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It’s time to end the mandates

By Steve Kirsch | January 24, 2022

Boris Johnson recently declared an end to the COVID restrictions in the UK. He said, “We will trust the judgment of the English people.”

Why can’t we do that in the US? Isn’t it time to trust the judgment of the American people?

Whether you ask a red or blue pill person, it’s clear that both sides have compelling rationales to end the mandates and the State of Emergency.

Interestingly, the rationale for each side is completely different, but the conclusion is the same. Here’s how they stack up.

Blue pill rationale

  1. We don’t need mandates for the vaccine or masks because we know they work. No need to sell us! Mandate or not, we will comply.
  2. We no longer fear those who are not compliant: we are all boosted up the wazoo using safe and effective vaccines with virtually no side effects AND we are wearing N95 or P100 masks at all times. And we always stay 6 feet from any other person. So there is basically no way to infect us.
  3. We have nothing to fear. Virtually none of us will be hospitalized, and none of us risk death. And the prevalence of Omicron makes our risk even lower.
  4. We think people who are not compliant are evil and deserve to die. Why force them to take life-saving medical interventions? We are better off as a society if these people are gone. Permanently.
  5. We trust our doctors to deliver quality medical advice. Our doctors always follow the CDC guidance which has been uniformly excellent. We all should be treated the same, no matter what our medical histories are. If the doctors follow the CDC guidelines, almost nobody dies. All the hospitals are filled with unvaccinated people.
  6. Just to be safe, we test ourselves every day using antigen tests for COVID. If we have a positive test result, we now have two new safe and effective drugs from the most trusted drug companies in the world so that in the rare chance that we get COVID, we can treat it with nearly 100% success.

Red pill rationale

  1. Mandates aren’t needed because we won’t comply with them anyway. They just create division and animosity in society. They divide us.
  2. We don’t fear the vaccinated.
  3. Cloth, surgical, and N95 masks don’t work so why should we wear them? P100 masks do work, but they are pretty cumbersome and not worth the trouble for a COVID variant that can’t hurt us.
  4. Social distancing is useless and doesn’t work. The 6 foot rule is not based on any science. Why isn’t it 5.2 feet? Nobody has seen the science justifying 6 feet so we aren’t going to comply with silly non-scientific rules.
  5. The current COVID vaccines are more likely to kill people than save them. In the Pfizer trial, 24% more people died in the group taking the vaccine! So it’s clear. If the vaccines don’t kill us, they will actually make the pandemic worse because they depress our immune system making us twice as likely to be infected with COVID as well as susceptible to other diseases (like reoccurrence of cancer). They also cause serious side effects. They are the most dangerous vaccines in human history. There is no way we will take them. Mandating them is just going to piss us off and hurt the economy. You will not get us to take them.
  6. Why would we take a drug that could kill us to prevent a variant that cannot? You’d have to be nuts. We will not comply so the mandates won’t make us.
  7. The primary variant is Omicron which if it happened today, we’d just ignore it since it is like getting a cold.
  8. If we get sick, we have very effective early treatment protocols using existing safe repurposed drugs like ivermectin, HCQ, aspirin, vitamin D, NAC, and Prozac. These protocols are 100% successful in preventing death from COVID when given early. We would never use Molnupiravir or Paxlovid; those drugs are both super dangerous.
  9. We use symptoms to determine if we have COVID. If we are unsure, we can use antigen tests. There is no need to test if we aren’t symptomatic because we know there is virtually zero asymptomatic spread and because the antigen tests almost never work reliably unless you are symptomatic so it’s a complete waste of money to test asymptomatic people. The testing companies don’t want anyone to know that, but we do.
  10. If we do get sick with COVID symptoms, we stay home and rest.
  11. Even if we had a truly safe vaccine, those of us who are recovered from COVID wouldn’t need it. A uniform mandate for everyone makes no sense.
  12. We believe doctors should be allowed to be doctors and that medical care should always be delivered by our healthcare professional we trust to use his professional judgement on our individual case. The CDC guidance is just awful.

January 25, 2022 Posted by | Civil Liberties, Science and Pseudo-Science | , , , | Leave a comment

The Emergency Must Be Ended, Now

BY HARVEY RISCH, JAYANTA BHATTACHARYA, PAUL ELIAS ALEXANDER | BROWNSTONE INSTITUTE | JANUARY 23, 2022

The time has come to terminate the pandemic state of emergency. It is time to end the controls, the closures, the restrictions, the plexiglass, the stickers, the exhortations, the panic-mongering, the distancing announcements, the ubiquitous commercials, the forced masking, the vaccine mandates.

We don’t mean that the virus is gone – omicron is still spreading wildly, and the virus may circulate forever.  But with a normal focus on protecting the vulnerable, we can treat the virus as a medical rather than a social matter and manage it in ordinary ways. A declared emergency needs continuous justification, and that is now lacking.

Over the last six weeks in the US, the delta variant strain – the most recent aggressive version of the infection – has according to CDC been declining in both the proportion of infections (60% on December 18 to 0.5% on January 15) and the number of daily infected people (95,000 to 2,100). During the next two weeks, delta will decline to the point that it essentially disappears like the strains before it.

Omicron is mild enough that most people, even many high-risk people, can adequately cope with the infection. Omicron infection is no more severe than seasonal flu, and generally less so. A large portion of the vulnerable population in the developed world is already vaccinated and protected against severe disease. We have learned much about the utility of inexpensive supplements like Vitamin D to reduce disease risk, and there is a host of good therapeutics available to prevent hospitalization and death should a vulnerable patient become infected. And for younger people, the risk of severe disease – already low before omicron – is minuscule.

Even in places with strict lockdown measures, there are hundreds of thousands of newly registered omicron cases daily and countless unregistered positives from home testing. Measures like mandatory masking and distancing have had negligible or at most small effects on transmission. Large-scale population quarantines only delay the inevitable.  Vaccination and boosters have not halted omicron disease spread; heavily vaccinated nations like Israel and Australia have more daily cases per capita than any place on earth at the moment. This wave will run its course despite all of the emergency measures.

Until omicron, recovery from Covid provided substantial protection against subsequent infection. While the omicron variant can reinfect patients recovered from infection by previous strains, such reinfection tends to produce mild disease. Future variants, whether evolved from omicron or not, are unlikely to evade the immunity provided by omicron infection for a long while. With the universal spread of omicron worldwide, new strains will likely have more difficulty finding a hospitable environment because of the protection provided to the population by omicron’s widespread natural immunity.

It is true that – despite emergency measures — hospitalization counts and Covid-associated mortality have risen. Since mortality tends to trail symptomatic infection by about 3-4 weeks, we are still seeing the delta strain’s remaining effects and the waning of vaccine immunity against serious outcomes at 6-8 months after vaccination. These cases should decline over time as delta finally says goodbye. It is too late to alter their course with lockdowns (if that were ever possible).

Given that omicron, with its mild infection, is running its course to the end, there is no justification for maintaining emergency status. The lockdowns, personnel firings and shortages and school disruptions have done at least as much damage to the population’s health and welfare as the virus.

The state of emergency is not justified now, and it cannot be justified by fears of a hypothetical recurrence of some more severe infection at some unknown point in the future. If such a severe new variant were to occur – and it seems unlikely from omicron – then that would be the time to discuss a declaration of emergency.

Americans have sacrificed enough of their human rights and of their livelihoods for two years in the service of protecting the general public health. Omicron is circulating but it is not an emergency. The emergency is over. The current emergency declaration must be canceled. It is time.

Authors

Harvey Risch is Professor of Epidemiology in the Department of Epidemiology and Public Health at the Yale School of Public Health and Yale School of Medicine. Dr. Risch received his MD degree from the University of California San Diego and PhD from the University of Chicago. After serving as a postdoctoral fellow in epidemiology at the University of Washington, Dr. Risch was a faculty member in epidemiology and biostatistics at the University of Toronto before coming to Yale.

Jay Bhattacharya, Senior Scholar of Brownstone Institute, is a Professor of Medicine at Stanford University. He is a research associate at the National Bureau of Economics Research, a senior fellow at the Stanford Institute for Economic Policy Research, and at the Stanford Freeman Spogli Institute.

Dr Alexander holds a PhD. He has experience in epidemiology and in the teaching clinical epidemiology, evidence-based medicine, and research methodology. Dr Alexander is a former Assistant Professor at McMaster University in evidence-based medicine and research methods; former COVID Pandemic evidence-synthesis consultant advisor to WHO-PAHO Washington, DC (2020) and former senior advisor to COVID Pandemic policy in Health and Human Services (HHS) Washington, DC (A Secretary), US government; worked/appointed in 2008 at WHO as a regional specialist/epidemiologist in Europe’s Regional office Denmark, worked for the government of Canada as an epidemiologist for 12 years, appointed as the Canadian in-field epidemiologist (2002-2004) as part of an international CIDA funded, Health Canada executed project on TB/HIV co-infection and MDR-TB control (involving India, Pakistan, Nepal, Sri Lanka, Bangladesh, Bhutan, Maldives, Afghanistan, posted to Kathmandu); employed from 2017 to 2019 at Infectious Diseases Society of America (IDSA) Virginia USA as the evidence synthesis meta-analysis systematic review guideline development trainer; currently a COVID-19 consultant researcher in the US-C19 research group.

January 23, 2022 Posted by | Civil Liberties, Economics, Science and Pseudo-Science | , , | Leave a comment

The Monumental Sacrifice of Novak Djokovic

BY STACEY RUDIN | BROWNSTONE INSTITUTE | JANUARY 17, 2022

Defending Australian Open Champion Novak Djokovic was deported from Australia, the day before commencement of 2022 tournament play. He entered the country on a visa including a medical exemption based on recent Covid infection. Due to public outry over “special treatment,” his visa was revoked upon arrival in the country, only to be reinstated by a court. It was later revoked by an immigration minister, whose decision was upheld by another court, sending Djokovic packing — potentially for three years.

