Louisiana Governor Reverses ‘Insane Mandate’ Requiring COVID Injections for Children

From [CHD] Children and students attending daycare, K-12 programs and college in Louisiana, at least for now, will not be required to get the COVID-19 vaccine, Gov. John Bel Edwards announced Wednesday.

The announcement reversed an earlier decision by the governor’s administration and the Louisiana Health Department (LHD) requiring students to be fully vaccinated beginning in the 2022-23 school year.

Edwards said he based the decision on the fact that the U.S. Food and Drug Administration (FDA) has not fully approved the vaccines for people under age 16.

The governor said his administration will continue to recommend all children age 5 and over get the vaccine, a recommendation the LHD endorsed Wednesday in a news release.

In their statements, the governor and the LHD implied COVID-19 vaccines for people over age 16 are fully approved. However, while the FDA did grant full licensing to Pfizer’s Comirnaty and Moderna’s Spikevax COVID-19 vaccines — for people 16 and older and 18 and older, respectively — those vaccines are not available in the U.S.

All COVID-19 vaccines being administered in the U.S. are still available only under Emergency Use Authorization.

Commenting on the governor’s announcement, Robert F. Kennedy, Jr., chairman and chief legal counsel for Children’s Health Defense (CHD), said:

“The science shows this age group is at zero risk from COVID-19 and at high risk of debilitating and sometimes deadly vaccine injury.

“The only thing driving these mandates is the deceptive campaign of orchestrated fear and deliberately induced confusion carried out by reckless and incompetent health officials, their Big Pharma overlords and the gullible politicians who do what they are told rather than conduct their own independent research.”

Kennedy added, “Hats off to Louisiana Attorney General Jeff Landry, who forced Gov. Edwards to back off this insane mandate.” [MORE]

Did Pfizer Commit Fraud in Its COVID Injection Research? Contrary to Its Claims, The Clinical Trials Failed to Demonstrate the Vaccine "Safes Lives" or that It is "Highly Effective"

STORY AT-A-GLANCE

  • In November 2021, Brook Jackson, a whistleblower who worked on Pfizer’s Phase 3 COVID jab trial in the fall of 2020, warned she’d seen evidence of fraud in the trial

  • With the release of Pfizer trial data — which they tried to withhold for 75 years — additional problems suggestive of fraud and data manipulation are coming to light

  • Trial site 1231, located in Argentina, somehow managed to recruit 10% of the total trial participants, 4,501 in all, and they did so in just three weeks, and without a contract research organization — a feat that has many questioning whether fraud was committed

  • The lead investigator for trial site 1231 is Dr. Fernando Polack, who also happens to be a consultant for the U.S. Food and Drug Administration’s Vaccines and Related Biological Products Advisory Committee (RBPAC), a current adjunct professor at Vanderbilt University in Tennessee, an investigator for Fundación Infant, funded by the Bill & Melinda Gates foundation, and the first author of Pfizer’s paper, “Safety and Efficacy of the BNT162b2 mRNA COVID-19 Vaccine,” published at the end of December 2021

  • Site 1231 held a second enrollment session, given the designation of “site 4444.” The 4444 trial site data raise another red flag. It supposedly enrolled 1,275 patients in a single week, from September 22 through 27, 2020 — the last week that recruitment could take place to meet the data cutoff for the FDA meeting in December 2020. Was “site 4444” fabricating data to create the appearance that the jab was having an effect?

From [MERCOLA] In November 2021, Brook Jackson, a whistleblower who worked on Pfizer's Phase 3 COVID jab trial in the fall of 2020, warned she'd seen evidence of fraud in the trial.

Data were falsified, patients were unblinded, the company hired poorly trained people to administer the injections, and follow-up on reported side effects lagged way behind. The revelation was published in The British Medical Journal. In his November 2, 2021, report, investigative journalist Paul Thacker wrote:1

"Revelations of poor practices at a contract research company helping to carry out Pfizer's pivotal COVID-19 vaccine trial raise questions about data integrity and regulatory oversight ...

[F]or researchers who were testing Pfizer's vaccine at several sites in Texas during that autumn, speed may have come at the cost of data integrity and patient safety ... Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding."

Jackson, a former regional director of Ventavia Research Group, a research organization charged with testing Pfizer's COVID jab at several sites in Texas, repeatedly "informed her superiors of poor laboratory management, patient safety concerns and data integrity issues," Thacker wrote.

When her concerns were ignored, she finally called the U.S. Food and Drug Administration and filed a complaint via email. Jackson was fired later that day after just two weeks on the job. According to her separation letter, management decided she was "not a good fit" for the company after all.

She provided The BMJ with "dozens of internal company documents, photos, audio recordings and emails" proving her concerns were valid, and according to Jackson, this was the first time she'd ever been fired in her 20-year career as a clinical research coordinator.

BMJ Report Censored

Disturbingly, social media actually censored this BMJ article and published pure falsehoods in an effort to "debunk" it. Mind you, the BMJ is one of the oldest and most respected peer-reviewed medical journals in the world! The Facebook "fact check" was done by Lead Stories, a Facebook contractor, which claimed the BMJ "did NOT reveal disqualifying and ignored reports of flaws in Pfizer's" trials.2

In response, The BMJ slammed the fact check, calling it "inaccurate, incompetent and irresponsible."3,4,5 In an open letter6 addressed to Facebook's Mark Zuckerberg, The BMJ urged Zuckerberg to "act swiftly" to correct the erroneous fact check, review the processes that allowed it to occur in the first place, and "generally to reconsider your investment in and approach to fact checking overall." As noted by The BMJ in its letter, the Lead Stories' fact check:7

  • Inaccurately referred to The BMJ as a "news blog"

  • Failed to specify any assertions of fact that The BMJ article got wrong

  • Published the fact check on the Lead Stories' website under a URL that contains the phrase "hoax-alert"

Pfizer Trial Data Raises Suspicions of Fraud

Now, with the release of Pfizer trial data8 — which they tried to withhold for 75 years — internet sleuths are finding additional problems suggestive of fraud and data manipulation. May 9, 2022, a Twitter user named Jikkyleaks posted a series of tweets questioning data from Pfizer trial sites 1231 and 4444.9

Trial site 1231, located in Argentina, somehow managed to recruit 10% of the total trial participants, 4,501 in all, and they did so in just three weeks, and without a contract research organization (CRO). CROs like the Ventavia Research Group, which Jackson worked for, provide clinical trial management services. The lead investigator for trial site 1231 is Dr. Fernando Polack,10 who also happens to be:11

  • A consultant for the U.S. Food and Drug Administration's Vaccines and Related Biological Products Advisory Committee (RBPAC) since 2017

  • A current adjunct professor at Vanderbilt University in Tennessee

  • An investigator for Fundación Infant,12 which is funded by the Bill & Melinda Gates foundation13

  • The first author of Pfizer's paper,14 "Safety and Efficacy of the BNT162b2 mRNA COVID-19 Vaccine," published at the end of December 2021

As noted by Jikkyleaks, Polack "is literally the busiest doctor on the planet," because in addition to all those roles, he also managed to single-handedly enroll 4,500 patients in three weeks, which entails filling out some 250 pages of case report forms (CRFs) for each patient. That's about 1,125,000 pages total. (CRFs are documents used in clinical research to record standardized data from each patient, including adverse events.)

This recruitment also took place seven days a week, which is another red flag. "Weekend recruitment for a clinical trial would be odd. Staff are needed to fill out that many record forms (CRFs) and there are potential risks to the trial, so you need medical staff. It would be highly unusual," Jikkyleaks notes.

Is Polack just a super-humanly efficient trial investigator, or could this be evidence of fraud? As noted by Steve Kirsch in the featured video and an accompanying Substack article,15 Polack is the coordinator for a network of 26 hospitals in Argentina, so perhaps it's possible he could have recruited 57 patients per week per hospital, but it seems highly unlikely.

Questions Surround Site 4444 Data

Now, "site 4444" does not exist. It's actually the same as site 1231. It appears site 1231 held a second enrollment session, and these were for some reason given the designation of 4444. The 4444 trial site data raise another red flag.

Site 4444 (the second enrollment session for site 1231) supposedly enrolled 1,275 patients in a single week, from September 22 through 27, 2020, and the suspicious thing about that — aside from the speed — is the fact that this was the last week that recruitment could take place to meet the data cutoff for the FDA meeting in December 2020. Jikkyleads writes:16

"My guess: they needed enough numbers of 'positive PCR tests' in the placebo group to show a difference between groups for that VRBPAC meeting on the 10th Dec, and they didn't have them. So, site 4444 appeared and gave them their 'perfect' result. Bravo."

Kirsch notes:17

"Was there fraud in the Pfizer trial? Without a doubt. The story of Maddie de Garay is a clear case of that. Brook Jackson has evidence of fraud; she has 17 lawyers working for her. If there wasn't fraud, these lawyers wouldn't be wasting their time.

This new data on Site 1231/4444 looks suspicious to me. It looks too good to be true. But we can't make the call without more information. Undoubtedly, the mainstream media will not look into this, Pfizer will remain silent, and Polack will be unreachable for comment. The lack of transparency should be troubling to everyone. That is the one thing we can say for sure."

Pfizer Documents Reveal COVID Jab Dangers

Among the tens of thousands of Pfizer documents released by the FDA so far, we now also have clear evidence of harm. For nurse educator John Campbell, featured in the video above, these documents appear to have served as a "red pill,"18 waking him up to the possibility that the jabs may indeed be far more dangerous than anyone expected, including himself.

In the video, Campbell reviews the documents listed as "5.3.6. Postmarketing Experience," which were originally marked "confidential." They reveal that, cumulatively, through February 28, 2021, Pfizer received 42,086 adverse event reports, including 1,223 deaths.

To have 1,223 fatalities and 42,086 reports of injury in the first three months is a significant safety signal, especially when you consider that the 1976 swine flu vaccine was pulled after only 25 deaths.

As noted by Campbell, "It would have been good to know about this at the time, wouldn't it?" referring to the rollout of the jabs. Campbell has been fairly consistent in his support of the "safe and effective" vaccine narrative, but "This has just destroyed trust in authority," he said.

158,000 Recorded Side Effects — A World Record?

The first really large tranche of more than 10,000 Pfizer documents was released March 1, 2022. (You can find them all on PHMPT.org.19) In this batch were no less than nine single-space pages of "adverse events of special interest," listed in alphabetical order20 — 158,000 in all!

The first side effect on this shockingly exhaustive list is a rare condition known as 1p36 deleti

Since the Vaccine Rollout Natural Deaths of All Kinds are Higher. Excess Death is 48% higher between 1/21 and 2/22 compared to 2020. COVID Deaths are 74% Higher and non-COVID deaths are 10% higher

Statistician Joel Smalley explains: It turns out that natural deaths of all kinds post-vaccine are higher than pre-vaccine.

As you can see, all natural causes excess death is 48% higher between the start of 2021 and mid-Feb 2022 compared to 2020. COVID deaths are 74% higher and non-COVID deaths are 10% higher.

Sure, it’s a longer time period and yes, COVID didn’t really hit until March 2020. Even so, due to many reasons (already noted below), cumulative excess deaths should have started trending lower ages ago, especially if this “vaccine” is so damned effective, right??

Even if we take average weekly COVID deaths, they are 7% higher in the post-vax era. Effective?!?!

Anyway, it’s also important to highlight the ratio of non-COVID excess deaths to COVID deaths. Before we even get to how many COVID deaths really were due to COVID and not just incidental, we’re already at 40% in 2020 and 30% in 2021/22.

Given that there are near enough a thousand independent studies and reports showing the complete ineffectiveness of any COVID intervention, we can’t do the real cost/benefit analysis of collateral deaths relative to COVID deaths saved. Can’t divide into zero!

Well, I can reject my first two hypotheses based on analysis at the state level. Excess deaths post-vax are positively correlated with excess deaths pre-vax, statistically significantly too.

So, whatever is killing people since 2021 seems to have a somewhat similar demographic propensity IMO. In other words, if you were susceptible to die of COVID, you were equally susceptible to die of the 2021 pathogen.

Not only that, the excess deaths really only ramp up after the summer - half a million in less than the time it took to rack up the first 275k. It’s like they were triggered by some event.

Now, you know, of course, exactly where I’m going with this. Just like a broken record, so many roads keep leading us back to the *not* safe and *not* effective “vaccine”.

If you plot monthly percentage excess death against percentage vaccinated population for each state, you get a remarkably similar picture… [MORE]

Dr Yeardon and Dr Blynd: Authorities Own the Minds of Those who Believe “The COVID Lies." The False Narratives are Enemy Outposts in the Believer's Mind, Giving Rise to More Coercive Political Systems

In the first part of the article (The Covid Lies), Dr. Yeadon counters the 12 widespread Covid narratives with the following arguments: 

1. The infection fatality rate of SARS-CoV-2 is 0.1 – 0.3%, which is not significantly different from some seasonal influenza epidemics.

2. Based on the peer-reviewed articles, at least 30 to 50% of the population has prior cross-immunity.

3. SARS-CoV-2 does discriminate. “The lethality of this virus, as is common with respiratory viruses, is 1000X less in young, healthy people than in elderly people with multiple comorbidities.”

4. Asymptomatic transmission is the “central conceptual deceit” used to “underscore almost every intrusion: masking, mass testing, lockdowns, border restrictions, school closures, even vaccine passports.”

5. PCR test is “the central operational deceit.”

6. Neither cloth nor surgical masks prevent respiratory virus transmission.

7. Lockdown is “epidemiologically irrelevant” and never works. “Only “stay home if you’re sick” works.

8. “Covid-19 is the most treatable respiratory viral illness ever”. Safe and effective early treatments are available.

9. Based on the peer-reviewed articles, very few clinically significant reinfections of SARS-Cov-2 have ever been confirmed.

10. SARS-CoV-2 mutates slowly, and no variant is even close to escaping naturally-acquired immunity. However, there is the possibility that the so-called vaccines prevent the establishment of immune memory, leading to the repeated infections, which would be a form of acquired immune deficiency.

11. Safety is the top priority in a public health mass intervention, even more than effectiveness. “It was NEVER appropriate to attempt to “end the pandemic” with a novel technology vaccine.”

12. The four gene-based “vaccines” are toxic. The basic rules of selecting vaccine candidates are: 1) the agent has no inherent biological action (non-toxic); 2) the agent should be the genetically most stable part of the virus; 3) the agent should be most different from human proteins. Spike protein as the vaccine does not fit any of the above criteria.

In the second part of the article he addresses How Much of the Covid-19 Narrative Was True. At the end of the article, Dr. Yeadon also provides a list of extra supplemental points to support his conclusions.

The Covid Lies

Working Draft, April 10, 2022 [PDF] [MORE]

By Dr. Mike Yeadon

Summary

I contend that all the main narrative points about the coronavirus named SARS-CoV-2 are lies. Furthermore, all the "measures" imposed on the population are also lies. In what follows, I support these claims scientifically, mostly by reference to peer-reviewed journal articles. In 2019, World Health Organization (WHO) scientists reviewed the

evidence for the utility of all non-pharmaceutical interventions, concluding that they are all without effect.

Given the foregoing, it is no longer possible to view the last two years as well-
intentioned errors. Instead, the objectives of the perpetrators are most likely to be totalitarian control over the population by means of mandatory digital IDs and cashless central bank digital currencies (CBDCs).

There is no medical or public health emergency. We can and should take back our freedoms with immediate effect. Testing healthy people stops. If you're sick, please stay

home. Masks belong in the trash. The Covid- 19 gene-based injections are not recommended and must not be coerced or mandated. Crucially, the vaccine passports database must be destroyed. Economic rectitude is recommended.

Serious crimes have obviously been committed. It is not the purpose of this document
to accuse anyone or to assemble the evidence against them at this time. However, when this is all resolved, We The People are strongly recommended to pay much more attention to Washington than previously.

TABLE OF CONTENTS

The Covid Lies pages 2-15

How Much of the Covid-19 Narrative Was True?

Additional Reflections pages 19-28

About Dr. Mike Yeadon page 29


THE NARRATIVE POINT

SARS-CoV-2 has such a high lethality that every measure must be taken to save lives.

Note: Covid-19 is the disease resulting from infection with the virus, SARS-CoV-2. They are often used interchangeably. Sometimes it doesn't much matter, but the confusion was sowed deliberately.

IMPORTANCE

Essential to claim high lethality in order that unprecedented responses may seem justified. To "pep up" the claim, recall "falling man" in Wuhan? The person was

allegedly sick but walking about, before falling dead on his face. That was never real. It was theatre.

THE REALITY

Early estimates of lethality were very high with, in some reports, an "infection fatality rate" (IFR) of 3%. Seasonal influenza is generally considered to have a typical IFR of 0.1%. That means some seasons, IFR for flu may be 0.3% and other times, 0.05% or lower.

In practise, and this was usual, estimates of IFR for Covid-19 were revised downwards repeatedly and now are generally recognised as in the range of 0.1-0.3%. It cannot now

be argued that it is significantly different from some seasonal influenza epidemics. Why, then, have we all but destroyed the modern world over it?

CONCLUSION AND VERDICT FALSE

The perpetrators knew that lethality estimates of new respiratory viral illnesses
ALWAYS start high and reduce. This is because, early on, we do not have any estimate of the number of people infected but not seriously ill and the number infected with no symptoms at all.

They created the impression of extreme danger, which was never true. This is such a crucial point, for once one sees it for what it is, the rest of the narrative is superfluous.

