around the world monitoring and potentially boosting their levels.

Read more …

So soon?

Is It Time To Stop Obsessing Over Covid Figures? (DM)

They’re the figures that have ruled our lives for the past 18 months; decided our freedoms; deepened our fears. The Covid dashboard published on the UK Government website has offered the public a window into the state of the UK’s epidemic, displaying daily Covid cases, hospitalisations and deaths, both nationally and regionally, since April 2020. Some people have avoided looking at the figures – published at 4pm every day, including weekends. But a surprising number of us have become secretly addicted to poring over them. Back in January, the dashboard attracted 76 million views in a single day. In more recent months, the dashboard has offered a source of celebration, thanks to the addition of the vaccination tally.

Scientists and politicians alike agree the UK’s Covid dashboard has been a resounding success, allowing the public to draw their own conclusions about the level of threat the virus poses to them. It’s also been a crucial yardstick for how stretched the NHS is, providing exact figures of how many Covid patients are in each hospital around the country. But now, with nearly eight in ten Britons protected against getting seriously ill, thanks to the vaccine, are daily Covid figures still necessary? After all, as Health Secretary Sajid Javid said of the virus earlier this summer: ‘We cannot eliminate it, instead we have to learn to live with it.’ There is growing concern from experts that the endless figures do more harm than good. Some have declared the tally of daily infections ‘completely meaningless’.

‘It shouldn’t really matter how many people are catching the virus – as long as they are protected,’ says Professor Jackie Cassell, public health expert at Brighton and Sussex Medical School. Other scientists have warned of the psychological impact of constant reminders of how many people are still catching Covid. ‘There’s a worry, that in the scramble to get out these daily updates, we’re alarming people disproportionately,’ says Professor Robert Dingwall, sociologist at Nottingham Trent University and former Government scientific adviser. ‘People see spikes in the data, and this is often the cause of great anxiety, which might lead them to limit their daily activities unnecessarily.

‘It stops people being able to acclimatise to a post-vaccine world, which is exactly what the jabs were intended to do. And if you look more widely you’ll find the majority of infections are in the younger, festival-going age groups, and didn’t reach the vulnerable or elderly.’ Others argue that the continued obsession over Covid figures overshadows the record-high demands on the NHS.

Read more …

Journal of Immunology.

Differentiation of Long-Lived SARS-CoV-2-Specific CD8+ T Cells (JoI)

CD8+ T cells can potentiate long-lived immunity against COVID-19. We screened longitudinally-sampled convalescent human donors against SARS-CoV-2 tetramers and identified a participant with an immunodominant response against residues 322 to 311 of nucleocapsid (Nuc322–331), a peptide conserved in all variants of concern reported to date. We conducted 38-parameter cytometry by time of flight on tetramer-identified Nuc322–331–specific CD8+ T cells and on CD4+ and CD8+ T cells recognizing the entire nucleocapsid and spike proteins, and took 32 serological measurements. We discovered a coordination of the Nuc322–331–specific CD8+ T response with both the CD4+ T cell and Ab pillars of adaptive immunity.


Over the approximately six month period of convalescence monitored, we observed a slow and progressive decrease in the activation state and polyfunctionality of Nuc322–331–specific CD8+ T cells, accompanied by an increase in their lymph node–homing and homeostatic proliferation potential. These results suggest that following a typical case of mild COVID-19, SARS-CoV-2–specific CD8+ T cells not only persist but continuously differentiate in a coordinated fashion well into convalescence into a state characteristic of long-lived, self-renewing memory.

Read more …

It reacts to magnets. Welcome to graphene oxide.

Contaminant In 1.63m Moderna Vaccine Doses In Japan Believed To Be Metal (R.)

A contaminant found in a batch of Moderna Inc’s COVID-19 vaccines delivered to Japan is believed to be a metallic particle, Japanese public broadcaster NHK reported, citing sources at the health ministry. Japan on Thursday suspended the use of 1.63 million doses shipped to 863 vaccination centres nationwide, more than a week after the domestic distributor, Takeda Pharmaceutical, received reports of contaminants in some vials. NHK, in a report published late on Thursday, cited ministry sources as saying the particle reacted to magnets and was therefore suspected to be a metal. Moderna has described it as “particulate matter” that did not pose a safety or efficacy issue. A health ministry official said the composition of the contaminant has not been confirmed.

In a statement, Takeda said it asked Moderna to investigate the issue and that it would work with the health ministry to replace the affected vaccine supply. News of the contaminant could provide a fresh setback for Japan’s inoculation drive as it struggles to persuade many – particularly young people — to get vaccinated. On Friday, eight more prefectures entered a state of emergency meaning about 80 per cent of Japan’s population is under coronavirus restrictions. The government reported nearly 25,000 new infections and severe cases at a record 2,000 for Thursday. The ministry has said the suspension of the Moderna batches was a precaution but it prompted several Japanese companies to cancel worker vaccinations and the European drugs regulator to launch an investigation.

Airline ANA Holdings Inc said it had secured more Moderna supplies and would resume inoculations on Saturday after a two-day suspension of the shots. Spanish pharma company Rovi, which bottles Moderna vaccines for markets other than the United States, said the contamination could be due to a manufacturing issue on a production line. A spokesperson said the company could not say anything more while it was investigating. Moderna put the lot in question and two adjacent ones on hold. Another health ministry official said it would take “some time” to confirm how many shots from the contaminated batch had been administered in Japan. Kyodo News reported that at least 176,000 shots have been used based on its own tally of figures reported by municipalities.

Read more …

Misinformation? Really?

Covid Vaccine Doubter Alex Berenson Permanently Banned From Twitter (NYP)

Conservative commentator and vaccine doubter Alex Berenson has reportedly been permanently suspended from Twitter for violating the social media platform’s COVID-19 misinformation rules. Berenson’s account was banned Saturday after “repeated violations” of the rules, a Twitter spokesperson told NBC News in a statement. Berenson, a one-time New York Times reporter, addressed the suspension in a Saturday night post to his Substack page, blaming his removal from Twitter on a recent post where he was critical of the coronavirus vaccine. “It doesn’t stop infection. Or transmission. Don’t think of it as a vaccine,” the tweet read.


