Sep 202021
 
 September 20, 2021  Posted by at 4:37 pm Finance Tagged with: , , , ,  22 Responses »


Thomas Cole The Course of Empire – Destruction 1836

 

 

Politicians and so-called experts across the planet increasingly want to force you to get inoculated with a substance that takes away at least twice the lives it saves, across all age groups. It doesn’t matter anymore if this is intentional or just sheer incompetence, we have no time left to discuss that. We’re killing people. Millions of people. Our loved ones, family, friends, and neighbors. It has to stop. Now. We have gone mad. Maybe Steve Kirsch’s access to the FDA can help.

And when Steve says the vaccines killed 200,000 Americans so far already, and permanently disabled 300,000, remember that this is just the tip of the iceberg: many if not most of the effects will only show up later. And then Pfizer today claims that their stuff is safe for kids 5 years old and up. Who are 99.9996% safe if they get infected, due to their immune system, which also gets killed by the vaccines.

And I would have some questions about the people “saved” by the vaccines. Because a recent Israel study suggests only that “a booster can strengthen protection for a few weeks in older adults.” A few weeks? And we call that a vaccine now?

Stop it. We have gone mad.

 

 

The US Food and Drug Administration (FDA) may have opened Pandora’s box on Covid. Not sure why, but for some reason they invited Steve Kirsch to a virtual meeting of the FDA Vaccine Advisory Committee, aka the Vaccines and Related Biological Products Advisory Committee, on September 17. The same committee that decided not to recommend booster shots for all Americans.

Kirsch is an entrepreneur who started several companies in the computing field, for instance Infoseek. He’s worth a few hundred million dollars. He also set up treatearly.org, which promotes early treatment for Covid. Didn’t anyone at the FDA know that in March, Kirsch offered $1 million to anyone who could prove fluvoxamine was not what saved 77 people in a trial, and identify what did?

Or that he offered $10,000 for a one hour debate on Covid? Or did someone at the FDA open Pandora’s box on purpose? And I know, officially the committee is independent from the FDA, and I don’t know what role Kirsch played in the 16-2 decision against boosters, but there are obviously some people there who feel uncomfortable with the current vaccine-at-all-costs approach. I wouldn’t rule out it was done on purpose. But the info is out there now, and YouTube and Twitter are not going to ban or shadowban the FDA.

Wikipedia about Kirsch is fun:

In April 2020, he started the COVID-19 Early Treatment Fund (CETF) with a personal donation of $1M in order to fund COVID-19 drug repurposing research. In May 2021, Kirsch posted an article online making an unfounded claim that COVID-19 vaccines affect fertility, while also underplaying the vaccines’ ability to prevent illness and death. The following month, Kirsch appeared in a YouTube video posted with Bret Weinstein and Robert W. Malone to discuss COVID-19 vaccines. In the video, Kirsch makes several false claims, including that spike proteins used in COVID-19 vaccines are “very dangerous”.

And he’s banned from YouTube and Twitter:

 

 

Here’s part of his presentation to the committee. The vaccines kill twice as many people as they save.

 

 

I summarized part of his latest slide deck here:

 

What You Need To Know About Covid Vaccine Safety

Censorship required The way to fight truth is using misinformation, intimidation, mandates, and censorship. Our government is ignoring early treatments and tells everyone that early treatment don’t work. They demonize the key treatment used by India to be COVID-free. Their agenda is to push the vaccine, not to cure COVID. Social media companies will censor, demonetize, and/or ban you for telling the truth. If you are a doctor, you can have your license revoked if you say the vaccines are unsafe.

COVID vaccines kill more people than they save for all age groups. On average, in the US, COVID vaccines kill 2 people for every person they save over a 6 month period.

To date
200K Killed
300K permanently disabled

Here’s how we compute the 2:1 ratio that shows the vaccines are nonsensical.

V:C defined

V:C is the ratio of the the number of vaccine-caused deaths (V) relative to the projected number of COVID deaths (C) that could be saved by the vaccine over a 6 month period. A number like 2:1 means we kill 2 people for every COVID death we save. That’s bad. For a COVID vaccine to be viable, you’re looking for V:C of 1:x where x > 100, i.e., you want the risk to be very small compared to the benefit. If you are saving the lives of >100,000 people, you don’t want to have to kill >1,000 people to have to do that. That would completely unacceptable in a civilized society and would be unprecedented in modern times, especially when we have early treatments that work with over 99% risk reduction that don’t have any safety issues.

V:C varies by place, time, age. V:C depends on the vaccine type, the rate of COVID deaths in your community at a particular time, and your age. For this presentation, we’ll compute this as a country-wide average for the US.

Determining V.
In general, the three vaccines in the US work through a very similar process. The vaccines have an estimated death rate of close to 1 death for every 1,000 people who are vaxed. Here, we calculate a deaths per million doses for each age range (using VAERS). For risk/reward assessments done by age, this gives the most precise guidance.

Determining C.
We use COVID mortality data from the CDC to determine the risk of death from COVID.

 

 

Is the vaccine safe for some age groups? The vaccines may have a positive risk/benefit for people in a certain demographic. The CDC and FDA think the vaccines are perfectly safe and have killed no one, so they have never done this analysis. For example, the VRBPAC unanimously approved boosters for people over 65. None of the panel members made the risk-benefit calculation. They were guessing. Were they right? No. They were dead wrong based on both our calculations and the real-world evidence. Here’s what the detailed calculations showed…

V:C in the US is not favorable for any age. The table shows the V:C numbers by age.

 

 

You can read this article which details how all these numbers were calculated. So for kids, we kill over 6 kids to save 1 kid from a COVID death. Mandating vaccination for anyone, especially school-age children, is proof of a corrupt society. Therefore, it’s nonsensical to vaccinate any age group. The FDA VRBPAC committee concluded that there is a benefit for 65 year old and older, but they refused to consider the mortality caused.

 

 

The full presentation, all 8+ hours of it. I set it to start at the point where Kirsch comes in, but knock yourself out.

 

 

 

Here are some earlier things by Kirsch.

 

From August 31:

Open Letter to CDC

I am the founder of the COVID-19 Early Treatment Fund (www.treatearly.org). Our work in funding early treatments for COVID was featured on 60 Minutes. I have been vaccinated and my entire family has been vaccinated. However, shortly after I was fully vaccinated, I began to hear stories from my friends that were very troubling. For example, one friend had three relatives who were formerly healthy die after getting the vaccine. Another friend had a heart attack 2 minutes after the injection and is now disabled, apparently for life. I assembled a team of over 19 doctors and scientists listed at the end of this comment to investigate the available evidence. Using the VAERS database and other official government data sources from the US and around the world (covering 35% of the world’s population), we found evidence that clearly demonstrates that the current vaccines are significantly more dangerous than has been previously believed.

Our most important findings include:

1/ The “real world” fatality data from VAERS does not match the fatality data from the Phase 3 trials. They aren’t even close. Using multiple independent methods, we estimate that over 150,000 Americans have already been killed. It is urgent to resolve this discrepancy as soon as possible as we strongly believe that the real world data is right and the vaccines should be immediately stopped.

2/ None of the COVID vaccines reduce all-cause morbidity. It’s the opposite: they all significantly increase all-cause morbidity by as much as 4.2 times baseline (p<=0.00001). The CDC must know this since this information is hiding in plain sight in the published literature. What is the point of offering an optional medical intervention which significantly increases all-cause morbidity when safer alternatives such as early treatment are available?

3/ There is an error in the adverse event detection formula used by the CDC that appears to have prevented the CDC from seeing the safety signals that were obvious to our VAERS experts.

4/ Early treatment and prophylaxis protocols are a superior option to the current vaccines, yet have been inexplicably ignored by the NIH:
• Higher relative risk reduction (over 99%)
• Greater safety (minor temporary side effects, known safety profile)
– They lower both all-cause mortality and all-cause morbidity
– They work equally well on all variants
– They do not promote escape variants
– They do not cause vaccine enhanced infectivity/replication
– They do not cause prion diseases
– They prevent long-haul COVID syndrome nearly 100% of the time
– They enable people to acquire recovered immunity which is both 13 times stronger and more durable than vaccine-induced immunity

We recommend the committee take the following actions:
• Require autopsies for all deaths within 4 weeks of any COVID19 vaccination so that data is available to compute an estimate of the true all-cause mortality.
• Make available the analysis of the 11,000 deaths investigation in VAERS for public inspection. It’s important for the public to understand why the CDC couldn’t attribute a single death to the vaccine whereas one of the world’s top pathologists ascribed at least 30% of all deaths to the vaccine.
• Explain publicly why there is a death peak on the second day after vaccination if the vaccinations are perfectly safe and not causing deaths.
• Explain publicly why the severe adverse side effects are dose dependent

[..] • Recommend that vaccine mandates should not be issued without evidence of a statistically significant all-cause morbidity decrease (which there is not in this case).
• Define a COVID vaccine stopping condition after which that vaccine should be halted until the stopping issues are addressed. In 1976, the stopping threshold was 35 deaths.

 

 

From June 12:

Should You Get Vaccinated?

  1. At least 6,000 deaths from the vaccine. The OpenVAERS team think it is over 20,000 due to under reporting.
  2. Biodistribution data shows massive accumulation in ovaries of the LNP (which instructs cells in ovaries to sprout toxic spike protein). Whoops. That was never supposed to be leaked out. We obtained it via FOIA request. The CDC never told you about that one, did they? Of course not!
  3. 82% miscarriage rate in first 20 weeks (10% is the normal rate). It is baffling that the CDC says the vaccine is safe for pregnant women when it is so clear that this is not the case. For example, one our family friends is a victim of this. She miscarried at 25 weeks and is having an abortion on 6/9/21. She had her first shot 7 weeks ago, and her second shot 4 weeks ago. The baby had severe bleeding of the brain and other disfigurements. Her gynecologist had never seen anything like that before in her life. They called in a specialist who said it was probably a genetic defect (because everyone buys into the narrative that the vaccine is safe it is always ruled out as a possible cause). No VAERS report. No CDC report. Yet the doctors I’ve talked to say that it is over 99% certain it was the vaccine. The family doesn’t want an autopsy for fear that their daughter will find out it was the vaccine. This is a perfect example of how these horrible side effects just never get reported anywhere.
  4. 25X the possibility of myocarditis for teen boys (can lead to heart failure and death)
  5. Kids already have natural immunity (Science Magazine article), so there is no benefit to vaccination, only risk. Have you ever seen the risk / benefit analysis by the CDC?? Ask for it before you consent.
  6. No point vaccinating those who’ve had COVID-19: Findings of Cleveland Clinic study. No benefit, only risk.
  7. Doctors who attribute adverse events to the vaccine are punished (such as Dr. Hoffe). So under reporting is incentivized.
  8. The CDC refuses to say how many people have died and is “still investigating” heart damage in kids even though it is obvious why (free spike protein causing clotting and inflammation). A 25X increase when the only “new” thing is the vaccine isn’t hard to figure out. Ask the CDC for their current top 5 hypotheses for the cause. It will be more than amusing to see what they say. If it isn’t the vaccine, heads should roll.
  9. The CDC is deliberately misleading the American people. Check out the side effects page. Death, disability, excessive miscarriage rates, heart attacks, stroke, inability to walk, talk, or see, Bell’s Palsy, persistent pain, Parkinson’s like symptoms, re-activation of shingles, blood clots, etc. are all missing.
  10. >500X more deadly than the flu vaccine
  11. COVID vaccines have generated more adverse reports in the last 6 months than all 70 vaccines over the past 30 years combined. They missed that one.
  12. Defective virus design (s1 was never supposed to be free, inclusion of PEG was unnecessary and allows LNP to be widely distributed)
  13. Strong opposition to vaccination by extremely credible voices like Malone, Geert Vanden Bossche, others
  14. NIAID (Cliff Lane) is improperly manipulating the COVID Treatment Guidelines to make it appear these drugs do not work, thus giving the world the false impression that the vaccine, even if imperfect, is the only way out. Ivermectin and fluvoxamine have been confirmed in Phase 3 trials. Ivermectin has a very high quality systematic review, the highest possible level in Evidence Based Medicine. Repurposed drugs are safer and more effective than the current vaccines. In general, early treatment with an effective protocols reduce your risk of dying by more than 100X so instead of 600,000 deaths, we’d have fewer than 6,000 deaths. NOTE: The vaccine has already killed over 6,000 people and that’s from the vaccine alone (and doesn’t count any breakthrough deaths).
  15. Vaccines skipped proper toxicology studies in order to bring to market faster. We don’t know what we don’t know.
  16. The unpredictable and horrifying side effects of this vaccine on heathy kids, such as the 16 year old girl who was unable to speak and see just 48 hours after being vaccinated
  17. Debilitating side effects can happen at any time because vaccine victims are very similar to COVID long haulers (Dr. Bruce Patterson has discovered this) and we all know that long haul can start at anytime (even when the disease is asymptomatic) and could be incurable.
  18. Because the vaccine is not perfectly safe, the government is required by law to warn people of the death and disability risks caused by the vaccine and to obtain informed consent. Always be sure to ask for the 50 most serious side effects and how often they happen. And find out whether they will compensate you if you are disabled for life from the vaccine. This is important because the blood clots can form anywhere with this very unsafe [vaccine] .