Dr. John Ioannidis is one of the world's most-published epidemiologists and he has been scathing about the inappropriate responses to a novel virus of not particularly unusual lethality. Like most respiratory viruses, SARS-CoV-2 represents no serious health threat to those under 60 years of age, certainly not children, and is a serious threat only to those nearing the end of their lives by virtue of age and multiple comorbidities.1

Dr. Ioannidis's current estimate of global IFR is around 0.15%. For reference, a typical seasonal influenza outbreak has a typical IFR of around 0.1%, but can be markedly worse in bad winters.2

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THE NARRATIVE POINT

Because this is a new virus, there will be no prior immunity in the population.

IMPORTANCE

Seems reasonable, doesn't it? This remark, made repeatedly early on, aimed to squash any notion that there was a degree of"prior immunity" in the population. Prior immunity and natural immunity are only now, two years in, not considered "misinformation".

THE REALITY

Within a few months, multiple publications showed that a large minority (ranging from 30%-50%, some later said even more) of the population had T-cells in their blood which recognised various pieces of the viral protein (synthesised, as no one seemed to have any real virus isolates to use).

While some people argued that recognition by T-cells didn't mean functional immunity, really it does.

We were prevented from learning that we already knew of six coronaviruses, four of which cause "common colds" which in elderly and infirm people can cause death.

CONCLUSION AND VERDICT FALSE

This was a straight lie. It's pretty much never true that there's no prior immunity in a population. This is because viruses are each derived from earlier viruses and some of the population had already defeated its antecedents, giving them either immunity or a big head start in defeating the new virus. Either way, a sizeable proportion of the population never had cause to worry.

This article includes all the important peer-reviewed articles to mid-2020, with many showing at least 30%-50% having prior immunity (it depends upon the measure used to assess it).3

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THE NARRATIVE POINT

This virus does not discriminate. No one is safe until everyone is safe.

IMPORTANCE

Intention was to minimise the numbers who might reason they're not "at risk" people.

THE REALITY

This claim was always absurd. The lethality of this virus, as is common with respiratory viruses, is IO00X less in young, healthy people than in elderly people with multiple comorbidities.

CONCLUSION AND VERDICT FALSE

In short, almost no one who wasn't close to the end of their lives was at risk of severe outcomes and death. In middle-aged individuals, obesity is a risk factor, as it is for a handful of other causes of death.

This intriguing review details how the initial modelling induced fear and provided the excuse for heavy-handed measures, especially "lockdowns".4 It was, however, )ust that: an excuse. All experienced public health experts knew that lockdowns were absurd, ineffective, and hugely destructive. There's no way to sugar-coat this. It was wrong before it was ordered, and it's necessary to examine why those who knew did not protest. It's almost as if they were complicit.

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THE NARRATIVE POINT

People can carry this virus with no signs and infect others: asymptomatic transmission.

IMPORTANCE

This is the central conceptual deceit. If true, then anyone might infect and kill you. Falsely claimed asymptomatic transmission underscores almost every intrusion: masking, mass testing, lockdowns, border restrictions, school closures, even vaccine passports.

THE REALITY

The best evidence comes from a meta-analysis of a larger number of good studies, examining how often a person testing positive went on to infect a family member (they compared as potential sources of infection people who had symptoms with those who did not have symptoms). ONLY those WITH symptoms were able to infect a family member at any rate that mattered.5

CONCLUSION AND VERDICT FALSE

Asymptomatic transmission is epidemiologically irrelevant. It's not necessary to argue it never happens; it's enough to show that if it occurs at all, it is so rare as not to be worth measuring.

In this video, we also have Fauci and a WHO doctor telling us exactly this.6 Also, I show why it is like it is. It's very clear.

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THE NARRATIVE POINT

The PCR test selectively identifies people with clinical infections.

IMPORTANCE
This is the central operational deceit. If true, we could detect risky people and isolate them. We could diagnose accurately and also count the number of deaths.

Polymerase chain reaction (PCR), at its best, can confirm the presence of genetic information in a clean sample and is useful in forensics for that reason. It involves cycle after cycle of amplification, copying the starting material at the beginning of each cycle. The inventor of the PCR test, Kary Mullis, won a Nobel Prize for it and often criticised Fauci for misusing that test to diagnose AIDS patients, which Mullis insisted was inappropriate.

THE REALITY

In a "dirty" clinical sample, there is more than a possible piece of, or a whole, virus which might replicate. There are bacteria, fungi, other viruses, human cells, mucus, and more. It's not possible unequivocally to know, if a test is judged "positive" after many cycles, what it was that was amplified to give the signal at the end that we call "positive".

In mass testing mode, commonly used, no one ever runs so-called "positive controls" through the chain of custody. That's diagnostic testing 101. It's a deception.

Every test has an "operational false positive rate" (oFPR), where some unknown percent of samples turns positive, even if there is no virus present. A good oFPR would be less than 1%, but is it 0.8% or 0.1%? If you test 100,000 samples daily, and the oFPR is 0.8%, you will get 800 positive tests or "cases" even if there is no virus in the entire community. Often, the "positivity" the fraction of tests that are positive, is in that range, sub-1% or low-single-digit percent. I believe much or all of that can be caused by false positives. Note, criminals can manipulate the content of the test kits because there are very few providers in a territory, often just one. The conditions for running the test are also subject to variation by the authorities, like the CDC.

CONCLUSION AND VERDICT FALSE

You can be genuinely positive, yet not ill. There is no lower limit of true detection below which you'd be declared to have some copies of the virus, but declared clinically well. It's an absurd idea.

You can have no virus yet test positive (with or without symptoms). All of these are swept together and called "confirmed Covid-19 cases". If you die in the next 28 days,

you're said to be a "Covid death" no matter what the cause.

Those using the test kits provided commercially are what are called "black box". They are unable to say what is in the kit, because this is proprietary. The original "methods paper" was published in 48 hours, making a mockery of claimed peer review, by a

Page6of31

Berlin lab headed by Professor Christian Drosten, scientific advisor to Angela Merkel of Germany. The paper was comprehensively rebutted by an international team.7

The WHO released a series of guidance notes on PCR,8 and it was clear that their technical staff did not approve of mass testing the population, because it's possible to return wholly false positives. Indeed, at times of low genuine prevalence, that's all they can be.

I often wonder if this 2007 real-life example of a PCR-based testing system which returned 100% false positives, yet convinced a major hospital that they had a huge disease outbreak for weeks, might have been the inspiration for the untrustworthy methods used in the Covid-19 deception?9

Drosten also led the TV publicity around the idea of asymptomatic transmission. One lucky scientist is at the centre of the two most important deceptions in the entire Covid- 19 event!

Professor Norman Fenton here presents a multi-part lecture with two main elements.I° First, he describes how mass testing of people with no symptoms unavoidably drives up the proportion of positive PCR test results that are false. The second part deals with the possibility that data fraud entirely accounts for the apparent efficacy of the vaccines, while attempting to hide vaccine deaths, by classifying them as unvaccinated for 14 days after injection.

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THE NARRATIVE POINT
Masks are effective in preventing the spread of this virus.

IMPORTANCE

This is mostly used to maintain the illusion of danger. You see others' masks and feel afraid. Complying is also a measure of whether you do what you're told, even if the measure is useless.

THE REALITY

We have known for decades that surgical masks worn in medical theatres do not stop respiratory virus transmission. Masks were tested across a series of operations by doctors at the Royal College of Surgeons (UK). No difference in post-operative infection rate was seen by mask use.

Cloth masks definitely don't stop respiratory virus transmission as shown by several large, randomised trials. If anything, they increase risk of lung infections. The

authorities have mostly conceded on cloth masks.

Some people speak of "source control" catching droplets. Problem is, there is no evidence that transmission takes place via droplets. Equally, there is no evidence it occurs via fine aerosols. No one finds it on masks, or on air filters in hospital wards of Covid patients, either. Where is the virus?

CONCLUSION AND VERDICT FALSE

It's not necessary to use up time on this topic. It was known long before Covid-19 that face masks don't do anything.

Many don't know that blue medical masks aren't filters. Your inspired and expired air moves in and out between the mask and your face. They are splashguards, that's all.

This is a good review of the findings with masks in respiratory viruses by a recognised expert in the field. No effect.11

Neither masks nor lockdowns prevented the spread of the virus. This review summarizes 400 papers. 12

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THE NARRATIVE POINT

Lockdowns slow down the spread and reduce the number of cases and deaths.

IMPORTANCE

The most impactful yet wasteful intervention, accomplishing nothing useful.

Useful to the perpetrators, however, wishing to damage the economy and reduce interpersonal contacts. This measure was surprisingly tolerated in many wealthy countries, because "furlough" schemes were put in place, compensating many people for not working, or requiring them to work from home.

THE REALITY

The measure, though among the most repressive acts ever imposed on citizens in a democracy, was intuitively reasonable to many. This is an example of how far off-course uninformed intuition can be.

The core idea was simple. Respiratory viruses are transmitted from person to person. Reducing the average number of contacts surely reduces transmission? Actually, it doesn't, because the transmission concept is wrong. Transmission is from a SYMPTOMATIC person to a susceptible person. Those with symptoms are UNWELL. They remain at home in most cases with no action from the government. Transmission occurred mostly in institutions where sick people and susceptible people were forced into contact: hospitals, care homes, and domestic settings.

CONCLUSION AND VERDICT FALSE

A general lockdown had no detectable impact on epidemic spreading, cases, hospitalisations, or deaths.

This is now widely accepted, after a meta-analysis by Johns Hopkins University (interestingly, as the JHU repeatedly features as an actor in a documentary about pandemic-related fraud by German journalist Paul Schreyer).13

This is because those involved in the vast bulk of human-to-human contacts are fit and well and such contacts didn't result in transmission. Essentially, if you're fooled by the "asymptomatic transmission" lie, then lockdown might make sense. However, since it is epidemiologically irrelevant, lockdowns can never work, and of course, all the voluminous literature confirms this.

This concept is unequivocally known to multiple public health scientists and doctors. This is why "lockdown" had never been tried before.

Importantly, WHO scientists drafted a detailed review of all the non-pharmaceutical interventions (NPIs) in 2019 and distributed copies of the report to all member states.14

This means that ALL member states already knew, late in 2019, that masks, lockdowns, border restrictions, and business or school closures were futile. Only "stay home if you're sick" works at all, and people don't need to be told this, for they are too unwell to go out.

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THE NARRATIVE POINT

There are unfortunately no treatments for Covid beyond support in hospital.

IMPORTANCE

Reinforced the idea that it was vital to avoid catching the virus.

Legally, it was essential for the perpetrators bringing forward novel vaccines that there be no viable treatments. Had there been even one, the regulatory route of Emergency

Use Authorisation would not have been available.

THE REALITY

In my opinion, while all these measures were destructive and cruel, active deprivation
of access to experimentally applied but otherwise known safe and effective early treatments led directly to millions of avoidable deaths worldwide. In my mind, this is a policy of mass murder.

Contrasting with the official narrative, the therapeutic value of early treatment was already understood and demonstrated empirically during spring 2020. Since then, a sizeable handful of well-understood, off-patent, low-cost and safe oral treatments have been characterised.

CONCLUSION AND VERDICT FALSE

The official position was that the disease Covid-19 could not be treated and the patient only "supported" often by mechanical ventilation. Ventilation is wholly inappropriate

because Covid-19 is rarely an obstructive airway disease, yet has a high associated morbidity and mortality. An oxygen mask is greatly preferred.

In my view, due to the very large amount of empirical treatment and good communication, Covid-19 is the most treatable respiratory viral illness ever. We knew in the first three months of 2020 that hydroxychloroquine, zinc, and azithromycin were empirically useful, provided treatment was started early and tackled rationally.15

It's very important to note that it has been known for a decade and more that elevating intracellular zinc acts to suppress viral replication.16

There is no question that senior advisors to a range of governments knew that so-called "zinc ionophores" compounds which open channels to allow certain dissolved minerals to cross cell membranes, were useful in severe acute respiratory syndrome (SARS) in 2003 and should be expected also to be therapeutically useful in SARS-CoV-2 infection.

This is a starting point for all of the clinical trials in Covid-19,17 including especially ivermectin and hydroxychloroquine (which are zinc ionophores).Is

It should be noted that using known safe agents for experimental purposes as a priority has always been an established ethical medical practice and is known as "off-label prescribing".

Page 10 of 31


THE NARRATIVE POINT
It's not certain if you can get the virus more than once.

IMPORTANCE

The idea of natural immunity was flatly denied and the absurd idea that you might get the same virus twice was established. This ramped up the fear, which might otherwise have passed swiftly.

THE REALITY

Those with even a basic grasp of mammalian immunology knew that senior advisors to government, speaking in uncertain terms on this question, were lying. Certainly, in the author's case, it was a pivotal point. I shared a foundational education in UK
universities at the same time as the UK government's Chief Scientific Advisor. This

shared education meant we'd have had the same set texts. I reasoned that he knew what I knew and vice versa. I was as sure as it is possible to be that it wouldn't be possible to get clinically unwell twice in response to the same virus, or close-in variants of it. I was right. He was lying.

CONCLUSION AND VERDICT FALSE

There have been scores of peer-reviewed )ournal articles on this topic.19 Very few clinically important reinfections have ever been confirmed.

Beating off a respiratory virus infection leaves almost everyone with acquired immunity, which is complete, powerful, and durable.

You wouldn't know it for the misdirection around antibodies in blood, but such antibodies are not considered pivotally important in host immunity. Secreted antibodies in airway surface liquid of the IgA isotype certainly are, but most important are memory T-cells.2°

Those infected with SARS in 2003 still had dear evidence of robust, T-cell mediated immunity 17 years later.21

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THE NARRATIVE POINT

Variants of the virus appear and are of great concern.

IMPORTANCE

I believe the purpose of this fiction was to extend the apparent duration of the pandemic--and the fear--for as long as the perpetrators wished it. While there is

controversy on this point, with some physicians believing reinfection by variants to be a serious problem, I think untrustworthy testing and other viruses entirely is the parsimonious explanation.

THE REALITY

I come at it as an immunologist. From that vantage point, there is very strong precedent indicating that recovery after infection affords immunity extending beyond the sequence of the variant that infected the patient to all variants of SARS-CoV-2.

The number of confirmed reinfections is so small that they are not an issue, epidemiologically speaking.

We have good evidence from those infected by SARS in 2003: they not only have strong T-cell immunity to SARS, but cross-immunity to SARS-CoV-2. This is very important because SARS-CoV-2 is arguably a variant of SARS, there being around a 20% difference at the sequence level.

Consider this: if our immune systems are able to recognise SARS-CoV-2 as foreign and mount an immune response to it, despite never having seen it before, because of prior immunity conferred by infection years ago by a virus which is 20% different, it's logical that variants of SARS-CoV-2, like delta and omicron, will not evade our immunity.

No variant of SARS-CoV-2 differs from the original Wuhan sequence by more than 3%, and probably less.

CONCLUSION AND VERDICT FALSE

Normal rules of immunology apply here)2 Despite the publicity to the contrary, SARS- CoV-2 mutates relatively slowly and no variant is even close to evading immunity acquired by natural infection.

This is because the human immune system recognises 20-30 different structural motifs in the virus, yet requires only a handful to recall an effective immune memory)3

The variants story fails to note "Muller's Ratchet" the phenomenon in which variants of a virus, formed in an infected person during viral replication (in which "typographical errors" are made and not corrected) trend to greater transmissibility but lesser lethality.
If this was not the case, at some point in human evolution, we would have expected a respiratory viral pandemic to have killed off a substantial proportion of humanity. There is no historical record for such an event.

I do not rule out the possibility that the so-called vaccines are so badly designed that they prevent the establishment of immune memory. If that is true, then the vaccines are worse than failures, and it might be possible to be repeatedly infected. This would be a form of acquired immune deficiency.

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THE NARRATIVE POINT
The only way to end the pandemic is universal vaccination.

IMPORTANCE

This, I believe, was always the ob)ective of the largely faked pandemic. It's NEVER been the way prior pandemics have ended, and there was nothing about this one that should have led us to adopt the extreme risks that were taken and which have resulted in hundreds of thousands, probably millions, of wholly avoidable deaths.

THE REALITY

The interventions imposed on the population didn't prevent spread of the virus. Only individual isolation for an open-ended period could do that, and that's clearly impossible (hospital patients and residents of care homes have to be cared for at very least and additionally, the nation has to be supplied with food and medicines).

All the interventions were useless and hugely burdensome.

Yet we have reached the end of the pandemic, more or less. We would have done so faster and with less suffering and death had we adopted measures along the lines

proposed in the Great Barrington Declaration and used pharmaceutical treatments as they were discovered, plus general improvements to public health, such as encouraging vitamin supplements.

CONCLUSION AND VERDICT FALSE

It was NEVER appropriate to attempt to "end the pandemic" with a novel technology vaccine. In a public health mass intervention, safety is the top priority, more so even

than effectiveness, because so many people will receive it.

It's simply not possible to obtain data demonstrating adequate longitudinal safety in the time period any pandemic can last.

Those who pushed this line of argument and enabled the gene-based agents to be injected needlessly into billions of innocent people are guilty of crimes against

humanity.

It quickly became apparent that natural immunity was stronger than any protection from vaccination,24 and most people were not at risk of severe outcomes if infected.25

Even children who were immunocompromised are not at elevated risk from Covid-19, so advice that such children should be vaccinated is lethally flawed36

These agents are clearly underperforming against expectationsY

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THE NARRATIVE POINT

The new vaccines are safe and effective.

IMPORTANCE

I feel particularly strongly about this claim. Both components are lies. I outline the inevitability of the toxicity of all four gene-based agents below.

Separately, the clinical trials were wholly inadequate. They were conducted in people
not most in need of protection from safe and effective vaccines. They were far too short in duration. The endpoints only captured "infection" as measured by an inadequate
PCR test and should have been augmented by Sanger sequencing to confirm real infection. Trials were underpowered to detect important endpoints like hospitalisation and death.