This draconian act puts Djokovic at a serious disadvantage in his Grand Slam rivalry with Rafael Nadal, who is competing in Australia this year after vocally supporting vaccines. Both champions, along with Roger Federer, currently hold 20 Grand Slam titles. Djokovic was favored to be the first to reach 21, but his decision to remain unvaccinated leaves Nadal alone with that opportunity for now. (Federer is out recovering from surgery.)

Djokovic was technically deported for not being vaccinated, but the decision lacks even a superficial “health and safety” justification. Djokovic already had Covid twice, once in early 2020 and again in December 2021. At the time of his deportation, he had been in Australia for ten days, and tested negative. He’s as healthy as a human being can be — you don’t earn “GOAT’ status in the difficult sport of tennis any other way.

Further proof that Djokovic poses no disease threat to anyone is the fact that this tournament was safely played in January 2021, before vaccines were available for any player or guest. Even if Djokovic had taken the vaccine, he’d be no “safer” in terms of his ability to transmit the virus, as the 100,000 daily cases in highly-vaccinated Australia attest.

Even the government that deported Djokovic didn’t try very hard to frame its decision as the elimination of a health threat. Rather, it stated that Novak could become an “icon of free choice” if allowed to stay. Ironically, he will undoubtedly become that now that he’s made the supreme sacrifice of forfeiting his chance to play in order to openly oppose mandatory vaccination.

It’s not a good look for the Covid Regime if an avowed “anti-vaxxer” dominates the sport. The world audience might start thinking about the relative health status of “unvaccinated” people, particularly since athletes have been experiencing heart trouble all over the world — several already at the Australian Open practice courts.

As it stands, Millions of Australians and others who have already taken the vaccine applaud the government’s decision. They can’t get the vaccine out of their bodies, so the next best thing is to make sure that everyone else has to put themselves into the same spot.

Nevermind the precedent it sets to allow a government to force people to choose between their health and their career. Such Sophie’s choices are normal these days.

The Regime would not have minded Djokovic playing in an unvaccinated state so long as he publicly expressed support for mandatory universal vaccination. He could have easily done this — a hero in Serbia, the wealthy star could have tapped any number of doctors to provide fake certification of vaccination. But that would have violated his principles.

In 2010, an “unwell” Djokovic was collapsing at tournaments, unable to complete strenuous matches. A doctor witnessing his condition on TV got in touch with the athlete, recommending that he eliminate gluten, dairy and processed sugar from his diet. Novak thought it sounded strange but agreed to try, and it’s hard to argue with his results. His 2011 season was one of the best in men’s tennis history. On his new fuel, he was unstoppable. He ended the season with an unbelievable 10–1 record against Nadal and Federer, and compiled a 41-match winning streak.

This experience changed not only the tennis player. It fundamentally changed the man, as Djokovic explains in his book “Serve to Win”:

When it’s not being cared for, your body will send you signals: fatigue, insomnia, cramps, flus, colds, allergies. When that happens, will you ask yourself the questions that matter? Will you answer honestly and with an open mind?

Open-minded people radiate positive energy. Closed-minded people radiate negativity. Eastern medicine teaches you to align mind, body, and soul. If you have positive feelings in your mind — love, joy, happiness — they affect your body… But a lot of people, especially closed-minded people, are led by fear. That and anger are the most negative energies we have. What are closed-minded people afraid of? It could be many things: Fear that they are wrong, fear that someone might have a better way, fear that something has to change. Fear limits your ability to live your life.

Some people at the top feed off of negativity. The way I see it, pharmaceutical and food companies want people to feel fear. They want people to be sick. How many TV ads are for fast foods and medicines? And what’s at the root of those messages? We’ll make you feel better with our products. But even deeper down: We’ll make you fear that you don’t have enough of the things we say you need. It’s crazy — even when you’re completely healthy, they say you need [products] to stay that way.

Here’s a pattern I’d rather embrace: good food, exercise, openness, positive energy, great results. I’ve been living that pattern for several years now. It works better than the alternative.

Djokovic rejects Big food, Big Ag, Big Chemical, and Big Pharma. He doesn’t need them. His practices allow him to be healthy without any of their products — in fact, he’s achieved an elite level of health by actively avoiding their products.

There is no greater threat to the bottom line of these companies than people like Novak Djokovic. He is not scared, he is not anxious, so he can’t be manipulated or sold an easy fix. He can see the path to health takes hard work, and he’s willing to put it in. When they tell him that he can’t be healthy without a vaccine, he laughs in their faces. They can send him packing, but they can never take away his integrity and self-worth.

Novak Djokovic doesn’t want to lie to the public, making it appear as if he agrees with The System’s “path to health.” If he did that, he would get to play his tournament, but he would have millions of lives on his conscience. He’d rather give up his career’s crowning achievement in order to stand in truth. To send people the message: you CAN reject this tyranny. You do NOT have to comply. You can SAY NO, and you will be okay.

It’s easier for him, yes, with his millions of dollars. Healthcare workers on a middle-class salary will have a harder go of it. Military members faced with dishonorable discharge absent vaccination have it worse. But Djokovic has made it easier, at least, for everyone to publicly reject vaccination. If Novak openly rejects this vaccine, they can too, without shame. His very public deportation will hopefully get many people thinking about his approach to health, which if widely understood and adopted, will finally burn the Covid Regime to the ground — once and for all.

Stacey Rudin is an attorney and writer in New Jersey, USA.

January 22, 2022 Posted by | Book Review, Science and Pseudo-Science, Timeless or most popular | , , , | Leave a comment

Novavax covid vaccine safe and effective?

By Sebastian Rushworth, M.D. | January 15, 2022

I’ve been getting frequent requests for at least the last six months to write about the Novavax covid vaccine. I’ve been resisting, mainly because it’s seemed uncertain whether it would ever actually be approved in the western world. Now that it’s been approved for use in the EU, however, that has changed, and I figure that I can put it off no longer.

I guess the reason so many people are excited about the Novavax vaccine is that it uses a traditional technology that’s been used many times previously, rather than the new-fangled technologies used in the mRNA and adenovector vaccines that have up to now been all that’s available in the US and EU. To many people, that apparently makes it feel inherently safer.

The Novavax vaccine consists of two parts: the Sars-Cov-2 spike protein and an adjuvant (a substance that causes the immune system to realize that a dangerous foreign entity is present, and which thus activates an immune response to the spike protein). So, rather than injecting genetic blueprints in to the body that get cells to make the viral spike protein themselves (as is the case with the four previously approved vaccines), the spike protein is injected directly.

The first country to approve the Novavax vaccine was Indonesia, which approved it for use in November. That means that there is no even slightly long term real world follow-up data available yet. All we have is the preliminary results from the randomized trials. That means we still have no idea about rare side-effects, and won’t for months. Several million people had already received the AstraZeneca vaccine before authorities realized it could cause serious blood clotting disorders, and millions had also received the Moderna and Pfizer vaccines before it became clear that they can cause myocarditis. With that cautionary point having been made, let’s take a look at what the preliminary results from the randomized trials show.

The first trial results concerning the Novavax vaccine appeared in the New England Journal of Medicine in May. 4,387 people in South Africa were randomized to receive either the vaccine or a saline placebo. The trial was conducted during the final months of 2020, when the beta variant was dominant in South Africa. Like the earlier covid vaccine trials, the objective of the study was to understand the ability of the vaccine to prevent symptomatic disease, which was defined as symptoms suggestive of covid-19 plus a positive covid test.

The average age of the participants was 32 years and chronic conditions were rare, so this was a group at low risk of severe disease. When this fact is combined with the relatively small total number of participants (for a vaccine trial), there was no possibility that the study was going to say anything useful about the ability of the vaccine to prevent severe disease. So this was really a trial looking at the ability of the Novavax vaccine to prevent the common cold in healthy young people.

Let’s look at the results.

As with the earlier published vaccine trials, data on efficacy was only provided two months out from receipt of the vaccine. At the two month mark, 15 people in the vaccine group had developed symptomatic covid-19, as compared with 29 people in the placebo group. This gives a relative risk reduction of 49% against the beta variant at two months post vaccination, which is disappointing. It’s below the 50% risk reduction that regulators have set as the minimum level required for them to approve a vaccine.

It’s even more disappointing when you consider that efficacy against symptomatic infection likely peaks at two months out from vaccination, and then drops rapidly – that is the pattern that’s been seen with all the other approved covid vaccines, and it’s very likely that the same is true for this vaccine.

Furthermore, the beta variant is long gone. The other approved vaccines appear to have little to no ability to prevent infection from the currently dominant omicron variant (although they do still seem to reduce the risk of severe disease to a large extent). Here in Sweden you are currently just as likely to get covid regardless of whether you’ve been vaccinated or not, but you’re still far less likely to end up in an ICU due to severe covid if you’ve been vaccinated. There’s no reason to assume that this vaccine is any different.

Let’s move on and look at safety. Safety data was only provided for a sub-set of patients, and for the first 35 days out from receipt of the first vaccine dose. What little there was though, was somewhat discouraging, with twice as many adverse events requiring medical attention in the group receiving the vaccine as in the group receiving the placebo (13 vs 6), and twice as many serious adverse events in the group receiving the vaccine (2 vs 1). To be fair though, the small absolute numbers make it impossible to draw any conclusions about safety based on this limited data. So we’ll wait to pass judgement.