“Think of it — at best — as a therapeutic with a limited window of efficacy and terrible side effect profile that must be dosed IN ADVANCE OF ILLNESS.” Berenson, in his Substack post, defended the tweet in question as “entirely accurate.” In a statement to The Post, the Yale-educated writer and novelist blasted Twitter’s decision. “We have reached a dangerous moment. Social media companies that have audiences which dwarf any other are now actively censoring reporters at the behest of governments,” he said. “I will continue to fight to get out the truth and am considering all legal options.”

Read more …

In the wire.

Escapes From Afghanistan, Coordinated From A Home Office In Connecticut (CTM)

Across the hall from his twin daughters’ sun-splashed bedroom, where Mickey Mouse and a menagerie of stuffed animals stand watch from bunk beds, Alex Plitsas typed furiously on his iPhone, relaying encrypted messages to a terrified Afghan family outside the airport at Kabul. The Afghan father had been beaten the previous day by the Taliban, his pregnant wife whipped across the back. Plitsas sent a signal to them to flash to American personnel who would admit them to the airport gate. To the Americans at the airport gate, he relayed a photo of the family, a hollow-eyed selfie. They were just four meters from the gate, an exit from Afghanistan.

Improbably, they had been guided there by Plitsas, an Army veteran and suburban dad standing in stocking feet in a home office in a tidy neighborhood on the other side of the world. He is one of the many players in a crowd-sourcing exercise that, at least for Plitsas, would reach a crescendo Thursday night. An interpreter he helped already had flown to safety. The pregnant woman was under the care of American medics. And a more difficult case, coordinating the rescue of four unaccompanied minors whose plight had been the subject of a CNN story, had found a happy ending. At 11:07 p.m., a text message arrived with a picture of four children and three words: “In the wire.”

The wire was the fence separating the American-controlled portion of Hamid Karzai International Airport from the chaos and carnage of Kabul. On a day when suicide bombers killed 13 U.S. troops and scores of Afghan civilians outside the airport gate, four kids were saved. There were others, their stories certain to unfold over time. All were beneficiaries of a network of military veterans and others with contacts in Afghanistan. They used social media, off-the-shelf encryption communication apps and satellite maps in what’s been dubbed the “Digital Dunkirk,” a nod to the civilian flotilla that evacuated trapped British troops after the fall of France. As midnight approached, the end of a frenetic 36 hours, Plitsas struggled to explain what he felt. It had been a day of frustration, false starts, grievous losses and scattered gains. Finally, he said, “I could throw up right now.”

Killed by US

Read more …

 

 

 

Eric Clapton – This Has Gotta Stop

 

 

 

 

Geese
https://twitter.com/i/status/1431521290922479616

 

 

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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 222021
 
 August 22, 2021  Posted by at 9:19 am Finance Tagged with: , , , , , , ,  76 Responses »


Salvador Dali Elephants 1948

 

Dr Reveals Stunning Truth About Covid Vaccine (RAV)
Simply Put: **** YOU (Denninger)
Moderna Knows Their Vaccine Has Caused Over 300,000 Injuries, Hides Info (DE)
No Test, Just Get Vax Card (RAV)
We Have ‘Leaky Vaccines’ (RAV)
Why Are Regulatory Agencies Hiding COVID Vaccine Safety Signals? (CHD)
There’s An Alternative And Ethical Strategy To The Jab (RAV)
What’s The Best Way To Top Up Our Immunity? (BBC)
Why Testing COVID Immunity is as Important as Vaccination (WA)
Bill Gates Has Major Shares In Pfizer, BioNTech, Is Primary Funder Of MHRA (DE)
Police Say Melbourne Anti-lockdown Protest ‘Most Violent In Nearly 20 Years’ (G.)

 

 

 

 

Karl Denninger, from his comments section:

There are two mechanisms for ADE, both related but distinct. The first is where the antibodies simply are all binding either due to mutational mismatch or simply the nature of the virus in question. This was what derailed attempts to produce both RSV and coronavirus vaccines in the past, and has bedeviled attempts at Dengue as well. The reason the vax makers used only the “S” protein was their BELIEF that this would evade the problem. They had no proof of that and in fact scant animal and in-vitro evidence, but that’s what they went with and then looked for signals in the (short) trials. That part looked good at the time.

But there’s a second, nasty way that ADE happens. As antibody titers wane they may not do so evenly. Mutational mismatch makes this dangerous because the neutralizing portion may wane faster than the binding portion. At some point there’s enough binding antibody remaining that you get ****ed because the neutralizing titer is too low to help, but the binding enhances the infection. This is almost as bad as the first form but it’s very hard to detect without extensive trials over time against the wild virus, and challenge trials in humans are never approved because if you do them and get hit with this you will kill a huge percentage of the subjects, thus you’ll never get ethical approval to do them.

There is ANECDOTAL evidence that this is showing up RIGHT NOW in a small percentage of people who got jabbed. It’s not conclusive but the signal is there, and it’s alarming as Hell. Figuring out WHO is in that bucket and potentially at risk, and whether there is stratification we can predictively use, had better be done — FAST — because there are over 150 million Americans who are potentially at risk of this happening to them.

 

 

Yes, good question:

What happens when the FDA approves Pfizer on Monday? Is that the end for all the other vaccines?

A series of short clips of Robert Malone on Bannon’s show.

Dr Reveals Stunning Truth About Covid Vaccine (RAV)

Read more …

“If it turns out that said person did in fact build a proper immune response then these cases are either OAS or ADE-enhanced disease..”

Simply Put: **** YOU (Denninger)

I believed I might have had Covid-19 in January of 2020, even though I tested negative for antibodies several months later. As it turns out my later antibody testing (negative) was correct and not a defective test; whatever I had in January of 2020 it was not Covid-19. But now having had Covid-19 (almost-certainly Delta too) and knowing damn well it was Covid-19, and surviving it, it is a clearly-distinct infection that I could not possibly mistake for anything else. Having had the infection and now having found IgG antibodies by test I am now known robustly immune to any and all variants; the immunity built from natural infection is conserved across the various epitopes of the virus in all cases because the “N” portion of the virus, which has to remain more-or-less intact for it to be able to be a virus, forms the backbone and bulk of the immune response built following natural infection.

This is not true for any of the vaccines, it was a critical error in what we did and it is why we are now seeing escape. It is not breakthrough folks, it is escape due to mismatch between the coded antibodies and circulating virus and it will both continue and accelerate as the match inexorably continues to degrade between what circulates and the original “wild type” out of Wuhan, which is what’s coded in ALL the jabs and which is long extinct. What’s worse is that if OAS or ADE really come out to play on top of it then if you have not been naturally infected and have been jabbed you are in for a world of **** if you get challenged by the virus in the wild. Even very, very small enhancement percentages from ADE-style reactions can completely overwhelm any sort of treatment possibility at all.