There's evidence of fraud in at least one of the pivotal clinical trials. I think there is also clear evidence of manufacturing fraud and regulatory collusion. They should never have been granted emergency use authorisations (EUAs).

THE REALITY

The design of the agents called vaccines is very bothersome. Gene-based agents are new in a public health application. Had I been in a regulatory role, I would have informed all the leading R&D companies that I would not approve these without extensive longitudinal studies, meaning they could not receive EUA before early 2022 at the earliest. I would have outright denied their use in children, in pregnancy, and in the infected-recovered. Point blank, rd need years of safe use before contemplating an alteration of this stance.

The basic rules of this new activity, gene-based component vaccines, are: (1) to select part of the virus that has no inherent biological action--that rules out spike protein, which we inferred would be very toxic, before theylt even started clinical trials;2s (2) select the genetically most stable parts of the virus, so we could ignore the gross misrepresentations of variants so slight in difference from the original that we were
being toyed with via propaganda--again, this rules out spike protein; (3) choose parts of the virus which are most different from any human proteins. Once more, spike protein is immediately deselected, otherwise unnecessary risks of autoimmunity are carried forward.

That all four leading actors chose spike protein, against any reasonable selection criteria, leads me to suspect both collusion and malign intent.

Finally, let nature guide us. Against which components of the virus does natural immunity aim? We find 90% of the immune repertoire targets NON-spike protein responses.29 1 rest my case.

CONCLUSION AND VERDICT FALSE

These agents were always going to be toxic. The only question was, to what degree? Having selected spike protein to be expressed, a protein which causes blood clotting to

be initiated, a risk of thromboembolic adverse events was burned into the design. Page 14 of 31

Nothing at all limits the amount of spike protein to be made in response to a given dose. Some individuals make a little and only briefly. The other end of a normal range results in synthesis of copious amounts of spike protein for a prolonged period. The locations in which this pathological event occurred, as well as where on the spectrum, in my view played a pivotal role in whether the victim experienced adverse events, including death.

There are many other pathologies flowing from the design of these agents, including,
for the mRNA "vaccines" that lipid nanoparticle (LNP) formulations leave the injection site and home to the liver and ovaries,3° among other organs,31 but this evidence is enough to get started.

See this interview for evidence of clinical trial and other fraud, publicised by Edward Dowd, a former BlackRock investment analyst.32

See this video for evidence of official data fraud (UK Office of National Statistics): especially at 2min 45sec for the heart of the matter.33

See here for evidence of manufacturing fraud.34 The same methodology was used to obtain regulatory authorisations, and so it is my contention that there is also regulatory fraud.

In the Pfizer clinical trial briefing document to FDA, which was used for issuing the EUA (on p. 40 or thereabout), there is a paragraph stating that there were approximately 2,000 "suspected unconfirmed Covid cases"--meaning people were sick with symptoms but were not tested (otherwise, it would be stated that the tests were negative). Of these, in the first seven days after injection, there were 400 in the vaccine arm and 200 in placebo. These subjects were excluded from the dataset used to assess efficacy. It's as clear evidence of fraud as you can get; they admit to it in the FDA briefing! Nobody paid any attention to this that I am aware of.

There's also evidence of data fraud in that clinical trial as summarised by Dr. Peter Doshi, associate editor of The BMJ (formerly called the British Medical Journal).

Though many people refuse to accept or even look at the evidence, it is clear that the number of adverse events and deaths soon after Covid-19 vaccination is astonishing and far in excess, in 2021 alone, than all adverse effects and deaths reported to the U.S. Vaccine Adverse Event Reporting System (VAERS) in the previous 30 years. Here is a simplified view of Covid vaccine-related mortality reports from VAERS.3s

This excellent presentation by a forensic statistician, well used to presenting analyses for court purposes, dismantles the claims that the vaccines are effective and shows how toxicity is hidden (see the second half of the recording).1° Another paper published by the same group questions vaccine efficacy.36

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References

1. Ioannidis JPA, Axfors C, Contopoulos-Ioannidis DG. Population-level COVID-19 mortality risk for non-elderly individuals overall and for non-elderly individuals

without underlying diseases in pandemic epicenters. Environ Res. 2020 Sep; 188:109890.

2. Ioannidis JPA. Reconciling estimates of global spread and infection fatality rates of COVID- 19: an overview of systematic evaluations. Eur ] Clin Invest. 2021 May;51(5):e13554.

3. Doshi P. Covid-19: Do many people have pre-existing immunity? BM]. 2020;370:m3563.

4. Joffe AR. COVID- 19: Rethinking the lockdown groupthink. Front Public Health. 2021 Feb 26;9:625778.

5. Madewell ZJ, Yang Y, Longini Jr IM, Halloran ME, Dean NE. Household transmission of SARS-Cov-2: a systematic review and meta-analysis. ]AMA Netw Open. 2020 Dec

1;3(12):e2031756.

6. "Exposing the lie ofasymptomatic transmission, once and for all:' May 10, 2021. https://www.bitchute.com/video/llj22KttYq7z/

7. https://cormandrostenreview.com/

8. World Health Organization. Diagnostic testing for SARS-CoV-2. Interim guidance, Sep. 11, 2020. https://apps.who.int/iris/bitstream/handle/lO665/334254/WHO-2019- nCoV-laboratory-2020.6-eng.pdf?sequence= 1 &isAllowed=y

9. Kolata G. Faith in quick test leads to epidemic that wasn't. New York Times, Jan. 22, 2007. Available at https://eumeswill.wordpress.com/2020/08/11/faith-in-quick-test-leads-to-epidemic-that-wasnt/

10. "Prof. Norman Fenton - Open science sessions: How flawed data has driven the narrative" PANDA, Feb. 3, 2022. https://rumble'c°m/vtxilh-°pen-science-sessi°ns how_flawed_data_has_driven_the_narrative.html

11. Jefferson T, Del Mar CB, Dooley L, et al. Physical interventions to interrupt or reduce the spread of respiratory viruses. Cochrane Database Syst Rev. 2020 Nov 20;11(11):CD006207.

12. Alexander PE. More than 400 studies on the failure of compulsory Covid interventions (lockdowns, restrictions, closures). Brownstone Institute, Nov. 30, 2021. https:// brownstone.org/articles/more-than-400-studies-on-the-failure-of-compulsory- covid-interventions/

13. Dinerstein C. The Johns Hopkins lockdown analysis. American Council on Science and Health, Feb. 16, 2022. https://www.acsh.org/news/2022/O2/16/johns-hopkins- lockdown-analysis- 16135

14. World Health Organization. Non-pharmaceutical public health measures for mitigating the risk and impact of epidemic and pandemic influenza: annex: report of systematic

15. McCullough PA, Kelly RJ, Ruocco G, et al. Pathophysiological basis and rationale for early outpatient treatment of SARS-CoV-2 (COVID-19) infection. Am 1 Meal. 2021 Jan;134(1):16-22.

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16. Te Velthuis AJW, van den Worm SHE, Sims AC, Baric RS, Snijder EJ, van Hemert MJ. Zn(2+) inhibits coronavirus and arterivirus RNA polymerase activity in vitro and zinc ionophores block the replication of these viruses in cell culture. PIoS Pathog. 2010 Nov 4;6(11):e1001176.

17. COVID-19 early treatment: real-time analysis of 1,609 studies. Retrieved Apr. 4, 2022 from https://c19early.com/.

18. Bryant A, Lawrie TA, Dowswell T, et al. Ivermectin for prevention and treatment of COVID-19 infection: a systematic review, meta-analysis, and trial sequential analysis to inform clinical guidelines. Am J Ther. 2021 Jun 21;28(4):e434-e460.

19. Alexander PE. How likely is reinfection following Covid recovery? Brownstone Institute, Dec. 29, 2021. https://brownstone.org/articles/how-likely.-is-reinfection- following - covid-recovery_/

20. Wyllie D, Mulchandani R, Jones HE, et al. SARS-CoV-2 responsive T cell numbers are associated with protection from COVID-19: a prospective cohort study in keyworkers. MedRxiv, Nov. 4, 2020.

21. Le Bert N, Tan AT, Kunasegaran K, et al. SARS-CoV-2-specific T cell immunity in cases of COVID-19 and SARS, and uninfected controls. Nature. 2020 Aug;584(7821):457-462.

22. Tarke A, Sidney J, Methot N, et al. Negligible impact of SARS-CoV-2 variants on CD4+ and CD8+ T cell reactivity in COVID-19 exposed donors and vaccinees. BioRxiv, Mar. 1,2021.

23. Tarke A, Sidney J, Kidd CK, et al. Comprehensive analysis ofT cell immunodominance and immunoprevalence of SARS-CoV-2 epitopes in COVID-19 cases. BioRxiv, Dec. 9, 2020.

24. Gazit S, Shlezinger R, Perez G, et al. Comparing SARS-CoV-2 natural immunity to vaccine-induced immunity: reinfections versus breakthrough infections. MedRxiv, Aug. 25, 2021.

25. Alexander PE. 150 plus research studies affirm naturally acquired immunity to Covid-19: documented, linked, and quoted. Brownstone Institute, Oct. 17, 2021. https://brownstone.org/articles/79-research-studies-affirm-naturally-acquired- immunity-to-covid- 19-documented-linked-and-quoted/

26. Chappell H, Patel R, Driessens C, et al. Immunocompromised children and young people are at no increased risk of severe COVID-19. J Infect. 2022 Jan;84(1):31-39.

27. Alexander PE. 46 efficacy studies that rebuke vaccine mandates. Brownstone Institute, Oct. 28, 2021. https://brownstone.org/artides/16-studies-on-vaccine-efficacy/

28. Grobbelaar LM, Venter C, Vlok M, et al. SARS-CoV-2 spike protein $1 induces fibrin(ogen) resistant to fibrinolysis: implications for microclot formation in COVID- 19. MedRxiv, Mar. 8, 2021.

29. Ferretti AP, Kula T, Wang Y, et al. Unbiased screens show CD8+ T cells of COVID-19 patients recognize shared epitopes in SARS-CoV-2 that largely reside outside the spike protein. Immunity. 2020 Nov 17;53(5): 1095-1107.

30. Schidlich A, Hoffmann S, Mueller T, et al. Accumulation of nanocarriers in the ovary: a neglected toxicity risk? J Control Release. 2012 May 30;160(1): 105-112.

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31. https://www.docdroid.net/xq0Z8B0/pfizer-report-japanese-government- pdf#page=14

32. "Edward Dowd interview portion on Steve Bannons War Room Ep #1602" https:/www.onenewspage.com/video/20220204114277521/Edward-Dowd-Interview- portion-on-Steve-Bannons-War.htm

33. "Norman Fenton interviewed by Majid Nawaz, LBC Radio 4 Dec 2021" Truth Archive 2030, Feb. 21, 2022. https://www.bitchute.com/video/KApFxhjiWLqI/

34. "COVID vax variability between lots - independent research by international team" Craig-Paardekooper, Dec. 15, 2021. https://www.bitchute.com/video/4HlIyBmOEJeY/

35. ht__tp.s://....__openvaers.com/covid- data/mort ality.

36. Neil M, Fenton NE, Smalley J, et al. Latest statistics on England mortality data suggest systematic mis-categorisation of vaccine status and uncertain effectiveness of Covid-19 vaccination. ResearchGate, December 2021. DOI:10.13140!RG.2.2.14176.20483


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How Much of the Covid-19 Narrative Was True? Additional Reflections

Introduction

The purpose of this document is to demonstrate that all of the key narrative points about the SARS-CoV-2 virus said to cause the disease Covid-19 and the measures

imposed to control it are incorrect. Given that the sources of these points are scientists, doctors, and public health officials, it is evident that they were not simply mistaken. Instead, they have lied in order to mislead. I believe the motivations of those who I call "the perpetrators" become clear, once it is internalised that the entire event is based on lies.

In recent days, breaking news indicates that coronavirus antibodies are present in blood stored in European blood banks from 2019.1 The implications are momentous.

Unprecedented Pronouncements

In the first three months of the Covid event, I started noticing senior scientific and medical advisors on UK television saying things that I found disturbing. It was hard to

put my finger on the specifics, but they included remarks like:
"Because this is a new virus, there won't be any immunity in the population". "Everyone is vulnerable".

"In view of the very high lethality of the virus, we are exploring how best to protect the population".

I had been reading extensively about the apparent spread of SARS-CoV-2 in China and beyond, and had already arrived at a number of important conclusions. Essentially, I
was sure that, objectively, we weren't going to experience a major event. I based some of my conclusions on the Diamond Princess cruise ship experience. Note that no crew members died, and only a minority on the ship even got infected, suggesting substantial prior immunity, a steep age-lethality relationship, and an infection fatality ratio (IFR) not much different, if at all, from prior respiratory virus infections. But what was happening was that, in my view, senior people were acting a lot more frightened than seemed appropriate.

It was with this heightened interest that I began to closely examine all aspects of the alleged pandemic. I suspected something very bad was happening when the Imperial College released its modelling paper by Neff Ferguson. This claimed that over 500,000 people in the UK would die unless severe "measures" were put in place. Ferguson had over-projected all of the last five disease-related emergencies in the UK and had been responsible for the destruction of the beef herd through his modelling of the spread of foot-and-mouth disease.

I had also been reading about all sorts of"non-pharmaceutical interventions" (NPIs), and what this had taught me was that there was absolutely no experimental literature around any of the NPIs being spoken of, except masks--which were clearly ineffective in blocking respiratory virus transmission. Moreover, the non-experts in the

Page 19 of 31

mainstream media drew on a very limited group of experts, and I noticed that none were immunologists.

I had, in parallel, watched the evolving scene in Sweden and was pleased to note that the Swedes' chief epidemiologist, Anders Tegnell, seemed to know what he was doing and had dismissed the panic. I knew he had been the deputy of his predecessor, ]ohan Gieseke, who was still around in an emeritus role. Gieseke was also reassuringly calm.

The final straw was when on March 23, 2020, the British prime minister initiated the first "lockdown". This was wholly without precedent. I knew Sweden had rejected

lockdown measures as wholly unnecessary and extremely damaging.

Instigating Fear

From that day forward, the team from the UK Scientific Advisory Group for Emergencies (SAGE) put up one or more members every day to appear alongside the

prime minister or the health minister. These press conferences were meandering affairs, and it wasn't clear what their purpose was. The questions asked never sought to place things in context, but instead seemed to always explore the outer edges of possible outcomes and then follow up with remarks that didn't seem adequately prepared.

In retrospect, I think the aim was to make the press conferences the only "must watch" thing on TV, and with such a large, captive audience, a form of fear-based hypnosis was instigated. Much later, Belgian professor and clinical psychologist Mattias Desmet informed us that this was indeed the aim, calling the process "mass formation".2 This process can become malignant, as have past beliefs in events that were later conceded to have been episodes of societal madness, like the Salem witch trials, satanic abuse of children, and other delusions.

Some experts believe that modern societies are more--and not less--susceptible to mass panics because of the ubiquity of easily-controlled messaging (properly termed "propaganda" since it was completely deliberate and carefully planned). An August
2021 animated video titled "Mass Psychosis - How an Entire Population Becomes Mentally Ill" illustrates this phenomenon; despite the animation format, the film leans heavily on academic research from luminaries such as Gustave Le Bon, Sigmund Freud, Edward Bernays, Stanley Milgram, and Solomon Asch, as well as later researchers and studies.3

It is important to be cautious about the purported importance of "mass formation" however. In a sense, it might be seen as wholly impersonal and something that is thrown at the population and lands more or less effectively on people at random. Worse, it comes with the notion that, if you are susceptible, it cannot be resisted. There is a contrasting school of thought that holds that information technology (IT), data, and artificial intelligence (AI) are capable of assembling a "digital prison" that is tailored to each individual and shaped over time by choices that we each make.4 The outcome isn't in any way preordained. However, incentives and deterrents are associated with innumerable decisions we make, such as how to pay for something, whether we sell our data for tiny rewards, whether we consciously decide to open links suggested for us, whether we leave location services running permanently, and more.5

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Using Mass Testing to Promote Fear

As soon as the UK lockdown was initiated, the focus turned full force onto mass testing, and especially on testing people without symptoms. I knew this didn't make any sense, because if a large enough number of people are tested daily, without knowledge of the

false-positive rate, it could certainly very quickly panic people into thinking there were lots of people walking around with the virus, unaware they had it and allegedly spreading it to others.

Once the lockdown was in place, in addition to testing, the press conferences focused
on numbers in hospital, numbers on ventilators, and ultimately, the daffy deaths "with Covid". Early treatments and improved lifestyle were never spoken of. The first lockdown lasted 12 weeks, with most office staff told to work from home while being paid "furlough" (a word never before used in Britain). The "fear porn" continued all the way into high summer, long after daily Covid deaths had reached approximately zero.

The introduction of mandatory masking in all public areas in the heat of summer, when they had never been required before, was the last straw for me. It was all theatre.

At that point, I set out to investigate a couple of core concepts: the "PCR test" and "asymptomatic transmission". I'm embarrassed to say, however, that it wasn't until the autumn of 2020 that I had clear in my mind, with mounting horror, that the entire event, if not completely manufactured, was being grossly exaggerated, with the intent of deceiving the entire "liberal democratic West". Scores of countries were economically being squeezed to death. I knew that from a financial perspective, borrowing or printing enough money to subsidize tens of millions to remain at home could not be long sustained without destroying the sovereign currency. Strangely, exchange rates didn't move much--another clue that powerful forces were managing this event as well as its consequences. Around this time, country leaders started talking about "Build Back Better" and Klaus Schwab's book, COVID-19: The Great Reset, appeared.

