Dr Peter McCullough reveals the Covid-19 Vaccines are Bioweapons and a CDC whistle-blower

Dr Peter McCullough reveals the Covid-19 Vaccines are Bioweapons and a CDC whistle-blower has confirmed 50,000 Americans have died due to the jabs

BY  ON 

The most highly cited physician on the early treatment of COVID-19 has come out with an explosive new interview that blows the lid off the medical establishment’s complicity in the unnecessary deaths of thousands.

Dr. Peter McCullough said these deaths have been facilitated by a false narrative bent on pushing an all-new, unproven vaccine for a disease that was highly treatable.

He said the alleged Covid-19 virus is a bioweapon and the vaccines represent “phase two” of that bioweapon.

“As this, in a sense, bioterrorism phase one was rolled out, it was really all about keeping the population in fear and in isolation and preparing them to accept the vaccine, which appears to be phase two of a bioterrorism operation,” McCullough said in a June 11 webinar with German attorney Reiner Fuellmich and several other doctors.

He noted:

“Both the respiratory virus and the vaccine delivered to the human body the spike protein, the gain of function target of this bioterrorism research.”

“Now I can’t come out and say all this on national TV today or at any time,” he continued. “But, what we had learned over time is that we could no longer communicate with government agencies. We actually couldn’t even communicate with our propagandised colleagues in major medical centres, all of which appear to be under a spell, almost as if they are hypnotized right now.”

He did not hold back in his criticism of his colleagues in the medical community.

“And doctors, good doctors, are doing unthinkable things, like injecting biologically active messenger RNA that produces this pathological spike protein into pregnant women. I think when the doctors wake up from their trance they’re going to be shocked to think what they’ve done to people.”

McCullough is professor of medicine and vice chief of internal medicine at Baylor University and also teaches at Texas A&M University. He is an epidemiologist, cardiologist and internist and has testified before the Texas State Senate related to COVID-19 treatments. He holds the distinction of being the most widely cited physician in the treatment of COVID-19 with more than 600 citations in the National Library of Medicine.

In the interview McCullough said:

“The first wave of the bioterrorism is a respiratory virus that spread across the world, and affected relatively few people—about one percent of many populations—but generated great fear.”

He said the virus targeted primarily people over 50 with multiple medical conditions. It poses almost no risk to children.

He said 85 percent of the more than 600,000 U.S. deaths could have been prevented with a multi-drug treatment given in the early to mid-point of the disease.

Instead, people were told to stay home and not return to the hospital unless their symptoms got worse, such as severe breathing problems. By then it was too late for many. They were placed on ventilators and died.

The vast majority of doctors jumped in lockstep to follow these erroneous “guidelines” handed down by the World Health Organisation and the U.S. Centre for Disease Control. Those guidelines neglected to place any focus on the treatment of sick patients and, from the beginning, as early as April 2020, started emphasizing the need for a vaccine as the only real hope of beating back the virus.

The federal Vaccine Adverse Event Reporting System [VAERS] logged 5,993 reports of deaths of people injected with the COVID vaccine between Dec. 14, 2020, and June 11, 2021. That’s more than all the deaths reported to VAERS from all other vaccines combined over the last 22 years.

But these numbers, as shocking as they are, don’t scratch the surface of the actual number of dead Americans, said McCullough.

“We have now a whistleblower inside the CMS, and we have two whistleblowers in the CDC. We think we have 50,000 dead Americans. Fifty thousand deaths. So we actually have more deaths due to the vaccine per day than certainly the viral illness by far. It’s basically propagandized bioterrorism by injection.

McCullough added that “every single thing that was done in public health in response to the pandemic made it worse.”

He said the suppression of early COVID treatments, such as hydroxychloroquine and especially Ivermectin, “was tightly linked to the development of a vaccine.”

Without the suppression of the already-available treatments, the government would not have been able to legally grant Emergency Use Authorisation to the three vaccines rushed to market in the USA by Moderna, Pfizer and Johnson and Johnson.