 

 

The vaccines kill at least twice as many people as they save. And if you don’t take them, you will be an outcast. We have gone outrageously mad.

 

 

 

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Sep 202021
 
 September 20, 2021  Posted by at 9:01 am Finance Tagged with: , , , , , , ,  53 Responses »


Claude Monet The sheltered path 1888

 

YouTube Is Always Right (Steve Kirsch)
Covid-19 Vaccines Are Killing At Least 2 People For Every 1 Life They Save (TE)
Counting Covid (Attkisson)
A Plausible Hypothesis, Based On Fact (Denninger)
Indian Bar Association Issues A Legal Notice To WHO (IF)
The Weaponisation of Vaccination (NoF)
Gaming Measurement of Vaccine Efficacy (Crawford)
Now The Lancet U-turns Over Covid Lab Leak Theory (DM)
This Week in the New Normal |(OffG)
Evergrande: Why Most Analysis Is Dead In The Water (Erba)
France Accuses Britain Of ‘Retreating To America’s Lap’ (Inews)
BlackRock and Citi Get on Board the Climate Nazi Train (IMan)

 

 

Fullmilch

 

 

Singapore stats. Completely out of hand. Vaccines, is there still any doubt about this? 82% fully vaccinated. Yet Eric Topol, who calls himself a physician-scientist, says:
“Delta can be daunting to contain. The situation in Singapore with over 1,000 new cases today and yesterday, 80% of total population fully vaccinated, 1 of top 3 countries in the world, is an important indicator of the challenge.”

How blind can one be?

And here’s the health minister. The vaccines saved us!

 

 

 

 

 

 

See Us. Hear Us. Believe Us. Heal Us.

 

 

Vaccine Truth tweets: “Steve Kirsch’s last video on YouTube where he admits “Ivermectin doesn’t work” in order to satisfy YouTube policies. It’s hilarious. Let’s see how long it takes before YouTube removes it.”

Note: Kirsch was suspended by Twitter too.

YouTube Is Always Right (Steve Kirsch)

STOP listening to the science! Whatever YouTube says is what you should believe. The science says that Ivermectin works. The science is wrong. What matters is what YouTube says, not science. Stop thinking for yourself and do whatever YouTube says. Otherwise, you will be banned, block, and demonitized.


Watch all my future content on Rumble.

Read more …

More Kirsch.

Covid-19 Vaccines Are Killing At Least 2 People For Every 1 Life They Save (TE)

FDA experts have unexpectedly voted against approving Covid-19 vaccination boosters for anyone over the age of 16 in the USA, citing a lack of long term data and stating that the risks do not outweigh any benefits because the Covid-19 vaccines are killing at least 2 people for every 1 life saved. In a live broadcast conducted on the 17th September the Food and Drug Administration vaccine advisory committee met to debate and vote on Pfizer and BioNTech’s application to offer booster shots to the general public. The meeting lasted over 8 hours and contained some shocking revelations. Dr Joseph Fraiman, an emergency medicine physician in New Orleans, spoke for several minutes during the meeting and revealed that no clinical evidence exists to disprove claims that the Covid-109 vaccines are harming more people than they save.


“We need your help on the front lines, to stop vaccine hesitancy. Demand the booster trials are large enough to find a reduction in hospitalisations. “Without this data we the medical establishment cannot confidently call out anti-Covid-vaccine activists who publicly claim the vaccines harm more than they save especially in the young and healthy. “The fact we do not have the clinical evidence to say these activists are wrong should terrify us all”. Dr Joseph Fraiman was then followed by Steve Kirsch, Executive Director of the Covid-19 Early Treatment Fund, who revealed that the Covid-19 vaccines more people than they are saving. “I’m going to focus my remarks today on the elephant in the room that nobody likes to talk about, that the vaccines kill more than they save.

“We were led to believe that the vaccines were perfectly safe but this is simply not true, for example there are four times as many heart attacks in the treatment group in the Pfizer 6 month file report, that wasn’t just bad luck.VAERS shows heart attacks happen 71 times more often following these vaccines compared to any other vaccine,” Steve Kirsch then continued his presentation by showing a slide titled ‘Excess Death: Life ratio is UNACCEPTABLE’. The slide shows how many excess deaths were required following vaccination to save one life due to Covid-19. “Only the VAERS (Vaccine Adverse Event Reporting System) are statistically significant, but the other numbers are troubling.” said Steve Kirsch.


“Even if the vaccines have 100% protection, it still means we kill 2 people to save 1 life. “Four experts did analysis using completely different non US data sources and all of them came up with approximately the same number of excess vaccine related deaths, about 411 deaths per million doses. That translates into 115,000 people have died (due to the Covid-19 vaccines).”

Read more …

“Oh, well that was a typo. They just got put in there by accident.”

Counting Covid (Attkisson)

As hindsight comes into clearer focus, we’re learning a lot about mistaken advice and policies amid the Covid-19 pandemic. One still murky and disputed area involves the death toll, now upwards of 640,000 in the U.S., according to CDC. Some insist the true count is much higher; others claim it’s lower. Today, we begin with the startling results of our investigation that found in some documented cases, news that Covid was the cause of death was greatly exaggerated. Grand County, Colorado, rural country a hundred miles outside of Denver. Thanksgiving 2020, Lucais Reilly shoots his wife Kristin in the head, then turns the gun on himself, committing suicide. They have alcohol and drugs in their system and a history of domestic troubles. Grand County coroner Brenda Bock explains how the small town tragedy is exposing serious questions about the way Covid deaths are counted.

Brenda Bock: I had a homicide-suicide the end of November, and the very next day it showed up on the state website as Covid deaths. And they were gunshot wounds. And I questioned that immediately because I had not even signed off the death certificates yet, and the state was already reporting them as Covid deaths. Bock says somebody, somewhere had apparently run the couple’s names through a database showing they’d tested positive for Covid within 28 days of their death. Then recorded them as Covid deaths even though they died of gunshots. Sharyl: If we look at the death certificates for the murder-suicide case, what will it say about Covid? Bock: Nothing, absolutely nothing. I paid a forensic pathologist to do the autopsies on those two cases. And nowhere is COVID mentioned on those death certificates. Nowhere.

Bock: This is a copy of the death certificate, and nowhere does it say COVID. So we have a homicide, suicide, nothing to do with COVID. Because there had been no Covid deaths within the geographic boundaries of Grand County in 2020, Bock was in a unique position to challenge the state’s accounting. In many cities and counties, the numbers are too big and the coroners would never know about discrepancies. Within a week of the murder-suicide, two more Grand County deaths popped up on the state’s Covid count. Bock investigated and found out why she had no record of them. Bock: Two of them were actually still alive, and yet they were counting them. Had I not called them on it and asked them who those were, where were they from, all the information about it and it’s like, “Oh, well that was a typo. They just got put in there by accident.”

Attkisson

Read more …

“Despite the presence of antibodies sufficient to suppress a virus with an R0 of nearly 6, twice that of the original strain [..] we had a wild outbreak of disease anyway”

A Plausible Hypothesis, Based On Fact (Denninger)

The recent JAMA article makes clear several things. First, likely as many as half of those who got a positive PCR test never had Covid-19 at all. The antibody counts they documented in that study do not square with the claimed infection rate nor the low-symptom prevalence where the person in question never sees a doctor and is never tested. Back in the fall of 2020 the folly of the so-called “tests” was laid bare on the table when Elon Musk took four in sequence on the same day and got two positive and two negative results — nothing better than a coin-toss. How many more people were labeled as “diseased” when they either had the flu, some other virus, or nothing? The data from JAMA strongly suggests the answer is “a huge percentage, likely roughly half of so-called positive tests, were in fact not from actual positive Covid-19 individuals.”

The danger of telling someone they had something when they didn’t is they have every reason to think they’re safe when they’re not and thus they are likely to put themselves at severe risk of getting hammered. That’s stupid and contrary to every principle of medicine, say much less ethical behavior. But antibody presence is dispositive. Pre-existing immunity is very, very hard to determine the presence of, since cross-reaction requires you know what you’re looking for — and we don’t. We didn’t do the work, beyond SARS. We didn’t want to do the work because discovering what it was (1) made possible a potential easy infection that would confer actual immunity (e.g. if it’s OC48 which usually causes colds, well, go get inoculated with it on purpose!) and (2) instantly deflates the fear porn, drive for vaccines and every single screaming idiot in the government, social media and on TV.

But then this summer something odd happened. Despite the presence of antibodies sufficient to suppress a virus with an R0 of nearly 6, twice that of the original strain and equal to that claimed for Delta, which I remind you is unsubstantiated and the data from the UK in fact suggests Delta is not materially more-infective than the original wild strain (it only has to be a bit more-so to out-compete, of course), we had a wild outbreak of disease anyway. Much worse is that in Britain it is impossible for there to be widespread communicable disease even for a a virus with an R0 worse than measles: “Based on antibody testing of blood donors, 97.7% of the adult population now have antibodies to COVID-19 from either infection or vaccination compared to 18.1% that have antibodies from infection alone.”

It is impossible for Britain to have any material Covid-19 infectious activity among adults given this level of prevalence unless the jabs are largely or entirely worthless, or much worse, enhance infection. It’s a hypothesis that fits the facts and you can bet not one single penny of government money will go toward proving or disproving it as if it was to be proved then what do you do with all the vaccine companies and every involved government at all levels, local, state and federal, who literally slaughtered their populations with their advocacy and even in some cases attempted mandates for these jabs. Do we have any independent medical science folks remaining, anywhere in the world, who will take this challenge on and prove it up? We’ll see.

But whether they do or not you can’t change facts and the facts are that either the jabs destroyed existing immunity, creating susceptible people out of resistant ones, or the virus has evolved to largely-evade the protection the jabs provided. Which it is doesn’t matter to the person who believed they were safe, and now learns — especially the hard way — that they are not.

Read more …

You go girl.

Indian Bar Association Issues A Legal Notice To WHO (IF)

Advocate Dipali Ojha of the Indian bar association and a team of young indian lawyers have issued a legal notice to the world health organization over their blatant campaign against any alternative treatments. Her legal action against WHO comes after the tweet from Soumya Swaminathan, WHO chief scientist, who issued tweet against Ivermectin backing it with a link, that was declaration from a private company. The team of indian lawyers seeks to make available all possible affordable options to the masses and hold the highest authorities accountable for their directives, and suspected submission to big pharma lobbying.

Timestamp :

00:00 Intro
01:14 Interview Start
02:03 Dipali Ojha background
03:58 Why did Indian Bar association sue WHO ?
11:08 WHO Scientist Twitter statement against treatments
13:04 History of Iver-mectin & Big Pharma profit motive
16:30 Can 8 billion people get vaccine ? options for poor countries
20:19 Dipali Ohja explains indian Protocol & Lawsuit
23:44 Media blackout on Iver-mectin
24:20 role of fact checkers
25:20 AI bias in social media
26:40 Where was the lawsuit filed?
27:10 Dipahli ojha explains cause of 2nd legal notice
32:38 Effects of legal notice
34:50 Many solutions to the crisis
37:14 Diplai ojha explains the Public Interest Litigation
38:52 Rajiv explains the two lawsuits in one
40:54 Challenging Compulsory Vaccine & civil rights
42:28 Role of Gates Foundation , Fauci & Wuhan lab funding
46:50 Dipali Ohja explains WHO’s compromised investigations
48:40 Vaccine and complementary treatments
50:24 Role of AI in information bias
51:19 Closing statement of Diplai Ojha

Read more …

“The vaccination pass is a mobilisation of state power, an extension of discipline and policing over the free life of civil society.”