All of this contributed to my developing the idea of"The Covid lies". It seemed to me that everything we had been told about the virus wasn't true, and also that all the NPIs imposed upon us couldn't work, and so were for nothing more than show.

One Dominant Narrative

As already mentioned, repetition and fear were key to instigating "mass formation" as described by Mattias Desmet.2 This narrowing of focus, according to Desmet, means those "in the mass" (crowd) literally are incapable of hearing anything that challenges
the narrative of which they've been convinced. Any explanation other than the truth is marshalled to dismiss rational counter-arguments. And indeed we saw that anyone challenging the dominant narrative was attacked, smeared, censored, and cancelled on social media, and no reasonable and independent voices were ever seen or heard on TV or radio.

Desmet argues that mass formation, to be successful, requires that certain conditions be in place: high levels of free-floating anxiety; a strong degree of social isolation (where devices replace real human interactions); and finally, low levels of "sense-making" that is, many things do not make sense to many people. When a crisis is dropped into a population where these conditions obtain and is repeated ad nauseam, it is possible in effect to hypnotise them.

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When the narrative has taken hold, what happens next?
Now, the population's anxiety has an obvious focus, which is felt as a relief.

The routines--masking, lockdowns, testing, hand sanitizing--become for some a ritual, which provides daily meaning.

Finally, so many people are acting the same way and echoing the same lines (the lines they've heard time and again on TV, radio, newspapers, and their devices), that people can feel part of a national effort in a way they've not felt before.

This combination, coupled with visible and strong punishment for anyone who questions the narrative or simply refuses to comply, reinforces the groupthink.

It is, according to crowd psychology experts, nearly impossible to extract those who are this deeply "in the mass". However, there is always another group of individuals who never fall for such tricks. Outwardly pleasant and easygoing, these individuals typically are sceptical and go along with things only if they make sense to them personally, and not because an authority figure tells them to.

There is also a third group in the middle--individuals who often sense that something is wrong but lack the courage of their own convictions and tend to side with whatever they're told to do, rather passively. They are not hypnotised, but to third parties, they
can seem to be.

Crowd psychology experts encourage those who've seen through the lies (the second group) to speak out and continue to do so. This legitimises speaking out by all others not persuaded by the narrative and might even extract some from the middle group. Even those in the "mass" group will be prevented from sinking yet more deeply into the narrative, from where those orchestrating events can otherwise prompt such people to commit atrocities.

Vaccine Lies

In the second half of 2020, the conversation turned to the oncoming vaccines. Having spent 32 years in pharmaceutical research and development (R&D), I knew that what we were being told about vaccines was )ust lies. It's not possible to bypass a dozen years of careful work or to compress it into a few months. The product that was to emerge was almost certain, to my mind, to be very dangerous. And after I began reading my way into this area, I grew more concerned still.

In my "Covid Lies" comments, I isolate ONLY the ma)or narrative points themselves
and show that none of them are true. In other words, this was not )ust a little lying here and there--no, the entire construct was false. After I describe all the main lies, I show how the perpetrators were able to get away with it. At the conclusion, I believe the reader will share my view that the whole event was manufactured or exaggerated from a mild situation.

Remember, no alternative views were permitted in the "public square". In fact, in July 2019--well before the declared pandemic--a group of powerful media organisations

had already assembled and founded the Trusted News Initiative (TNI). The purpose of TNI was both to control mass media messages and crush alternative voices from any direction.6

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Again, all of the Covid narrative was lies. Not mistakes. Many of the politicians who repeated others' lines might try to offer as defence that they relied on experts to inform them. U.S. Centers for Disease Control and Prevention (CDC) director Rochelle Walensky recently did )ust that when she said that the CDC made vaccination recommendations because CNN published Pfizer's press release saying that their Covid-19 vaccine was 95% effective. (You can't make this up.) However, the true sub)ect matter experts who promoted the false narrative from the public health departments-- such as Chief Scientific Advisor Sir Patrick Vallance in the UK and National Institute of Allergy and Infectious Diseases (NIAID) director Dr. Anthony Fauci in the U.S.--knew their statements were untrue.

The Question of Motive

The question of motive has to arise. What possible motive might there have been to create this state of fear? Who must have been involved to have granted authorisation to do it?

I have tried to find benign explanations and have failed to do so. The logical conclusions I'm drawn to make for very disturbing reading. I look forward to discussing them with you and indeed with anyone. Although it's unlikely I am correct on every point, what I

am sure of is that the overall picture is one of extreme deception and a highly-organised fraud. Moreover, I am not alone in reaching this view. For example, in an essay titled "if
I were going to conquer you" one author walks us through what the perpetrators would do in order to take over the world through a simultaneous "coup d~tat" of the liberal democracies.7 Robert F. Kennedy, Jr. summarised a plausible explanation in a speech in Milan in November 2021.8

I appear to be the ONLY former executive-level scientist from big pharma anywhere in the world speaking out. I have invested two years pro bono in identifying the key elements of the fraud, in the sincere hope I can connect with upright individuals who can help bring this to wider attention and, ultimately, to a halt and to )ustice. As a result of these efforts, I can describe a global fraud operating for two years at tremendous cost in lives, the economy, and the very structure of human societies, which could only have been undertaken by powerful people, organised for a purpose that is not to the benefit of ordinary people.

Additional Observations

Though not all central, there are a large number of ancillary points that reinforce my conclusions. I have assembled some of them below. This list is not exhaustive and may

be added to.

Fraud Assessed

In a series of five short videos,9 you will find remarkable similarities in a Canadian team's interpretation of the same fraud. Note, in particular, the second film (3.5 minutes) on non-pharmaceutical interventions.1°

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Fraud Rehearsed

German investigative journalist Patti Schreyer shows that this fraud was rehearsed for many years, increasingly, with all the stakeholders now running the alleged Covid-19 fraud,n

Autopsies

Why were autopsies strongly discouraged worldwide in 2020 and still today? My conclusion is that this was to cover up the lack of Covid-19 deaths. After vaccination, a

large fraction of deaths have been judged to be due to the vaccines, and the lack of autopsies covers them up, too.12

PCR Test

The Nobel-prize-winning inventor of the PCR test, Dr. Kary Mullis, stated definitively that PCR must not be used to diagnose viral illnesses.13 On what basis, therefore, were "cases" determined purely by the restflts of this one test, much disputed as to its appropriateness?

Cause of Death

A death from any cause, within 28 days of a positive test for SARS-CoV-2, is recorded
as a "Covid death". It's absurd--we have never assigned cause of death like this before, ever. The effect of untrustworthy PCR tests and the arbitrary assignment of a dubious "positive" as somehow causative of death has been a very effective way to fool and frighten people. Most do not know that there are literally scores of viruses, even
common cold viruses, which can infect human airways, some of which--in elderly and infirm people--can give rise to severe illness.

Hospital Protocols

Hospital treatment protocols, where I have explored them, look designed to kill:

In the UK, the pathway starts with everyone being tested with untrustworthy PCR tests, which are applied repeatedly for an inpatient. Given that 2% of hospital admissions end in a hospital death, repeated poor testing guarantees a lot of"Covid deaths".

A patient "diagnosed" as "positive" Covid is then placed in isolation, and visitors are not allowed until the patient is moribund.

A standard treatment involves intravenous midazolam (a benzodiazepine used for sedation) and morphine from a syringe driver, at doses up to 10 times greater than advisable for a patient capable of breathing unaided. This often results in respiratory failure and either immediate death or mechanical ventilation, accompanied by withdrawal of an care; of course, these patients then expire. It's murder.

In the UK, we have documentary evidence that the UK National Health Service (NHS) stockpiled a year's supply of midazolam by ordering it normally but banning 2019 prescriptions. By April 2020--over no more than two months--the entire supply was exhausted. Another year's supply was then bulk-purchased from a generics company in France, cleaning out their stock.

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Something similar occurred in U.S. hospitals, with ramped-up cash bonuses for each stage passed, up to and including mechanical ventilation.

Mechanical ventilation is rarely appropriate, because Covid-19 is NOT an obstructive lung disorder. Blood oxygen desaturation is best addressed using non-invasive masks with elevated oxygen levels. When hospitals tried this in Italy in February 2020, they ceased mechanical ventilation within a week, so stark were the differences in outcomes; that is, most ventilated patients died, while most masked patients survived. Apparently, the method of treatment the Italian health care providers had been given from "colleagues in Wuhan" was what they called "the Wuhan protocol". In this, the guidance given was that the sooner they sedated and ventilated an agitated patient, the better the patient's chances. This was a lie. Panicked patients needed anxiolytics (anti-anxiety drugs) and an oxygen mask, but instead, they were killed.

Experimental Vaccines

I have been incensed by the misuse of novel, experimental "vaccines" particularly in Covid-recovered individuals, pregnant women, and children.

Recovered individuals are immune, and the risks of adverse events are greatly increased because the body is already poised to attack any cells expressing spike protein.

Pregnant women are not at greatly elevated risks from Covid-19 because they tend
to be young and healthy. NEVER, since thalidomide (1956-1962), have we approved the use of experimental agents in pregnant women, and certainly not without reproductive toxicology studies. None of the vaccines have a completed "Reprotox" package (summaries on the reproductive effects of chemicals, medications, physical agents, or biologics). I filed a short expert opinion in court with America's Frontline Doctors (AFLDS) on this topic.14 The vaccine makers also didn't complete something called an ADME-Tox (Absorption Distribution Metabolism Excretion- Toxicity) package. Documents obtained in March 2022 through Freedom of Information Act (FOIA) requests show that Pfizer was "planning to study" vaccination in maternity as of April 30, 2021--that is, after they had already manufactured and shipped close to 100 million doses.

The misuse of these agents in healthy children has, without question, reverse risk/ benefit: the injections kill far more children than the virus could.

The whole thing stinks of a purpose different from public health, because if it was a legitimate public health effort, we definitely would NOT do any of these things. When I co-authored the world's first treatise explaining some of these concerns, officials lied on the nationally broadcast BBC and other media outlets, smearing me and others like me who were raising questions. Note that the petition in question, filed with the European Medicines Agency (EMA), was co-authored by Dr. Wolfgang Wodarg, the public health doctor and minor politician from Germany who stopped the fraudulent "swine flu pandemic" in 2009.15

Revised Definitions

I observed two strange occurrences. First, the WHO altered the definition of "immunity" from "that obtained after natural infection or vaccination" only mentioning vaccination and excluding "natural immunity". 16 That meant that only

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vaccination could accomplish the goal. They eventually changed this back, but for many, the damage was done, leaving non-experts not trusting natural immunity, even though it is superior to that from vaccination because the body has been exposed to all parts of the virus and will, therefore, respond to any part of it if reinfected. The definition of a "vaccine" was also changed, so that it wasn't necessary to prevent infection or transmission, whereas traditional vaccines almost always do this. They do so because they prevent the development of clinical illness and, in the case of respiratory viruses at least, lack of symptoms renders the person all but incapable of infecting anyone else.

In addition, the WHO changed the definition of "pandemic:' Previously, "pandemic" meant the simultaneous spreading across many countries of a pathogen, causing many cases and deaths. The definition was changed to eliminate the need for many deaths. (See Dr. Wolfgang Wodarg [at 45 min, 50 sec], interviewed on UK TV in 2010 after the exaggerated swine flu pandemic, which I now believe was something of a rehearsal for the 2020 Covid-19 pandemic.)17

This is a critical point, because PCR can be designed against any pathogen, and protocols can be adopted such that a large number of false positives appear. This grants bad actors the ability, relatively easily, to create the illusion of a pandemic, almost to order. Dr. Wodarg recaps his 2009 experiences and shows interesting similarities with recent events in an January 2021 interview,is

Many people simply don't believe experts when they talk of a "very high fraction of positive test results being false positives". I assure you, however, there have genuinely been a number of events where the entire suspected epidemic was an illusion, and 100% of positives were false positives. In 2007, the New York Times reported on an example of "an epidemic that wasn't" which, when I first read it, gave me a crawling sensation.19 I wonder if it was this genuine event--a false alarm in which experts admitted placing
"too much faith in a quick and highly sensitive molecular test that led them astray"-- that birthed the method for exaggerating (or even fully faking) a pandemic such as the one we are currently living?

Bizarre Statements

I noticed early on that Bill Gates said, "We won't return to normal until pretty much the whole planet has been vaccinated". This is a bizarre statement from a person with no

medical or scientific training (or indeed a college degree in anything). It is never necessary to vaccinate the entire population, when only the elderly and infirm are at serious risk of death if infected. Note, too, that the median age of deaths from/with Covid was the same or even older than the median age of death due to all causes.

For his part, former UK prime minister Tony Blair insisted that vaccine passports would be essential to restore confidence. Again, this was absurd, especially once we learned that these vaccines do not prevent transmission. Once this became clear, the case for coerced vaccination vanished, and this is still the present position. Yet, my unvaccinated relatives may not enter the U.S. If you fear infection, the safest person to be around isn't a vaccinated person but a person who is fit and well, with no respiratory symptoms.

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Boosters and Antibodies

The practise of"boosting"--giving people dose after dose of poorly-designed agent, ostensibly to reinforce their immunity--has no immunological basis. No genuine immunity wanes in a few months, or sometimes even in a few weeks. The perpetrators have exploited the public's understanding of the annual influenza vaccine to somehow normalise something that is both dangerous and ineffective.

I also noticed that early on, in discussing immunity, antibodies were the discussion
topic, whereas T-cells were an "extremist plot". This is another absurdity. I can assemble expert witnesses who will attest alongside me that blood-based antibodies are relatively unimportant, potentially irrelevant to infection by respiratory viruses. This is because the virus infects the air side of the airways and blood-based antibodies cannot leave the blood and enter this "compartment". Blood antibodies and respiratory viruses never meet except under unusual circumstances. On the contrary, T-cells leave the blood and migrate through infected airway tissue, removing infected cells.

Ferguson Track Record

Professor Neff Ferguson at Imperial College has a poor record of modelling and predictions.2°

Prescient Testimony

A former WHO staffer, lane Bfirgermeister, shared frighteningly prescient testimony in 2010. Her understanding was that respiratory virus pandemics will be used to force
near universal vaccination and that this had sinister motives.21 1 dismissed this the first time I saw it. Many of us turn away instinctively from evil because we cannot or do not want to believe that other humans are capable of that which our logic tells us is happening. I now no longer reject it. It fits far too well with the totally independent Paul Schreyer documentary. 11

More Prescient Testimony

Another doctor, Dr. Rima Laibow, made similar claims.22 This testimony speaks of population rejection, and like lane Biirgermeister, locates the fraud in a conceptual world government. Again, one can reject it, or consider it alongside other pieces of information.


Conclusions

I think it's worth developing the theme of turning away from evidence of sheer evil, and I have to say more, because it is THE pressing issue today. The evidence I set forth
makes it perfectly plain that the entire world is being lied to in ways that led-- predictably--to huge suffering and death. Given that none of the "measures" imposed could have mitigated illness and death from a respiratory virus, the only outcome was to be the fracturing of civil society and damage, potentially fatal, to the economy and financial system. I emphasise again here that WHO scientists had conducted a detailed review of control measures for respiratory virus epidemics and pandemics as recently as 2019, and they concluded that no imposed NPI measures make any difference at all.23 The claims made for control in Wuhan are not credible.

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The stakeholders who must have approved this action own or control the majority of the world's capital and assets. Their motivation cannot be for money, for they stand astride the money-creating apparatus in the central and private banks. Equally, it cannot be to obtain gross control over the population, since they already demonstrably have that. This is what leads me inexorably to propose that the motives behind this are terrible--at the very least, to secure totalitarian control through mandatory, digital IDs (in the guise of useless "vaccine passports" useless because none of these so-called vaccines reduce transmission, the only possible justification for them). Add to this a "financial great reset" with withdrawal of cash and introduction of central bank digital currencies (CBDCs), and we have a wholly controlled population, controlled automatically without human intervention on the ground. All that's needed is to require the population to show their health passport or else they will not be allowed to cross a regulated threshold, like accessing a food store, or make a transaction using digital money unless the AI algorithm permits it. If those operating this takeover of humanity wished then to eliminate a portion of the population, with plausible deniability, I doubt a more propitious starting point could be had.

I do not believe it's a fault in those who fall for the narrative that they cannot see the lies. People want to believe that governments and experts, for all their well-known flaws and occasionally uncovered corruption, are trying to do the best they can. They cannot accept the truth, that there is a group of powerful people who regard the ordinary members of the public as surplus to requirements. They want to deny evil because it makes them feel bad, sad, and uncomfortable to think about the world this way. They want to deny reality; that's their coping mechanism, which is being exploited by the perpetrators of evil. It gives a cloak of invisibility to those who want to commit mass murder, quite literally, since so many people are so willing to imagine that it is not happening.

It is not clear to me what to do with the information I've gathered here. I believe that a calm review of the summary that I call "The Covid Lies" will result in any open-minded person agreeing that we all have been subjected to a monstrous fraud with lethal consequences, and that there is overwhelming evidence of long-term planning and deliberately injurious acts. There is no easy way to say that, but it could be represented objectively and taught, in the manner of a workshop, so that participants get to derive their own conclusions (albeit being led by the evidence).

I doubt just talking to a group of people who hold the dominant narrative view as "true" would respond at all well to this, delivered as a lecture. Nobody wants to accept that they've been fooled, even if the blow is softened by telling them that this has been brought about by highly experienced professionals in the covert services and has required huge amounts of money to buy off several groups. On the positive side, an increasing number of people have detected that fraud is ongoing. A particularly good example comes from the financial analyst community and refers to life insurance claims among many other pieces of evidence of wrong-doing. 24 Ignoring this and hoping it will go away is naive and very dangerous for us all. The perpetrators have not gone away and will likely return in the fall. I expect this year or the next will see them assume totalitarian tyranny, if we have not, before then, "inoculated" important stakeholder groups to understand what has happened so far and cautioned them to be alert to the many potential presentations of the next fear- provoking episode.