In the case of Moderna, the U.S. government is co-patent holder through the National Institutes of Health, a clear conflict of interest, and confidential documents reveal Moderna sent a coronavirus mRNA vaccine candidate was sent to a US University in December 2019, weeks before Covid-19 was allegedly known to even exist.

“I published basically the only two papers that teach doctors how to treat COVID-19 at home to prevent hospitalisation and death…If treated early, it results in an 85 percent reduction in hospitalisations and death,” McCullough said.

So not only were the vaccines rolled out unnecessarily by suppressing already available, effective treatments, but the FDA and CDC are now covering up tragic numbers of deaths caused by their experimental mRNA injections.

McCullough said he has organized groups around the world that emphasise early treatment.

“Governments have actually tried to block early treatment of Covid patients, so we created a home patient guide,” he said.

“We broke through to the people, and the people who got sick with COVID called in to get medications from mail-order distribution pharmacies. So without the government even knowing what went on, we crushed the epidemic here in the United States towards the end of December and January.

“We basically took care of the pandemic with about 500 doctors and telemedicine services. And to this day we treat about 25 percent of the US COVID-19 population that actually are at high risk, over age 50 with medical problems or present with severe symptoms. And we basically handled the pandemic, and at the same time we’ve tried to keep ourselves above the political fray.”

McCullough said his focus has recently turned to the unnecessary and dangerous injections.

“We are working to change the public view of the vaccine. The public initially accepted the vaccine and we had to kind of slowly turn the ship. Now, in the U.S. the rates of vaccination have been dropping since April 8. Most of the vaccination centres are empty.

“We have a lot going on in the United States. We are engaging more and more attorneys.

Source

COVID-19 Origins Revealed

COVID-19 Origins Revealed


By Mike Adams

June 8, 2021

The cover-up has imploded. Covid-19 was engineered in a lab, and the desperate attempts to hide its true origins are rapidly collapsing.

Over the weekend, even the Wall Street Journal is now catching up to what Natural News reported a year ago, admitting that covid-19 came from a lab. The article is entitled, “The Science Suggests a Wuhan Lab Leak” and carries the subhead, “The Covid-19 pathogen has a genetic footprint that has never been observed in a natural coronavirus.”

Authored by Steven Quay and Richard Muller, the article discusses the genetic fingerprint of the “double CGG” combination that appears in the virus:

Although the double CGG is suppressed naturally, the opposite is true in laboratory work. The insertion sequence of choice is the double CGG. That’s because it is readily available and convenient, and scientists have a great deal of experience inserting it. An additional advantage of the double CGG sequence compared with the other 35 possible choices: It creates a useful beacon that permits the scientists to track the insertion in the laboratory. Now the damning fact. It was this exact sequence that appears in CoV-2.

Despite this, the virologists involved in the gain-of-function research on coronavirus sought to hide the existence of this double CGG fingerprint:

When the lab’s Shi Zhengli and colleagues published a paper in February 2020 with the virus’s partial genome, they omitted any mention of the special sequence that supercharges the virus or the rare double CGG section. Yet the fingerprint is easily identified in the data that accompanied the paper. Was it omitted in the hope that nobody would notice this evidence of the gain-of-function origin?

But in a matter of weeks virologists Bruno Coutard and colleagues published their discovery of the sequence in CoV-2 and its novel supercharged site. Double CGG is there; you only have to look. They comment in their paper that the protein that held it “may provide a gain-of-function” capability to the virus, “for efficient spreading” to humans.

So it’s not just that SARS-CoV-2 was engineered in a lab; the scientists involved in that effort also tried to cover their tracks and deceive the world as millions died.

“The scientific evidence points to the conclusion that the virus was developed in a laboratory,” write Quay and Muller. Yes, we knew that a year ago. Now, the mainstream media is finally beginning to admit to the reality that those of us in the independent media have known all along.