Let’s move on to the second trial, which was published in the New England Journal of Medicine in September. This was a much larger trial than the first, with 15,187 people in the UK who were randomized to either the Novavax vaccine or a saline placebo. Like the earlier study, it was looking at the ability of the vaccine to prevent symptomatic disease. The study ran from late 2020 to early 2021, during a time when the alpha variant was dominant, so the results of the study apply primarily to that variant. 45% of the participants had at least one risk factor that would predispose them to severe disease, and the average age was 56 years.

Ok, so what were the results?

Among participants who received two doses of the vaccine, there were 96 covid infections in the placebo group, but only 10 in the vaccine group during the three month period after receipt of the second dose. This gives an efficacy during the first few months of 90%, similar to what was found in the Moderna and Pfizer vaccine trials. One person ended up being hospitalized for covid-19 in the placebo group, while no-one was hospitalized in the vaccine group – so unfortunately there again weren’t enough hospitalizations to be able to say anything about the ability of the vaccine to prevent severe disease (although it’s pretty clear from this study that even for a relatively high risk group, the overall risk of hospitalization due to covid is low – of 96 people in the placebo group who got covid, only one required hospitalization).

Let’s turn to safety. Safety data is only provided for the period from receipt of the first dose to 28 days out from receipt of the second dose, so we don’t learn anything about the longer term, but at least for that shorter period, there was no signal of serious harm. There were 44 serious adverse events in the vaccine group, and 44 serious adverse events in the placebo group. One person in the vaccine group developed myocarditis three days after receipt of the second dose, which suggests that the Novavax vaccine might cause myocarditis, just like the Pfizer and Moderna vaccines do.

Let’s turn to the final trial, which was published in the New England Journal of Medicine in December. It was carried out in the United States and Mexico during the first half of 2021. Just as with the previous trial, the results apply primarily to the alpha variant. 29,949 participants were randomized to either the Novavax vaccine or a saline placebo. Like the other two trials, the purpose was to see if the vaccine prevented symptomatic disease, again defined as symptoms suggestive of covid-19 plus a positive PCR test. The median age of the participants was 47 years, and 52% had an underlying condition that would predispose them to more severe disease if infected with covid-19.

So, what were the results?

At 70 days out from receipt of the second dose, 0.8% of participants in the placebo group had developed covid-19, compared with only 0.1% in the vaccine group. This gives a relative risk reduction of 90%, a result that is identical to that seen in the previous trial. Unfortunately, no information is provided on hospitalizations, which I assume means that not one of the 29,949 people included in the study was hospitalized for covid-19, so, just as with the earlier trials, it’s impossible to tell if the vaccine results in any meaningful reduction in hospitalizations.

At 28 days post receipt of the seond dose, 0.9% of participants in the vaccine group had suffered a serious adverse event, compared with 1.0% of participants in the placebo group. That is encouraging.

Ok, let’s wrap up. what can we conclude about the Novavax vaccine after looking at the results of these three trials?

First, we can conclude that it effectively protected people from symptomatic covid due to the alpha variant at two-three months post vaccination (which of course tells us nothing about how effective the vaccine is after six months or a year). That information is now mostly of historical interest, since alpha is long gone and we’re living in the era of omicron. If the Novavax vaccine is similar to the four previously approved vaccines, then it’s likely useless at preventing infection due to omicron.

Second, it’s impossible to conclude from these trials whether the Novavax vaccine results in any reduction in risk of hospitalization due to covid, for the simple reason that not enough people ended up being hospitalized. Having said that, my guess would be that it probably does protect against hospitalization and need for ICU treatment, just as the other approved vaccines do. At its heart, it’s doing the same thing as they are – generating an immune response to the spike protein found on the original Wuhan covid variant, and the overall trial results are very similar to the trial results for the Moderna and Pfizer vaccines.

The overall safety data suggests that the vaccine is pretty safe, with serious adverse events being balanced between the vaccine group and the placebo group. Rare side-effects are however not detectable in randomized trials with a few tens of thousands of participants. For that longer term follow-up with much larger numbers of people is necessary. So it’s currently impossible to know whether the Novavax vaccine can cause myocarditis, like the mRNA vaccines, or blood clotting disorders, like the adenovector virus vaccines, or some other type of rare adverse event entirely. It’s therefore impossible to say at the present point in time whether it will turn out to be more safe, or less safe, or equivalent to the already approved vaccines.

January 22, 2022 Posted by | Science and Pseudo-Science, Timeless or most popular | , | Leave a comment

Ethical concerns arising from the Government’s use of covert psychological ‘nudges’

Health Advisory and Recovery Team | January 20, 2022

Letter to Mr William Wragg, MP

18th January 2022

Mr William Wragg, MP

Chair of the Public Administration & Constitutional Affairs Committee (PACAC)

Dear Mr Wragg,

Re: Ethical concerns arising from the Government’s use of covert psychological ‘nudges’ in their COVID-19 communications strategy

We are writing to you as a group of psychological specialists and health professionals to highlight our major ethical concerns about the deployment of covert behavioural-science techniques (commonly referred to as ‘nudges’) in the Government’s COVID-19 communications strategy. Our view is that the use of these behavioural strategies – which often operate below people’s conscious awareness and frequently rely on inflating emotional distress to change behaviour – raises profound moral questions. In light of these pressing concerns we respectfully request that, in your role as chair of the Public Administration & Constitutional Affairs Committee (PACAC), you instigate a comprehensive inquiry into the acceptability of using these strategies on the British people as a means of promoting compliance with public health directives.

Background

The appetite for using covert psychological strategies as a means of changing people’s behaviour was boosted by the emergence of the ‘Behavioural Insights Team’ (BIT) in 2010 as ‘the world’s first government institution dedicated to the application of behavioural science to policy’ (1). The membership of BIT rapidly expanded (2) from a seven-person unit embedded in the UK Government to a ‘social purpose company’ operating in many countries across the world. A comprehensive account of the psychological techniques recommended by the BIT is provided in the Institute of Government document, MINDSPACE: Influencing behaviour through public policy (3), where the authors claim that their strategies can achieve ‘low cost, low pain ways of nudging citizens … into new ways of acting by going with the grain of how we think and act’.

Since its inception in 2010, the BIT has been led by Professor David Halpern who is currently the team’s chief executive. Professor Halpern and two other members of the BIT also currently sit on the Scientific Pandemic Insights Group on Behaviours (SPI-B) (4), a subgroup of SAGE that advises the Government on its COVID-19 communications strategy. Most of the other members of the SPI-B are prominent British psychologists who have expertise in the deployment of behavioural-science ‘nudge’ techniques.

It is important to emphasise that the use of behavioural science in this way represents a radical departure from the traditional methods – legislation, information provision, rational argument – used by governments to influence the behaviour of their citizens. By contrast, many of the ‘nudges’ delivered by the BIT are – to various degrees – acting upon us automatically, below the level of conscious thought and reason.

The ‘nudges’ of concern

The BIT and the SPI-B have encouraged the deployment of many techniques from behavioural science within the Government’s COVID-19 communications. However, there are three ‘nudges’ which have evoked most of our alarm: the exploitation of fear (inflating perceived threat levels), shame (conflating compliance with virtue) and peer pressure (portraying non-compliers as a deviant minority) – or “affect”, “ego” and “norms”, to use the language of the MINDSPACE document.

AFFECT/FEAR

Aware that a frightened population is a compliant one, a strategic decision was made to inflate the fear levels of all the British people. The minutes of the SPI-B meeting (5) dated the 22nd March 2020 stated, ‘The perceived level of personal threat needs to be increased among those who are complacent’ by ‘using hard-hitting emotional messaging’. Subsequently, in tandem with a subservient mainstream media, the collective efforts of the BIT and the SPI-B have inflicted a prolonged and concerted scare campaign upon the British public. The methods used have included:

  • Daily statistics displayed without context: the macabre mono focus on showing the number of COVID-19 deaths without mention of mortality from other causes or the fact that, under normal circumstances, around 1600 people die each day in the UK.
  • Recurrent footage of dying patients: images of the acutely unwell in Intensive Care Units.
  • Scary slogans: for example, ‘IF YOU GO OUT YOU CAN SPREAD IT, PEOPLE WILL DIE’, typically accompanied by frightening images of emergency personnel in masks and visors.

EGO/SHAME

We all strive to maintain a positive view of ourselves. Utilising this human tendency, behavioural scientists have recommended messaging that equates virtue with adherence to the Covid-19 restrictions and subsequent vaccination campaign. Consequently, following the rules preserves the integrity of our egos while any deviation evokes shame. Examples of these nudges in action include:

  • Slogans that shame the non-compliant: for example, ‘STAY HOME, PROTECT THE NHS, SAVE LIVES’.
  • TV advertisements: actors tell us, ‘I wear a face covering to protect my mates’ and ‘I make space to protect you’.
  • Clap for Carers: the pre-orchestrated weekly ritual, purportedly to show appreciation for NHS staff.
  • Ministers telling students not to ‘kill your gran’.
  • Shameevoking adverts: close-up images of acutely unwell hospital patients with the voice-over, ‘Can you look them in the eyes and tell them you’re doing all you can to stop the spread of coronavirus?’