The Weaponisation of Vaccination (NoF)

The vital public health measure of vaccination is being transformed into a project of the extension of state control, with measures such as covid passports and mandatory vaccination. The Israeli minister of health was caught confiding to the minister of the interior that ‘there is no medical or epidemiological justification for the Covid passport, it is only intended to pressure the unvaccinated to vaccinate’. France – the European country with the harshest covid pass laws – shows how this ‘pressure to vaccinate’ is driven by a political rather than a medical impulse. The vaccination pass is a mobilisation of state power, an extension of discipline and policing over the free life of civil society. This rides roughshod over individual liberty, unions, scientific committees and medical logic alike.

Currently, all over-12s in France must present a vaccine passport (‘pass sanitaire’) in order to access restaurants, museums, long-distance trains, and outdoor and indoor sports facilities. All civil society bodies take on a policing function. Covid pass checks are installed at the entrance of open-air horse riding facilities, in bars, at the entrance of swimming pools. The sports instructor checks your covid pass at the start of every class or term. The riding school asks you to ‘prepare your health certificate’ before you are allowed to walk into the open field where the horses are held. The cafe asks you to scan your QR code before sitting down at a table.

The vaccinated person is treated as safe, and the unvaccinated person as risky. This distinction is made not on public health grounds, since vaccinated and unvaccinated transmit the delta variant at similar rates, but because the unvaccinated person stands as the figure that has resisted state authority. The unvaccinated becomes the dissident, the person who refused to roll over. A young French woman who tried to enter a shopping centre without a covid pass was set upon and beaten by a group of armed police. She was beaten not because she is a public health risk, but because she represents a threat to public order. The push for 100% vaccination has become a project of incorporating the whole population, whether it is in their interests to be vaccinated or not.

It is this political impulse that lies behind the hasty extension of vaccination to younger age groups, who stand to benefit little from the vaccine and could suffer from short-term or future side effects. Macron apparently made the decision to extend vaccines to 12-15 year olds suddenly one morning, when he was told by his scientific advisory committee that he had ‘free rein’ to decide whether to vaccinate the young, partly in order to ‘avoid the slowing down of vaccination’. A more reflective scientific ethics advisory committee complained that it has not been given time to make its recommendations, and criticised the ‘hasty’ decision; it judged that the benefits of the vaccine to adolescents were ‘very limited’ and the existing safety data to be too slim to judge its suitability for this age group. Yet now, this age group is forced to take the vaccine.

Read more …

Statistician Mathew Crawford on the problem with the first 14 days after vaccination.

Gaming Measurement of Vaccine Efficacy (Crawford)

Suppose that tomorrow it is announced that in a Wuhan laboratory—located somewhere between the French-designed Wuhan Institute of Virology and the fabled wet market—that an NIH funded project results in highly valuable intellectual property in the form of the Morris Therapy. After rigorous mandatory testing of the Morris Therapy on Uyghurs, including the high risk elderly, pregnant women, and also children, the Morris Therapy demonstrates 100% efficacy in preventing COVID-19…after day 13. NIAID Princeling, Dr. Anthony Fauci quackly announces an EUA both for the Morris Therapy, and also swift approval of the as of yet unavailable COMorrisY Therapy. Nobody was reached at any governmental organization who could explain which of these has indemnity, and whether citizens pay for those liabilities by giving up their children as they drop them off at school where they are to be treated by swiftly trained gym teachers.

During the first two weeks, 80 million Americans jump at the opportunity to receive Morris Therapy. However, 79.2 million of those Americans seem to be…well…missing. With doctors and morgue owners tight lipped, the CDC reports that indeed, the Morris Therapy has resulted in 100% efficacy in preventing COVID-19 after the first 13 days. Scientists and other people who pay attention to things rush to post videos on YouTube, Twitter, and Facebook pointing out that there are nearly a million reports of death in the Highly Profitable Therapy Adverse Events Reporting System (HPTAERS). Fact checkers [just doing their job] point out that causality of those deaths HPTAERS hasn’t been proved, and censor all those reports. University faculty petitioned to silence, reprimand, or simply harass their colleagues who participated in those reports, labeling them with the pejorative “anti-Morrisers”. No autopsies are performed on the 79.2 million Americans who died during the first 13 days after a dose of Morris Therapy.

What happened is that 99% of the people who received the Morris Therapy dropped dead during the first few days. Even worse, many were taken to the hospital, entered into a database as non-Morrised, and as hospital beds filled up, media outlets declared a “pandemic of the un-Morrised”. All the social pressure makes it hard to talk about the problem. Meanwhile, nobody does autopsies on the bodies that might reveal clues to the deaths, such as the presence of spike-Morris protein in organs all over the body. All the 79.2 million deaths are presumed to be COVID-19 deaths, and the media dedicates itself to a 48 hour marathon of fear porn, lamenting that poorer nations are not receiving their equitable share of limited supplies of Morris Therapy.

Meanwhile, health officials and all those devoted to the success of the Morris Therapy as the final solution to the COVID-19 pandemic…”correctly” point out none of the 800,000 survivors of the Morris Therapy have COVID-19 (though nobody really wants to talk about disease etiology as it might link Morris Therapy as a Type II COVID-19). In the end, the entire population of the SARS-CoV-2 virus decided as a “species” (if we can call a virus a species), that invading the U.S. just wasn’t worth it at all, deciding instead to go live amongst the flies, minks, bats, and pangolins.

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Have they apologized yet?

Now The Lancet U-turns Over Covid Lab Leak Theory (DM)

The Lancet medical journal has bowed to pressure over its heavily-criticised coverage of the disputed origins of the Covid pandemic by publishing an ‘alternative view’ from 16 scientists – calling for an ‘objective, open and transparent debate’ about whether the virus leaked from a Chinese laboratory. It was revealed earlier this year that Peter Daszak – a British scientist with long-standing links to the Wuhan Institute of Virology – had secretly orchestrated a landmark statement in The Lancet in February 2020 which attacked ‘conspiracy theories suggesting that Covid-19 does not have a natural origin’. The now-infamous letter, signed by 27 leading public health experts, said they stood together to ‘strongly condemn’ the theories which they said ‘do nothing but create fear, rumours, and prejudice’.

They also lavished praise on Chinese scientists who they said had ‘worked diligently and effectively to rapidly identify the pathogen behind this outbreak… and share their results transparently with the global health community’. Now, The Lancet has agreed to publish an alternative commentary which discusses the possibility that laboratory research might have played a role in the emergence of the SARS-CoV-2 virus. It also directly confronts the efforts of science journals to stifle debate by labelling such theories as ‘misinformation’. In the article, the authors argue that ‘there is no direct support for the natural origin of SARS-CoV-2, and a laboratory-related accident is plausible’. They add that the February 2020 statement ‘imparted a silencing effect on the wider scientific debate’.

[..] The new commentary, published in The Lancet on Friday, said: ‘The world will remain mired in dispute without the full engagement of China, including open access to primary data, documents, and relevant stored material to enable a thorough, transparent and objective search for all relevant evidence.’ One of the signatories, Professor Nikolai Petrovsky of Flinders University in Adelaide, Australia, told The Mail on Sunday: ‘It might seem small, but after 18 months of complete denial, the very act of [The] Lancet agreeing to publish this letter acknowledging the origins of Covid-19 remains an open verdict, is a very big deal. ‘For a leading medical journal like Lancet to agree to finally open its doors to a letter from scientists highlighting the ongoing uncertain origins of Covid-19, indicates how far we have come in 18 months in requesting an open scientific debate on the topic, but also indicates just how far we still have to go’.

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“..once we’ve established “anti-vaxxers” don’t deserve healthcare, those other people she’s so careful to mention – smokers and drunk drivers – they’re next. Along with the obese, or the clumsy, or the religious, or the politically inconvenient.”

This Week in the New Normal |(OffG)

Ruth Marcus, a deputy editor at the Washington Post, has had enough of people pussy-footing around this issue and is going “come right out and say it” – unvaccinated people deserve healthcare less than vaccinated people. She at least admits this “conflicts radically with accepted medical ethics”, which is completely true but for some reason that doesn’t seem to change her mind: “..under ordinary circumstances, I agree with those rules. The lung cancer patient who’s been smoking two packs a day for decades is entitled to the same treatment as the one who never took a puff. The drunk driver who kills a family gets a team doing its utmost to save him..”

To be clear then – Ruth considers the unvaccinated as morally inferior to a drunk driver who ran over some kids. Which says a lot more about her, than the unvaccinated. This is one of this feeler pieces. An antennae article, gently feeling the ground to see if can bear the weight of the agenda coming behind it. It’s setting up the conversation. Because once we’ve established “anti-vaxxers” don’t deserve healthcare, those other people she’s so careful to mention – smokers and drunk drivers – they’re next. Along with the obese, or the clumsy, or the religious, or the politically inconvenient.

If you don’t believe me, just check the comments under the article. The WaPo has one of the most scripted comments sections on the internet, whose usual job is to play the “bad cop” to the author’s “good cop”. And, sure enough, BTL is full of hundreds of supposedly real humans saying the author doesn’t go far enough, and we should ration all kinds of healthcare based on personal choices. This particular talking point is already being aired on CNN and by late-night talkshow hosts too. Expect it to spread quickly, especially when the flu season starts.

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Twitter thread by Girolamo Pandolfi da Casio ditto Carlo Dossi Erba.

Evergrande: Why Most Analysis Is Dead In The Water (Erba)

Evergrande: why most analysis is dead in water and how best to understand and navigate what’s happening? Both denialists and alarmists are getting it wrong. Let’s start by understanding this: what is happening is the result of a CCP-initiated policy change to curb leverage. It started a while back and has seen other defaults, including SOEs. What are the specific policy changes? Most important is the introduction of the 3 red lines a year ago: – L/A < 70% – net leverage < 100% – cash to ST debt > 1. What’s the point of the 3 red lines? First and foremost to forestall a systemic crisis that could have brought down the whole financial sector if left unchecked. Real estate amounts to a significant chunk of China GDP with strong linkages upstream and downstream.


And believe it or not, the sector was levered to the gills. The 3 red lines are hardly draconian, yet all the CCC, a large chunk of the B and a good 1/3 of the BB did not pass them a year ago. Needless to say, it was really not too early. But there is more to it than leverage. One common practice of these construction companies,a game Evergrande excelled at, was to bid land at prices significantly higher than market. It didn’t matter to them, coz the risk got transferred to flat buyers and banks that financed the purchase. That model worked well for local governments, banks and households because house prices were going up. So much so over the last 15 years, that a serious affordability crisis emerged in major cities AND HH debt soared way above disposable inc – below HH debt as % GDP.

So it wasn’t hard to figure out the economic disaster in the making: exponential price rises with explosive HH and Construction leverage. But that’s not all. There is another problem that escapes most China analysts. As a result of years of seeking easy growth through construction and leverage, the misallocation of capital was : 1- capital starving more innovative and high tech sectors (see chart) and 2- creating a headwind for a re-balancing towards a more consumption driven growth. At some point, reigning in lending to the RE sector became vital in order to address the structural issue of capital misallocation. That also explains the curbs on VC investments in RE and most importantly, a curb on all the irregularities that characterized RE.


The issue of irregularities is at the core of what is happening with Evergrande. More on that later. It’s a long introduction, but it seemed important to explain these issues to understand the long term nature of this problem and why its resolution will be tedious. So there is a new paradigm dictated by a set of economic realities that CCP could no longer ignore and most importantly, they can relax the rules a bit, but can’t reverse course. They can’t allow consumers to be bust nor a rogue unproductive sector to balloon further.