Names you need to know: Peter Daszak (EcoHealth Alliance), Anthony Fauci, Ralph Baric

Some good sources of information about the communist Chinese bioweapons program that was funded by Daszak, Fauci and even the Pentagon:

RedState.com: EXCLUSIVE: High-Ranking Chinese Defector Has ‘Direct Knowledge’ of Several Chinese Special Weapons Programs

Wall Street Journal: The Science Suggests a Wuhan Lab Leak

UK Daily Mail: The Pentagon secretly funneled $39 to Peter Daszak, his charity funded the Wuhan lab

The National Pulse: Fauci’s Boss Admits Funding Wuhan Lab: ‘We Had No Control Over What They Were Doing.’

LifeSiteNews: China Virus “Smoking Gun” Found

The Bulletin of the Atomic Scientists: The origin of COVID: Did people or nature open Pandora’s box at Wuhan?

From the UK Daily Mail:

The Pentagon gave $39 MILLION to Dr. Peter Daszak’s EcoHealth Alliance – the charity that funded coronavirus research at the Wuhan lab accused of being the source of the outbreak, federal data reveals… Federal data seen by DailyMail.com reveals The Pentagon gave $39 million to EcoHealth Alliance, which funded a lab in Wuhan, China, between 2013 and 2020. The Wuhan Institute of Virology is accused of being the source of Covid-19.

From LifeSiteNews:

The Australian Strategic Policy Institute (ASPI) has just uncovered a Chinese book that proves that Chinese military scientists have been working towards the development of a “new era of genetic weapons.” These weapons, the Chinese scientists promised, could be “artificially manipulated into an emerging human disease virus, then weaponized and unleashed.”

In the 2015 volume, called The Unnatural Origin of SARS and New Species of Man-Made Viruses as Genetic Bioweapons, the Chinese military scientists begin by suggesting that World War III would be fought with biological weapons.

And not just any bioweapons.

Coronaviruses, a number of which cause respiratory illnesses in people, were mentioned as a class of viruses that could be readily weaponized. Indeed, the Chinese scientists were even more explicit, pointing out in their paper that the coronavirus that causes Severe Acute Respiratory Syndrome, or SARS, was an ideal candidate for a bioweapon.

From The Bulletin:

It later turned out that the Lancet letter had been organized and drafted by Peter Daszak, president of the EcoHealth Alliance of New York. Daszak’s organization funded coronavirus research at the Wuhan Institute of Virology. If the SARS2 virus had indeed escaped from research he funded, Daszak would be potentially culpable. This acute conflict of interest was not declared to the Lancet’s readers. To the contrary, the letter concluded, “We declare no competing interests.”

Virologists like Daszak had much at stake in the assigning of blame for the pandemic. For 20 years, mostly beneath the public’s attention, they had been playing a dangerous game. In their laboratories they routinely created viruses more dangerous than those that exist in nature. They argued that they could do so safely, and that by getting ahead of nature they could predict and prevent natural “spillovers…”

Researchers at the Wuhan Institute of Virology, led by China’s leading expert on bat viruses, Shi Zheng-li or “Bat Lady,” mounted frequent expeditions to the bat-infested caves of Yunnan in southern China and collected around a hundred different bat coronaviruses.

Shi then teamed up with Ralph S. Baric, an eminent coronavirus researcher at the University of North Carolina. Their work focused on enhancing the ability of bat viruses to attack humans so as to “examine the emergence potential (that is, the potential to infect humans) of circulating bat CoVs [coronaviruses].” In pursuit of this aim, in November 2015 they created a novel virus by taking the backbone of the SARS1 virus and replacing its spike protein with one from a bat virus (known as SHC014-CoV). This manufactured virus was able to infect the cells of the human airway, at least when tested against a lab culture of such cells.

Baric had developed, and taught Shi, a general method for engineering bat coronaviruses to attack other species. The specific targets were human cells grown in cultures and humanized mice.