NORMS/PEER PRESSURE

Awareness of the prevalent views and behaviour of our fellow citizens can pressurise us to conform and knowledge of being in a deviant minority is a source of discomfort. The Government has repeatedly encouraged peer pressure throughout the COVID-19 crisis to gain the public’s compliance with their escalating restrictions, an approach that – at higher levels of intensity – can morph into scapegoating. The most straightforward example is how, during interviews with the media, ministers have often resorted to telling us that the vast majority of people are ‘obeying the rules’ or that almost all of us are conforming. However, in order to enhance and sustain normative pressure, people need to be able to instantly distinguish the rule breakers from the rule followers; the visibility of face coverings provides this immediate differentiation. The switch to the mandating of masks in community settings in summer 2020, without the emergence of new and robust evidence that they reduce viral transmission, strongly suggests that the mask requirement was introduced primarily as a compliance device to harness normative pressure.

Ethical questions

Compared to a government’s typical tools of persuasion, the covert psychological strategies (outlined above) differ in both their nature and subconscious mode of action. Consequently, we believe there are three main areas of ethical concern associated with their use: problems with the methods per se; problems with the lack of consent; and problems with the goals to which they are applied.

First, it is highly questionable whether a civilised society should knowingly increase the emotional discomfort of its citizens as a means of gaining their compliance. Government scientists deploying fear, shame and scapegoating to change minds is an ethically dubious practice that in some respects resembles the tactics used by totalitarian regimes such as China, where the state inflicts pain on a subset of its population in an attempt to eliminate beliefs and behaviour they perceive to be deviant.

Another ethical issue associated with these covert psychological techniques relates to their unintended consequences. Shaming and scapegoating have emboldened some people to harass those unable or unwilling to wear a face covering. More disturbingly, the inflated fear levels will have significantly contributed to the many thousands of excess non-COVID deaths (6) that have occurred in people’s homes, the strategically-increased anxieties discouraging many from seeking help for other illnesses. Furthermore, a lot of older people, rendered housebound by fear, may have died prematurely from loneliness (7). Those already suffering with obsessive-compulsive problems about contamination, and patients with severe health anxieties, will have had their anguish exacerbated by the campaign of fear. Even now, when all the vulnerable groups have been offered vaccination, many of our citizens remain tormented by ‘COVID-19 Anxiety Syndrome’ (8), characterised by a disabling combination of fear and maladaptive coping strategies.

Second, a recipient’s consent prior to the delivery of a medical or psychological intervention is a fundamental requirement of a civilised society. Professor David Halpern (the BIT Chief Executive and prominent member of SPI-B) explicitly recognised the significant ethical dilemmas arising from the use of influencing strategies that impact subconsciously on the country’s citizens. The MINDSPACE document (9) – of which Professor Halpern is a co-author – states that, ‘Policymakers wishing to use these tools … need the approval of the public to do so’ (p74). More recently, in Professor Halpern’s book, Inside the Nudge Unit, he is even more emphatic about the importance of consent: ‘If Governments … wish to use behavioural insights, they must seek and maintain the permission of the public. Ultimately, you – the public, the citizen – need to decide what the objectives, and limits, of nudging and empirical testing should be’ (p375).

As far as we are aware, no attempt has yet been made to obtain the public’s permission to use covert psychological strategies.

Third, the perceived legitimacy of using subconscious ‘nudges’ to influence people may also depend upon the behavioural goals that are being pursued. It may be that a higher proportion of the general public would be comfortable with the government resorting to subconscious nudges to reduce violent crime as compared to the purpose of imposing unprecedented and non-evidenced public-health restrictions. Would British citizens have agreed to the furtive deployment of fear, shame and peer pressure as a way of levering compliance with lockdowns, mask mandates and vaccination? Maybe they should be asked before the Government considers any future imposition of these techniques.

The position of the British Psychological Society

The British Psychological Society (BPS) is the leading professional body for psychologists in the UK. According to their website (10), a central role of the BPS is, ‘To promote excellence and ethical practice in the science, education and application of the discipline’. [Our emphasis]. Mindful of their important position as the guardian of ethical psychological practice, on the 6th January 2021 46 psychologists and therapists (including many of the signatories of the present letter) wrote to the BPS (11) raising the ethical questions outlined above.

A month later, on the 5th February 2021, a reply (12) was received from Dr Debra Malpass (Director of Knowledge and Insight at the BPS) which failed to directly address our ethical concerns and was, in our view, evasive and disingenuous. Dr Malpass’s response included questioning whether the strategies deployed by Government psychologists were actually covert, stating that the role of specific psychologists had not been evidenced, and expressing how ‘incredibly proud’ the BPS was about the ‘fantastic work done by psychologists throughout the pandemic’.

Dissatisfied with this initial reaction, we contacted the BPS again to question whether our expressed concerns had actually been considered by their ethics committee. We received a brief reply from Dr Malpass on the 16th February 2021 informing us that our initial letter would be considered at their next BPS Ethics Committee on the 1st March; we understood this to be an admission that the covert psychological strategies recommended by psychologists had yet to be scrutinised in regards to their ethical acceptability.

By 12th March, and not having received any further communication from the BPS, we prompted them again. On the 23rd March a message was received from Dr Roger Paxton (Chair of the BPS Ethics Committee) apologising that ‘owing to a very full agenda and an oversight’ no discussion about our concerns had taken place but that they would be included on the agenda of their June meeting.

On the 30th June, and not having received any further communication from the BPS, we prompted them again. On the 1st July we received a response (13) from Dr Paxton, comprising three paragraphs, informing us that the issues we raised had been considered and that their ethics committee had endorsed all previous BPS responses. In this communication, Dr Paxton acknowledged that he had received a large number of recent emails raising the same issues, but rejected our ethical concerns arguing that the strategies referred to were ‘indirect’ rather than covert, the application of psychology in this instance fell outside the realm of individual health decisions (so informed consent was not an issue), levels of fear within the general population were proportionate to the objective risk posed by the virus, and the psychologists’ role in the pandemic response demonstrated ‘social responsibility and the competent and responsible employment of psychological expertise’.

We believe the BPS responses to our ethical concerns about the deployment of covert psychological strategies throughout the COVID-19 pandemic have been defensive and disingenuous. Also we believe the BPS is impeded by a major conflict of interest on this issue in that several members of the SPI-B are also influential figures within the BPS. As such, the impartiality of the BPS in addressing the ethical issues we raised is highly questionable.

Finally, it is worth noting that serious concerns about the Government’s use of behavioural science have previously been raised in relation to other spheres of government activity. An All Parliamentary Group Report (APGR) (14) analysing the recommendations of the Morse Report (15) (a Treasury-commissioned review into the Loan Charge, published in December 2019) found that the distress evoked in those people targeted by behavioural insights may, in some instances, have led to victims taking their own lives. In the words of the APGR:

HMRC continue to apply pressure to taxpayers by using 30 behavioural insights in communications, something that has been cited in one of the seven known suicides of people facing the Loan Charge’.

In further recognition of the suffering and anguish associated with these ‘nudge’ techniques, the APGR recommends:

An independent assessment and suspension of HMRC’s use of behavioural psychology/behavioural insights in light of the ongoing suicide risk to those impacted by the Loan Charge’.

Clearly, a truly independent and comprehensive evaluation of the ethics of deploying psychological ‘nudges’ on the British people – during public health campaigns and in other areas of government – is now urgently required. We respectfully ask the PACAC to consider performing this important role.

Co-Signatories

Psychology/therapy/mental health

  • Dr Gary Sidley (M.Sc., ClinPsy, PhD) Retired Consultant Clinical Psychologist
  • Ms Jen Ayling (UKCP registered counsellor) Psychotherapeutic Counsellor
  • Dr Faye Bellanca (DClinPsy) Clinical Psychologist
  • Dr Christian Buckland ((PsychD) Psychotherapist
  • Alison Burnard (Dip Gestalt Therapy) Gestalt Psychotherapist
  • Daran Campbell (PG Dip Counselling) Substance Misuse Practitioner
  • Dr Tom Carnwath (FRCPsych, FRCGP) Consultant Psychiatrist
  • Dr Maria Castro Romero (DClinPsy) Senior Lecturer in Clinical Psychology
  • Gillian England (PG Dip Cognitive Behavioural Psychotherapy) Cognitive Behavioural Therapist
  • Dr Elizabeth English (M.Phil, DPhil) Mindfulness Teacher & Trauma Therapist
  • Mr Patrick Fagan (M.Sc.) Chief Scientific Officer, Capuchin Behavioural Science
  • Dr Tracey Grant Lee (DClinPsy) Chartered Clinical Psychologist
  • Andy Halewood (Advanced M.Sc. in Counselling Psychology) Chartered Psychologist
  • Sue Parker Hall (CTA, MSc, PGCE) Psychotherapist
  • Andrew D Harry (RPP PTP) NLP Master Practitioner
  • Mrs Nicole Harvey (B.Sc, Pg Dip) Mental Health Practitioner/CBT Therapist
  • Ms Julie A Horsley (Advanced Diploma in Counselling) Counsellor/Therapist
  • Dr Richard House (MA, Ph.D, C.Psych. AFBPsS) former Senior Lecturer in Psychology
  • Emma Kenny (MA Counselling, Advanced Diploma Counselling) Media Psychologist & Psychological Therapist
  • Rachel Maisey (MA, PGCE, PgDip Counselling) Integrative Counsellor
  • Jane Margerison (PG Dip Integrative Psychotherapy, RMN) Psychotherapist
  • Kate Morrissey (Advanced Diploma in Counselling, MA Social Work) Counsellor
  • Lucy Padina (Diploma in Psychology, Advanced Diploma in the Management of Psychological Trauma) Independent Consultant & Registered Social Worker
  • Carolyn Polunin (M.Sc.) Integrative Psychotherapist
  • Dr Livia Pontes (DClinPsy) Clinical Psychologist
  • Dr Kate Porter (DClinPsy) Clinical Psychologist
  • Ian Price (M.Sc. Organisational Behaviour) Business Psychologist
  • Dr Bruce Scott (B.Sc., PhD) Psychoanalyst
  • Professor David Seedhouse (PhD) Honorary Professor of Deliberative Practice
  • Deborah Short (MA Gestalt Psychotherapy) Psychotherapist
  • Ms Deborah Sharples (B.A. [Hons] Social Work) Mental Health Social Worker
  • Susan Sidley (RMN) Retired Psychiatric Nurse
  • Dr Angela Smith (DClinPsy, PhD) Psychology Lead
  • Dr Helen Startup (DClinPsy, PhD) Consultant Clinical Psychologist
  • Dr Dov Stein (MA, MB, BCh, BAO DCH Dobs) Consultant Psychiatrist & Psychotherapist
  • Dr Zenobia Storah (DClinPsy) Child & Adolescent Clinical Psychologist
  • Professor Ellen Townsend (PhD) Professor of Psychology
  • Sarah Waters (BA, Dip Counselling & Therapy) Psychotherapist
  • Dr Alice Welham (MA, DClinPsy, PhD) Clinical Psychologist
  • Dr Damian Wilde (DClinPsy) Highly Specialist Clinical Psychologist