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“It shows our readiness to be hard-headed in defending our interests and challenging unfair practices and malign acts.”

France Accuses Britain Of ‘Retreating To America’s Lap’ (Inews)

France has continued its war of words in the increasingly bitter diplomatic row over the UK’s new defence pact with the US and Australia. Europe Minister Clement Beaune said Britain had returned into the “American lap” after Australia announced it was scrapping its £30 billion French submarine deal in favour of more powerful nuclear-powered vessels acquired with the help of the UK and US. The announcement prompted President Emmanuel Macron to order the recall of the French ambassadors from Washington and Canberra – a move virtually unheard of among such close allies. However, there was no similar order for the French envoy to London to return to Paris for consultations.

But in a series of interviews with French television, Mr Beaune suggested it was because the UK was the “junior partner” which had accepted its “vassalisation” by the US. “Our British friends explained to us they were leaving the EU to create Global Britain. We can see that this is a return into the American lap and a form of accepted vassalisation,” he said. “The UK is clearly trying to find its feet, perhaps there was a lack of thought about the strategic future. Today they are hiding in the American fold. I hope that will not be their policy for the decades to come.” He later added: “We see through this partnership, this strategic alliance and after the Kabul crisis, that Global Britain seems to be more about a US junior partner than working with different allies.”

New Foreign Secretary Liz Truss has defended the pact, saying it showed Britain would be “hard-headed” in defending its interests. Writing in The Sunday Telegraph, Ms Truss said the UK was a “fierce champion” of freedom and democracy around the world. “It shows our readiness to be hard-headed in defending our interests and challenging unfair practices and malign acts. It also shows our commitment to security and stability in the Indo-Pacific region,” she wrote.

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Wait. China takes it all over, and that’s supposed to benefit Citi?

BlackRock and Citi Get on Board the Climate Nazi Train (IMan)

There are some things that bring joy to my soul. My pleasures are simple ones. Peanut butter on toast (the food of gods), witnessing Macron getting a slap, and this…

The awesome thing here is that what is taking place is that our competition on bidding for coal assets has disappeared in a cloud of woke smoke. This will quickly become geopolitical, and the question is this: can BlackRock, Citi, Prudential, HSBC, and their other woke mates decide the fate of nations? They are already affecting the fate of nations. Witness Canada and all of Western Europe. But will they do the same to China? Will they do the same to Russia? The answer to that will only be fully revealed in the due course of time, but we don’t really need any crystal balls here as we just watch actions, not words.

“China put 38.4 gigawatts (GW) of new coal-fired power capacity into operation in 2020, according to new international research, more than three times the amount built elsewhere around the world and potentially undermining its short-term climate goals.” Nearly all of the 60 new coal plants planned across Eurasia, South America and Africa — 70 gigawatts of coal power in all — are financed almost exclusively by Chinese banks” We see all of this on the ground, and while it is taking place, formerly reputable media outlets such as the FT, Reuters, and Bloomberg tell us that: “China’s belt and road initiative creates a problem for China with respect to their climate goals.”

Really? There is no conflict or problem. Let me explain. Here is what is transpiring. They will keep paying lip service to the woke ideology while capturing the bulk of the energy market, and by the time we all wake up, they’ll control the world’s energy and logistics chains. And once they’ve done that, they’ll be able to control the reserve currency and once they’ve done that… well, they will be the dominant power. Game over. At this rate they’ll get there in a frighteningly rapid period of time. No more than a couple of decades.

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Before machines the only form of entertainment people really had was relationships.”
~ Douglas Coupland

 

 

 

 

Chris Rock: “there’s no money in the cure. The money’s in the medicine. That’s how a drug dealer makes his money… that’s all the government is, a bunch of drug dealers.”
https://twitter.com/i/status/1439792949404045314

 

 

 

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

 

Sep 162021
 


Pablo Picasso In “Le Lapin Agile” or harlequin with a glass 1905

 

The Spike Will Not Be Found In The Blood. It Travels “Incognito” (Chesnut)
Are Booster Shots Increasing Covid Spread And Covid Deaths? (Gato Malo)
CDC Now Lists Vaccinated Deaths as Unvaccinated (Mercola)
So You’d Like To NOT Have Society Collapse? (Denninger)
39% of Australians Unable To Perform Daily Activities After Vaccine (TE)
Mask Mandates And Vaccine Passports Are A Performance (Stuart Waiton)
91% Of China’s Youth Aged 12-17 Are Fully Vaccinated Against Covid (RT)
Are You Kidding Me, Pfizer, Volume 1 Gazillion (Berenson)
A Slog Vaxicide Special (Ward)
France Leads The Way In Holding Covid Incompetents To Account (RT)
33 Districts In Uttar Pradesh Are Now Covid-free (HT)
EU Red Tape Prevents Russia From Boosting Gas Supplies To Europe – Lavrov (RT)
US ‘Lost Focus’ In War On Terror – Oliver Stone (RT)
Durham Reportedly Seeking Indictment Against Clinton Campaign Lawyer (JTN)

 

 

Looking worse, fast. I’m starting to think you will need ivermectin -and/or HCQ- to fight off the vaccine. Preferably, don’t get vaccinated, but if you have been, get ivermectin. And whatever you do, stay away from booster shots.

“We are very certain about this, the vaccine is directly killing individuals”.

“The growing consensus among vaccination researchers is that exposure to 5-8 of these mRNA jabs over a relatively brief period of time will – dependent on the underlying health of the individual – result in death.”

 

 

McCullough NZ the vaccine is directly killing individuals

 

 

Thread by @Parsifaler (Walter Chesnut). Yikes.

The Spike Will Not Be Found In The Blood. It Travels “Incognito” (Chesnut)

The Autoimmune Mechanism. THE SPIKE WILL NOT BE FOUND IN THE BLOOD. IT IS TRAVELLING “INCOGNITO” INTRACELLULARLY. WE KNEW IT ENTERED CELLS VIA ENDOCYTOSIS IN 2008! Yesterday I observed that every cell the Spike Protein invades seems to cause the body to develop autoimmunity against it. I believe I have discovered the mechanism. It is a very brief and straightforward mechanism. Most likely many spikes do NOT stay on the cell surface, once they are expressed via spike protein therapied. The Spike is proven to be brought into the cell by Endocytosis. The spike protein is internalized into cells rapidly and is detected in cells within 5 mi, a hallmark of endocytosis. The amount of spike protein in cells continues to increase for up to 30 min. Thus, SARS-CoV-2 spike protein enters cells via endocytosis.

Once it is in the cell, its signaling damages mitochondria. The team then replicated this process in the lab, exposing healthy endothelial cells (which line arteries) to the spike protein. They showed that the spike protein damaged the cells by binding ACE2. This binding disrupted ACE2’s molecular signaling to mitochondria (organelles that generate energy for cells), causing the mitochondria to become damaged and fragmented. Once the mitochondria are damaged, this then activates the autoimmune response of the body. The accumulation of defective mitochondria led to overproduction of an inflammatory protein called type 1 interferon.

The findings suggest that failed quality control of mitochondria may cause Sjogren’s, lupus, and other autoimmune diseases through production of interferon. The Spike Protein then proceeds to travel from cell to cell via EXTRACELLULAR VESICLES. This means, of course, they will NOT BE FOUND IN THE BLOOD. We would not have been aware all this time. As the S1 unit has been found in monocytes 15 months post infection, it may be traveling intracellularly, executing a “Sherman’s March Through Georgia” on the mitochondria, resulting in multisystemic autoimmunity. Again, we have known the spike enters cells via endocytosis since 2008.

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“..we are seeing such a strong surge in deaths from a delta variant that looks to have a much lower CFR than prior variants..”

Are Booster Shots Increasing Covid Spread And Covid Deaths? (Gato Malo)

israel has been playing an interesting role as a bit of a canary in the coal mine. They have been pushing vaccines, vaccine passports, and now boosters harder than just about anyplace else on earth. They also make a good lab as they report solid (by covid standards) data and occupy only one regional climate zone so we do not need to adjust for heterogeneous seasonal surges within the aggregate (as we do in the US). And one thing is becoming very clear: whatever they are doing is not working and even their health ministers are having to admit this. This dip was (as i expected) driven by a drop in testing and reporting due to rosh hashanah (and will likely dip again late this week for yom kippur) but next week, we should be starting to get clearer data again.

With over 30% of the total population now having had a booster shot since the commencement of that program in earnest on august 1st, we should be able to get a sense of efficacy. I ran the series of booster uptake and plotted it vs deaths per day. What i saw looked like cause for concern and appears to validate calls from the departing FDA vaccine experts to get a good, hard look at this data before doing anything aggressive. Boosters began to rise and by the time they hit even 0.5%, deaths were starting to rise with them. the two move in near perfect lockstep. Clearly, correlation is not proof of causality, but this is an awful lot of signal to ignore out of hand especially given our strong reasons to presume causal linkage. (that said, the alignment with seasonal surge poses difficulties in separating signal source)


It’s further worrying that even with a 67% vaccination rate at the beginning of this rise and a significant portion of the population having already had exposure to covid and cohorts of the highest risk already having been depleted in past waves, that we are seeing such a strong surge in deaths from a delta variant that looks to have a much lower CFR than prior variants. (0.4% vs 1.1% per UK variants of concern data) It has barely attenuated at all (and it’s not clear we’ve reached highs. Consider the “false flat” from last year and how much later this surge was this year. We could be at the half way mark. This will bear watching.)

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“..if you have received a COVID injection, the CDC’s guidelines call for your PCR test to be run at a CT of 28 or less. If you are unvaccinated, your PCR test is to be run at a CT of 40..”

CDC Now Lists Vaccinated Deaths as Unvaccinated (Mercola)

According to the CDC,6 you’re not counted as fully vaccinated until a full 14 days have passed since your second injection in the case of Pfizer or Moderna, or 14 days after your first dose of Janssen. This is how the CDC defines a vaccine breakthrough case: “… a vaccine breakthrough infection is defined as the detection of SARS-CoV-2 RNA or antigen in a respiratory specimen collected from a person ≥14 days after they have completed all recommended doses of a U.S. Food and Drug Administration (FDA)-authorized COVID-19 vaccine.” In other words, if you’ve received one dose of Pfizer or Moderna and develop symptomatic COVID-19, get admitted to the hospital and/or die from COVID, you’re counted as an unvaccinated case. If you’ve received two doses and get ill within 14 days, you’re still counted as an unvaccinated case.

The problem with this is that over 80% of hospitalizations and deaths appear to be occurring among those who have received the jabs, but this reality is hidden by the way cases are defined and counted. A really clever and common strategy of the CDC during the pandemic has been to change the definitions and goalposts so it supports their nefarious narrative. For example, the CDC has quietly changed the definition of “vaccine,” apparently in an attempt to validate calling the COVID mRNA gene therapies vaccines. In an August 26, 2021, archived version7 of vaccine, the CDC defines it as a “product that stimulates a person’s immune system to produce immunity to a specific disease, protecting the person from that disease.”

But a few days later, a new definition appeared on the CDC’s website,8 which now says a vaccine is a “preparation that is used to stimulate the body’s immune response against diseases.” The differences in the definitions are subtle but distinct: The first one defined a vaccine as something that will “produce immunity.” But, since the COVID-19 vaccines are not designed to stop infection but, rather, to only lessen the degree of infection, it becomes obvious that the new definition was created to cover the COVID vaccines. It’s not just the CDC’s definition of a breakthrough case that skews the data. Even more egregious and illogical is the fact that the CDC even has two different sets of testing guidelines — one for vaccinated patients and another for the unvaccinated.

Since the beginning of the pandemic, the CDC has recommended a PCR test cycle threshold (CT) of 40.9 This flies in the face of scientific consensus, which has long been that a CT over 35 will produce 97% false positives, essentially rendering the test useless. In mid-May 2021, the CDC finally lowered its recommended CT count, but only for patients who have received one or more COVID shots. So, if you have received a COVID injection, the CDC’s guidelines call for your PCR test to be run at a CT of 28 or less. If you are unvaccinated, your PCR test is to be run at a CT of 40, which grossly overestimates the true prevalence of infection. The end result is that unvaccinated individuals who get tested are FAR more prone to get false positives, while those who have received the jab are more likely to get an accurate diagnosis of infection.