We do not yet know if this is happening as we are deliberately not autopsying and investigating cases where someone was vaccinated, got infected anyway and then rapidly crashed going from being moderately ill to in an ICU or dead within 72 hours. There are multiple reports of this happening already. If this was someone who had a defective immune response then that’s very unfortunate but it does happen. We had damned well better prove that, however, and we’re not going the pathology work to do so. If it turns out that said person did in fact build a proper immune response then these cases are either OAS or ADE-enhanced disease and while this outcome is clearly not universal in those who got jabbed if it is happening even once in a while we had better figure it out right ****ing now or there is going to be a pile of dead bodies this fall and winter and it will be the direct responsibility of those who advocated for and in fact are trying to, in many cases, FORCE mass-jabbing of the population that caused it.

Read more …

They have a special service to do it for them.

Moderna Knows Their Vaccine Has Caused Over 300,000 Injuries, Hides Info (DE)

A leaked report from Moderna’s data collection company reveals that the Moderna Covid-19 vaccines have caused upwards of 300,000 vaccine injuries in a three-month time span – dwarfing the number of vaccine injuries Moderna actually reported to VAERS in that time frame. Moderna is new to the vaccine industry, and they are part of a global effort to introduce new mRNA spike protein replication technology to the field of vaccination. The company is also new to the Vaccine Adverse Events Reporting System (VAERS), a government reporting database that collects incidences of vaccine injury and death. The CDC and the FDA manage VAERS and are well aware of the widespread injuries and deaths caused by these vaccines.


VAERS is required to make these injuries public each and every week, even as the medical establishment continues to yawn and turn the other way. The VAERS database has published hundreds of thousands of vaccine injury reports in 2021, but the CDC and the FDA haven’t done anything significant to address the wide-scale medical malpractice and wrongful death perpetuated by this experimental gene gtherapy. The CDC and the FDA refuse to take the vaccines off the market, and only warn young adults that the vaccines “rarely” cause heart problems, anaphylactic shock, and blood clots. Moderna is legally required to forward all vaccine injury reports directly to VAERS, but they apparently aren’t doing their part and are concealing massive amounts of vaccine injury data.

If this data was shared in a timely and transparent manner, it would further corroborate the numerous, wide-scale injuries already being reported to VAERS. According to the most recent data from VAERS, Moderna has only reported 110,500 adverse events reports from January through March for their SpikeVax COVID-19 vaccine. Most of these injuries occurred in the United States. VAERS also reports another 78,000 reports of vaccine injury from SpikeVax from April through June, with 71,400 of those injuries coming from the United States. Of these 188,500 vaccine injuries reported to VAERS, Moderna themselves only reported a fraction of them. Most of the reports came from patients, physicians, and other health care providers, who documented the adverse events in a medical report filed with VAERS.


Most shocking yet, a data collection service that works for Moderna sent out an internal memo highlighting up to 300,000 adverse events that occurred in a three-month span in 2021. Moderna’s data collection company is called IQVIA. This company helps drug-makers manage clinical trials. IQVIA employs 74,000 people and grossed $ 11 billion in sales last year. The company’s President for Research and Development Solutions sent out a Quarter Two update that was labeled “Confidential – for internal distribution only.” The report includes upwards of 300,000 incidences of vaccine injury reported directly from injured consumers. The memo states that IQVIA applied more than 12 automation’s to drive greater efficiencies and quality “to ensure regulatory compliance for the Moderna pharmacovigilance program.”

Read more …

Homer the pathologist.

No Test, Just Get Vax Card (RAV)

Read more …

And leaky vessels.

We Have ‘Leaky Vaccines’ (RAV)

Read more …

“..more and more people recognize that the premise that vaccine adverse events are “one in a million” is an utter fiction.”

Why Are Regulatory Agencies Hiding COVID Vaccine Safety Signals? (CHD)

A few months before the first COVID-19 vaccines received Emergency Use Authorization (EUA) in late 2020, a global vaccine safety expert cautioned the rushed circumstances made it essential to “get [safety monitoring] right” by “intensively” and “robustly” scrutinizing adverse events following the experimental rollout. As this expert stated, “Deploying any new vaccine based on data from expedited clinical trials into a population without a functioning safety monitoring system in place is reckless and irresponsible given the tools that are available.” Moreover, she added, any investments needed to beef up safety monitoring would be “inexpensive in comparison” to the massive funding allocated to COVID-19 vaccine development and scale-up.

In theory, the U.S. has had a national vaccine safety monitoring system in place since 1990 — the Vaccine Adverse Event Reporting System (VAERS) — intended to function as an “early warning system.” VAERS and its U.S. Food and Drug Administration (FDA) counterpart FAERS (FDA Adverse Event Reporting System) constitute the principal data sources that regulators rely on when pulling drugs or vaccines from the market for safety reasons. Not only has VAERS never lived up to its promise, but there can be little doubt its glaring failures are largely, and malignantly, by design.

For example, when a government-commissioned study highlighted VAERS inadequacies in 2010 — estimating more than 99% of vaccine adverse reactions were going unreported and that one of every 39 doses of vaccine administered was linked to adverse events corroborated in vaccine package inserts — the Centers for Disease Control and Prevention (CDC) simply shut the project down. Now, in less than a year, more than half a million reports of injuries have flooded into VAERS following experimental COVID jabs, including thousands of deaths. Yet a deafening regulatory silence has greeted this record-setting volume of adverse reactions, which accounts for nearly a third of all reports accumulated by VAERS over its entire three-decade lifespan.

Statistical tricks (and conflicts of interest) are not new to the vaccine or pharmaceutical industries, which have used them for decades to successfully mask the “chasm between vaccine rhetoric and reality.” Even when drug warning systems seem to “work,” the lag time between reports of harm and regulatory action is, on average, 20 years. In that light — with FDA speeding toward full approval of the Pfizer injection, Moderna gaining fast-track designation to test other experimental mRNA vaccines in children and adults and CDC benignly maintaining that the results of COVID vaccine safety monitoring are “reassuring” — it is not hard to be discouraged about the agencies’ continued ability to get away with misusing and abusing safety data from VAERS and other sources.