Other health professionals

  • Mr John Collis (PGCert in Advanced Practice, BSc [Hons] Nursing, BA [Hons] Retired Nurse Practitioner
  • James Cook (Bachelor of Nursing [Hons], Master of Public Health [MPH]) Registered Nurse
  • Dr Clare Craig (BM, BCh, FRCPath) Consultant Pathologist
  • Dr David Critchley (BSc, PhD) Clinical Pharmacologist
  • Roisin Dargan-Peel (MA) Former Registered General Nurse, Midwife & Health Visitor
  • Mr Paul Goss (MCSP, HCPC, KCMT) Clinical Director & Chartered Physiotherapist
  • Dr Ros Jones (MD, FRCPCH) Retired Consultant Paediatrician
  • Mrs Alison Langthorne (RGN) Staff Nurse
  • Jenna Leith (RGN) Advanced Nurse Practitioner
  • Dr Sam McBride (MB, BCh, MRCP, FRCP, FRCEM) Clinical Gerontologist
  • Mrs Julie Noble (M.Sc, RN) Senior Forensic Nurse Examiner & Advanced Practitioner
  • Mrs Christine Mary Proctor (RGN) Former Registered General Nurse
  • Dr Annabel Smart (MBBS, BSc, DFSRH) Retired General Practitioner
  • Nat Stephenson (B.Sc Audiology) Paediatric Audiologist
  • Dr Helen Westwood (MBChB, MRCGP, DCH, DRCOG) General Practitioner

January 22, 2022 Posted by | Civil Liberties, Science and Pseudo-Science, Timeless or most popular | , , | Leave a comment

On The Eve of Washington March, COVID Declaration

Now Backed by More Than 17,000 Doctors and Medical Scientists Around the World

By Robert W Malone MD, MS | January 22, 2022

Following Dr. Robert Malone’s appearance on The Joe Rogan Experience, more physicians and medical scientists have joined with their colleagues from around the world in signing the Physicians Declaration. Now with more than 17,000 signatures confirmed through a rigorous validation process, these physicians and scientists are represented by Dr. Malone as he speaks at the march to Defeat the Mandates on Sunday, January 23 in Washington, D.C.

The over 17,000 signers to the declaration have reached consensus on three foundational principles:

  1. Healthy children should not be subject to forced vaccination: they face negligible risk from covid, but face potential permanent, irreversible risk to their health if vaccinated, including heart, brain, reproductive and immune system damage.
  2. Natural Immunity Denial has prolonged the pandemic and needlessly restricted the lives of Covid-recovered people. Masks, lockdowns, and other restrictions have caused great harm especially to children and delayed the virus’ transition to endemic status.
  3. Health agencies and institutions must cease interfering with the physician-patient relationship. Policymakers are directly responsible for hundreds of thousands of deaths, as a result of institutional interference and blocking treatments proven to cure at a near 100% rate when administered early.

Led by Dr. Malone and staying loyal to the Hippocratic oath, the declaration’s signers have resisted financial inducements, threats, unprecedented censorship, and reputational attacks to remain committed first to patient health and well-being. After 23 months of research, millions of patients treated, hundreds of clinical trials performed and scientific data shared, and after demonstrating and documenting their success in combating COVID-19, the 17,000+ physicians and medical scientists who signed the declaration support the core principles Dr. Malone and many other doctors have been speaking out about since late last year.

The 17,000+ signatures of the declaration are authentic and must pass a screening process before being officially identified as signing the declaration. Signatories are required to supply their affiliation and a link to their medical organization, facility, or profile. Nurses, non-MD practitioners and non-medical scientists are removed from the list signatories, as are duplicate entries and “bot” emails. The emails of the signatories have been separately and repeatedly tested and verified by a 3rd-party provider.

As the number of signatures to the declaration continues to rise, we have published a select group of world famous, highly credentialed physicians and scientists who authored the declaration. Many other doctors who have spoken out against the corruption, censorship and hypocrisy by authorities have been threatened, fired, censured, lied about, intimidated, and harassed – all while saving patients’ lives daily. Never has the public been forced to become lab rats, for a vaccine 5 years away from adequate testing, violating basic principles of informed consent. Moreover, the medical and scientific evidence on the efficacy and safety of the COVID- 19 vaccine do not support mandating its use for anyone, especially healthy children.

January 23 March on Washington

The over 17,000 signers of the declaration will be represented on Sunday, January 23, when Dr. Malone stands with fellow doctors and scientists on stage in Washington DC, as part of the Defeat the Mandates march Sunday, January 23, 2022. At the Lincoln Memorial, they will be joined by a wide range of featured guests for a series of inspiring talks and musical performances. Join us!

About the Global COVID Summit

Global Covid Summit is the product of an international alliance of doctors and scientists, committed to speaking truth to power about Covid pandemic research and treatment.

Thousands have died from Covid as a result of being denied life-saving early treatment. The Declaration is a battle cry from physicians who are daily fighting for the right to treat their patients, and the right of patients to receive those treatments – without fear of interference, retribution or censorship by government, pharmacies, pharmaceutical corporations, and big tech. We demand that these groups step aside and honor the sanctity and integrity of the patient- physician relationship, the fundamental maxim “First Do No Harm”, and the freedom of patients and physicians to make informed medical decisions. Lives depend on it. More information here: https://globalCovidSummit.org


An events page is available to alert you to upcoming Summits and other events, most prominent of which is the January 23 March on Washington, an “American Homecoming” to protest overreaching medical mandates.

But you can also view some amazing video from past summits including Florida and San Juan, Puerto Rico. Please spread the word about this site – it’s important!

Remember – if you are a physician, nurse, medical scientist or medical care professional, please wear a white coat to the march (or carry it). Let’s all work to make this march peaceful in solidarity for all those marching around the world.

January 22, 2022 Posted by | Science and Pseudo-Science, Solidarity and Activism | , , | Leave a comment

How Billions in COVID Stimulus Funds Led to Dangerous, Tyrannical Policies in U.S. Schools

The Defender | January 20, 2022

In a January interview on Del Bigtree’s “The Highwire” —“COVID-19: Following the Money” — policy analyst A.J. DePriest, a member of the grassroots Tennessee Liberty Network, shared the group’s jaw-dropping findings about the undue influence of federal relief monies on school and hospital policies.

In this article, The Defender covers how federal money affected schools. We will cover the impact of federal money on hospitals in a separate article to follow.

In 2020 and 2021, Congress passed trillions in COVID-related stimulus through the Coronavirus Aid, Relief and Economic Security (CARES) Act, the Coronavirus Response and Relief Supplemental Appropriations (CRRSA) Act and the American Rescue Plan (ARP) Act.

Sizeable portions of those funds went to schools.

Digging into the education allotment, the Tennessee network discovered public, charter and nonprofit private schools in the U.S. received nearly $190.5 billion during three rounds of Elementary and Secondary School Emergency Relief (ESSER) funding (called ESSER I, II and III).

One of DePriest’s disquieting take-home messages is that this education lucre came with major strings attached — federal strings that are persuading ignominious school board members to adopt policies unfavorable and even dangerous to student health and well-being.

While DePriest characterized the stimulus bonanza as a “BIG carrot” for cash-strapped schools, that assessment may be too generous. If one examines the disturbing conditions attached to the U.S. Department of Education’s (DOE’s) dazzling largesse, the government billions seem closer to a godfather-like “offer they can’t refuse.”

The $190 billion ‘carrot’

The size of the federal “carrot” increased with each ESSER iteration. The $1.9 trillion ARP package alone assigned state educational agencies and school districts a whopping $122 billion (ESSER III).

On Jan. 18, the U.S. Department of Education (DOE) crowed about its disbursement of the final chunk of ESSER III monies, claiming the funds were “critical” for addressing “recent challenges” such as the putative and much-ballyhooed Omicron variant.

In Tennessee, the state’s initial take from ESSER I was nearly $260 million, but ESSER II quadrupled that amount to over $1.1 billion. By ESSER III, Tennessee’s educational haul had reached almost $2.5 billion.

The school district encompassing Memphis received roughly three-quarters of a billion dollars, DePriest noted, while Nashville schools pocketed a cool half a billion.

Schools and COVID vaccines

In DePriest’s view, there’s a catch that explains why school boards in every state have been so coldly unresponsive to parental pleas to unmask their children and abandon other COVID restrictions.