Analysis of COVID Deaths by Country Income Levels: The higher the income, the higher the deaths. The higher the income, the higher the vaccinations. The higher the vaccinations, the higher the deaths

From [JOELSMALLEY] The higher the income, the higher the deaths. The higher the income, the higher the vaccinations. The higher the vaccinations, the higher the deaths.

It’s a curious thing that the higher the income level of a country, the higher the number of COVID deaths they experienced.

In terms of the high income countries, the ratios of upper middle, lower middle and low income countries are 100:39:16:3 respectively.

I say curious because you would think that higher income countries would have better resources to deal with a public health emergency? I wouldn’t dare suggest that the countries as a whole are more intelligent. You mean to tell me that all those sophisticated traffic light and one-way systems didn’t “beat the virus”??

It’s perhaps not so curious that the same pattern plays out in terms of COVID vaccination rates.

The vaccine is up to 100% effective in reducing COVID mortality (allegedly). This is the last claim, the pro-vaxxers cling to now that transmission reduction is well and truly debunked.

Inevitably, given the significant “inequality” between the rich countries and the poor in terms of vaccine availability and administration, we should, therefore, expect to see a massive reversal in COVID deaths in the post-vax period.

But we don’t.

The ratios post-vax are 100:60:25:4 (compared to 100:39:16:3). The upper middle income countries have massively caught up the high income countries but they attained the same level of vaccination. That’s not supposed to be how it happens!

The low income countries have attained a mere 12% of the vaccination rate of the high income countries but their relative COVID death rate has only risen by a relative 1%. When you factor in that the high income countries ought naturally to have lower relative death given the magnitude of the excess in the pre-vax period, this, again, is not exactly a ringing endorsement of vaccine effectiveness.

David Martin’s "Proposed Indictment" Claims Govt/Big Pharma Weaponized COVID and then Hyped a Manufactured Crisis to Create Dependency on their Deadly "Vax," which was Created Prior to the Plandemic

From David Martin’s organization [PROSECUTE NOW]

The Proposed Indictment

Throughout the decade of the 90s, Pfizer sought to research, develop and patent a coronavirus (CoV) vaccine. Their first patent filing specifically recognizing the S-protein as the immunologic target for vaccines was filed on November 14, 1990 (U.S. Patent 6,372,224). With a focus on swine and canine gastroenteritis, these efforts showed little commercial promise and the patent was abandoned in April of 2000. During the same period, the National Institute for Allergy and Infectious Disease (NIAID), under the vaccine obsession of Dr. Anthony Fauci, funded Professor Ralph Baric at the University of North Carolina Chapel Hill. This program, designed to commercially weaponize a naturally occurring toxin, is the beginning of the criminal conspiracy and violates 18 USC § 175, 15 USC § 1-3, and 15 USC § 8). Dr. Baric’s expertise was understanding how to modify components of the coronavirus associated with cardiomyopathy. NIAID Grants AI 23946 and GM63228 (leading to patent U.S. 7,279,327 “Methods for Producing Recombinant Coronavirus”) was the NIH’s first Gain-of-Function (GOF) project in which Dr. Baric created an “infectious, replication defective” clone of recombinant coronavirus. This work clearly defined a means of making a natural pathogen more harmful to humans by manipulating the Spike Protein and other receptor targets. A year after filing a patent on this GOF CoV, the world experienced the first outbreak of Severe Acute Respiratory Syndrome (SARS).

Under the guise of responding to a public health emergency, the United States Centers for Disease Control and Prevention (CDC) filed a patent application on the genome of SARS CoV on April 25, 2003. By accessing and manipulating the Chinese genomic data (which came from China making an “invention” claim by a U.S. entity illegal violating 35 USC §101, 103), Dr. Baric, Dr. Fauci, and the CDC violated 18 USC § 175 (a felony). One year earlier, Dr. Baric and his team had already filed a patent which was clearly the pathogen CDC claimed as novel in 2003. Three days after filing a patent on the genome, NIH-funded Sequoia Pharmaceuticals filed a patent for the vaccine on the virus invented a mere three days earlier. At the same time, in violation of 15 USC § 19, Dr. Fauci was appointed to a board position with the Bill and Melinda Gates Foundation (a competitor in vaccine manufacturing) thereby beginning the interlocking directorate1 anti-trust crime.

In 2005, the DARPA and MITRE hosted a conference in which the intentions of the U.S. Department of Defense was explicit. In a presentation focused on “Synthetic Coronaviruses Biohacking: Biological Warfare Enabling Technologies”, Dr. Baric presented the malleability of CoV as a biological warfare agent. Violating 18 USC § 175 and inducing the non-competitive market allocation (violating 15 USC § 8) for years to follow, Dr. Baric and the U.S. Department of Defense spent over $45 million in amplifying the toxicity of CoV and its chimeric derivatives.

From 2011 until the alleged COVID-19 pandemic, Dr. Fauci has routinely lamented the inadequacy of public funding for his vaccine programs and the public’s general unwillingness to succumb to his insistence that everyone MUST be vaccinated against influenza. Despite repeated appropriations to advance vaccine dependency, his efforts have been largely unsuccessful. NIAID – under Dr. Fauci’s direct authorization – encouraged UNC Chapel Hill and Dr. Baric’s lab to ignore the GoF moratorium in a letter dated October 21, 2014. At that time, Drs. Fauci, Baric and EcoHealthAlliance’s Peter Daszak were in possession of an extremely dangerous Chinese pathogen identified a year earlier in Wuhan.2

While many illegal acts were committed by the conspirators leading up to 2015, the domestic terrorism program (in violation of 18 USC § 2339) was announced by NIAID-funded Daszak at the National Academy of Sciences. Here, he announced what was to become the domestic and global terrorism event branded COVID-19.

...until an infectious disease crisis is very real, present, and at an emergency threshold, it is often largely ignored. To sustain the funding base beyond the crisis, he said, we need to increase public understanding of the need for MCMs such as a pan-influenza or pan- coronavirus vaccine. A key driver is the media, and the economics follow the hype. We need to use that hype to our advantage to get to the real issues. Investors will respond

if they see profit at the end of process, Daszak stated.”3

It is not surprising that one year later NIAID’s funding paid off with Dr. Baric’s lab announcing that the Wuhan- derived pathogen was “poised for human emergence”.4

Knowing that the U.S. Department of Health and Human Services (through CDC, NIH, NIAID, and their funded laboratories and commercial partners) had patents on each proposed element of medical counter measures and their funding, Dr. Fauci, Dr. Gao (China CDC), and Dr. Elias (Bill and Melinda Gates Foundation) conspired to commit acts of terror on the global population – including the citizens of the United States – when, in September 2019, they published the following mandate in A World At Risk:

“Countries, donors and multilateral institutions must be prepared for the worst. A rapidly spreading pandemic due to a lethal respiratory pathogen (whether naturally emergent or accidentally or deliberately released) poses additional preparedness requirements. Donors and multilateral institutions must ensure adequate investment in developing innovative vaccines and therapeutics, surge manufacturing capacity, broad-spectrum antivirals and appropriate non-pharmaceutical interventions. All countries must develop a system for immediately sharing genome sequences of any new pathogen for public health purposes along with the means to share limited medical countermeasures across countries.
Progress indicator(s) by September 2020

• Donors and countries commit and identify timelines for: financing and development of a universal influenza vaccine, broad spectrum antivirals, and targeted therapeutics. WHO and its Member States develop options for standard procedures and timelines for sharing of sequence data, specimens, and medical countermeasures for pathogens other than influenza.

• Donors, countries and multilateral institutions develop a multi-year plan and approach for strengthening R&D research capacity, in advance of and during an epidemic.
• WHO, the United Nations Children’s Fund, the International Federation of Red Cross and Red Crescent Societies, academic and other partners identify strategies for increasing capacity and integration of social science approaches and researchers across the entire preparedness/response continuum.”5

As if to confirm the utility of the September 2019 demand for “financing and development of” vaccines and the fortuitous SARS CoV-2 alleged outbreak in December of 2019, Dr. Fauci began gloating that his fortunes for additional funding were likely changing for the better. In a February 2020 interview in STAT, he was quoted as follows:

The emergence of the new virus is going to change that figure, likely considerably, Fauci said. “I don’t know how much it’s going to be. But I think it’s going to generate more sustained interest in coronaviruses because it’s very clear that coronaviruses can do really interesting things.”6

In November 2019 – one month before the alleged “outbreak” in Wuhan, Moderna entered into a material transfer agreement – brokered by the Vaccine Research Center at NIAID (at which UNC Chapel Hill alum Dr. Kizzy Corbett worked) – to access Dr. Baric’s Spike Protein data to commence vaccine development. In his own written statement obtained by the Financial Times, he refers to this agreement as being the foundation for the mRNA Moderna vaccine.7

To finalize the nature of the racketeering and anti-trust criminal conspiracy, when it came time to commercialize the NIH and DARPA owned spike protein and pass it off as a “vaccine” (in conflict with the standard for vaccines in statutory and scientific application), the Operation Warp Speed contract was awarded to DoD contractor ATI, a subsidiary of ANSER. In a graph reminiscent of the anti-trust hearings at the formation of the Clayton Act in the early 20th century, the identity of the interlocking conflicts of interests are presented in graphic relief. It is with no surprise that the result of this price-fixing conspiracy was the enrichment of the conspiring parties and the harm of consumers.

Indeed, the money followed the hype and they used the hype to get to the real issues. Investors follow where they see profit at the end of the process.

And real Americans are dying each day because a criminal organization unleashed terror resulting in the deaths of Americans.

18 U.S.C. § 2331 §§ 802 – Acts of Domestic Terrorism resulting in death of American Citizens

Pub. L. No. 107-52 expanded the definition of terrorism to cover "domestic," as opposed to international, terrorism. A person engages in domestic terrorism if they do an act "dangerous to human life" that is a violation of the criminal laws of a state or the United States, if the act appears to be intended to: (i) intimidate or coerce a civilian population; (ii) influence the policy of a government by intimidation or coercion;

Every single Act, the declaration of the State of Emergency, the Emergency Use Authorization, the fraudulent face masks, the business closures, and the OSHA and CMS vaccine mandates are ALL admitted by the conspirators to be acts to coerce the population into taking a vaccine. Further, these acts disrupted the democracy of the United States of America and resulted in the violation of 18 USC § 2384. The conspirators announced it in 2015, then prepared the pathogen in 2016, and laid out the terror campaign in September 2019. And now they profit from the death of Americans.


Footnotes

FN 1. 1 We note that gain-of-function specialist, Dr. Ralph Baric, was both the recipient of millions of dollars of U.S. research grants from several federal agencies and sat on the World Health Organization’s International Committee on Taxonomy of Viruses (ICTV) and the Coronaviridae Study Group (CSG). In this capacity, he was both responsible for determining “novelty” of clades of virus species and directly benefitted from determining declarations of novelty in the form of new research funding authorizations and associated patenting and commercial collaboration. Together with CDC, NIAID, WHO, academic and commercial parties (including Johnson & Johnson; Sanofi and their several coronavirus patent-holding biotech companies; Moderna; Pfizer; Merck; BioNTech; AstraZeneca; Janssen; Ridgeback; Gilead (Dr. Baric’s alter ego); Sherlock Biosciences; and others), a powerful group of interests constituted what are “interlocking directorates” under U.S. anti-trust laws. Further, most of these entities, including the Federal Government, violated 35 USC § 200-206 by failing to disclose Federal Government interest in the remedies proposed.

These entities were affiliated with the WHO’s Global Preparedness Monitoring Board (GPMB) whose members were instrumental in the Open Philanthropy-funded global coronavirus pandemic “desk-top” exercise EVENT 201 in October 2019. This event, funded by the principal investor in Sherlock Biosciences (a beneficiary of the SARS CoV-2 EUA for CRISPR technology) and linking interlocking funding partner, the Bill and Melinda Gates Foundation into the GPMB mandated a respiratory disease global preparedness exercise to be completed by September 2020 and alerted us to anticipate an “epidemic” scenario. We expected to see such a scenario emerge from Wuhan or Guangdong China, northern Italy, Seattle, New York or a combination thereof, as Dr. Zhengli Shi and Dr. Baric’s work on zoonotic transmission of coronavirus identified overlapping mutations in coronavirus in bat populations located in these areas.

2 By October 2013, the Wuhan Institute of Virology 1 coronavirus S1 spike protein was described in NIAID’s funded work in China. This work involved NIAID, USAID, and Peter Daszak, the head of EcoHealth Alliance. This work, funded under R01AI079231, was pivotal in isolating and manipulating viral fragments selected from sites across China which contained high risk for severe human response. (

The GoF work NIAID allowed to persist in the face of the moratorium was Dr. Baric’s work with this pathogen

3 Forum on Medical and Public Health Preparedness for Catastrophic Events; Forum on Drug Discovery, Development, and Translation; Forum on Microbial Threats; Board on Health Sciences Policy; Board on Global Health; Institute of Medicine; National Academies of Sciences, Engineering, and Medicine. Rapid Medical Countermeasure Response to Infectious Diseases: Enabling Sustainable Capabilities Through Ongoing Public- and Private-Sector Partnerships: Workshop Summary. Washington (DC): National Academies Press (US); 2016 Feb 12. 6, Developing MCMs for Coronaviruses. Available from: https://www.ncbi.nlm.nih.gov/books/NBK349040/

4 Menachery VD, Yount BL Jr, Sims AC, Debbink K, Agnihothram SS, Gralinski LE, Graham RL, Scobey T, Plante JA, Royal SR, Swanstrom J, Sheahan TP, Pickles RJ, Corti D, Randell SH, Lanzavecchia A, Marasco WA, Baric RS. 2016. SARS-like WIV1-CoV poised for human emergence. Proc Natl Acad Sci U S A. 2016 Mar 14. pii: 201517719

5 https://apps.who.int/gpmb/assets/annual_report/GPMB_annualreport_2019.pdf (page 8)

Dr. Ryan Cole says the Coerced COVID Vax Policy will Cause a Surge in Cancer Rates

From [HERE] America’s mass Wuhan coronavirus (COVID-19) vaccination programs are poor and unscientific policy decisions that will lead to surges in cancer rates among the vaccinated.

This is according to Dr. Ryan Cole, a board-certified and expert pathologist trained at the Mayo Clinic. Cole was among the first physicians in the United States to openly warn about how the COVID-19 vaccines may be associated with serious health risks, such as an elevated risk of developing cancer, which he observed in his patients. (Related: COVID-19 mass vaccination programs violate bioethics principles.)

During an interview with journalist Veronika Kyrylenko of the New American, Cole said the mRNA in COVID-19 vaccines suppresses the immune system and “all sorts of cell cycle pathways.”

Cole explained that cells have “little pattern receptors” that are responsible for communicating with the immune system. The mRNA in COVID-19 vaccines downregulates these cells – meaning the number of surface receptors they have decreases.

When more and more of a vaccinated person’s cells experience downregulation due to the mRNA in the COVID-19 vaccines, their risk of cancer spikes upward.

“A couple of these downregulated receptors are responsible for keeping cancer in check,” said Cole.

This is just one way the COVID-19 vaccines are responsible for increasing cancer ratesamong the fully vaccinated. Cole further explained that the spike proteins in the COVID-19 vaccines can bind to the body’s genes, including several genes that are related to cancer and tumors.

For example, when the spike proteins bind to P53 genes, a family of genes known as tumor suppressor genes, a person’s risk of developing cancerous tumors increases. When the spike proteins bind to BRCA1 and BRCA2 genes, the risk of women developing breast or ovarian cancer increases.

“So, that’s just the tip of the iceberg in terms of what the spike protein can do,” warned Cole. “The other huge problem is the fact – and this was a study out of [Stanford University] … in the journal Cell – the synthetic mRNA can persist in the body, we know, for at least 60 days. That’s the point at which they stopped their study so they could publish.”

COVID-19 vaccines alter the immune system

At every opportunity that is available to him, Cole speaks out against the COVID-19 vaccines and about how they are responsible for the alarming uptick in cancers that the U.S. is currently experiencing.

“We’re seeing an alteration of the innate immune response,” said Cole. He added that scientists all over America are also witnessing this and that the uptick in these strange immune responses coincides with the rollouts of COVID-19 vaccines.

Some of the strange medical phenomena Cole has witnessed include the appearance of a childhood disease in adults and the uptick in rare cancers.

All of his observations have also been echoed by other physicians, but rigorous studies are not being conducted because of a lack of funding and because mainstream scientific institutions are unwilling to study these phenomena.

“You cannot find that for which you do not look,” he said.

COVID Injection Caused Spinal Cord Injury that Ended Surgeon’s 20-Year Career. 'There was No Paperwork, No Asking about My History, No Consent Form, No Anything.'

From [CHD] Dr. Joel Wallskog was once a successful orthopedic surgeon. A joint replacement specialist for 20 years, he had a large and busy practice in Wisconsin, where he saw almost 6,000 patients each year.

Married to his college sweetheart for almost 30 years and the father of four children, Wallskog had a “fantastic” life, he said. He enjoyed his career and balanced it with fun, active time with his family.

But the Moderna COVID-19 vaccination changed his life forever, Wallskog said. His health deteriorated rapidly and his career came to an end.

He recently told his story to Stephanie Locricchio, an advocacy liaison for Children’s Health Defense (CHD), on CHD.TV’s “The People‘s Testaments.”