However, the safety narrative started imploding in a big way in late 2019, when the world’s top vaccine experts gathered at the World Health Organization and admitted, almost to a person, that vaccines are sometimes fatal and that safety monitoring is failing to capture the dangers. COVID may have provided these worried experts with a temporary and convenient reprieve, but more and more people recognize that the premise that vaccine adverse events are “one in a million” is an utter fiction. With injuries from COVID vaccines occurring on an unprecedented scale — and credible doctors and scientists issuing urgent warnings about short-term and longer-term damage — it may become increasingly difficult for the vaccine establishment to shove its problems under the statistical carpet.

Read more …

IVM.

There’s An Alternative And Ethical Strategy To The Jab (RAV)

Read more …

The BBC can’t say “Stop Mass Vaccination”. So they try a way around it. And get lost.

What’s The Best Way To Top Up Our Immunity? (BBC)

There are marked differences in your immune system after a natural infection with coronavirus and after vaccination. Which is better? Even asking the question bordered on heresy a year ago, when catching Covid for the first time could be deadly, especially for the elderly or people already in poor health. Now, we’re no longer starting with zero immunity as the overwhelming majority of people have either been vaccinated or have already caught the virus. It is now a serious question that has implications for whether children should ever be vaccinated. And whether we use the virus or booster shots to top up immunity in adults. Both have become contentious issues. “We could be digging ourselves into a hole, for a very long time, where we think we can only keep Covid away by boosting every year,” Prof Eleanor Riley, an immunologist from the University of Edinburgh, told me.

Prof Adam Finn, a government vaccine adviser, said over-vaccinating people, when other parts of the world had none, was “a bit insane, it’s not just inequitable, it’s stupid”. We need to understand a little bit about the key building blocks of both our immune system and the virus it is attacking. The power-couple of the immune system that clears the body of infection are antibodies and T-cells. Antibodies stick to the surface of the virus and mark it for destruction. T-cells can spot which of our own cells have been hijacked by the virus and destroy them. For all the trouble the virus has caused, it is spectacularly simple. It has the famous spike protein, which is the key it uses to unlock the doorway into our body’s cells. And 28 other proteins that it needs to hijack our cells and make thousands of copies of itself. (For comparison it takes about 20,000 proteins to run the human body).

[..] There is clear evidence that adults who have not had any vaccine dose will have stronger immune defences if they do get vaccinated, even if they have caught Covid before. But there are two big questions: 1/ do vaccinated adults need to be boosted, or is exposure to the virus enough? 2/ do children need vaccinating at all, or does a lifetime of encountering build a good immune defence? The idea of regularly topping up immunity throughout life is not radical in other infections, such as RSV (respiratory syncytial virus) or the four other coronaviruses that infect people and cause common cold symptoms. Each time you’re exposed, the immune system gets a little bit stronger, and this continues until old age, when the immune system starts to fail and the infections become a problem again.

“This isn’t proven, but it could be a lot cheaper and simpler to let that happen than spend the whole time immunising people,” said Prof Finn, who warns we could end up “locked into a cycle of boosting” without seeing if it was necessary. However, he said the argument in children had “already been won” as “40-50% have already been infected and most weren’t ill or particularly ill”. There are counter-arguments. Prof Riley points to long-Covid in children, and Prof Openshaw to nervousness around the long-term effects of a virus that can affect many of the body’s organs. But Prof Riley said there was potential in using vaccines to “take the edge off” Covid, followed by infection, to broaden the immune response.

Read more …

“..we’re not testing antibodies, because they’re worried that a substantial number of people are going to find out that the vaccine didn’t work for them.” – Dr. Holman Noorchashm”

Why Testing COVID Immunity is as Important as Vaccination (WA)

Antibody testing is the gold standard for determining immunity, says immunologist and physician, Dr. Hooman Norchashm. Yet, the CDC and FDA are actively deterring people from testing their immunity. Why? Dr. Noorchashm suggests that the answer to this could lie partly in the phenomena of vaccine spoilage. “It’s a medicine, just like any other medicine. It’s got a failure rate…, and we should accept that.” “They’re worried that a substantial number of people are not going to find out that the vaccine didn’t work for them.” Currently, the delta variant of COVID-19 is being used by the Government to explain the high occurrence of breakthrough infections. However, Dr. Noorchashm suggests, vaccine spoilage is a more likely explanation. While a strong believer in vaccination, Dr. Noorchashm argues that determining individual immunity rather than blanket vaccination is the ‘Achilles heel’ to overcoming COVID-19.

Read more …

Owning shares is one thing, but funding the goverment?!

Bill Gates Has Major Shares In Pfizer, BioNTech, Is Primary Funder Of MHRA (DE)

An investigation has revealed that the Bill & Melinda Gates Foundation are the primary funders of the UK’s Medicine & Healthcare products Regulatory Agency, and that the Foundation also owns major shares in both Pfizer and BioNTech. The Medicine & Healthcare products Regulatory Agency (MHRA) extended the emergency authorisation of the Pfizer / BioNTech mRNA jab in the UK to allow it to be given to children between the ages of 12 – 15 on the 4th June 2021. At the time, the Chief Executive of the MHRA, Dr June Raine said the MHRA had “carefully reviewed clinical trial data in children aged 12 to 15 years and have concluded that the Pfizer vaccine is safe and effective in this age group and that the benefits outweigh any risk”.

We are left wondering if Dr June Raine and the MHRA have even read the results of the extremely short and small study. If they have then they would have seen that 86% of children in the study suffered an adverse reaction ranging from mild to extremely serious. Just 1,127 children took part of the trial, however only 1,097 children completed the trial, with 30 of them not participating after being given the first dose of the Pfizer jab. The results do not state why the 30 children did not go on to complete the trial. The information is publicly available and contained within an FDA fact sheet which can be viewed here (see page 25, table 5 on-wards).

There was never any doubt that the MHRA would give emergency authorisation for the Pfizer / BioNTech vaccine to be used in children when you consider that a certain Mr Bill Gates owns shares in both Pfizer and BioNTech and is the primary funder of the MHRA. The Bill & Melinda Gates Foundation bought shares in Pfizer back in 2002, and back in September 2020 Bill Gates ensured the value of his shares went up by announcing to the mainstream media in a CNBC interview that he viewed the Pfizer jab as the leader in the Covid-19 vaccine race.