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“I give this right up into the Christmas season when Biden’s mandate allegedly will go into effect before it totally screws the economy.”

So You’d Like To NOT Have Society Collapse? (Denninger)

Go ahead Governors, let businesses mandate jabs and masks. Let Biden get away with his bull****. Don’t put in place E/Os and don’t call back the legislature into special session right here and now, today, and put a conclusive stop to all of it. I give this right up into the Christmas season when Biden’s mandate allegedly will go into effect before it totally screws the economy. With that, down goes the market, commercial real estate detonates (what happens when that Lowes closes due to lack of staff and so do another couple of nice big-box stores for the same reason down the street — everywhere at once!) and with it the debt markets.

There are already places where WalMarts are being forced to close to restock shelves as they’re so short of people and can’t hire more, having put in place employee mandates which enough prospective and current employees are responding to with “**** that!” that the only option remaining to them is to lock the doors and repurpose the few people they do have. This area is tourist-heavy and now, with schools allegedly back open, the traffic shifts — down a bit now, down more as we go into the winter. That local places still can’t manage to hire tells the tale — the people are tired of the abuse and, for the offered wage, they won’t apply or work. Give someone 18 months to figure out how to give you the finger and many will do exactly that.

On top of this you have all of those who complied with said mandates and now are out sick, many with the coof which, the company and the government assured us all would not happen if you just rolled up your sleeve. Of course they lied and still are, trying to claim it’s “rare” that people get materially ill after being vaccinated against Covid. That’s just the latest line of bull**** and, given the sick rate among those who have been jabbed it’s obvious if you pay a single bit of attention. Good luck Biden along with governors and local officials — you’re going to need it, and were I you in this market today I’d be rather careful if you’re not ok with a 201k — which is what you might have left of your 401k as we approach Christmas.

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It gets worse fast.

39% of Australians Unable To Perform Daily Activities After Vaccine (TE)

The National Centre for Immunisation and Research (NCIRS) in Australia are currently leading a collaboration with the Australia’s Government known as AusVaxSafety. The group has been conducting active vaccine surveillance of the Covid-19 vaccines in use in Australia to “ensure their ongoing safety”. Up to the 16th August 2021 over 1.4 million Austalians had partipated in the surveillance completing more than 2.4 million safety surveys, outlining their experience following the Covid-19 vaccination and the published results show the following –


Pfizer Vaccine – 1st DoseFollowing the first dose of the Pfizer vaccine 1,007,479 people responded to an SMS/email about their health in the three days after having the jab. The results show that 37.2% reported having an adverse reaction, with 374,832 reporting at least one adverse event. 0.5% of participants also reported seeing a doctor or attending hospital in the three days following vaccination due to an adverse reaction. This equates to 5,037 people. Whilst 6.7% of participants reported missing work, study or routine duties for a short period – meaning 67,501 people were left unable to perform daily activities following their first dose of the Pfizer mRNA Covid-19 injection.

Pfizer Vaccine – 2nd Dose Following the 2nd dose of the Pfizer vaccine 770,864 people responded to an SMS/email about their health in the three days after having the jab. The results show that 56.4% reported having an adverse reaction, a significant increase on the percentage of people who reported having an adverse reaction after having their first dose of the Pfizer jab. 1.3% of participants also reported seeing a doctor or attending hospital in the three days following vaccination due to an adverse reaction. This equates to 10,021 people – double the number of people who reported seeking medical attention after having the first dose despite there being 237,000 less particants in the 2nd dose survey. However, a huge 21.2% of participants were left unable to perform daily activities, that’s 163,423 people who reported missing work, study or routine duties.

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Dr Stuart Waiton is a senior lecturer in sociology and criminology at Abertay University. He is a columnist for the Glasgow Herald, author of three books, and is currently writing a book entitled The Criminalisation of Everything.

Mask Mandates And Vaccine Passports Are A Performance (Stuart Waiton)

The illiberal actions of Western nations over Covid are as much about a worrying shift in politics as it is about ‘the science’. Some very basic freedoms that we have traditionally enjoyed are in grave danger. In America, Joe Biden is putting pressure on workers to get the vaccine. Without proof that you do not have Covid, or evidence of vaccination, you will no longer be able to enter a workplace that has more than 100 staff. This policy will affect two-thirds of the workforce – around 100 million people. While many liberals in America have understandably reacted with outrage at changes to abortion regulations in places such as Texas, the idea of bodily autonomy as a basic human right, a right that should apply to vaccinations, barely gets a mention.

In France, vaccine passports have been introduced in cultural and leisure venues – cinemas and museums, as well as bars, restaurants, cafés, trains… Basically anywhere and everywhere you go in that country, you will be expected to show your papers. In England, thus far, vaccine passports have been ruled out. However, in Scotland, the governing Scottish National Party (SNP) have once again shown that it is always prepared to take authoritarian measures one step further than their English counterparts by introducing passports for major venues. Suggesting a puritanical dimension to this policy, not only are outdoor venues of 10,000 people and indoor venues of 500 being targeted, but all “sexual entertainment venues” will need evidence of vaccination.

Despite the fact that 84% of over-18s have had both jabs, the policy in Scotland is being introduced, in part, and arguably in large part, to put pressure on younger people to get a vaccination for a virus that has little or no effect on them.

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Again: Yikes!

91% Of China’s Youth Aged 12-17 Are Fully Vaccinated Against Covid (RT)

Just over 90% of students in China aged 12-17 have received two doses of a Covid-19 vaccine, state media has revealed. Despite the high inoculation rate, the Ministry of Education has urged caution in schools over the virus.
On Wednesday, People’s Daily shared that the two-dose vaccination rate of teachers and students over 18 years old stands at 95%, slightly higher than the rate among younger pupils. Despite the wide vaccine coverage among China’s school children, the Ministry of Education has issued a notice imploring institutes and schools to make Covid prevention and control a top priority.

The statement came after China’s National Health Commission warned that coronavirus infections were circulating at a primary school in Putian, a city home to three million in East China’s Fujian Province. The region has recorded over 150 local cases in five days, prompting some cities in other parts of the country to impose travel warnings before major holidays. A number of cities in Fujian province, such as Quanzhou and Fuzhou, have decided to suspend primary schools and kindergartens, with others switching classes to online learning.

The Chinese government has manufactured and authorized two of its own Covid jabs. While the domestically produced vaccines have been given the green light for administration to children as young as three, authorities have yet to expand the inoculation campaign to the under-12s. Several regions across China started vaccinating its teenagers against Covid in July, including the capital Beijing. Figures from the National Health Commission showed that China has so far managed to administer close to 2.16 billion vaccine doses.

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“..it conducted a single “Phase 1” trial that covered 12 people over 65..”

Are You Kidding Me, Pfizer, Volume 1 Gazillion (Berenson)

The FDA just released its briefing book for Pfizer’s request for a third dose of Comirnaty (or is that BNT162b2? No matter! It’s approved either way, sorta). It is every bit the mess we all expected. Let’s go to the highlights: Pfizer basically hasn’t bothered to test the booster AT ALL in the people actually at risk – it conducted a single “Phase 1” trial that covered 12 people over 65. The main Phase 2/3 booster trial (beware efforts to cover multiple “phases” of drug research at once, you want it bad you get it bad) included no one over 55. No one. As in NONE. Which makes total sense – why test the booster in people who actually need it because they’re at high risk from the ro? Nothing good can come of that. So that’s our trial design. Now safety:

Of the 300 people who received the booster, one had a heart attack two months later. No worries, Pfizer concluded it wasn’t related. Yay! Five percent of recipients had enlarged lymph nodes. How about effectiveness? Well, we don’t have enough data – or any data, really – telling us how well the booster will work. But the FDA made Pfizer go back and review its data from the pivotal clinical trial from last year. Pfizer compared people who received the vaccine with those who received the placebo and THEN the vaccine (the best we can do at this point, since Pfizer blew up the trial by giving placebo subjects the vaccine, double-yay!) Pfizer concluded that your annual risk of getting Covid-19 IF YOU ARE VACCINATED is about 7 percent.

Further: “An additional analysis appears to indicate that incidence of COVID-19 generally increased in each group of study participants with increasing time post-Dose 2 at the start of the analysis period.” Oh. But don’t worry, Uncle Joe already told you you can get your booster on September 20. If it’s good enough for our fearless leader, it should be good enough for the FDA, amirite? SCIENCE!

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“The growing consensus among vaccination researchers is that exposure to 5-8 of these mRNA jabs over a relatively brief period of time will – dependent on the underlying health of the individual – result in death.”

A Slog Vaxicide Special (Ward)

One can observe categorically that medical researchers in Australia, India, France, the US, Germany and Japan are showing why the mRNA Covid “vaccines” tested by Oxford Recovery on dogs killed all the vaccinated animals. The detailed nature of deadly Cytokinic overreaction is closely allied to the study of how ‘autoantibodies’ develop. These little mothers are not always good news. Antibodies are produced by our B cells in two ways: (i) randomly, and (ii) in response to a foreign protein or substance within the body. Initially, one B cell produces one specific kind of antibody. In either case, the B cell is allowed to proliferate or is killed off through a process called clonal deletion. Normally, the immune system is able to recognise and ignore the body’s own healthy proteins, cells, and tissues.

But sometimes, the immune system ceases to recognise one or more of the body’s normal constituents as “self,” leading to production of pathological autoantibodies. When this happens, these psycho antibodies go into a frenzy of destruction. The more the body is exposed to mRNA formulations, the more certain death becomes. That certainty helps to explain the emerging narrative about “booster” shots of “vaccine”. This is Anthony Fauci of the US CDC from a live media interview five days ago: “You know, I think we are going to need boosters. And I think very likely, when we look back on this, the proper complete regimen for good full protection will almost certainly be three shots – the first two that we’ve spoken about and a late third boost several months later.”

For the already vaxxed, that would make five jabs in all….and no doubt, a new strain would miraculously appear to justify a 6th and 7th top-up. The growing consensus among vaccination researchers is that exposure to 5-8 of these mRNA jabs over a relatively brief period of time will – dependent on the underlying health of the individual – result in death. In a bid to head off awkward questions about the efficacy of such drugs, Fauci then resorted to the current default lie: “This is still an outbreak, a pandemic of the unvaccinated. And when you look at the percentage of cases, particularly those that wind up with severe consequences leading to hospitalization, it is overwhelmingly among the unvaccinated.”

Read more …

That would be Macron?!

France Leads The Way In Holding Covid Incompetents To Account (RT)

Former French Health Minister Agnès Buzyn faces a possible prison term and heavy fine for “endangering the life of others” in her mishandling of the coronavirus pandemic, as France leads the way in making its leaders accountable. Despite the massive failures by governments and public health officials across the globe in dealing with the pandemic, it’s only the dead that really pay any sort of price. Most of the so-called experts simply move on, retire, or fade back into academia or big pharma where many of them came from. Not so in France, where the appetite for accountability has landed former Health Minister Agnès Buzyn in la merde,having just been indicted by the Court of Justice of the Republic – a special court established specifically to hold government ministers accountable for their actions – for “endangering the life of others” through mismanagement of the Covid-19 pandemic, which has cost the French 115,000 lives. If found guilty, she faces a year in jail and a €15,000 fine.

Buzyn, a former doctor, did not have a good pandemic. She stood on the steps of the Elysee Palace in January last year and foolishly declared, “The risks of the coronavirus spreading to the population are low.” Ooops. But Buzyn is not the only French politician with their neck on the block. Her successor, Health Minister Olivier Véran, is also under investigation, along with former Prime Minister Edouard Phillippe. Surely, this is the sort of ministerial accountability that every democratic nation should be enforcing. Too often, incompetent, bungling, and plainly dishonest politicians escape sanction when they step aside, trying to present their resignation – or sacking – as some kind of noble gesture for which they should be congratulated, not imprisoned.