In September 2020, Wallskog said, staff members in the clinic he referred patients to began coming down with COVID-19. He did not feel ill (“maybe in retrospect I had a runny nose for a couple days,” he said) but got an antibody test, which was positive.

When a close friend came down with COVID-19 and had to be intubated, Wallskog decided he should get vaccinated, despite his reservations.

“I was part of the healthcare system. I believed in the system,” he told Locricchio.

Still, Wallskog said, “I had some second thoughts. It just didn’t seem right. I just had COVID, I proved that I had antibodies … I had natural immunity. …But again, I was part of the system that I trusted.”

He received his vaccine through his employer, one of the 10 largest healthcare systems in the country. Despite this, when he got the shot, “there was no paperwork, there was no asking my history, there was no consent form, there was no anything,” he said.

About a week later, Wallskog’s feet became numb. Then he started getting “electrical sensations” down his legs when he bent his head forward. He compared the sensation to “putting your finger in an outlet.”

When he began having trouble standing, he ordered emergent MRIs and was found to have a lesion on his spinal cord.

A neurologist diagnosed transverse myelitis, a disorder caused by inflammation of the spinal cord. Myelin is the protective covering over the nerves, and without it, electrical impulses are not transmitted correctly, resulting in loss of feeling and mobility.

Wallskog noted that he was quickly diagnosed because he is a physician. “Being in the healthcare system, I can navigate the system like not many people can,” he said.

“That’s why I’m worried about so many [other people’s] injuries that are going to take months to get worked up. If the providers don’t know what to look for, [others] will maybe never get a diagnosis.”

Despite various treatments and rest, Wallskog suffers pain and numbness and is unable to stand long enough to perform surgery. His career came to an end in early 2021.

‘Look at the data yourself’

Wallskog said he is now embarrassed for his profession.

“I feel like I’ve been unblinded …  like I got off the hamster wheel and I stopped drinking the Kool-Aid and I started asking questions,” he said. “I started looking. I started talking to people.”

“Look at the data yourself,” he advised. “Don’t wait for the media, who will twist every data point.

Despite what we’ve been told for more than two years now, “science is a dynamic process,” he said:

“Science isn’t settled. Science is a process of exploration, of admitting when you’re wrong, finding out what you’re right on. You have hypotheses, you test them … move forward. And people need to realize that and not necessarily trust these people that are so-called experts.

“I am open to learning and seeing the truth. If there are things that I’m wrong [about], that’s fine, that’s part of science.”

“I’m so thankful that you’re saying this,” Locricchio told Wallskog. “Because it really means something … you’re a citizen, you’re an injured person, but you’re also a physician.”

Wallskog has now taken matters into his own hands in an effort to help others. “We’re sick and tired of waiting for other people to do the right thing,” he said. “We’re just going to do it ourselves.”

He is now co-chairman, along with Brianne Dressen, of REACT19, a “science-based nonprofit” offering financial, physical and emotional support for those suffering from long-term COVID-19 vaccine adverse events.

The REACT19 website states:

“​​React19 works with both patients and providers as well as research teams. Our programs all fall within our 3 categories of assistance (financial, physical, and emotional).

“Programs include funding, promoting, and sharing relevant scientific research; bringing the right medical teams together with patients; direct financial assistance; educational outreach; and supporting communities where impacted people can begin to heal physically and emotionally.”

Financial support is important, said Wallskog, but acknowledgment of vaccine injuries is just as vital.

He spoke with Dr. Peter Marks, director of the Center for Biologics Evaluation and Research (CBER) at the U.S. Food and Drug Administration. According to Wallskog, “[Marks] privately said, ‘I acknowledge these injuries,’ but he won’t publicly acknowledge them.”

“This was a quote on video,” said Wallskog. “And I said, ‘well, that’s too bad because acknowledgment is important.’”

Wallskog added:

“Without the [Centers for Disease Control and Prevention], the [U.S. Food and Drug Administration], the [National Institutes of Health] and other governmental agencies acknowledging these injuries, the conditions won’t be communicated to the healthcare community. If the healthcare community doesn’t know what to look for … when these people present [to a doctor with symptoms], then they’re just gaslit,” he said.

“Acknowledgment leads to the development of evaluation and treatment protocols for these people. That’s why it’s important … And the other thing is to support these people. And that’s what I’m hoping to do through REACT.”

Professor John W. Oller - ‘Creating and Containing Monsters: Weaponized Pathogens and the SARS-CoV-2 Plandemic’

ABSTRACT

This review zeros in on the aspect of vaccine theory, practice, and research that is the most dangerous, the most controversial, and that is at the epicenter of the alleged SARS-CoV-2 “pandemic”. Regardless whether the “pandemic” itself is real or an illusion manufactured out of fear by vested interests, it is central to ethics and policy discussions seeking to understand bioweapons research in general. The official involvement of the USA in civilian bioweapons research dates at least from World War II under President Franklin Delano Roosevelt. The historical records, cloaked in secrecy until after the Anthrax mailing of 2001, reveal an intimate connection to vaccine research and development, its governmental protection from public scrutiny, and from citizen initiated lawsuits. It is an industry that has released dangerous weaponized pathogens by accident and by sinister designs supposedly compensated in the peace-loving nations by unrealistic hopes in non-existent counter-measures for outbreaks, including epidemiological tracking after the fact, vaccines being researched to counter the weaponization of pathogens being studied, immunity enhancing drugs, and downstream hoped for blood sera containing antibodies. Critical questions concern the ratio of real-risks to hoped-for-benefits, the “mitigating” measures “governments” (especially in the USA) have supposedly established to prevent pandemic outbreaks from bioweapons research, and how all that has played out in the instance of SARS-CoV-2.

Keywords: avian influenza (HPAI), bioweapons research, coronaviruses, COVID-19 pandemic, chronic noncommunicable diseases, dual use research, flu vaccines, gain of function, H1N1, H5N1, H7N9, Middle East respiratory syndrome (MERS), severe acute respiratory syndrome (SARS), SARS-CoV-2, weaponized pathogens

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Dr Gilbert Berdine: Clearly there is a Very Significant Above Average Number of People Dying Across the US that Cannot be Attributed to COVID

By Gilbert G. Berdine, M.D. Gilbert Berdine is an associate professor of internal medicine at the Texas Tech University Health Sciences Center (TTUHSC)and a faculty affiliate with the Free Market Institute.

Dr. Berdine earned his B.S. degrees in chemistry and life sciences from the Massachusetts Institute of Technology in Boston and his M.D. degree from Harvard University School of Medicine in Boston. He completed residency in Internal Medicine and fellowship in Pulmonary Diseases at the Peter Bent Brigham Hospital (Now called Brigham and Women’s Hospital) in Boston.

From [HERE] The CEO of the OneAmerica insurance company recently disclosed that mortality in the 18-64 age group was 40 percent higher during the 3rd and 4th quarters of 2021 than during pre-pandemic levels. For reference, the CEO indicated that a 10 percent increase would have been a 1-in-200-year event. Furthermore, most of the deaths were not attributed to Covid.

The CEO of the OneAmerica insurance company recently disclosed that mortality in the 18-64 age group was 40 percent higher during the 3rd and 4th quarters of 2021 than during pre-pandemic levels. For reference, the CEO indicated that a 10 percent increase would have been a 1-in-200-year event. Furthermore, most of the deaths were not attributed to Covid.

Clearly there is a very significant above average number of deaths across the US that cannot be attributed to Covid. As was the case for the Age Group graphs, data for the last 10 weeks are incomplete due to delays in reporting of death certificates. Deaths attributed to Malignant Neoplasms were average during the entire pandemic period. Although there was an increase in deaths from Alzheimer Disease and dementia in 2020 after the onset of the pandemic, this was less apparent during 2021. There was an increase in deaths attributed to Other select causes (which include suicides and drug overdoses), but the magnitude was much smaller than what is seen in the Circulatory diseases category. Deaths attributed to Circulatory diseases include strokes, heart attacks, and heart failure (including myocarditis). The Circulatory diseases category is clearly the most important category for excess deaths during 2020 and 2021. Notably, deaths attributed to Respiratory diseases were below average during 2021 for the period of interest between Week 10 and Week 24 of 2021. Covid is a respiratory disease and leads to acute respiratory distress syndrome with hypoxemia and respiratory failure in severe cases. During the period of interest between Week 10 and Week 24 of 2021, Covid deaths were steadily declining, deaths attributed to Respiratory diseases were below average, but deaths due to Circulatory diseases were significantly above average. It is difficult to explain the data between Week 10 and Week 24 of 2021 on the basis of lung injury caused by Covid infection.

The spike protein enables entry of the virus into the host cells. The spike protein targets the angiotensin converting enzyme-2 (ACE-2) receptor. Angiotensin converting enzymes play an important role in the regulation of blood pressure. Angiotensin receptor blockers (ARB) and angiotensin converting enzyme (ACE) inhibitors are both important classes of drugs used to treat hypertension. It does not require a stretch of the imagination to suspect that the spike protein could cause elevation of blood pressure. Acute elevation in blood pressure is known to be a risk factor for stroke, acute myocardial infarction (heart attack), and congestive heart failure. Spike protein is also associated with clotting, presumably due to endothelial injury, which would also increase risk for myocardial infarction and stroke. It is not clear why spike protein from the Covid virus would explain above average deaths attributed to Circulatory diseases during a time period when Covid cases and deaths were declining. However, the Covid virus was not the only source of spike protein during this time period. The mRNA vaccines led to the production of spike protein by host cells and Weeks 10-24 of 2021 were immediately followed by the mass introduction of mRNA vaccines to the US public. The data is not proof, but it is certainly a red flag.

The appropriate method to assess vaccine efficacy and safety is all cause mortality. Deaths from all causes are compared between the vaccine group and a control unvaccinated group. This method has not been used. Rather, the CDC and FDA determine on a case-by-case basis whether reported adverse events can be attributed to the vaccine. If a footballer drops dead during a game, one would not be inclined to attribute the cause to a vaccine given 10 weeks earlier. However, when 5 footballers drop dead every week, one will be looking for ANY common denominator between the dead footballers. Neither the CDC nor the FDA are impartial observers of vaccine safety. Both agencies have vested interests in promoting the vaccines. When the CDC or FDA analyze events on a case-by-case basis, they are inclined to say that an event was not due to a vaccine (especially if the people at the CDC and FDA include former executives from Pfizer). However, when the entire US population has a significant number of events compared to historic basis, one must look for the common denominators in the people with the events. The existing data is not proof that the vaccines are causing deaths due to Circulatory diseases. The burden of proof, however, lies with the CDC and FDA to prove that the vaccines are not causing deaths due to spike protein. It is scientific irresponsibility to eliminate the control group via vaccine mandates and make future assessment of vaccine safety scientifically impossible. 

Dr Robert Malone Claims Pfizer and the CDC Committed Criminal Fraud when they Withheld Critical Data from the Public, resulting in Harm and Death to Thousands from COVID Injections

From [HERE] It’s been shown that Pfizer and the CDC committed fraud when they willfully withheld critical data from the public, resulting in harm and death to thousands from the injections.

What’s going on here is criminal. For the people close to the data who said nothing, there will be legal consequences. They will either be witnesses or defendants.

The FDA and the CDC had to be sued to release the data on a biological product that every person is being asked, if not forced to take. This should make everyone very concerned.

DoD data shows clear increase in disease after injection and WorldInData.org reports a 73% of the COVID deaths in both high income and middle-high income nations (that could afford vaxx) occurred AFTER vaxx was released. In a pandemic, the most deaths should occur at the beginning, before treatment is available. However, the COVID vaxxines failed to improve health, which was apparently by design.

Dr Malone reacted to the latest Pfizer data dump, telling The New American’s Veronika Kyrylenko, “In my opinion, withholding scientific data constitutes fraud. This is scientific fraud, in my opinion.

“If I was to publish a study in which I had a large body of epidemiological data and I decided to only publish part of it, because I wanted to advance some agenda, I would be guilty of scientific fraud. The paper would be withdrawn, I would be kicked out of my academic institution, I would be guilty of scientific fraud. That’s what this is.

“And the CDC, I’ve watched them over the years become more and more and more a political arm and not serving its function. This is the Centers of Disease Control and Prevention. They are the archive of information, which physicians have relied upon for decades, through the MMWR Publication. They are the ones responsible for providing us with the frontline data about what’s going on and where it’s happening. They have stopped performing that function.

“They no longer release that detailed information through MMWR. hey have become a purely political organization; and arm of the Executive Branch and what they have done, in my opinion is obscene.

“And it’s part of what’s underlied the attacks against [Dr Peter McCullough] and I have sustained from the press. If you think about it, ‘The CDC didn’t say that, therefore, you’re spreading medical misinformation,’ but now we learn who’s really been spreading medical misinformation! It’s the CDC!

“I think we’re all owed an apology, I think that this data that they have been withholding – it’s not just the 18 to 49 triple-boost efficacy data, it is a ton of information, intentionally withholding it – that’s why we’ve bee attacked, it is unjust, we are the ones, it turns out we’re completely vindicated, we have been speaking truth and it’s the truth that’s been hidden from the American public and more important, it’s been hidden from other physicians and it’s been hidden from public health authorities.

“That article was powerful, if you look through it. The New York Times tried to hide it and they dropped it on President’s Day and they wrote it in ways that ties to obscure what’s really going on. But what’s going on here is criminal, in my opinion,” he says.

Veronika asks him if there will be consequences for the Federal Government for what they have done.

He replies, “I’ve spoken repeatedly: for those people that are within the Government – we call them ‘Govvies’ for slang – the folks working at the CDC, that gave interviews for The New York Timesbut wouldn’t share their names, I think they are now at a point of choosing.

“There are going to be legal consequences and I believe they do have a choice. These government employees that have been participating in hiding this data: They can either be defendants or they can be witnesses. It is time for them to step up and speak out.

“And if they want to do a whistleblower action, speak to Senator Ron Johnson, his office is in business, looking for this and when the Midterms are done and he’s re-elected and the Republicans take the Senate, he’s going to be in charge of the Senate Subcommittee on Investigations and I can tell you that he is ready to go.”

Dr Malone hands the mic to Dr McCullough, who says, “I’d just add to that that this isn’t the only area of concern about data transparency. The FDA and Pfizer are being sued for release of their full dossier. Many of you know, there is now an accelerated release of the data – but the reluctance to release information on a biological product that each and every American is being asked, if not mandated to take – the reluctance to do so should make everyone concerned.

“The other area of data transparency we’re extremely concerned about is the Department of Defense Epidemiological Database [DMED] information that was released on the January 24th Senate Panel: A Second Opinion, chaired by Senator Ron Johnson and their lead attorney, Tom Renz Co-Counsel, Leigh Dundas presented the data and the whistleblowers, in fact did disclose their names; lead whistleblower being Flight Surgeon Theresa Long and it’s clear: there’s a manifold increase, across many disease categories among our servicemen, year over year.

“The only thing thats changed is the administration of the vaxxines in large numbers. So data transparency, at this point in time will be an area that I believe Dr Malone is correct, will be intensely investigated and for those who are close to the data, I think they do have a choice coming up and it’s going to be a matter of making the right choice and where they want to end up; on what side of history.

Denmark’s Pandemic of the Vaccinated. Research Shows that "the Vaccinated" in Denmark Account for more Cases, Hospitalizations and Deaths than the Unvaccinated (2022)

From [HERE] Kristoffer Torbjørn Bæk’s research reveals the vaccinated in Denmark account for more cases, hospitalisations and deaths than the unvaccinated and have done all year.

Now that vaccination statuses are stable enough that the tomfoolery of misclassification no longer meddles with the analysis, we can see a clear picture of the ineffectiveness of the Covid vaccine, Joel Smalley commented.

In this article, Joel Smalley summarised and commented on Danish data collated and made publicly available by Danish molecular biologist Kristoffer Torbjørn Bæk

Bæk has also co-authored a pre-print study published on medRxiv, ‘Estimates of excess mortality for the five Nordic countries during the Covid-19 pandemic 2020-2021’, comparing Nordic all-cause deaths using “other estimates” to a recent study in the Lancet, “which is a clear outlier” and “most likely substantially overestimates excess deaths of Finland and Denmark, and probably Sweden.”

“Other estimates are more consistent and suggest a range of total Nordic excess deaths of approximately half of that in the Lancet study,” the authors of the study wrote. [MORE]

The Experimental Drug Remdesivir is ‘Disastrous’ as a COVID Treatment b/c It Causes Death and Organ Damage, But the US Government Pays Hospitals to Use It on Unvaxxed Persons

From [chd] Story at a glance:

  • So far, all of the drugs developed against COVID-19 have been disastrous in one way or another. Remdesivir, which to this day is the primary COVID drug approved for use in U.S. hospitals, routinely causes severe organ damage and, often, death.

  • Despite that, the U.S. Food and Drug Administration has approved remdesivir for in-hospital and outpatient use in children as young as 1 month old.

  • Another COVID drug, Paxlovid, will in some cases cause the infection to rebound when the medication is withdrawn.

  • Molnupiravir (sold under the brand name Lagevrio) also has serious safety concerns. Not only might it contribute to cancer and birth defects, it may also supercharge the rate at which the virus mutates inside the patient, resulting in newer and more resistant variants.

  • The fact that U.S. health authorities have focused on these drugs to the exclusion of all others, including older drugs with high rates of effectiveness and superior safety profiles, sends a very disturbing message. They’ve basically become extensions of the drug industry, protecting the drug industry’s interests at the cost of public health.

So far, all of the drugs developed against COVID-19 have been disastrous in one way or another. Remdesivir, for example, which to this day is the primary COVID drug approved for use in U.S. hospitals, routinely causes severe organ damage, and, often, death.