“The only vaccine that, if everything went perfectly, might seek the emergency use license by the end of October, would be Pfizer.” The Bill & Melinda Gates Foundation also “coincidentally” bought $55 million worth of shares in BioNTech in September 2019, just before the alleged Covid-19 pandemic struck. The MHRA received a grant from the Bill & Melinda Gates Foundation in 2017 to the tune of £980,000 for a “collaboration” with the foundation. However, a Freedom of Information request which the MHRA responded to in May 2021 revealed that the current level of grant funding received from the Gates Foundation amounts to $3 million and covers “a number of projects”.

Read more …

“They don’t care about their freedom, they’re just looking for trouble…”

Police Say Melbourne Anti-lockdown Protest ‘Most Violent In Nearly 20 Years’ (G.)

An anti-lockdown protest held in Melbourne on Saturday was one of the most violent the city has seen in 20 years, Victoria’s top police officer says. Chief commissioner Shane Patton said his officers had no choice but to use non-lethal weapons to defend themselves from an angry mob that came armed and appeared intent on attacking them. It is the first time during a lockdown protest, police have used such tactics that included rounds of pepper spray projectiles and canisters. At least nine officers ended up in hospital after being pelted with projectiles, punched and kicked by some members of a 4,000 strong crowd who turned out to protest the city’s Covid-19 lockdown. The mostly unmasked protesters let off flares, yelled slogans and blasted music as they moved through the CBD.

More than 700 extra Victorian police officers were deployed to contain the lockdown protest. Patton said he was nothing short of disgusted with the conduct of some in the crowd. “What we saw yesterday … was probably one of the most violent protests we’ve seen in nearly 20 years,” he told reporters on Sunday. More than 200 people were arrested including some on remand for previous crimes. At least 19 will be taken to court rather than issued with fines in excess of $5,000. Two people will face assault charges. He said many in the crowd came armed with projectiles that were hurled at police and it was clear they were there not to protest for personal freedom but to “confront and attack”.

[..] “I just hope it doesn’t result in the mass spread of Covid-19. The risk that those people have now posed to the rest of the community, by their conduct yesterday, was disgraceful and selfish.” Patton also revealed 48 people have been fined almost $5,500 each over an illegal engagement party in Caulfield North, including the future bride and groom. That number is expected to rise with eight other attendees yet to be interviewed. The rest of the people at that party were children. They’ve been warned and won’t receive fines..

Read more …

 

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Golden oldie.

 

 

 

 

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Jul 242021
 


René Magritte Le Mal du Pays (Homesickness) 1940

 

Vast Majority Of Unvaccinated Americans Say They Won’t Be Getting Jabs (RT)
Alabama Governor Declares ‘It’s Time To Blame The Unvaccinated For COVID’ (SN)
Israel Finds Pfizer Jab Only 39% Effective At Stopping Delta Variant (ZH)
Vaxxed Employees Of CA City Must Wear Stickers To Work Without Masks (RT)
EU Watchdog Approves Moderna Jab For Ages 12 And Up (Y!)
French Hospital Goes On Indefinite Strike To Protest Vaccination Mandate (RT)
Big Fail (Jim Kunstler)
CDC Quietly Deletes 6,000 COVID Vaccine Deaths From Its Website
Biden DOJ Drops Investigations Into Nursing Home Covid-19 Deaths (RT)
Greece Invokes Constitution to Impose Compulsory Vaccination (GR)
Science vs. Religion As Greek Priests Lead The Anti-vax Movement (Pol.eu)
Hugely Experienced Nfl Coach Leaves Job After Refusing To Take Jab (RT)
Cleveland Indians Change Name To The “Guardians” (ZH)

 

 

 

 

Verkerk

 

 

Israel severe hospitalized patients yesterday 5, all vaxxed

 

 

Fleming VAERS

 

 

So far it’s about half?!

Vast Majority Of Unvaccinated Americans Say They Won’t Be Getting Jabs (RT)

The Biden administration faces an uphill battle to meet its goals for Covid-19 vaccinations, as a newly released poll shows that 80% of American adults who haven’t yet recived the jab have no intention of doing so. The results of the Associated Press-NORC poll, which was released on Friday, revealed that 45% of unvaccinated respondents said they “definitely” wouldn’t be getting inoculated against the virus, with 35% indicating they “probably” wouldn’t do so. Only 19% of those who hadn’t been vaccinated intended to get the shots, and just 3% consider those plans definite. The responses suggest there is little room for growth in US vaccination rates, because 67% of participants had already received the jab, and only 1% of overall respondents said they would definitely get inoculated.

Just 5% said they would probably get vaccinated. Other unvaccinated Americans don’t plan to get jabbed, meaning around 73% is the apparent upside for the nation’s adult vaccination rate. President Joe Biden had aimed to have 70% of US adults vaccinated with at least their first dose by July 4, but fell short, at 67%. Nearly three weeks beyond his target date, some 69% of adults have received a Covid-19 shot, according to CDC data. Nearly 60% of adults are fully vaccinated, and the rate is 49% for the overall population. Perhaps more troubling for vaccine proponents is the declining rate of new vaccinations. After the rollout hit a one-day record of 4.6 million doses delivered on April 10, the daily pace has slowed to around 500,000 in recent weeks.

In Alabama, which ranks last in the nation, with just 34% of its population fully vaccinated, and only a trickle of residents rolling up their sleeves to get the shots, Governor Kay Ivey became so frustrated on Thursday that she said it’s “time to blame the unvaccinated folks” for rising Covid-19 infections. While 83% of Democrat adults have been vaccinated, according to the Associated Press-NORC poll, just 51% of Republicans have been. And Republicans are more skeptical that the vaccines will be effective against the highly infectious Delta variant of Covid-19, which has driven the country’s recent jump in new cases. The poll found that 58% of Republicans expect the vaccines to work well against new variants, while 81% of Democrats expressed confidence. Among unvaccinated Americans, 64% don’t trust the shots to prevent the spread of Delta.

Read more …

Let’s turn that around.