[..] But what about the rest of the Covid clowns around the world, with their misinformation, backtracking on guidance, exaggeration, underestimation, and sheer, cack-handed incompetence? Right up there is WHO Director-General Tedros Adhanom Ghebreyesus who, when meeting with Chinese President Xi Jinping, was full of praise for China’s containment of the coronavirus. The very least we could expect would be the WHO boss clearing his desk. In the US, Dr Anthony ‘Flip-flop’ Fauci faced his own messaging problems, having initially announced that the pandemic posed a “very, very low risk to the United States,” in January 2020. Since then, there have been more than 40 million reported covid cases in the US and around 652,000 deaths. I hope he likes golf, because Dr Fauci might soon have a lot more time to work on his handicap.

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Ivermectin.

33 Districts In Uttar Pradesh Are Now Covid-free (HT)

There are no active cases of the coronavirus disease (Covid-19) in 33 districts of Uttar Pradesh, the state government informed on Friday. About 67 districts have not reported a single new case of the viral infection in the last 24 hours, the government said, noting the steady improvement of the Covid-19 situation in the state. [..] Overall, the state has a total of 199 active cases, while the positivity rate came down to less than 0.01 per cent. The recovery rate, meanwhile, has improved to 98.7 per cent. As per the state’s health bulletin, Uttar Pradesh reported only 11 new Covid-19 cases and zero deaths in the last 24 hours. The fresh cases came out of 2.26 lakh samples that were tested in the last 24 hours.


As of Friday, the state government has conducted 7.42 crore tests, according to the data published by Uttar Pradesh’s health department. On the vaccination front, around 7 crore people in the state have received their first dose of the jab. The vaccination coverage in the state has exceeded 8.47 crores, out of which, 12 lakh people have been inoculated in the last 2 hours. Meanwhile, the overall nationwide tally climbed to 33,174,954 after recording 34,973 cases in the last 24 hours. This was around 19% lower than Thursday when the country had logged 43,263 fresh infections. The death toll stands at 442,009.

India home kit.

Read more …

As prices are soaring all over Europe, the EU keeps playing politics. My guess is Merkel will put a stop to that. She does’t want to leave her country in a state of huge unrest.

EU Red Tape Prevents Russia From Boosting Gas Supplies To Europe – Lavrov (RT)

Despite the completion of Nord Stream 2, Europe should not expect the Russian pipeline to start deliveries this year due to bureaucracy within the EU, Russian Foreign Minister Sergey Lavrov warned on Wednesday. “Now the process of obtaining the necessary permits from the German regulator is underway. The process is not fast. The beginning of 2022 has been indicated,” Lavrov told the press. Experts say this could be the reason behind the current surge in gas prices, which have been smashing records for several days now. According to the press secretary of the German Federal Network Agency (BNetzA), Fita Wolf, Nord Stream 2’s certification may take several months, a prospect which practically forces market participants to raise prices.


To add to the problem, the pipeline’s main adversaries, Ukraine and the United States, have both vowed to complicate the certification procedure. According to Lavrov, there will be many roadblocks before certification is finally granted. “I have no doubt that attempts to attack this gas pipeline will continue,” the Russian foreign minister said. Gas prices in Europe have risen 20% since the start of trading on Wednesday. The price of October futures on the Dutch TTF exchange exceeded $964 per 1,000 cubic meters by 11am GMT, ICE data shows.

Read more …

There was ever any focus.

US ‘Lost Focus’ In War On Terror – Oliver Stone (RT)

On the 20th anniversary of the 9/11 terror attacks, in a conversation with RT, award-winning director Oliver Stone condemned the US response as rooted in “exaggerated hype to go to war” and a misguided attempt at revenge-seeking. Stone condemned the bloody-minded drive for vengeance that characterized the US’ reaction to the attacks from the outset. “‘We’ve gotta get them for this’ – [but] we didn’t even know who ‘them’ were!” he exclaimed to Going Underground’s Afshin Rattansi on Wednesday, pointing out that it was Khalid Sheikh Mohammed, rather than the better-known terrorist bogeyman Osama Bin Laden, who put together the entire plan “in his brain.”

“We lost focus in that moment – we were terrified, horrified, but we didn’t really look at what happened. We should have looked at why. A lot of [the government’s reasoning] was BS. A lot of it was exaggerated hype to go to war by the US and Israel,” Stone explained. Regarding US President Joe Biden’s controversial pullout from Afghanistan, Stone’s was a rare voice of support, insisting he “didn’t think it was a bad withdrawal at all” and that the sense of crisis was inflated by the media. “I appreciate a man who isn’t rushing to judgment like Bush was or Trump would be. A man who thinks about things and is deliberate … Most American presidents would fold – change their minds because of the polls,” which are “always tough on presidents.”

Stone observed that the reasons the terrorists gave for the 9/11 attacks were relatively simple: former president George H.W. Bush’s decision to station US troops on Saudi holy land and the US’ increasingly ‘one-sided’ support for Israel, despite international law. “We should have looked at why [the attacks occurred]. Bush said they envy our freedoms, but that was nonsense. They did it because of two reasons, as Osama stated very clearly,” Stone continued. “Instead of disengaging when the war was over in November, we sent in a huge amount of troops, didn’t understand the landscape, went out again and again on patrols, and, as we did in Vietnam, [the US Army] antagonized people by just being there.”

Read more …

Coming too close to Clinton?

Durham Reportedly Seeking Indictment Against Clinton Campaign Lawyer (JTN)

Special counsel John Durham reportedly is seeking a grand jury indictment against Michael Sussmann, a cybersecurity lawyer at a Democratic-allied law firm that represented Hillary Clinton’s 2016 campaign. According to the New York Times, the charge is said to be related to an alleged false statement to the FBI about a client’s identity when Sussmann pushed now-debunked claims about secret communications between Russia’s Alfa Bank and the Trump Organization in the lead-up to the 2016 presidential election. Durham “has told the Justice Department that he will ask a grand jury to indict a prominent cybersecurity lawyer on a charge of making a false statement to the FBI,” the New York Times reported on Wednesday, citing “people familiar with the matter.”

Prior testimony and documents show Sussmann, who worked at Perkins Coie, delivered allegations about the Alfa server to then-FBI General Counsel James Baker in fall 2016. Baker has told invetsigators Sussman told him his approach was not on behalf of any client. But Sussmann told Congress he made the approach on behalf of a computer security client. The newspaper said Durham’s team has obtained records showing Sussmann billed work on the Alfa Bank matter to the Clinton campaign, the newspaper said. Sussmann’s lawyers, Sean M. Berkowitz and Michael S. Bosworth, acknowledged Wednesday that they expected him to be indicted, but denied wrongdoing.

“Mr. Sussmann has committed no crime,” they told the Times. “Any prosecution here would be baseless, unprecedented and an unwarranted deviation from the apolitical and principled way in which the Department of Justice is supposed to do its work. We are confident that if Mr. Sussmann is charged, he will prevail at trial and vindicate his good name. Durham has until the weekend to charge Sussmann because of a five-year statute of limitations, the newspaper said.

Read more …

 

 

 

 

 

McCullough Delta
https://twitter.com/i/status/1438056517001904130

 

 

 

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


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

 

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

 

 

Update from the CDC:

 

 

 

 

 

 

 

“FDA approval is checkmate for Pfizer.”

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

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

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

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

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

Read more …

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

Here’s where those numbers come from.

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

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

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

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

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

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


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

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

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

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

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

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

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

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

Denmark To Scrap All Covid-19 Restrictions (ZH)

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


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

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Crazy, that’s the only word.

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

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

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

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

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

US Mandates Vaccinations For Marines (PPundit)

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

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

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

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

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

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

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

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

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

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

Low and Dark (Kunstler)

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

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

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

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

Read more …

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

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

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

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

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

Read more …

 

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Aug 262021
 
 August 26, 2021  Posted by at 9:21 am Finance Tagged with: , , , , , , ,  83 Responses »


Vasily Polenov Christ among the teachers (doctors) 1896

 

67% Of UK Covid-19 Deaths Since February 2021 Were Vaccinated (DE)
McCullough: ‘The Vaccines Are Failing’ (CHD)
2 Things MSM Didn’t Tell You About FDA’s Approval of Pfizer Vaccine (CHD)
Comparing SARS-CoV-2 Natural Immunity To Vaccine-induced Immunity (Medrxiv)
Safety of the BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Setting (NEJM)
Real-World Study Links Pfizer Vax to High Risk of Myocarditis (MPT)
Delta Will Charge Unvaccinated Employees $200 Per Month For Health Plan (AP)
Texas Gov. Greg Abbott Bans Covid-19 Vaccine Mandates (TT)
New Zealand Could Be Split Into North And South Island Bubbles (G.)
Origins of SARS-CoV-2: Window Is Closing For Key Scientific Studies (Nature)
Early Wuhan COVID Samples Contained Genetically Modified Viruses (ET)
Tucker Carlson Warns “Elitist Dems” Want You To “Shut Up And Obey” (SN)
“I Was Living Like Scarface” (MPN)
“Leftie” Is Now A Slur In Working-Class Towns (G.)

 

 

 

 

 

 

 

 

 

 

Comment on the same Public Health England (PHE) briefing the Daily Sceptic addressed yesterday, saying “Calculating the vaccine effectiveness against Delta infection in the over-50s [..] gives a figure of just 15%..”

67% Of UK Covid-19 Deaths Since February 2021 Were Vaccinated (DE)

The latest Public Health England report on Covid-19 infections, hospitalisations, and deaths show that the Covid-19 injections do not work, and quite possibly make the recipient worse if exposed to the alleged Covid-19 virus due to the fully vaccinated population accounting for 21% of all infections but 58% of all Covid-19 deaths. PHE release a technical briefing on Covid-19 variants of concern every two weeks, and the 21st update released on the 20th August 2021 provides further proof; just as previous reports have, that the Covid-19 vaccines are in fact increasing the risk of hospitalisation and death, rather than reducing it by the 95% claimed by the vaccine manufacturers.

According to the report since the 1st February 2021 and the 15th August 2021 there have been 183,133 confirmed cases among the unvaccinated population, an increase of 32,079 on the last count made in the previous report where the confirmed figure was 151,054 up to the 2nd August 2021. There have also been 26,194 confirmed cases among people who had received a single dose of a Covid-19 vaccine, 21 days prior to their positive test, an increase of 2,176 on the last count made in the previous report where the confirmed figure was 24,018 up to the 2nd August 2021.

Confirmed cases among people who had received a single dose of a Covid-19 vaccine more than 21 days prior to their positive test total 62,763 up to the 15th August 2021. This is an increase of 17,674 on the previous report where the confirmed figure was 46,089 up to the 2nd August 2021. Finally, the latest report reveals that there have been 73,372 confirmed cases of the Delta Covid-19 variant among the fully vaccinated population, an increase of 26,364 on the last count made in the previous report where the confirmed figure was 47,008 up to the 2nd August 2021.

Read more …

Are we getting McCullough overkill?

McCullough: ‘The Vaccines Are Failing’ (CHD)

Why is the world experiencing such a “prominent outbreak” of the Delta variant when so many people have been vaccinated? Cardiologist Dr. Peter McCullough addressed those questions and more on the “RFK Jr. The Defender Podcast.” New research shows people who are vaccinated against COVID are more susceptible to the Delta variant, said McCullough, pointing to a pre-print study by the prestigious Oxford University Clinical Research Group published Aug. 10 in The Lancet. The paper’s authors demonstrated widespread vaccine failure and transmission under tightly controlled circumstances in a hospital lockdown in Ho Chi Minh City, Viet Nam. The study found vaccinated people carry 251 times the load of COVID-19 viruses in their nostrils compared to the unvaccinated, the study found.

“They had an outbreak and they locked down the hospital where the workers could not get out,” said McCullough. “They were assiduously checking the workers and testing them for COVID, as well as doing sequencing.” The researchers found workers were still getting COVID during the lockdown period, said McCullough, and they were passing it to one another. The study’s big finding is their calculation of viral load, McCullough said: “This group had actually calculated viral load from oral and nasal secretions in the past. The viral load was 251 times that of the previous unvaccinated era where they had used the same methodology. So, they had previous workers and patients who had COVID-19 before any exposure to the vaccines. And now the vaccinated were carrying a massive viral load and passing it to one another.”