Despite its horrible track record, the U.S. government actually pays hospitals a 20% upcharge for sticking to the remdesivir protocol, plus an additional bonus. Hospitals must also use remdesivir if they want liability protection.

Incentives like these have turned U.S. hospitals into veritable death traps, as more effective and far safer drugs are not allowed, and hospitals are essentially forced to follow the recommendations of the U.S. Centers for Disease Control and Prevention.

If you are at the hospital and your hear “Remdesivir,” It Means RUN DEATH IS NEAR. Don’t let them do this to you or your family

As reported by Forbes science reporter JV Chamary back in January 2021, in an article titled, “The Strange Story of Remdesivir, a COVID Drug That Doesn’t Work”:

“Remdesivir is an experimental drug developed by biotech company Gilead Sciences (under the brand name Veklury) in collaboration with the US Centers for Disease Control and Army Medical Research Institute of Infectious Diseases …

“The drug proved ineffective against the Ebola virus … yet was still subsequently repurposed for SARS-CoV-2 coronavirus. News media prematurely reported that patients were responding to treatment.

“But the published data later showed that ‘remdesivir was not associated with statistically significant clinical benefits [and] the numerical reduction in time to clinical improvement in those treated earlier requires confirmation in larger studies’ …

“What’s weird about remdesivir is that it hasn’t been held to the same standards as other drug candidates. Normally, a drug is only approved for use by a regulatory body like the U.S. Food and Drug Administration if it meets the two criteria for safety and efficacy.

“Nonetheless, in October 2020, remdesivir was granted approval by FDA based on promising data from relatively small trials with about 1,000 participants. A large-scale analysis by the World Health Organization’s Solidarity trial consortium has cleared up the confusion.

“Based on interim results from studying more than 5,000 participants, the international study concluded that remdesivir ‘had little or no effect on hospitalized patients with COVID-19, as indicated by overall mortality, initiation of ventilation and duration of hospital stay.’ As a consequence of being mostly ineffective, WHO recommends against the use of remdesivir in COVID-19 patients.”

Shockingly, US approves remdesivir for babies

Curiously, while Big Tech — aided and abetted by the U.S. government — has spent the last two years censoring and banning any information that doesn’t jibe with the opinions of the WHO, the U.S. government has completely ignored the WHO’s recommendation against remdesivir.

In fact, in late April, the FDA approved remdesivir as the first and only COVID-19 treatment for children under 12, including babies as young as 28 days, which seems beyond Orwellian and crazy considering it’s the worst of both worlds: It’s ineffective AND has serious side effects.

What’s worse, the drug is also approved for outpatient use in children, which is a first. In an April 30 blog post, Dr. Meryl Nass expressed her concerns about the FDA’s approval of remdesivir for outpatient use in babies, stating:

“Remdesivir received an early EUA (May 1, 2020) and then a very early license (October 22, 2020) despite a paucity of evidence that it actually was helpful in the hospital setting. A variety of problems can arise secondary its use, including liver inflammation, renal insufficiency and renal failure …

“WHO recommended against the drug on November 20, 2020. Few if any other countries used it for COVID apart from the US. A large European trial in adults found no benefit. The investigators felt 3 deaths were due to remdesivir (0.7% of subjects who received it). However, on April 22, 2022 the WHO recommended the drug for a new use: early outpatient therapy in patients at high risk of a poor COVID outcome.”

Remdesivir — a reckless choice for children

Nass goes on to recount how monoclonal antibody treatment centers have been turned into outpatient treatment centers using remdesivir instead, but we still don’t have a lot of data on its effectiveness in early treatment. She continues:

“The FDA just licensed Remdesivir for children as young as one month old. Both hospitalized children and outpatients may receive it. The drug might work in outpatients, but the vast majority of children have a very low risk of dying from COVID.

“If 7 deaths per 1,000 result from the drug, as the European investigators thought in the study of adults cited above, it is possible it will harm or kill more children than it saves.

“Shouldn’t the FDA have waited longer to see what early outpatient treatment did for older ages? Or studied a much larger group of children? Very little has been published on children and remdesivir …

“When we look at the press release issued by Gilead, we learn the approval was based on an open label, single arm trial in 53 children, 3 of whom died (6% of these children died); 72% had an adverse event, and 21% had a serious adverse event.”

Overall, remdesivir appears to be an exceptionally risky treatment choice for young children. Certainly, there are safer early treatment protocols that are very effective. Two other COVID drugs, Paxlovid and Molnupiravir, also have serious safety concerns.

Post-Paxlovid COVID rebound

As reported by Bloomberg, COVID patients treated with a five-day course of Paxlovid sometimes experience severe rebound when the medication is withdrawn.

U.S. government researchers are now planning to study the rate and extent to which the drug is causing SARS-CoV-2 infection to rebound, and whether a longer regimen might prevent it.

Bloomberg describes the post-Paxlovid rebound of David Ho, a virologist at the Aaron Diamond AIDS Research Center at Columbia University:

“Ho said he came down with COVID on April 6 … His doctor prescribed Paxlovid, and within days of taking it, his symptoms dissipated and tests turned negative. But 10 days after first getting sick, the symptoms returned and his tests turned positive for another two days.

“Ho said he sequenced his own virus and found that both infections were from the same strain, confirming that the virus had not mutated and become resistant to Paxlovid. A second family member who also got sick around the same time also had post-Paxlovid rebound in symptoms and virus, Ho says.

“‘It surprised the heck out of me,’ he said. ‘Up until that point I had not heard of such cases elsewhere.’ While the reasons for the rebound are still unclear, Ho theorizes that it may occur when a small proportion of virus-infected cells may remain viable and resume pumping out viral progeny once treatment stops.”

Clinical Director of the Division of Infectious Diseases at Brigham and Women’s Hospital, Dr. Paul Sax, told Bloomberg:

“Providers who are going to be prescribing this should be aware that this phenomenon occurs, and if people have symptoms worsening after Paxlovid, it’s probably still COVID. The big problem is that when this drug was released, this information wasn’t included [on the label].”

Pfizer defends Paxlovid

The U.S. Food and Drug Administration has stated it is “evaluating the reports of viral load rebound after completing Paxlovid treatment and will share recommendations if appropriate.”

The U.S. Centers for Disease Control and Prevention has not yet commented on the findings.

Pfizer, meanwhile, insists the increase in viral load post-treatment “is unlikely to be related to Paxlovid” because viral rebound was found in “a small number” of both the treatment and placebo groups in Pfizer’s final-stage study.

Clifford Lane, deputy director for clinical research at the National Institute of Allergy and Infectious Diseases (NIAID), told Bloomberg that some people may simply “need longer dosing of Pfizer’s drug than the standard five days.”

“There’s two things that suppress the virus: the drug and the host immune response,” he said. “If you stop the drug before the host immune response has had a chance to kick in, you may see the virus come back.”

Molnupiravir supercharges viral mutation

Molnupiravir (sold under the brand name Lagevrio) also has serious safety concerns. This drug was developed by Merck and Ridgeback Therapeutics and approved for emergency use by the FDA December 23, 2021, for high-risk patients with mild to moderate COVID symptoms.

However, not only might it contribute to cancer and birth defects, it may also supercharge the rate at which the virus mutates inside the patient, resulting in newer and more resistant variants. As reported in November 2021 by Forbes contributor and former professor at Harvard Medical School, William Haseltine, Ph.D.:

“… I believe the FDA needs to tread very carefully with molnupiravir, the antiviral currently before them for approval. My misgivings are founded on two key concerns.

“The first is the drug’s potential mutagenicity, and the possibility that its use could lead to birth defects or cancerous tumors. The second is a danger that is far greater and potentially far deadlier: the drug’s potential to supercharge SARS-CoV-2 mutations and unleash a more virulent variant upon the world …

“My concern with molnupiravir is because of the mechanism by which this particular drug works. Molnupiravir works as an antiviral by tricking the virus into using the drug for replication, then inserting errors into the virus’ genetic code once replication is underway. When enough copying errors occur, the virus is essentially killed off, unable to replicate any further …

“But my biggest concern with this drug is … molnupiravir’s ability to introduce mutations to the virus itself that are significant enough to change how the virus functions, but not so powerful as to stop it from replicating and becoming the next dominant variant.”

Haseltine cites prepandemic experiments showing MERS-CoV and the mouse hepatitis virus (MHV) both developed resistance against the drug, thanks to mutations that occurred.

While the central idea behind the drug is that the genetic errors will eventually kill the virus, these experiments showed the viruses were in fact able to survive and replicate to high titers despite having large numbers of mutations throughout their genomes.

The drug did slow down replication, but as noted by Haseltine, “outside of the lab, as the drug is given to millions of people with active infections, this disadvantage may quickly disappear as we would likely provide a prime selection environment to improve the fitness of the virus.”

This risk may be particularly high if you fail to take all the prescribed doses (typically 800 milligrams twice a day for five days).

Experts question usefulness of Molnupiravir

More recently, in a January 10 article, Newsweek cited concerns by professor Michael Lin of Stanford University:

“‘I am very concerned about the potential consequences now that molnupiravir has been approved … It would only be a matter of time, perhaps a very short time, before a lucky set of mutations occurs to create a variant that is more transmissible or immunoevasive …

“The drug simply speeds up that natural process. The hope is that over enough days all the viral copies will have so many mutations that none of the copies can function.’ But Lin said he was concerned that in the real world, there is a possibility that a mutated virus could jump from a patient taking molnupiravir to another individual, citing the relatively modest efficacy of the drug.

“‘For cases that get worse so that people have to go to the hospital, this drug only prevents that from happening 30% of the time. That means 70% of the time the virus isn’t being eliminated quickly enough to make a difference. And we know COVID patients going to hospitals are highly contagious.’

“Lin said the risks could be heightened when a patient does not comply exactly with the dosing schedule of the drug … ‘In any of those situations viruses will have picked up some mutations but not enough to kill all the virus copies,’ he said. ‘The survivors are now mutated, perhaps have picked up immunoevasion and can go on to infect others’ …

“According to Lin, the ‘very low efficacy alone’ should have disqualified the drug from approval … ‘Even if the drug were great we wouldn’t take such a risk, but this drug is worse than any other drug that’s sought approval for COVID-19. It’s completely not worth it.’”

Haseltine also told Newsweek that, “Of all the antiviral drugs I have ever seen, this is by far the most potentially dangerous,” and “The more people that take it, the more dangerous it will be.”

One of the FDA panel members who actually voted against the approval of molnupiravir, James Hildreth, president of Meharry Medical College in Tennessee, wanted Merck to do a better job of quantifying the risk of mutations before approval.

During the panel meeting, he noted that:

“Even if the probability is very low, 1 in 10,000 or 100,000, that this drug would induce an escape mutant which the vaccines we have do not cover, that would be catastrophic for the whole world.”

Government has sold out to Big Pharma

Widespread use of a drug that turbocharges mutation of an already rapidly mutating virus probably isn’t the wisest strategy. Likewise, using drugs that cause high rates of organ failure, like remdesivir, and drugs that causes the virus to rebound with a vengeance, like Paxlovid, don’t seem to be in the best interest of public health either.

The fact that U.S. health authorities have focused on these drugs to the exclusion of all others, including older drugs with high rates of effectiveness and superior safety profiles, sends a very disturbing message.

They’ve basically become extensions of the drug industry and have abandoned their original purpose, which is to protect public health — by ensuring the safety and efficacy of drugs, in the case of the FDA, and by conducting critical science and data analysis in the case of the CDC.

Instead, they seem to be doing everything they can to protect Big Pharma profits, even if it costs you your life. Remdesivir, for example, is an extremely expensive drug, costing between $2,340 and $3,120 depending on your insurance.

Ivermectin, meanwhile — which has been very effective against COVID and shown to outperform at least 10 other drugs, including Paxlovid — costs between $48 and $94 for 20 pills depending on your location. The average cost is said to be about $58 per treatment.

Paxlovid costs $529 per five-day course of treatment, and molnupiravir is around $700. While not quite as expensive as remdesivir, both are still nearly 10 times costlier than ivermectin, which is more effective.

Paxlovid alone has cost U.S. taxpayers $5.29 billion. Just imagine the billions we could have saved had we saner leadership.

Since the FDA and CDC cannot be trusted, it’s imperative to take responsibility for your own health. Do your own research and follow your own conscience and conviction.

Remember, when it comes to COVID-19, early treatment is crucial, and effective protocols are readily available — just not from the FDA, CDC or even most hospitals.

New UK Government Data Shows COVID Injections Kill More People than They Save

Figure 6. Only at the start of the data collection period did the numbers look favorable for the vaccine. They all turn negative over time for Doses 1 and 2 over time meaning the vaccines are nonsensical. No cherry picking required. You can see it visually. Source: All-Cause Mortality by Vaccination Status

From [HERE] and [HERE] New UK government data allows us to analyse the data in a way we couldn’t before. This new analysis shows clearly that the Covid vaccines kill more people than they save for all age groups. In other words, they shouldn’t be used by anyone. The younger you are, the less sense it makes.

“The bottom line is this: finally, the data is publicly available in plain sight that shows clearly that our governments have been publicly killing us with these vaccines and vaccine mandates.” – Steve Kirsch

Anyone can validate the data and methodology. The results make it clear that the Covid vaccines should be halted immediately.

If the vaccines really work, then why hasn’t any government anywhere in the world produced a proper risk-benefit analysis that shows the opposite result?

If the vaccines work, then why do all the lines in Figure 6 below show that Dose 1 and Dose 2 of the vaccines kill more people than they save?

What the data shows

Here’s the result of the analysis.

What this means is that if you are 25 years old, the vaccine kills 15 people for every person it saves from dying from Covid. Below 80, the younger you are, the more nonsensical vaccination is. The cells with * means that the vaccine actually caused more Covid cases to happen than the unvaccinated.

Above 80, the UK data was too confounded to be useful. Until we have that data, it’s irresponsible to make a recommendation.

I describe below how you can compute this yourself from the UK data.

Introduction

One of my friends recently sent me a link to the mortality data from the UK government Office of National Statistics from 1 January 2021 to 31 January 2022. I had not seen this data before so I analysed it.

What I found was absolutely stunning because it was consistent with the VAERS risk-benefit analysis by age that I had done in November 2021.

Where to get the UK government source data

The government data is archived here. You want to open the spreadsheet and look at the spreadsheet tab labelled Table 6.

You can also access the original source at: ONS dataset, Deaths by vaccination status, England, which you can see at the top of the page.

In either case, you click the green button labelled “xlsx” to get the spreadsheet, then go to tab “Table 6”:

England.
Death by vaccination status dataset. Table 6. All-cause, Covid 19, Non-Covid 19 age-specific mortality rates per 100k Person Years.
All age groups (*exc. 10-14yo: Too few deaths. 'Error bars' too wide).https://t.co/fuKiimFqJU
All-cause. pic.twitter.com/7d4ciM9Sr4

— O.S. (@OS51388957) March 22, 2022
Note: The data is from England only, not all of the UK.

Where to get my analysis of the data

I annotated the UK source data and you can download it here. This makes it easier to see what is going on. You can see all the original data and my formulas for calculating the ACM ratios and risk benefit analysis on the Table 6 tab.

It is all in plain sight for everyone to see. I then copied values to the Summary and Exec Summary tabs.

Methodology

I compared the all-cause mortality (“ACM”) for people who got 2 shots at least 6 months ago with the unvaccinated. The 6-month time frame provides a minimum reasonable “runway” to observe the outcomes for the typical “fully vaccinated” person.

Summary of the data

This summary below (which I put on the Summary tab which is to the right of the Table 6 tab) shows the rates of all- cause mortality per 100,000 person-years for each age range and also shows the risk benefit ratio.

The data clearly shows that any mortality benefit you get from taking the vaccine and lowering your risk of death from Covid is more than offset by the mortality you lose from the vaccine itself. This isn’t new. It is something I have been saying since May, 2021. But now I finally found the data where I could calculate it reliably.

In the Pfizer Phase 3 trial, there was a 40% increase in ACM in the vaccinated group. They killed an estimated 7 people for every person they saved from Covid!

In the Pfizer Phase 3 trial, there were a total of 21 deaths in the vaccine group and 15 deaths in the placebo group.

This 40% increase in the all-cause mortality in the trial (21/15=1.4) was of course dismissed as not statistically significant. While that is true, that doesn’t mean we shouldn’t pay attention to the number.

But now, based on the UK data, we know that the result in the Phase 3 trial wasn’t a statistical fluke. Not at all.

In fact, if we look at the risk benefit, we see that we saved 1 life from dying from Covid (1 Covid death in the treatment group vs. 2 Covid deaths in the placebo group= 1 life saved), but there were 7 excess non-Covid deaths (20 – 13).

So, the Pfizer trial showed that for every person we saved from Covid, we killed 7 people. However, the numbers were too small to place a high confidence in this point estimate.

However, I’d argue that Pfizer trial was a best case because:

1. The trial enrolled abnormally healthy people who died at a 10X lower rate than the population (there is a 1% US average death rate per year, yet there were just 15 deaths in the 22,000 placebo arm in 6 months which is a .1% death rate)

2. They were able to get rid of anyone who had a reaction to the first dose without counting them

The most important point though is that the Pfizer trial killed:save ratio of 7:1 and the ACM ratio of 1.4 is consistent with the hypothesis that the vaccine kills more people than it saves.

My ACM risk/benefit estimate using VAERS

This is from a risk/benefit computation I did on 1 November 2021 using the VAERS data to compute the ratio of the # of people killed from the vaccine (V) to the # of people who might be saved from Covid (C) if they took the vaccine and it had 90% effectiveness over 6 months (since we knew it waned over time and variants would change). Of course, that was a conservative estimate of the benefit, but that’s because I wanted to make sure I was on solid ground if attacked.