Alabama Governor Declares ‘It’s Time To Blame The Unvaccinated For COVID’ (SN)

The governor of Alabama stated Thursday that it is “time to start blaming the unvaccinated folks” for rising cases of COVID in the state, adding that “These folks are choosing a horrible lifestyle of self-inflicted pain.” Governor Kay Ivey made the comments during a press briefing, declaring “Let’s be crystal clear about this issue. The new cases of Covid are because of unvaccinated folks.” “Almost 100% of the new hospitalizations are with unvaccinated folks. And the deaths are certainly occurring with the unvaccinated folks,” Ivey added. She continued, “We got to get folks to take the shot. The vaccine is the greatest weapon we have to fight COVID. There is no question about that the data proves it. I’ve taken the shot back in December, both shots. It’s just the thing to do. The unvaccinated is who we need to focus on.”


“Folks are supposed to have common sense. But it’s time to start blaming the unvaccinated folks, not the regular folks. It’s the unvaccinated folks that are letting us down,” Ivey further proclaimed. She added, “I’ve done all I know how to do. I can encourage you to do something, but I can’t make you take care of yourself.”

Read more …

“..perhaps as low as 30%..”

Israel Finds Pfizer Jab Only 39% Effective At Stopping Delta Variant (ZH)

Over the past month, Israel, the world’s most heavily vaccinated country (with leading mRNA jabs, no less) has seen the number of positive COVID tests has risen by more than 30x as the number of active infections in the country has surpassed 10K. Meanwhile, the Israeli Health Ministry, which has previously estimated the true efficacy of the Pfizer jab against the delta variant at only 64% (while still more than 90% effective at preventing serious illness and death), just released new data purporting to show that while the Pfizer jab is still 88% effective at preventing serious illness, it’s only 39% effective at preventing infection with delta.


Alex Berenson, a former NYT journalist who has often reported on scientific findings that don’t support the official narrative on masks and vaccines, shared the findings in a tweet, and speculated that the true efficacy in offering protection against the Delta variant might be even lower – perhaps as low as 30%. [..] The Israeli numbers are much lower than other recent studies, including one study recently published in the New England Journal of Medicine, which found that two doses offers 88% protection against the Delta variant causing symptomatic disease, while offering 94% protection against the alpha variant.

Read more …

Nice that they didn’t make them yellow. Or star-shaped.

Vaxxed Employees Of CA City Must Wear Stickers To Work Without Masks (RT)

A California city has ordered its employees to wear a sticker identifying their fully vaccinated status if they choose to come to work without a mask, amid a growing global trend of distinguishing the vaxxed from the uninjected. The city of Montclair, located in California’s Pomona Valley, has decreed that starting next week, employees who want to work without a mask will have to wear a sticker showing they’ve had a Covid shot. According to City Manager Edward Starr, the policy is designed to ensure that Montclair is in compliance with a June directive issued by California’s workplace safety board, which instructs all vaccinated workers in the state to submit evidence or sign a pledge they have been vaccinated if they choose to abstain from wearing a face mask.

In response to recommendations from the Centers for Disease Control and Prevention, California issued new guidance in April stating that fully vaccinated individuals could forgo masks in most settings. The city official claimed that California’s Department of Public Health was encouraging the use of stickers on employee ID badges “to demonstrate they have been fully vaccinated.” He dismissed the notion that the labels could be seen as potentially problematic, and stressed that the policy would help the city to fulfill state and federal guidelines. Starr also pointed to the fact that the CDC offers a selection of printable stickers that workplaces can provide to employees who get vaccinated. However, it doesn’t appear that the public health authority has issued guidance recommending stickers be used as forms of identification.

[..] In Switzerland, the head of the country’s centrist Green Liberal Party advocated for people working in hospitals and other healthcare facilities to wear identification showing their vaccination status, purportedly as a way to reduce the possibility of transmission in high-risk settings. The use of Star of David badges or other labels has become popular among protesters who object to global vaccine rollouts and other Covid measures. Such demonstrators have been routinely criticized and shamed by the media for their allegedly extremist views about worldwide vaccination drives, many of them now openly coercive.

Read more …

This cannot be based on science. There are no data for mid or long term. This is politics plain and simple.

EU Watchdog Approves Moderna Jab For Ages 12 And Up (Y!)

The European medicines watchdog on Friday approved the use of Moderna’s coronavirus vaccine for children aged 12 to 17, making it the second jab for adolescents for use on the continent. “The use of the Spikevax vaccine in children from 12 to 17 years of age will be the same as in people aged 18 and above,” the European Medicines Agency (EMA) said, using the vaccine’s brand name. The vaccine will be given in two injections, each four weeks apart. The decision by the Amsterdam-based agency follows the approval of the first vaccine for European youngsters, by Pfizer/BioNTech in May. The effects of the jab have been studied among 3,732 children aged 12 to 17 years, the EMA said. “The study showed that Spikevax produced a comparable antibody response in 12- to 17-year-olds to that seen in young adults aged 18 to 25 years,” it said.

The Moderna jab employs the same mRNA technology as Pfizer/BioNTech, using genetic material to deliver instructions to human cells to create coronavirus spike proteins. It thereby trains an immune response without exposing the host to a real infection. The EMA said there were common side effects in children similar to those in adults. This included pain and swelling at the injection site, tiredness, headache, muscle and joint pain, enlarged lymph nodes, chills, nausea, vomiting and fever. “These effects are usually mild or moderate and improve within a few days from the vaccination,” the EMA said. But it noted that due to the “limited number of children and adolescents included in the study, the trial could not have detected new uncommon side effects”.

Nor could it estimate the risk of known side effects such as myocarditis (inflammation of the heart muscle) and pericarditis (inflammation of the membrane around the heart). “However, the overall safety profile of Spikevax determined in adults was confirmed in the adolescent study,” it said. “The benefits of Spikevax in children aged 12 to 17 outweigh the risks, in particular in those with conditions that increase the risk of severe Covid-19.”

Read more …

Macron will remember today’s protests.

French Hospital Goes On Indefinite Strike To Protest Vaccination Mandate (RT)

The staff of the hospital in Montelimar, in the French department of Drome, have gone on indefinite strike to protest the new rules demanding they take a vaccine against Covid-19 by mid-September or face losing their jobs. The strike against “forced vaccination” was announced on Thursday by the CGT-GHPP trade union, and affects some 200 doctors and 1,500 nurses in the southeastern French city. Hundreds of them gathered outside the hospital on Friday, denouncing lockdowns and vaccine mandates and chanting “liberté!” (freedom). The French legislature is finalizing the proposal that would require all medical professionals in contact with the vulnerable to be fully vaccinated by September 15, or else lose their salaries and even their jobs.