The catch is that federal generosity for state educational agencies is contingent on states proving to DOE (in reports submitted twice a year through fall 2023) they are meeting requirements synced with the Centers for Disease Control and Prevention’s (CDC’s) “safety recommendations.”

The CDC’s aggressive “recommendations” include:

  • Enforcing “universal and correct wearing of masks”
  • Physically modifying schools to facilitate “distancing”
  • Ensuring “respiratory etiquette” and handwashing (likely with carcinogenic sanitizers)
  • Implementing strenuous cleaning protocols to maintain “healthy facilities”
  • Facilitating contact tracing, “in combination with isolation and quarantine”
  • Conducting testing (both screening and diagnosis), helped along by additional resources from a federal-CDC-Rockefeller Foundation partnership to “ensure that all schools can access and set up screening testing programs as quickly as possible”
  • Coordinating with state and local health officials
  • Engaging in “efforts to provide vaccinations to school communities”

In its Jan. 18 press release, DOE took pains to emphasize that expanding access to vaccinations is “critical” for “safely reopening schools and sustaining safe operations.” And it furnished two ominous illustrations of how its stimulus monies are supporting vaccination efforts on the ground.

First, DOE noted, the Vermont Agency of Education is partnering with other statewide agencies “to vaccinate all Vermonters, including eligible students.” DOE approvingly stated that three-fourths of 12- to 17-year-olds in Vermont already received at least one dose.

DOE also considered the Hawaii Department of Education’s hosting of dozens of vaccination clinics for students, staff and “school communities” to be exemplary.

Further evidence of the feds’ hold over schools comes from the fact that some school districts have already taken steps to mandate COVID shots for some or all K-12 students, even in advance of formal U.S. Food and Drug Administration (FDA) approval.

Weaponizing HVAC systems?

More than 40% of school districts plan to spend some of their ESSER funds on “improvements” to heating, ventilation and air conditioning (HVAC) systems.

This raises a potential red flag in light of the Environmental Protection Agency’s (EPA) authorization in February 2021 — through a slippery “Public Health Emergency Exemption” — of a potentially hazardous, nanoparticle-based “air treatment” called Grignard Pure.

Dispersal of the chemical, authorized for indoor use in public spaces, occurs primarily “in-duct” via HVAC systems.

EPA’s authorization allows for Grignard Pure’s use in indoor spaces “when adherence to current public health guidelines … is impractical or difficult to maintain.”

As examples of spaces where the chemical’s use is permitted, the agency lists government facilities, healthcare facilities, food processing facilities and public transit.

EPA’s definition of “government facilities” does not appear to include schools, but the agency does admit to studying use of “air treatment technologies” on school buses.

A senior EPA scientist conceded last August, “how safe [the technologies] are, particularly for sensitive populations such as children, is not fully understood.” Given the experimental use of “air treatments” on school buses, it would behoove parents to query schools’ motives for upgrading their HVAC systems.

Moreover, though EPA initially green-lighted Grignard Pure in just two states (Georgia and Tennessee), it added four more states — Maryland, Nevada, Pennsylvania and Texas — last July.

The manufacturer’s website indicates that applications for Public Health Emergency Exemption are pending in another 15 states.

Nor does EPA’s vaguely worded list of indoor spaces seem to preclude use of the chemical in facilities not on that list. For example, Grignard Pure’s CEO is openly publicizing his product’s use in religious spaces, and a member of the company’s engineering steering committee elatedly stated last year, “There’s no limit to where we can use it!”

St. Simons Presbyterian Church in Georgia paved the way for church use, with the facility’s HVAC vents, which “run the length of both sides of the sanctuary’s ceiling,” apparently having been deemed ideal for spritzing congregants during services. This generates “a light haze [that] comes from the air vents and settles over the sanctuary.”

According to news accounts, the Georgia church’s pastor views Grignard Pure as “an added layer of safety,” a fact that the church emphasizes in its weekly bulletins. The pastor also is considering using the chemical-dispensing system during flu season.

Health risks associated with triethylene glycol

As The Defender previously reported, Grignard Pure’s supposedly virus-killing active ingredient is triethylene glycol (TEG), a chemical whose prior claim to fame was its use in theatrical fog machines.

Shortly before EPA reached its upbeat decision to approve TEG, the UK’s Scientific Advisory Group for Emergencies (SAGE) recommended against TEG’s use as a virucide due to its limited effectiveness and “potential health effects for those exposed over a long period of time.”

After WWII and in the early 1950s, there was an attempt to deploy TEG for “air disinfection” purposes in school settings. However, “wartime and post-war authors would not have had access to much of the toxicological and health data now available for this chemical,” said the UK SAGE group.

These data show “a number of potential acute health effects,” including respiratory tract irritation in case of inhalation.

A Berkeley, California lab — the Indoor Air Quality Scientific Findings Resource Bank — recently expressed multiple concerns about TEG in relation to air disinfection.

The indoor air quality experts cautioned, “careful attention should be given to dosage of triethylene glycol in indoor settings in order to minimize potential health effects caused by chemical exposure,” particularly in light of evidence of health effects with repeated exposure.

The Berkeley group also warned “TEG could react with other indoor chemicals” — including common disinfectants — “leading to additional and perhaps unexpected adverse health effects,” including toxic effects on human airway epithelial cells.

In light of these “uncertainties about TEG dosing, chemical mixtures, and health risks,” they suggested TEG should be viewed as a “lower priority” option.

In similar comments about the use of TEG “or other similar chemicals” for air disinfection (p. 23), SAGE wrote in November 2020:

“There is currently no strong evidence that using a continuous spray chemical in the air will be an effective control against SARS-CoV-2 transmission. … [T]here is no precedent for such an approach to be used as a continuous spray in an occupied space for infection control. Cleaning the air by spraying it with a chemical is a misnomer – it is simply swapping one contaminant for another.”

TEG’s cousin polyethylene glycol (PEG)

As The Defender reported a year ago, TEG is a chemical cousin to and sometime-component of polyethylene glycol (PEG), a synthetic, nondegradable polymer of questionable biocompatibility.

PEG is known to be associated with adverse immune responses, including anaphylaxis.

Both the Pfizer and Moderna COVID jabs use PEG to make their mRNA “carrier systems” work, and the compound is also present in numerous other drugs and consumer products.

Up to 72% of the U.S. population may have anti-PEG antibodies — including an estimated 8% with highly elevated levels — that could lead to life-threatening anaphylactic reactions. Research is needed to assess potential TEG-PEG cross-reactivity.

Children’s Health Defense (CHD) in August 2020 first sounded the alarm about the risks of PEG in COVID shots, pointing out that well before COVID, PEG had already been flagged, including by Moderna itself, for its potential to trigger immediate hypersensitivity reactions.

CHD was so concerned about the potential for anaphylaxis that it followed up with a letter to the FDA on Sept. 25, 2020, outlining the need for critical safeguards for Moderna clinical trial participants.

Those concerns have since been borne out by repeated reports of PEG-linked anaphylaxis that began surfacing concurrent with the two mRNA vaccines’ rollout.

Resistance is NOT futile

In mid-August, Tennessee’s governor issued an executive order giving parents ultimate decision-making authority over their children’s masking behavior at school.

U.S. Secretary of Education Miguel Cardona evinced no compunction about immediately chastising the governor and his education commissioner for taking matters into their own hands.

In a letter dated two days later, Cardona wrote that the Tennessee governor’s action was “at odds with the school district planning process embodied in the U.S. Department of Education’s. . . interim final requirements,” pointedly adding that CDC safety recommendations include “universal and correct wearing of masks.”

Meanwhile, Treasury Secretary Janet Yellen warned Arizona Gov. Doug Ducey on Jan. 14 that the Biden administration is prepared to take back Arizona’s relief funds — and also withhold future federal aid — due to the state’s active discouragement of school mask mandates.

Yellen offered no explanation as to why the Treasury Department, rather than DOE, was issuing the warning.

In response, Ducey emphasized Arizona’s focus on “things that matter” — math, not masks. Attorney General Mark Brnovich urged Yellen to rescind the threat, arguing that Treasury is “trying to overstep its constitutional bounds” by dictating how the state should run and fund its schools.

These types of intimidation tactics are also evident at the school-district level, prompting parents’ growing frustration.

Rather than continue to beg for mask lenience, DePriest reminds parents they have every right to confront school board members about the feds’ cash-in-exchange-for-obedience arrangements.

“They’re getting the money to mask your kids. It has nothing to do with health and safety,” DePriest said.

As evidenced by the quadrupling of homeschooling since the beginning of COVID, many families have simply had it. However, for parents for whom homeschooling is not an option, there is every reason to push local school boards to address their student-unfriendly behavior more transparently.

Here are a handful of possible questions and actions:

  1. Borrowing DePriest’s no-nonsense wording, a first step is to ask, “How much money are you taking from the federal government to commit this egregious, tyrannical behavior on our kids?” If school board members profess not to know, prepared citizens can easily present them with the financial information listed here.
  2. As one state describes it, “The governance of local school boards by democratically-elected individuals remains at the heart of two vital United States structures: the public education system and democracy itself.” Remind school board members that when they put politics and financial arm-twisting ahead of their relationship with the public and the students they are supposed to serve, they are engaging in a fundamental betrayal of trust and ethics.
  3. Emphasize to school board members that the damage caused by COVID restrictions has far outweighed any threat from the illness, turning schools into “a physically, spiritually, and emotionally unsafe place” for children. Moreover, none of the restrictions are genuinely evidence-based.
  4. Continue to present school board members with evidence about the experimental COVID injections’ dangers (see sample talking points here).
  5. Ask schools whether they are planning for or engaging in HVAC “improvements.” If yes, ask them to describe the purpose of the “improvements” and whether schools intend to use HVAC systems to disseminate unsafe chemicals. Tell them EPA is doing research on “air treatments” in school buses, and let them know about the risks — both known and hypothesized — of chemicals like TEG.
  6. Finally, for officials who claim that their hands are tied, A.J. DePriest has a ready solution: Tell them to “give the money back”!

© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

January 21, 2022 Posted by | Civil Liberties, Science and Pseudo-Science | , , | Leave a comment

Yohan Tengra Exposes the Public Health Mafia in India

Corbett • 01/19/2022

How does the global public health mafia direct the health policy of nations around the world? In today’s conversation, James talks to Yohan Tengra of the Awaken Indian Movement to discuss Tengra’s article breaking down the Indian Covid-19 Task Force and how its members’ conflicts of interest relate to the decades-long takeover of India’s public health system.

Watch on Archive / BitChute / Minds / Odysee or Download the mp4

SHOW NOTES:
Yohan Tengra: AnarchyForFreedom.in / AwakenIndiaMovement / Telegram channel

Who Is Bill Gates?

India’s Covid-19 Task Force & “Experts” Exposed : Conflicts of Interest in Our Public Health System

HPV vaccine deaths: Parliament panel indicts PATH, health officials

Govt cancels FCRA licence of top public health NGO

NITI Aayog Launches Behaviour Change Campaign

A State of Fear: How the UK Weaponized Fear by Laura Dodsworth

Swedish company showcases microchip that can download COVID-19 passport status

Fact Check: Polio Vaccines, Tetanus Vaccines, and the Gates Foundation

Demonetization and You

January 21, 2022 Posted by | Corruption, Timeless or most popular, Video | , , , | Leave a comment

Was Peter Daszak Working For The Central Intelligence Agency?

An EcoHealth Alliance whistleblower steps forward

Dr. Shi Zhengli, Dr. Peter Daszak, and the Wuhan Institute of Virology
Kanekoa TheGreat | January 18, 2022

“We found other coronaviruses in bats, a whole host of them, some of them looked very similar to SARS. So we sequenced the spike protein: the protein that attaches to cells. Then we… Well, I didn’t do this work, but my colleagues in China did the work. You create pseudo particles, you insert the spike proteins from those viruses, see if they bind to human cells. At each step of this, you move closer and closer to this virus could really become pathogenic in people. You end up with a small number of viruses that really do look like killers.”

This statement was said by EcoHealth Alliance President Peter Daszak at a 2016 forum discussing “emerging infectious diseases and the next pandemic”. Daszak, who received more than $118 million in grants and contracts from federal agencies, including $53 million from USAID, $42 million from DOD, and $15 million from HHS, appeared to boast about the manipulation of “killer” SARS-like coronaviruses carried out by his “colleagues in China” at the now infamous Wuhan Institute of Virology.

According to investigative research done by independent-journalist Sam Husseini and The Intercept, much of the money awarded to EcoHealth Alliance did not focus on health or ecology, but rather on biowarfare, bioterrorism, and other dangerous uses of deadly pathogens.

EcoHealth Alliance received the majority of its funding from the United States Agency for International Development (USAID), a State Department subsidiary that serves as a frequent cover for the Central Intelligence Agency (CIA). Their second largest source of funding was from the Defense Threat Reduction Agency (DTRA), which is a branch of the Department of Defense (DOD) which states it is tasked to “counter and deter weapons of mass destruction and improvised threat networks.”

The United States Agency for International Development (USAID) has a long history of acting as a contract vehicle for various CIA covert activities. With an annual budget of over $27 billion and operations in over 100 countries, one former USAID director, John Gilligan, once admitted it was “infiltrated from top to bottom with CIA people.” Gilligan explained that “the idea was to plant operatives in every kind of activity we had overseas; government, volunteer, religious, every kind.”

In 2013, a US cable published by WikiLeaks outlined the U.S. strategy to undermine Venezuela’s government through USAID by “penetrating Chavez’s political base”, “dividing Chavismo”, and “isolating Chavez internationally.” In 2014, the Associated Press disclosed that USAID contracted out a project to develop a rival to Twitter in order to foment a rebellion in Cuba.

From 2009 to 2019, USAID partnered with EcoHealth Alliance on their PREDICT program which identified over 1,200 new viruses, including over 160 coronavirus strains; trained roughly 5,000 people around the world to identify new diseases; and improved or developed 60 research laboratories.

What better way for the CIA to collect intelligence on the world’s biological warfare capabilities?


Source: The Intercept

Dr. Andrew Huff received his Ph.D. in Environmental Health specializing in emerging diseases before becoming an Associate Vice President at EcoHealth Alliance, where he developed novel methods of bio-surveillance, data analytics, and visualization for disease detection.

On January 12, 2022, Dr. Andrew Huff issued a public statement (on Twitter) in which he claimed, Peter Daszak, the President of EcoHealth Alliance, told him that he was working for the CIA.

Dr. Andrew Huff’s full statement below:


Source: Dr. Andrew Huff

Dr. Huff continued, “… I wouldn’t be surprised if the CIA / IC community orchestrated the COVID coverup acting as an intermediary between Fauci, Collins, Daszak, Baric, and many others. At best, it was the biggest criminal conspiracy in US history by bureaucrats or political appointees.”

What exactly did they cover-up?

Peter Daszak’s EcoHealth Alliance—financed by USAID, DOD, and other U.S. Government agencies—partnered with Dr. Ralph Baric of the University of North Carolina and Dr. Shi Zhengli of the Wuhan Institute of Virology to conduct gain-of-function research on bat-borne coronaviruses.

Baric successfully created a “chimeric” coronavirus in 2015. There is a well-documented scientific paper trail that details how Dr. Baric and Dr. Zhengli continued to collaborate on gain-of-function research together to create what went on to be a potential precursor to the SARS-CoV-2 virus.

Dr. Anthony Fauci, Dr. Francis Collins, and Dr. Peter Daszak, who were proponents of this type of international collaboration on gain-of-function research were heavily incentivized to cover up the possibility of a lab origin because they previously had funneled U.S. taxpayer money to the Chinese lab.

At the start of 2020, there was a lot of chatter about where the virus SARS-CoV-2 actually originated from. Two papers published in March 2020—one in Nature Medicine and one in The Lancet—controlled the direction of the dialogue on the origin of the virus.

Both papers were repeatedly cited by Fauci, Collins, Daszak, the corporate media, and big tech as evidence to shut down and even censor any discussion of the possibility that the virus originated at the Wuhan Institute of Virology.

Only later through redacted emails released by FOIA did we learn that Fauci, Collins, and Daszak were intimately involved in crafting the two papers which dismissed the lab origin hypotheses as “conspiracy theory.”

In February 2020, Daszak told University of North Carolina coronavirus researcher Dr. Ralph Baric that they should not sign the statement condemning the lab-leak theory so that it seems more independent and credible. “You, me and him should not sign this statement, so it has some distance from us and therefore doesn’t work in a counterproductive way,” Daszak wrote.

More unredacted emails have revealed that while these scientists held the private belief that the lab release was the most likely scenario, they still worked to seed the natural origin narrative for the public through the papers published in Nature Medicine and The Lancet.

In April 2020, Daszak opposed the public release of Covid-19-related virus sequence data that has been gathered from China, as part of the U.S. Agency for International Development (USAID) PREDICT program because he said it would bring “very unwelcome attention” to the aforementioned “PREDICT and USAID” programs.


Source: U.S. Right To Know FOIA

In September 2020, scientists were outraged when Daszak was chosen to lead the World Health Organization task force examining the possibility that Covid-19 leaked from the Wuhan Institute of Virology.

Despite many clear attempts to cut off a legitimate scientific inquiry into the Wuhan lab origin hypothesis, the theory continued to persist predominantly due to the fact that the Chinese government was unable to provide a single shred of evidence in support of the natural origin theory.

In May 2021, the narrative turned when, Nicholas Wade, a former science reporter at the New York Times published his seminal column outlining the case for the Covid lab-leak theory.

For SARS1, an intermediary host species was identified within four months of the epidemic’s outbreak and the host of MERS was identified within nine months. Yet some 15 months after the SARS2 outbreak began, and a presumably intensive search, Chinese researchers had failed to find either the original bat population, or the intermediate species to which SARS2 might have jumped, or any serological evidence of a natural origin.

Every step of the way, Fauci, Collins, and Daszak have done everything in their power to obfuscate, mislead, and misinform the world about the possibility of SARS-CoV-2 originating at the Wuhan Institute of Virology.

If Dr. Andrew Huff is telling the truth, Fauci, Collins, and Daszak are not covering up the lab origin only for themselves, but also for the Central Intelligence Agency, the Department of Defense, and the U.S. Government.

January 20, 2022 Posted by | Deception, War Crimes | , , , , | Leave a comment

Covid-19 vaccines and treatments: we must have raw data, now

Data should be fully and immediately available for public scrutiny

Peter Doshi, senior editor, Fiona Godlee, former editor in chief, Kamran Abbasi, editor in chief | BMJ | January 19, 2022

In the pages of The BMJ a decade ago, in the middle of a different pandemic, it came to light that governments around the world had spent billions stockpiling antivirals for influenza that had not been shown to reduce the risk of complications, hospital admissions, or death. The majority of trials that underpinned regulatory approval and government stockpiling of oseltamivir (Tamiflu) were sponsored by the manufacturer; most were unpublished, those that were published were ghostwritten by writers paid by the manufacturer, the people listed as principal authors lacked access to the raw data, and academics who requested access to the data for independent analysis were denied.1234

The Tamiflu saga heralded a decade of unprecedented attention to the importance of sharing clinical trial data.56 Public battles for drug company data,78 transparency campaigns with thousands of signatures,910 strengthened journal data sharing requirements,1112 explicit commitments from companies to share data,13 new data access website portals,8 and landmark transparency policies from medicines regulators1415 all promised a new era in data transparency.