So now we know that my VAERS calculations approximately match the actual UK data in Figure 1. Since my analysis was deliberately conservative, many of the numbers are smaller than the actuals.

This is another example that people who claim (without evidence) that the VAERS data is too “unreliable to use” are wrong. If it is so unreliable, how did it match the real-world UK results so well?

Note how that VAERS showed exactly the same effect back then that we just learned from this UK data: that the younger you are, the more nonsensical getting vaccinated is.

Our V:C column decreases as you get older (from 6:1 down to 1.8:1) just like column E decreases (from 1.9:1 to 1:1 over the same range) in Figure 2.

Isn’t that an interesting “coincidence”? They are within a factor of 3 of each other.

Confirmation from others

I’m hardly the only person noting that the Covid vaccines kill more people than they save. Other articles show either no benefit at all or a negative benefit.

For example, check out:

  1. 99.6% of Covid deaths in Canada were among fully vaccinated people between April 10-17 which can only happen if the vaccinated have a great ACM than the unvaccinated since there is only an 86% vaccination rate in Canada. This is hard for anyone to explain.

  2. Fully Vaccinated 6x Higher Overall Mortality Than Non-Vaccinated (October 30, 2021)

  3. Follow-up of trial participants found ‘no effect on overall mortality’

Figure 4. Table from the Denmark paper published as a pre-print in the Lancet

4. Horowitz: The failure of the mRNA shots is on display for all with open eyes

Note that the Denmark paper (pre-published in the Lancet) showed overall zero all-cause mortality benefit based on clinical trial data. That’s certainly more optimistic than the UK numbers, but the problem for the vaccine makers is that the UK numbers showed up to 38% of the deaths were from Covid so if the vaccines actually worked and were safe, you’d see a huge ACM benefit and you saw nothing.

Why are we mandating a vaccine with a zero ACM benefit?? No public health official wants to answer questions about that.

What makes this analysis different than previous work

The dataset used here contains both Covid and non-Covid deaths by age. We haven’t had that before.

This enables us, for the first time, to validate the data as we explain in the next section.

In short, the data we have in this dataset is more detailed than in the more frequently cited UK Health Security Agency summaries. [MORE]

CDC Authorities Tracked Millions of Phones to See If Americans Obeyed Useless COVID Shelter in Place Orders which Destroyed People's Livelihoods During Government's COVID Vax Dependency Promotion

From [HERE] The Centers for Disease Control and Prevention (CDC) bought access to location data harvested from tens of millions of phones in the United States to perform an analysis of compliance with curfews, track patterns of people visiting K-12 schools and specifically monitor the effectiveness of policy in the Navajo Nation, according to CDC documents obtained by Motherboard.

The documents also show that although the CDC used COVID-19 as a reason to buy access to the data more quickly, it intended to use it for more general CDC purposes.

Location data is information on a device’s location sourced from the phone, which can then show where a person lives, works and where they went. The sort of data the CDC bought was aggregated — meaning it was designed to follow trends that emerge from the movements of groups of people — but researchers have repeatedly raised concerns about how location data can be deanonymized and used to track specific people.

The documents reveal the expansive plan the CDC had last year to use location data from a highly controversial data broker. SafeGraph, the company the CDC paid $420,000 for access to one year of data, includes Peter Thiel and the former head of Saudi intelligence among its investors. Google banned the company from the Play Store in June.

COVID Shots are Killing People w/o Anyone Noticing. CDC Data Shows Record Numbers (1 Million) of Non-COVID, Excess Deaths Since the Plandemic Began (heart disease, high blood pressure, dementia, etc)

STORY AT-A-GLANCE

  • According to U.S. Centers for Disease Control and Prevention data, more than 1 million excess deaths — that is, deaths in excess of the historical average — have been recorded since the COVID-19 pandemic began two years ago, and this cannot be explained by COVID-19. Deaths from heart disease, high blood pressure, dementia and many other illnesses rose during that time

  • Across the world, death rates have also risen in tandem with COVID shot administration, with the most-jabbed areas surpassing the least-jabbed in terms of excess mortality and COVID-related deaths

  • According to Walgreens data, during the week of April 19 through 25, 2022, 13% of unvaccinated persons tested positive for COVID. Of those who received two doses five months or more ago, 23.1% tested positive, and of those who received a third dose five months or more ago, the positive rate was 26.3%. So, after the first booster shot (the third dose), people are at greatest risk of testing positive for COVID

  • U.K. government data show the all-cause mortality rate is between 100% and 300% greater among people who got their first COVID shot 21 days or more ago. The risk for all-cause death is also significantly elevated among those who got their second dose at least six months ago, and mildly elevated among those who got their third dose less than 21 days ago. As of January 2022, all who got one or more doses at least 21 days ago were dying at significantly elevated rates

  • Other data also show that COVID mortality rates are far higher in areas with high vaccination rates, and risk-benefit analyses reveal the jabs do more harm than good in most age groups

FROM [MERCOLA -PDF] According to U.S. Centers for Disease Control and Prevention data(1), more than 1 million excess deaths — that is, deaths in excess of the historical average — have been recorded since the COVID-19 pandemic began two years ago, and this cannot be explained by COVID-19.

Deaths from heart disease, high blood pressure, dementia and many other illnesses rose during that time.2 "We've never seen anything like it," Robert Anderson, CDC's head of mortality statistics, told The Washington Post in mid-February 2022.3

According to University of Warwick researchers, "the scale of excess non-COVID deaths is large enough for it to be seen as its own pandemic."4 A number of explanations have been offered, including the fact that lockdowns and other COVID restrictions discouraged or prevented people from seeking care. But another, less discussed factor may also be at play.

Across the world, death rates have risen in tandem with COVID shot administration, with the most-jabbed areas surpassing the least-jabbed in terms of excess mortality and COVID-related deaths. This flies in the face of official claims that the shots prevent severe COVID infection and lower your risk of death, be it from COVID or all causes.5

Boosted? You're Now at Highest Risk of COVID

Ever since the announcement that the COVID "vaccines" would be using novel mRNA gene transfer technology, I and many others have warned that this appears to be a very bad idea.

Numerous potential mechanisms for harm have been identified and detailed in previous articles, and we're now seeing some of our worst fears come to bear. "Fully vaccinated" individuals are both more likely to be infected with SARS-CoV-2 and more likely to die, whether from COVID or some other cause.

As reported by investigative journalist Jeffrey Jaxen in the April 22, 2022, Highwire video above, data from Walgreens' COVID-19 tracker6 reveal that COVID-jabbed individuals are testing positive for COVID at higher rates than the unjabbed. What's more, people who got their last shot five months or more ago have the highest risk.

As you can see in the screenshot below, during the week of April 19 through 25, 2022, 13% of unvaccinated tested positive for COVID (with Omicron being the predominant variant). (The data reviewed by Jaxen are from the week of April 10 through 16.)

Of those who received two doses five months or more ago, 23.1% tested positive, and of those who received a third dose five months or more ago, the positive rate was 26.3%. So, after the first booster shot (the third dose), people are at greatest risk of testing positive for COVID.

A deeper dive into the data7 reveals that two doses appear to have been protective for a short while, but after five months, it becomes net harmful. The group faring worst of all is the 12 to 17 cohort, where no one with one dose tested positive, but after the second dose, cases suddenly appear, and get higher still after five months. After the third dose, positive cases drop a bit, but then shoot up higher than ever after five months.8

Deaths by Vaccination Status in the UK

Data sets from the U.K. government reveal an equally disturbing trend. The raw data from the Office for National Statistics9 is difficult to interpret, so Jaxen had data analysts create a bar graph to better illustrate what the data actually tell us. A screenshot from Jaxen's report is below.

Bars going upward are a good thing, as it indicates the risk for all-cause mortality based on vaccination status is either normal or reduced. Bars that dip below zero percent are indicative of increased all-cause mortality, based on vaccination status.

As you can see, the all-cause mortality rate is between 100% and 300% greater among people who got their first dose 21 days or more ago. The risk for all-cause death is also significantly elevated among those who got their second dose at least six months ago, and mildly elevated among those who got their third dose less than 21 days ago. As of January 2022, all who got one or more doses at least 21 days ago were dying at significantly elevated rates.

More Jabs, More COVID Deaths


Everywhere we look, we find trends showing the COVID shots are resulting in higher death rates. Above is an animated illustration10 from Our World In Data, first showing the vaccination rates of South America, North America, Europe and Africa, from mid-December 2020 through the third week of April 2022, followed by the cumulative confirmed COVID deaths per million in those countries during that same timeframe.

Africa has had a consistently low vaccination rate throughout, while North America, Europe and South America all have had rapidly rising vaccination rates. Africa has also had a consistently low COVID mortality rate, although a slight rise began around September 2021. Still, it's nowhere near the COVID death rates of North America, South America and Europe, all of which saw dramatic increases.

Here's another one,11 also sourced from Our World In Data, first showing the excess death rate in the U.S. (the cumulative number of deaths from all causes compared to projections based on previous years), between January 26, 2020, and January 30, 2022, followed by an illustration of the tandem rise of vaccine doses administered and the excess mortality rate. It clearly shows that as vaccination rates rose, so did the excess mortality rate.

Risk-Benefit Analysis Condemns the COVID Jabs

At this point, we also have the benefit of more than one risk-benefit analysis, and all show that, with very few exceptions, the COVID jabs do more harm than good. For example, a risk-benefit analysis12by Stephanie Seneff, Ph.D., and independent researcher Kathy Dopp, published in mid-February 2022, concluded that the COVID jab is deadlier than COVID-19 itself for anyone under the age of 80.

They looked at publicly available official data from the U.S. and U.K. for all age groups, and compared all-cause mortality to the risk of dying from COVID-19. "All age groups under 50 years old are at greater risk of fatality after receiving a COVID-19 inoculation than an unvaccinated person is at risk of a COVID-19 death," Seneff and Dopp concluded. And for younger adults and children, there's no benefit, only risk.

"This analysis is conservative," the authors note, "because it ignores the fact that inoculation-induced adverse events such as thrombosis, myocarditis, Bell's palsy, and other vaccine-induced injuries can lead to shortened life span.

When one takes into consideration the fact that there is approximately a 90% decrease in risk of COVID-19 death if early treatment is provided to all symptomatic high-risk persons, one can only conclude that mandates of COVID-19 inoculations are ill-advised.

Considering the emergence of antibody-resistant variants like Delta and Omicron, for most age groups COVID-19 vaccine inoculations result in higher death rates than COVID-19 does for the unvaccinated."

The analysis is also conservative in the sense that it only considers COVID jab fatalities that occur within one month of injection. As demonstrated by the U.K. data above, the risk of all-cause death is nearly 300% greater for those who got a second dose at least six months ago.

Teens Are at Dramatic Risk of Death From the Jabs

Similarly, an analysis13 of data in the U.S. Vaccine Adverse Events Reporting System (VAERS) by researchers Spiro Pantazatos and Herve Seligmann suggests that in those under age 18, the shots only increase the risk of death from COVID, and there's no point at which the shot can prevent a single COVID death, no matter how many are vaccinated.

If you're under 18, you're 51 times more likely to die from the COVID jab than you are to die from COVID if not vaccinated.

If you're under 18, you're a whopping 51 times more likely to die from the jab than you are to die from COVID if not vaccinated. In the 18 to 29 age range, the shot will kill 16 for every person it saves from dying from COVID, and in the 30 to 39 age range, the expected number of vaccine fatalities to prevent a single COVID death is 15.

Only when you get into the 60 and older categories do the risks between the jab and COVID infection even out. In the 60 to 69 age group, the shot will kill one person for every person it saves from dying of COVID, so it's a tossup as to whether it might be worth it for any given person.

How Many Are We Willing to Sacrifice?

We also have a risk-benefit analysis by researchers in Germany and The Netherlands. The analysis was initially published June 24, 2021, in the journal Vaccines.14 The paper caused an uproar among the editorial board, with some of them resigning in protest.15 In the end, the journal simply retracted it — a strategy that appears to have become norm.

After a thorough re-review, the paper was republished in the August 2021 issue of Science, Public Health Policy and the Law.16 The analysis found that, "very likely for three deaths prevented by vaccination we will have to accept that about two people die as a consequence of these vaccinations," the authors wrote in a Letter to the Editor17 of Clinical and Translational Discovery. Defending their work, they went on to note that:18

"The database we based our analysis on was a large naturalistic study of the BioNTech vaccine in Israel. This was the only study at the time that allowed for a direct estimation of an absolute risk reduction (ARR) in mortality.

Admittedly, the ARR estimate was only available for a short observation period of 4 weeks after the first vaccine dose, a point raised by critics. One might have wanted a longer observation period to bring out the benefit of vaccinations more clearly, and our estimate of a number needed to vaccinate (NNV) of 16 000 to prevent one death might have been overly conservative.

The recently published 6-month interim report of the BioNTech-regulatory clinical trial now covers a period long enough to let us look at this risk benefit ratio once again. In Table S4 of this publication, 14 deaths are reported in the placebo group (n = 21 921) and 15 in the vaccination group (n = 21 926).

Among them, two deaths in the placebo-group were attributed to COVID-19, and one in the vaccination group was attributed to COVID-19 pneumonia. This leads to an ARR = 4.56 × 10–5, and conversely to an NNV = 1/ARR = 21 916 to prevent one death by COVID-19. This shows that our original estimate was not so far off the mark.

The most recent safety report of the German Paul Ehrlich Institute (PEI) that covers all reported side effects since the vaccination campaign began (27 December 2020 until 30 November 202119 ... reports 0.02 deaths per 1000 BioNTech vaccinations or 2 per 100 000 vaccinations.

We had gleaned four mortality cases per 100 000 vaccinations (all vaccines) from the Dutch pharmacovigilance database LAREB. Using the data of Thomas et al., a liberal NNV = 20 000, we can calculate that by 100 000 vaccinations we save five lives.

Using the PEI pharmacovigilance report for the same product, we see that these 100 000 vaccinations are associated with two deaths, while using the LAREB database back in June 2021, they were associated with four deaths across all vaccines and are associated with two deaths in the most recent reports concerning the BioNTech vaccine ... In other words, as we vaccinate 100 000 persons, we might save five lives but risk two to four deaths."

The risk-benefit ratio may be even worse than that, though, as these calculations do not take into account the fact that passive pharmacovigilance data "are notorious for underestimating casualties and side effects," the authors note, or the fact that severe side effects such as myocarditis are affecting young males at a staggering rate, which can reduce lifespan in the longer term.

We Do Not Have a Functioning Pharmacovigilance System

In an August 2021 editorial, editor-in-chief of Science, Public Health Policy and the Law, James Lyons-Weiler, Ph.D., wrote:20

"There are two messages from those who hold appointed offices or other influential positions in Public Health on long-term vaccine safety.

The first message is that long-term randomized double-blinded placebo-controlled clinical trials are not necessary for the long-term study of vaccine safety because we have 'pharmacovigilance'; i.e. long- term post-market safety surveillance that is supported by widely accessible, passive vaccine adverse events tracking systems.

The second message is that any use of those very same vaccine adverse events tracking systems that leads to the inference or conclusion that vaccines might cause serious adverse events or death is unsupported by such systems ...

When those seeking support for public health initiatives, such as a new vaccination program, offer evidence that long-term vaccine safety studies are well in hand due to the possibility of detecting adverse events that happened following vaccination, they are either:

(a) unaware that the vaccine adverse events tracking systems upon which they are basing their confidence about society's ability to detect and track vaccine adverse events are alleged to be unable to be used to infer causal links between health outcomes and vaccination exposure, or:

(b) participating in a disinformation campaign to end scrutiny over the absence of properly controlled long-term randomized clinical trials to assess long- term vaccine safety. Neither of these is sufficient empirical basis for the knowledge claim of long- term safety ...

There must be room for disagreement in science; otherwise, science does not exist. It is sad to bear witness to the fact that science has degenerated into a war against unwanted and inconvenient results, conclusions and interpretations via the process of post-publication retraction for issues other than fraud, grave error in execution, and plagiarism.

The weaponization of the process of retraction of scientific studies is well underway, and it induces a bias that could be called "retraction bias", or, in the case in which a few persons haunt journals in search of studies that cast doubt on their commercial products, a 'ghouling bias,' which leads to biased systematic reviews and warped meta-analyses."

In his editorial, Lyons-Weiler specifically criticized the Vaccine journal for its retraction of the risk-benefit analysis cited above, and mocked the editorial board members who quit in protest, noting that "Rage-quitting is not science."

"The resigning editorial board members' knowledge claim is that no deaths have occurred due to the vaccination program. As helpful as that claim might be to a prescribed narrative, it is not based on empirical evidence, and it is, therefore, unwarranted," Lyons-Weiler wrote.21

"From a Popperian view of science, one can see the fatal flaw in the editorial board members' knowledge claim: if, as they insist, passive vaccine adverse events tracking systems cannot test the hypothesis of causality, then how can editorial board members, resigning or otherwise, know that the events were NOT caused by the vaccine? ...

It is logical to conclude that since passive vaccine adverse event tracking systems do not lend themselves well to testing hypotheses of causality, they do not provide the opportunity to design and conduct sufficiently critical tests of causality, and therefore a replacement system is needed ... one that is suitable to detect risk."

While we may indeed need better pharmacovigilance, there's really no doubt at this point that the COVID jabs are ill-advised for most people. I believe that in the years to come, people will look back at this time and vow to never repeat it. In the meantime, all we can do is look at and assess the data we do have, and make decisions accordingly.

- Sources and References