“We are against mandatory vaccination and vaccine coercion,” Elsa Ruillere, local union representative, told Sputnik France. “There is no choice between tests or vaccination: vaccination is compulsory. No, we don’t agree. We want to have the choice like the rest of the world and we do not want compulsory vaccination.” Ruillere says her union supports “free and informed consent” and is not against vaccination on principle but is against coercion. Some of the medical workers said they are waiting for the French-made Sanofi-GSK vaccine, promised for December.

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“..they will deny that such deaths are related to the ‘vax’ given the time distance from the injection.”

Big Fail (Jim Kunstler)

Poor Mr. Trump was hustled into the “Warp Speed” cover story for these shenanigans — which perhaps explains why he never looked entirely comfortable onstage with Dr. Fauci and the rest of the White House “team.” Meanwhile news about the efficacy of the vaccines, and especially any adverse reactions to the vaccines, has been very carefully managed by the government, the captive news media, and the — let’s just say it — the evil social media including Facebook, Twitter, and Google’s YouTube. How much are they squelching the actual numbers of deaths directly related to the vaccines? A savvy correspondent with a medical license writes:

“…the rate of reporting [adverse reactions] to the VAERS system in the US and Europe is very poor: somewhere between 1 and ten percent of actual events being reported. This obviously means that the actual death rate is likely much higher. So, I would not be surprised if the real number of ‘vax’ induced deaths in the US is in the range of 100,000 or more, much more. This is very reasonable when you take into account the shockingly frequent effects involving myocardial inflammation and blood clotting. Both of these pathologic processes logically stem from inflammation stimulated by massive production of the S1 spike protein by the injected mRNA.

The S1 spike protein, as you know, is the inflammation-inducing toxin in Covid infections. There was a major fuck-up by focusing on stimulating the production of S1; they, the PTB researchers, thought that the S1 protein was just a marker for SARs-COV, not the pathogenic toxin. In my opinion, most of the deaths from the mRNA ‘vax’ are going to take much longer via long-term inflammatory damage to the vascular system (including heart tissue, brain blood vessels, etc.). Of course, they will deny that such deaths are related to the ‘vax’ given the time distance from the injection. Too many people, making too much money from the mRNA shot….”

This is where things stand at the apogee of summer. Every day we are learning more about the spike protein time-bombs the vaxed population is walking around with in their veins. And now its coming clear why science has been made such a fetish of lately: because science has failed spectacularly, which is an even greater tragedy because when this stupendous calamity is over, what’s left of the civilized world will, by default, turn to superstition as its logical replacement.

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“..a strange thing happened..”

CDC Quietly Deletes 6,000 COVID Vaccine Deaths From Its Website

As reported earlier the CDC-linked VAERS website released its weekly numbers last Friday. The website has now recorded 11,140 reported deaths from the COVID vaccine in the United States. This is up from 9,125 reported deaths from the COVID-19 vaccinations total from last week. The number of deaths linked to vaccines this year has absolutely skyrocketed. According to the CDC’s own data. On Wednesday the CDC posted on its own website that there were 12,313 reported deaths from the COVID Vaccine since December. This number would track with the VAERS website number.

But then a strange thing happened. After the CDC posted this number they went back hours later and switched it to 6,079 reported deaths in the US from the COVID Vaccine. Infowars posted video of screengrabs from the CDC website on Wednesday. The CDC deleted 6,000 vaccine deaths from its website in 6 hours. What gives?

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“..their review of data about the deaths was stopped because it was too “time-consuming.”

Biden DOJ Drops Investigations Into Nursing Home Covid-19 Deaths (RT)

The Biden administration has decided not to investigate the Democrat governors of Michigan, Pennsylvania, and New York over claims their Covid-19 policies led to the deaths of thousands of vulnerable people in nursing homes. Deputy Assistant Attorney General Joe Gaeta informed House Republicans on Friday that the Justice Department had decided not to open an investigation into any public nursing facilities in the three states “at this time.”= In August 2020, the Trump administration requested data about nursing home deaths from Michigan, Pennsylvania, New Jersey, and New York – states that had policies ordering nursing homes to take in Covid-19 patients.

“We have reviewed the information you provided along with additional information available to the Department. Based on that review, we have decided not to open a [civil rights] investigation of any public nursing facility within Michigan at this time,” said the letter sent to Governor Gretchen Whitmer by Steven Rosenbaum, chief of the litigation section in the DOJ’s civil rights division, on Thursday. The same letter was sent to Tom Wolf of Pennsylvania. Whitmer’s April 2020 executive order required nursing homes to accept Covid-19 patients discharged from hospitals and place them in dedicated isolation units. Melissa Samuel, president of the Health Care Association of Michigan, claims the order was never fully implemented, however.

Wolf’s former health secretary, Rachel Levine – who withdrew her own mother from a nursing home even as overseeing the state policy of mandating homes take in Covid-19 patients – has since been confirmed as the first transgender assistant secretary at President Joe Biden’s Department of Health. The DOJ apparently sent the same letter to New York’s Andrew Cuomo. The only remaining governor who could be under investigation at this point is New Jersey’s Phil Murphy. Michigan’s official figures say that 87% of Covid-19 deaths were among people aged 60 and older, and about a third of the state’s total deaths were “linked to” long-term care facilities, amounting to 5,754 residents and staff. However, investigative journalist Charlie LeDuff claims the numbers might have been undercounted by as much as 100%, and that officials at the Michigan Department of Health and Human Services told him their review of data about the deaths was stopped because it was too “time-consuming.”

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Any lawyers left here?

Greece Invokes Constitution to Impose Compulsory Vaccination (GR)

Greece’s Prime Minister Kyriakos Mitsotakis defended compulsory vaccination for some groups in the country by referencing Article 25 of the Greek constitution on Friday. Mitsotakis spoke with the President of the Hellenic Republic Katerina Sakellaropoulou in front of the media about the coronavirus and the rate of vaccination in Greece. Both high-ranking politicians appeared to be in agreement about the need for a majority of the Greek populace to become inoculated. Mitsotakis highlighted that the Delta variant of the virus, which is much more transmissible than the original virus, means that it is more important than ever before for all Greeks who can get vaccinated to do so.