Progress was made, but clearly not enough. The errors of the last pandemic are being repeated. Memories are short. Today, despite the global rollout of covid-19 vaccines and treatments, the anonymised participant level data underlying the trials for these new products remain inaccessible to doctors, researchers, and the public—and are likely to remain that way for years to come.16 This is morally indefensible for all trials, but especially for those involving major public health interventions.

Unacceptable delay

Pfizer’s pivotal covid vaccine trial was funded by the company and designed, run, analysed, and authored by Pfizer employees. The company and the contract research organisations that carried out the trial hold all the data.17 And Pfizer has indicated that it will not begin entertaining requests for trial data until May 2025, 24 months after the primary study completion date, which is listed on ClinicalTrials.gov as 15 May 2023 (NCT04368728).

The lack of access to data is consistent across vaccine manufacturers.16 Moderna says data “may be available … with publication of the final study results in 2022.”18 Datasets will be available “upon request and subject to review once the trial is complete,” which has an estimated primary completion date of 27 October 2022 (NCT04470427).

As of 31 December 2021, AstraZeneca may be ready to entertain requests for data from several of its large phase III trials.19 But actually obtaining data could be slow going. As its website explains, “timelines vary per request and can take up to a year upon full submission of the request.”20

Underlying data for covid-19 therapeutics are similarly hard to find. Published reports of Regeneron’s phase III trial of its monoclonal antibody therapy REGEN-COV flatly state that participant level data will not be made available to others.21 Should the drug be approved (and not just emergency authorised), sharing “will be considered.” For remdesivir, the US National Institutes of Health, which funded the trial, created a new portal to share data (https://accessclinicaldata.niaid.nih.gov/), but the dataset on offer is limited. An accompanying document explains: “The longitudinal data set only contains a small subset of the protocol and statistical analysis plan objectives.”

We are left with publications but no access to the underlying data on reasonable request. This is worrying for trial participants, researchers, clinicians, journal editors, policy makers, and the public. The journals that have published these primary studies may argue that they faced an awkward dilemma, caught between making the summary findings available quickly and upholding the best ethical values that support timely access to underlying data. In our view, there is no dilemma; the anonymised individual participant data from clinical trials must be made available for independent scrutiny.

Journal editors, systematic reviewers, and the writers of clinical practice guideline generally obtain little beyond a journal publication, but regulatory agencies receive far more granular data as part of the regulatory review process. In the words of the European Medicine Agency’s former executive director and senior medical officer, “relying solely on the publications of clinical trials in scientific journals as the basis of healthcare decisions is not a good idea … Drug regulators have been aware of this limitation for a long time and routinely obtain and assess the full documentation (rather than just publications).”22

Among regulators, the US Food and Drug Administration is believed to receive the most raw data but does not proactively release them. After a freedom of information request to the agency for Pfizer’s vaccine data, the FDA offered to release 500 pages a month, a process that would take decades to complete, arguing in court that publicly releasing data was slow owing to the need to first redact sensitive information.23 This month, however, a judge rejected the FDA’s offer and ordered the data be released at a rate of 55 000 pages a month. The data are to be made available on the requesting organisation’s website (phmpt.org).

In releasing thousands of pages of clinical trial documents, Health Canada and the EMA have also provided a degree of transparency that deserves acknowledgment.2425 Until recently, however, the data remained of limited utility, with copious redactions aimed at protecting trial blinding. But study reports with fewer redactions have been available since September 2021,2425 and missing appendices may be accessible through freedom of information requests.

Even so, anyone looking for participant level datasets may be disappointed because Health Canada and the EMA do not receive or analyse these data, and it remains to be seen how the FDA responds to the court order. Moreover, the FDA is producing data only for Pfizer’s vaccine; other manufacturers’ data cannot be requested until the vaccines are approved, which the Moderna and Johnson & Johnson vaccines are not. Industry, which holds the raw data, is not legally required to honour requests for access from independent researchers.

Like the FDA, and unlike its Canadian and European counterparts, the UK’s regulator—the Medicines and Healthcare Products Regulatory Agency—does not proactively release clinical trial documents, and it has also stopped posting information released in response to freedom of information requests on its website.26

Transparency and trust

As well as access to the underlying data, transparent decision making is essential. Regulators and public health bodies could release details27 such as why vaccine trials were not designed to test efficacy against infection and spread of SARS-CoV-2.28 Had regulators insisted on this outcome, countries would have learnt sooner about the effect of vaccines on transmission and been able to plan accordingly.29

Big pharma is the least trusted industry.30 At least three of the many companies making covid-19 vaccines have past criminal and civil settlements costing them billions of dollars.31 One pleaded guilty to fraud.31 Other companies have no pre-covid track record. Now the covid pandemic has minted many new pharma billionaires, and vaccine manufacturers have reported tens of billions in revenue.32

The BMJ supports vaccination policies based on sound evidence. As the global vaccine rollout continues, it cannot be justifiable or in the best interests of patients and the public that we are left to just trust “in the system,” with the distant hope that the underlying data may become available for independent scrutiny at some point in the future. The same applies to treatments for covid-19. Transparency is the key to building trust and an important route to answering people’s legitimate questions about the efficacy and safety of vaccines and treatments and the clinical and public health policies established for their use.

Twelve years ago we called for the immediate release of raw data from clinical trials.1 We reiterate that call now. Data must be available when trial results are announced, published, or used to justify regulatory decisions. There is no place for wholesale exemptions from good practice during a pandemic. The public has paid for covid-19 vaccines through vast public funding of research, and it is the public that takes on the balance of benefits and harms that accompany vaccination. The public, therefore, has a right and entitlement to those data, as well as to the interrogation of those data by experts.

Pharmaceutical companies are reaping vast profits without adequate independent scrutiny of their scientific claims.33 The purpose of regulators is not to dance to the tune of rich global corporations and enrich them further; it is to protect the health of their populations. We need complete data transparency for all studies, we need it in the public interest, and we need it now.

Footnotes

  • Competing interests: We have read and understood BMJ policy on declaration of interests and declare that The BMJ is a co-founder of the AllTrials campaign. PD was one of the Cochrane reviewers studying influenza antivirals beginning in 2009, who campaigned for access to data. He also helped organise the Coalition Advocating for Adequately Licensed Medicines (CAALM), which formally petitioned the FDA to refrain from fully approving any covid-19 vaccine this year (docket FDA-2021-P-0786). PD is also a member of Public Health and Medical Professionals for Transparency, which has sued the FDA to obtain the Pfizer covid-19 vaccine data. The views and opinions do not necessarily reflect the official policy or position of the University of Maryland.

  • Provenance and peer review: Commissioned; externally peer reviewed.

References

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Author affiliations

Correspondence to: P Doshi Pdoshi@bmj.com

January 20, 2022 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular | , , | Leave a comment

Unboostered Brits Infected and Dying at Higher Rates than Unvaccinated

UKHSA Vaccine Efficacy Statistics: Week 3

eugyppius | January 20, 2022

The UK Health Security Agency has been condemned for literally months now to report incredibly inconvenient vaccine efficacy statistics. How they have struggled. They have composed disclaimer after disclaimer. They filled a whole blog post with special pleading. They have greyed out the inconvenient numbers.

In their latest report, published just this evening, they’ve tried something new and bold. They now only calculate case, hospitalisation and death rates for the unvaccinated and the triple vaccinated. The double vaccinated have been banished entirely from Table 12. This will make the evil negative efficacy go away, right?

Ha, no:

The numbers are unadjusted, it is true; much certainty surrounds the size of the unvaccinated population and therefore case rates within that group. What is more, these are cases, not true infection statistics. Nevertheless, res ipsa loquitur. It does not look great.

In fact, the UKHSA have given us a great gift, in that they finally provide separate case and severe outcome statistics for the triple-vaccinated and the double vaccinated, allowing us to compare rates across all three groups. They don’t do that themselves, of course, but no matter. We can use the raw numbers and rates from last week’s report to derive the total number of double and triple vaccinated, and the rates in this week’s report to derive the triple vaccinated population. A little subtraction then gives us a decent estimate of how many double but not triple vaccinated people there are in each age bracket.

Here is the graph the UKHSA don’t want you to see:

This is plainly a pandemic of the vaccinated.

The double vaccinated death rate is also a problem. You can tell this just from looking at the numbers in each category:

The crucial 70+ demographic is over 90% boostered, and yet the very few double vaccinated in this cohort manage to match or exceed theeir death numbers.

The death rates have the double vaccinated worse than the unvaccinated in the 70+ cohort, and roughly matching the unvaccinated in the 60–69 group:

This isn’t all that surprising, given that Public Health Scotland data has shown across-the-board negative efficacy for the unboostered for some weeks now:

This is also true of deaths, but beware of the extremely low numbers, particularly in the singly vaccinated:

January 20, 2022 Posted by | Science and Pseudo-Science | , , | Leave a comment

The Super Hero Film Era: How Political Dissent Is Neutralised

The Dave Cullen Show – Computing Forever | September 23, 2021

BitChute: https://www.bitchute.com/channel/thedavecullenshow/
Gab: https://gab.ai/DaveCullen
Minds.com: https://www.minds.com/davecullen

January 20, 2022 Posted by | Civil Liberties, Film Review, Mainstream Media, Warmongering, Timeless or most popular, Video | , | Leave a comment