The efficacy for the Pfizer vaccine is measured as being anywhere from 17% to 42% effective. “These levels are far below the 50% regulatory standard to even have a vaccine on the market,” said McCullough. Regardless of the variant or the vaccine, McCullough said the bottom line is that “the vaccines are failing.”

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“If it doesn’t say Comirnaty, you have not been offered an approved vaccine.”

2 Things MSM Didn’t Tell You About FDA’s Approval of Pfizer Vaccine (CHD)

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. 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.

Read more …

Vaccinated people are 13x more likely to get infected than those with natural immunity.

Comparing SARS-CoV-2 Natural Immunity To Vaccine-induced Immunity (Medrxiv)

Reports of waning vaccine-induced immunity against COVID-19 have begun to surface. With that, the comparable long-term protection conferred by previous infection with SARS-CoV-2 remains unclear. Methods: We conducted a retrospective observational study comparing three groups: (1)SARS-CoV-2-naive individuals who received a two-dose regimen of the BioNTech/Pfizer mRNA BNT162b2 vaccine, (2)previously infected individuals who have not been vaccinated, and (3)previously infected and single dose vaccinated individuals. Three multivariate logistic regression models were applied. In all models we evaluated four outcomes: SARS-CoV-2 infection, symptomatic disease, COVID-19-related hospitalization and death.


The follow-up period of June 1 to August 14, 2021, when the Delta variant was dominant in Israel. Results: SARS-CoV-2-naive vaccinees had a 13.06-fold (95% CI, 8.08 to 21.11) increased risk for breakthrough infection with the Delta variant compared to those previously infected, when the first event (infection or vaccination) occurred during January and February of 2021. The increased risk was significant (P<0.001) for symptomatic disease as well. When allowing the infection to occur at any time before vaccination (from March 2020 to February 2021), evidence of waning natural immunity was demonstrated, though SARS-CoV-2 naive vaccinees had a 5.96-fold (95% CI, 4.85 to 7.33) increased risk for breakthrough infection and a 7.13-fold (95% CI, 5.51 to 9.21) increased risk for symptomatic disease.

SARS-CoV-2-naive vaccinees were also at a greater risk for COVID-19-related-hospitalizations compared to those that were previously infected. Conclusions: This study demonstrated that natural immunity confers longer lasting and stronger protection against infection, symptomatic disease and hospitalization caused by the Delta variant of SARS-CoV-2, compared to the BNT162b2 two-dose vaccine-induced immunity.

Read more …

New England Journal of Medicine. Israel study. Drowning in numbers.

“Vaccination was most strongly associated with an elevated risk of myocarditis, lymphadenopathy, appendicitis, and herpes zoster infection”

Safety of the BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Setting (NEJM)

Table S6 shows the effect of SARS-CoV-2 infection on the incidence of various adverse events. Infection substantially increased the risk of many different adverse events, including myocarditis (risk ratio, 18.28; 95% CI, 3.95 to 25.12; risk difference, 11.0 events per 100,000 persons; 95% CI, 5.6 to 15.8), acute kidney injury (risk ratio, 14.83; 95% CI, 9.24 to 28.75; risk difference, 125.4 events per 100,000 persons; 95% CI, 107.0 to 142.6), pulmonary embolism (risk ratio, 12.14; 95% CI, 6.89 to 29.20; risk difference, 61.7 events per 100,000 persons; 95% CI, 48.5 to 75.4), intracranial hemorrhage (risk ratio, 6.89; 95% CI, 1.90 to 19.16; risk difference, 7.6 events per 100,000 persons;


95% CI, 2.7 to 12.6), pericarditis (risk ratio, 5.39; 95% CI, 2.22 to 23.58; risk difference, 10.9 events per 100,000 persons; 95% CI, 4.9 to 16.9), myocardial infarction (risk ratio, 4.47; 95% CI, 2.47 to 9.95; risk difference, 25.1 events per 100,000 persons; 95% CI, 16.2 to 33.9), deep-vein thrombosis (risk ratio, 3.78; 95% CI, 2.50 to 6.59; risk difference, 43.0 events per 100,000 persons; 95% CI, 29.9 to 56.6), and arrhythmia (risk ratio, 3.83; 95% CI, 3.07 to 4.95; risk difference, 166.1 events per 100,000 persons; 95% CI, 139.6 to 193.2).

Read more …

About that same Israel study.

Real-World Study Links Pfizer Vax to High Risk of Myocarditis (MPT)

The Pfizer COVID-19 mRNA vaccine was found to be associated with a threefold increased risk of myocarditis, according to a real-world case-control study from Israel. Vaccination had a strong association with an increased risk of myocarditis (risk ratio [RR] 3.24, 95% CI 1.55-12.44), as well as increased risks of lymphadenopathy (RR 2.43, 95% CI 2.05-2.78), appendicitis (RR 1.40, 95% CI 1.02-2.01), and herpes zoster infection (RR 1.43, 95% CI 1.20-1.73), reported Ran Balicer, MD, of Clalit Health Services in Tel Aviv, and colleagues.

However, in a separate cohort, infection with SARS-CoV-2 was associated with a higher risk of myocarditis (RR 18.28, 95% CI 3.95-25.12), as well as other cardiovascular complications, including acute kidney injury (RR 14.83, 95% CI 9.24-28.75), pulmonary embolism (RR 12.14, 95% CI 6.89-29.20), and intracranial hemorrhage (RR 6.89, 95% CI 1.90-19.16), the authors wrote in the New England Journal of Medicine. They noted that vaccination was “substantially protective” against anemia, acute kidney injury, intracranial hemorrhage, and lymphopenia. Balicer’s group examined data from the largest healthcare organization in Israel to compare incidence of adverse events among vaccinated individuals versus unvaccinated individuals, and estimated the effects of SARS-CoV-2 infection on these adverse events.

Participants in the vaccination cohorts were 16 years old and older, had been in the health organization for a full year, had no prior COVID-19 infection, and had no contact with the healthcare system in the last 7 days. Notably, populations with confounders, such as healthcare workers, long-term care facility residents, or people confined to their home for medical reasons, were excluded.

Read more …

As vaccinated people are 13x more likely to get infected than those with natural immunity. Logos.

Delta Will Charge Unvaccinated Employees $200 Per Month For Health Plan (AP)

Delta Air Lines will charge employees on the company health plan $200 a month if they fail to get vaccinated against COVID-19, a policy the airline’s top executive says is necessary because the average hospital stay for the virus costs the airline $50,000. CEO Ed Bastian said that all employees who have been hospitalized for the virus in recent weeks were not fully vaccinated. The airline said Wednesday that it also will stop extending pay protection to unvaccinated workers who contract COVID-19 on Sept. 30, and will require unvaccinated workers to be tested weekly beginning Sept. 12, although Delta will cover the cost. They will have to wear masks in all indoor company settings.

Delta stopped short of matching United Airlines, which will require employees to be vaccinated starting Sept. 27 or face termination. However, the $200 monthly surcharge, which starts in November, may have the same effect. “This surcharge will be necessary to address the financial risk the decision to not vaccinate is creating for our company,” Bastian said in a memo to employees. The surcharge will only apply to employees who don’t get vaccinated and won’t be levied for spouses or dependents, a Delta spokeswoman said. [..] Bastian said that 75% of Delta employees are vaccinated, up from 72% in mid-July. He said the aggressiveness of the leading strain of the virus “means we need to get many more of our people vaccinated, and as close to 100% as possible.”

“I know some of you may be taking a wait-and-see approach or waiting for full (Food and Drug Administration) approval,” he told employees. “With this week’s announcement that the FDA has granted full approval for the Pfizer vaccine, the time for you to get vaccinated is now.” A growing number of companies including Chevron Corp. and drugstore chain CVS announced they will require workers to get vaccinated after Monday’s FDA decision. United and Delta already require new hires to be vaccinated. Two smaller carriers, Hawaiian and Frontier, have said they will require either vaccination or regular testing for current employees. Other major U.S. airlines, including American and Southwest, said Wednesday that they are encouraging employees to get vaccinated but have not required it.

Read more …

“Vaccine requirements and exemptions have historically been determined by the legislature, and their involvement is particularly important to avoid a patchwork of vaccine mandates across Texas..”

Texas Gov. Greg Abbott Bans Covid-19 Vaccine Mandates (TT)

Gov. Greg Abbott on Wednesday announced an executive order banning COVID-19 vaccine mandates regardless of a vaccine’s approval status with the U.S. Food and Drug Administration. He also said he was adding the issue to the agenda for the current special session of the Texas Legislature. The order comes two days after the FDA granted full approval to the Pfizer vaccine. That raised questions about the fate of a previous Abbott order that prohibited vaccine mandates, but only for those under emergency authorization. Abbott’s latest order is simple, saying “no governmental entity can compel any individual to receive a COVID-19 vaccine.” The order preserves exceptions for places like nursing homes and state-supported living centers.

At the same time, Abbott asked lawmakers to consider legislation addressing whether state or local governments could issue vaccine mandates and, if so, which exemptions should apply. “Vaccine requirements and exemptions have historically been determined by the legislature, and their involvement is particularly important to avoid a patchwork of vaccine mandates across Texas,” Abbott said in a statement. Lawmakers are currently in their second special session, and time is limited to make progress on the 17-item agenda that Abbott previously announced. The House finally restored quorum last week after Democrats staged a nearly six-week protest of the GOP’s elections bill, and the current session is set to end Sept. 5.

Abbott’s last order regarding vaccine requirements, issued July 29, said “no governmental entity can compel any individual to receive a COVID-19 vaccine administered under an emergency use authorization.” While there is a new state law that acted as a backstop for Abbott’s previous order if a vaccine received full approval, it was not as sweeping as the order and left the door open to new mandates. There specifically appeared to be the fresh potential for cities, counties and school districts to require their employees to get vaccinated against COVID-19. San Antonio Independent School District had already announced mandatory employee vaccinations, prompting a lawsuit from Attorney General Ken Paxton. District officials said Wednesday they will move forward with the mandate — despite Abbott’s latest order.

Read more …

Says the “Covid modeller”. Get a life.

New Zealand Could Be Split Into North And South Island Bubbles (G.)

A Covid-19 modeller has suggested New Zealand’s North and South islands could become separate bubbles as the country grapples with a coronavirus outbreak, although South islanders with hopes of being fully released from lockdown should not hold their breath just yet. New Zealand is battling to contain an outbreak of the Delta variant that swiftly led to a nationwide, level four lockdown – the highest setting – which has been extended until at least the end of the week. There are now 210 cases in the community. Auckland – the largest city, where the majority of cases have been detected – will remain in lockdown until the end of the month.


There have been no cases in the South Island, but the 20,000-strong list of close contacts linked to the current outbreak extends across both islands. Around 120 people, who were potentially exposed to the virus at locations in Auckland, are isolating in the South Island. Auckland could expect to stay in lockdown for a number of weeks , but a North Island and South Island split could make sense, Covid-19 modeller at the University of Auckland, Shaun Hendy, told TVNZ. “I think at this stage, a North Island and South Island split is probably what we’d be looking at,” Hendy said. In order for the alert levels to drop in the South Island, any wastewater tests would need to come back clear, Hendy said.

Read more …

Daszak gets another shot at whitewashing Daszak, and Nature provides a podium to do it on.

Origins of SARS-CoV-2: Window Is Closing For Key Scientific Studies (Nature)

Our group was convened by the World Health Organization (WHO) in October 2020. We have been the designated independent international members of a joint WHO–China team tasked with understanding the origins of SARS-CoV-2. Our report was published this March1. It was meant to be the first step in a process that has stalled. Here we summarize the scientific process so far, and call for action to fast-track the follow-up scientific work required to identify how COVID-19 emerged, which we set out in this article.

The window of opportunity for conducting this crucial inquiry is closing fast: any delay will render some of the studies biologically impossible. Understanding the origins of a devastating pandemic is a global priority, grounded in science. We, all the members of the international expert team, each submitted detailed, confidential statements to the WHO on potential conflicts of interest, including funding, collaborative studies, public statements and other issues around the origins of COVID-19 that could be perceived as conflicts. After the WHO had reviewed these, team members were appointed in their individual capacity, not as representatives of their employers.