“The state has the right to demand the all citizens to pay their debt of social and national solidarity back,” noted Mitsotakis, referring to Article 25, Paragraph 4 of the Constitution. He then claimed that this part of Greek law is more relevant today than ever. “This is what we demand from our fellow citizens. The debt of social and national solidarity. The battle of our generation is tackling the pandemic. We will beat it. “But we must win it by taking all the responsibility of their citizens towards themselves, their families and society as a whole,” Mitsotakis said, arguing that people have a moral duty to become vaccinated.

[..] President Sakellaropoulou also spoke at length on Friday, and encouraged those who have yet to get inoculated to do so. She agreed with Mitsotakis that it was constitutional for the Greek government to coerce people who work in sectors where they endanger others to get inoculated. “The Constitution does not recognize anyone’s right, in the context of his own freedom, to endanger the life and health of his fellow human beings. This is because the rights outlined in the Constitution are granted not only because we are individuals with human value, which of course applies, but also because we are part of society as a whole,” the former Supreme Court justice explained. “And as part of society as a whole, precisely because we have the obligation of solidarity, that is, to take care of public health and the lives of our fellow human beings, we are obliged to accept restrictions on our own rights,” Sakellaropoulou added.

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“God does not force us to follow him, unlike those supporting vaccination.”

Science vs. Religion As Greek Priests Lead The Anti-vax Movement (Pol.eu)

Anti-vaxxers and churchgoers are out in force on a warm July Sunday morning in central Athens — and, for the most part, they are the same people. For the Greek authorities, one of the major sources of opposition to lockdowns, mask-wearing, social distancing and vaccination is influential Greek clerics and the power they wield from the pulpit. “The church authorities refuse to police the churchgoers, respecting the personality of the faithful,” reads a sign at the main entrance of Saint Nicholas’ Church in the capital. Inside the packed church, you could count the number of people wearing a face mask on the fingers of one hand. The priest, Vasileios Voloudakis, used his sermon to lash out against the government, doctors and church leadership.

“They want to treat the churches the same way they do gyms, but we believe that in here we are in heaven,” he told the congregation. “Scientists cannot explain some things, so they prefer to hush it up.” Voloudakis is one of the most prominent critics of coronavirus restrictions and vaccines in the Greek Orthodox Church and has even said that those who “alas” have the vaccine “will bitterly regret it.” He has a lot of supporters. “We stand up to protect human rights, the same rights that have been ratified by Christianity,” said Maria, a middle-aged woman attending the service with her husband who did not want to give her last name. “God does not force us to follow him, unlike those supporting vaccination.” “I fully trust my priest,” said Maria Papadopoulou, shortly after receiving Holy Communion.

“I don’t want to have an experimental vaccine. My parents are fully vaccinated, but I didn’t force them to do so; why should they do this to me? “They want to divide us and we shouldn’t allow that. Everyone should be free to do whatever they think is good for their health.” The church leadership officially supports vaccination. The head of the Greek Orthodox Church, Archbishop Ieronymos, spent several days in intensive care with coronavirus last November. A month later, he said: “I would be the first to go and get vaccinated if I had not been sick.” The archbishop announced he had received the vaccine on May 12. However, several influential archbishops and clerics repeatedly tell the flock not to get vaccinated, while some refuse to let people into church if they are wearing a mask or have had the jab.

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Some people pay big.

Hugely Experienced Nfl Coach Leaves Job After Refusing To Take Jab (RT)

Minnesota Vikings assistant Rick Dennison has reportedly left the team after refusing to take a vaccine for Covid-19, potenitally representing the first exit of its kind in the sport since jabs were made a requirement for staff.
In a ruling announced this summer, NFL bosses have ordered all staff at the designated ‘Tier 1′ elite coaching level of the sport to provide a valid religious or medical reason for not being vaccinated. 63-year-old Dennison, who won the Super Bowl three times as a coach with the Denver Broncos, where he also spent his entire playing career, has ended his two-season spell as the Vikings’ offensive line coach and run game co-ordinator because he chose not to take the treatment, according to ESPN sources. Coaches who lose top-tier status cannot be on the field, in meeting rooms or have direct interactions with players, leading to assistant offensive line coach Phil Rauscher filling Dennison’s position, the report claimed.

[..] Fans were divided as the report spread that Dennison had become the first NFL coach to lose their job after refusing to be vaccinated, with many rowing about whether the measure would be a breach of rights and others claiming the veteran had been free to make a choice the team may not have agreed with. “They didn’t fire him due to medical status,” argued one, speaking among an apparent majority of critics who showed little sympathy towards Dennison. “They are firing him because he can’t do the job due to a personal choice, which he has every right to make. “If he doesn’t want to get vaxed, based on the NFL guidelines, he could jeopardize the team, so they move on.”

Another echoed: “He wasn’t terminated. He chose to quit because he refused to follow mandatory NFL protocols outlined for the safety of players and staff during a global deadly pandemic. We cannot move on from this unless we contain it.” A self-described US Navy veteran retorted: “Society has lost their collective mind over a virus that kills far less than one percent [of people]. “Can’t watch any sport without being bombarded with woke bullsh*t and now this is the step towards corporate totalitarianism that will end my and many others’ NFL fandom.” A media host said: “Imagine throwing away the bag [money] over two shots that take 10 minutes of your time, protect yourself and others and set a good example.”

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I continue to find it strange that the cancel culture thinks that if they try to erase history, that somehow makes things better. What these teams should do is wear their names with pride, by reaching out to native communities, set up support projects, get involved in business, invest in the future of the children, so that the communities in turn feel pride in being represented by the teams.

Cleveland Indians Change Name To The “Guardians” (ZH)

After years of protests from Native American groups and some fans, Cleveland’s Major League Baseball team has officially changed its name after more than 100 years. According to the Major League Baseball (MLB) website, the team announced Friday morning that Cleveland Indians is no more, and the new name, drum roll… is Cleveland “Guardians.” Cleveland first announced last summer that it would begin having conversations with local community members and Native American groups about the possibility of a name change. The organization announced in December that it was beginning a search for a new nickname.


More than 4,000 fans signed up to be part of the conversation, and over 40,000 fans were surveyed, including 140 hours of interviews with fans, staff and community members. The organization determined that the name should connect to the city of Cleveland, preserve the team’s rich baseball history and unite the community. -MLB This follows the Washington Redskins, who changed their name “Washington Football Team” in the summer of 2020. Both of these teams have ditched Native American terminology because in today’s “woke” culture it’s considered racist.

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