So far, our mission has been guided by terms of reference agreed between the WHO and China in 2020, before our involvement1. These terms tasked us with making a detailed reconstruction of the early phase of the pandemic, beginning in Wuhan, China, where the first known cases were reported. Our mandate was to conduct a collaborative study with leading scientists in China to review data they had generated on the basis of initial questions from the WHO. We refined the generic list of questions described in the mandate into a detailed workplan described in the mission report.

Read more …

Bet this is also Daszak.

“We found genetic manipulation of the Nipah virus, which is more lethal than Ebola.”

Early Wuhan COVID Samples Contained Genetically Modified Viruses (ET)

Samples from early Wuhan COVID-19 patients show the presence of genetically modified Henipah virus, an American scientist has found. Henipah was one of the two types of viruses sent to China by Chinese-born scientists from a Canadian laboratory at the centre of a controversy over the firing of the scientists and collaboration with Chinese military researchers. It is not clear whether the virus found in the Chinese samples is related to the virus samples sent by the Canadian lab, which were shipped in late March 2019. The finding was confirmed for The Epoch Times by another qualified scientist.

The evidence was first found by Dr. Steven Quay, a Seattle-based physician-scientist and former faculty member at the Stanford University School of Medicine, who looked at early COVID-19 samples uploaded by scientists at the Wuhan Institute of Virology (WIV) shortly after China informed the WHO about the SARS-CoV-2 outbreak. The samples from the patients, who reportedly were found to have an “unidentified pneumonia disease” in December 2019, were uploaded to the genetic sequence database, GenBank, on the website of the U.S. National Institute of Health (NIH). Quay says that while other scientists around the world were mostly interested in examining the genome of SARS-CoV-2 in the samples uploaded by the WIV scientists, he wanted to see what else was in the samples collected from the patients.

So he collaborated with a few other scientists to analyze sequences from the samples. “We started fishing inside for weird things,” Quay told The Epoch Times. What they found, he says, are the results of what could likely be contamination from different experiments in the lab making their way into the samples, as well as evidence of Henipah virus. “We found genetic manipulation of the Nipah virus, which is more lethal than Ebola.” Nipah is a type of Henipah virus. [..] Documents released by the Canadian government state that the WIV’s intended use of the virus samples sent by Canada was “stock virus culturing,” which in simpler terms means storing the viruses while keeping them alive. Genetic manipulation would not be within the scope of this description.

Read more …

Worth watching.

Tucker Carlson Warns “Elitist Dems” Want You To “Shut Up And Obey” (SN)

Fox News host Tucker Carlson issued a stark warning Tuesday, emphasising that “we’re seeing now what happens when countries tolerate authoritarians, even for a moment” as people worldwide are being told to submit to increasingly draconian “rules” in the wake of the pandemic. Carlson noted “Has there ever been a clearer window into the society they’re trying to build? Our formerly middle-class nation now has a serf class. They’re the ones wearing the masks, being forced to take drugs they don’t want, being told not to communicate with one another, except through digital channels the Democratic Party controls.”


He continued, “We now have two groups of Americans, not a broad middle. The favored and the unfavored. The saved and the damned. The vaccinated and the unvaccinated. That’s how the architects of all this see the country.” Carlson also pointed to former NSA head Michael Hayden’s assertion that Trump supporters should be sent to Afghanistan to die. “That’s how contemptuous they feel about you,” Carlson noted, adding “Shut up and fetch another glass of Riesling, serf. And be sure not to breathe on me, or you’ll be deported.” “These are bad attitudes and are accelerating. How far can this go, you wonder?” he questioned. Carlson also described some of the insane policies being put into place in Australia and New Zealand, describing them as akin to North Korea.

Read more …

“Holy cow, I was living like Scarface…I was paying out anywhere between $300-400,000 per week to $5 million per week at times. All in cash.” Matthew Hoh, U.S. Marine Corps Captain and former State Department official

“I Was Living Like Scarface” (MPN)

The conflict in Afghanistan — for the U.S. at least — appears to be over. Essentially admitting defeat, American planes are beating a hasty and ignominious retreat from Kabul, with images of the withdrawal bearing a striking resemblance to those from the fall of Saigon 46 years previously. As the Taliban complete their takeover, many Americans are wondering what it was all about. For what, and on what, did the United States spend more than $2 trillion? A newly published study from the Special Inspector General for Afghanistan Reconstruction (SIGAR) — a U.S. government body — lays bare the waste and corruption of the whole affair, drawing parallels with famous satires such as “Catch 22” and “M*A*S*H*.” Uncompromising in its frankness, the 124-page report outlines the incompetence, venality and dark absurdity of the whole endeavor.

“When you look at how much we spent and what we got for it, it’s mind boggling,” one senior Department of Defense administrator admitted to SIGAR in 2015. Congress founded SIGAR in 2008 to provide neutral and objective oversight into the U.S.’ handling of Afghan reconstruction programs. The new report is the latest — and perhaps most critical — of 13 yearly offerings analyzing U.S. efforts in the country. At no point did the U.S. truly control all of Afghanistan. But officials in Washington wanted to see quantifiable results. In a region where American troops were barely able to leave their bases without being attacked, “cash spent” became one of the few concrete metrics commanders could report back with any accuracy. As the report concluded:

Perversely, because it was the easiest thing to monitor, the amount of money spent by a program often became the most important measure of success. A USAID official told SIGAR, ‘The Hill was always asking, ‘Did you spend the money?’…I didn’t hear many questions about what the effects were. Program budgets were massively expanded, often over the objections of USAID and others on the ground, who argued that inundating the country with dollars was not truly winning hearts and minds, and was a wasteful and ineffective strategy. There was no incentive to report on financial excesses, fraud or abuse, and barely any oversight over where the money was actually going. Contractors, NGOs and others who were aboard the seemingly endless gravy train also kept quiet as they stuffed their pockets with billions of dollars of public money.

MintPress spoke to a person who had been a central part of this bizarre story. Matthew Hoh was a captain in the U.S. Marine Corps and an official with both the Department of Defense and the State Department, spending almost 12 years in the U.S. military and government focusing on Iraq and Afghanistan. In 2009, he resigned from his position in the State Department in Zabul Province, Afghanistan, over U.S. policy in the country. “The way to prove that you were doing your job was by spending money,” Hoh told MintPress, continuing: Money being spent on an institutional level was a metric of success. Somehow in the minds of the U.S. political leaders, in Iraq and Afghanistan, dollars spent equated to things being constructed and effective counterinsurgency [against the Taliban]…But the Taliban themselves were taking the money! The Taliban guys were doing the construction work. It was absolutely nuts!”

Read more …

I don’t have time for the very few.

“Leftie” Is Now A Slur In Working-Class Towns (G.)

In 2011, Sam Fender was, by his own admission, “a little stoner” who had flunked out of his A-Levels in his hometown of North Shields, living with his mother in a flat with black mould on the walls. A decade later, he’s one of the UK’s best and most successful singer-songwriters: his 2019 debut album Hypersonic Missiles went to No 1, he won a Brit award, and his knack for writing songs about 21st-century disaffections marked him out from cheerier peers such as Ed Sheeran and George Ezra. His second album Seventeen Going Under, a superb record that channels the sound of Bruce Springsteen and the War on Drugs into an examination of his family, youth and frailty, is out in October.

[..] You’ve also written about politics – Aye, from the new album, is probably the angriest song you’ve ever written.

Because of the polarity between the left and the right, I don’t feel I have an identity with politicians on either side. The left wing have abandoned the working classes, and with a lot of the left – I don’t want to sound like Piers Morgan when I say this – I feel like there is too much nitpicking and stupid fights, especially online. But I hate the Tories with a passion. I was raised to hate them, I still hate them, and I always will. They clearly know who they stand for and they don’t represent people like us. A quarter of the kids in working families in my region are in poverty. Nobody sticks their neck out for the north-east. The line in Aye – “I don’t have time for the very few” – that’s the one thing that always going to be my main gripe on this planet, the sheer disparity between the 1% and the rest of the world. These culture wars are valid wars that need to be fought – there’s a lot of bigotry, a lot of racism and homophobia. But in order to get the Tories out, you’ve got to start representing the working class people of this country.

The right are sitting back and laughing, sweeping up every election. Blyth Valley up here went Tory. It’s a shipbuilding town. That’s insanity. Working-class people up here think the Tories are on their side – which shows how completely the left have fucked themselves. I’ve had arguments with people who say Jeremy Corbyn’s a twat, regurgitating Daily Mail headlines that he’s a terrorist sympathiser. I’m like: how? Tell me in your own words. And they go, “Ah you’re just one of them lefties”. “Leftie” is now a slur in working-class towns – what happened there? It upsets me that we’re in a place where the media have so much control over these blokes who have grafted all their life in a system that would benefit them if someone like Corbyn was in.

Read more …

 

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Aug 252021
 


Vincent van Gogh The red tree house 1890

 

 

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

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

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

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

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

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

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

 

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

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

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


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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

And Jill Malone.

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

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

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

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

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

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

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

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

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

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

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

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

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

 

 

 

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Aug 252021
 


Salvador Dali The Madonna of Port Lligat 1950

 

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

 

 

Yesterday I posted this on mandates:

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

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

 

 

A New York Post tweet:

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

 

 

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

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

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

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

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

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

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

Read more …

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

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

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

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


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

Read more …

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

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

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

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

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

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

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

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

Read more …

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

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

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


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

Read more …

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

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

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


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

Read more …

Pretty good!

A Most Unusual Thing in Australia, Alice (CTH)

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


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

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


So here we are. Cheers !

Read more …

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

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

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


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

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

Unvaccinated Removed From Transplant Waiting Lists (JTN)

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

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

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

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The long background story of ivermectin, before Covid.

From Nature, The Journal of Antibiotics, February 2017.

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

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

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

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

And ivermectin today:

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

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

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

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

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

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The Dems have sleepless nights over Kamala stepping up.

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

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


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

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

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

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

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

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

Read more …

 

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Aug 242021
 


George Caleb Bingham The verdict of the people 1854

 

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

 

 

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

 

 

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

 

 

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

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

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

 

 

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

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

 

 

Conditions Related to Printed Matter, Advertising, and Promotion

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

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

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

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

 

 

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

 

 

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

 

 

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

Well, not really, because they stopped those trials.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

FDA Ignores Both Science and Law (Denninger)

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Statistical Fraud in the FDA Vaccine Approval Process (JoshM)

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

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

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

For example, suppose we have 2 vaccines:

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

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

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

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

Read more …

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

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

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

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


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

Read more …

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

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

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


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

Read more …

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

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

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

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

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

Read more …

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

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

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


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

Read more …

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

Keeping Fear Alive (Tierney)

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

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

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

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

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

Read more …

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

Throwdowns and Showdowns (Kunstler)

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

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

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

Read more …

 

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Aug 212021
 
 August 21, 2021  Posted by at 6:04 pm Finance Tagged with: , , , , , ,  21 Responses »


René Magritte The false mirror 1928

 

 

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

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

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

 

 

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

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

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

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

 

 

And its European sister, EudraVigilance, on August 14:

 

 

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

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

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

 

 

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

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

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

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

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

 

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

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

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

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

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

 

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

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

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

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

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

 

 

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

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

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

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

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

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

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

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

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

 

Comments:

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

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

 

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

Dr Mike Yeadon

 

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

 

 

 

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Aug 212021
 


Salvador Dali Swans reflecting elephants 1937

 

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

 

 

Quite the paradox. That not even everybody recognizes.

 

 

 

 

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

And remember what Yeadon said:

 

 

 

 

How little managers become mass murderers.

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

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

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

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

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

Read more …

They don’t want anyone to see the paperwork.

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

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

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

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

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

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October 2020.

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

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

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

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

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

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

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

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Tragic, of course it is. But:

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

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

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

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

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

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

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

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

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

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

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

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

Director Of Yale University Research Center About Ivermectin (CdS)

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

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

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

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

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The protests will now grow fast. In many countries.

French Businesses Are Refusing to Enforce Vaccine Passport (SN)

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

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

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

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


French Health Pass has space for 8 shots

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A country inhabited by spike protein reservoirs.

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

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


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

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

The Heebie-Jeebies of August (Kunstler)

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

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

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

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

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

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

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

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

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

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