Peter Daszak celebrates (brags) about engineering the SARS coronavirus to attack human cells

Also from TheBulletin.org:

Shi set out to create novel coronaviruses with the highest possible infectivity for human cells. Her plan was to take genes that coded for spike proteins possessing a variety of measured affinities for human cells, ranging from high to low. She would insert these spike genes one by one into the backbone of a number of viral genomes (“reverse genetics” and “infectious clone technology”), creating a series of chimeric viruses. These chimeric viruses would then be tested for their ability to attack human cell cultures (“in vitro”) and humanized mice (“in vivo”).

On December 9, 2019, before the outbreak of the pandemic became generally known, Daszak gave an interview in which he talked in glowing terms of how researchers at the Wuhan Institute of Virology had been reprogramming the spike protein and generating chimeric coronaviruses capable of infecting humanized mice.

“And we have now found, you know, after 6 or 7 years of doing this, over 100 new SARS-related coronaviruses, very close to SARS,” Daszak says around minute 28 of the interview. “Some of them get into human cells in the lab, some of them can cause SARS disease in humanized mice models and are untreatable with therapeutic monoclonals and you can’t vaccinate against them with a vaccine. So, these are a clear and present danger….

“Daszak: Well I think…coronaviruses?—?you can manipulate them in the lab pretty easily. Spike protein drives a lot of what happen with coronavirus, in zoonotic risk. So you can get the sequence, you can build the protein, and we work a lot with Ralph Baric at UNC to do this. Insert into the backbone of another virus and do some work in the lab.

In disjointed style, Daszak is referring to the fact that once you have generated a novel coronavirus that can attack human cells, you can take the spike protein and make it the basis for a vaccine.

Full details in today’s length Situation Update podcast

Today’s podcast provides the full details, covering the origins of covid, the cover-up attempt and the collapse of the cover-up. Now we know that the spike protein used in covid vaccines is actually a communist Chinese military bioweapon.

We also therefore know that covid-19 vaccines are biological weapons designed to exterminate humanity, since they contain the weaponized spike protein that was specifically engineered to attack human ACE2 receptors, which exist all over the body (not just the lungs).

Remember, Fauci and Daszak helped fund the development of genetically engineered “humanized mice” — mice with human lung tissue — in order to maximize the ability of the virus to infect human beings. This is all now admitted.

Hear the full podcast on Brighteon.com:

 

COVID Vaccine Spike Protein Travels From Injection Site, Can Cause Organ Damage

‘We Made a Big Mistake’ — COVID Vaccine Spike Protein Travels From Injection Site, Can Cause Organ Damage

Research obtained by a group of scientists shows the COVID vaccine spike protein can travel from the injection site and accumulate in organs and tissues including the spleen, bone marrow, the liver, adrenal glands and in “quite high concentrations” in the ovaries.

By Megan Redshaw

COVID vaccine researchers had previously assumed mRNA COVID vaccines would behave like traditional vaccines. The vaccine’s spike protein — responsible for infection and its most severe symptoms — would remain mostly in the injection site at the shoulder muscle or local lymph nodes.

But new research obtained by a group of scientists contradicts that theory, a Canadian cancer vaccine researcher said last week.

“We made a big mistake. We didn’t realize it until now,” said Byram Bridle, a viral immunologist and associate professor at University of Guelph, Ontario. “We thought the spike protein was a great target antigen, we never knew the spike protein itself was a toxin and was a pathogenic protein. So by vaccinating people we are inadvertently inoculating them with a toxin.”

 

Bridle, who was awarded a $230,000 grant by the Canadian government last year for research on COVID vaccine development, said he and a group of international scientists filed a request for information from the Japanese regulatory agency to get access to Pfizer’s “biodistribution study.”

Biodistribution studies are used to determine where an injected compound travels in the body, and which tissues or organs it accumulates in.

“It’s the first time ever scientists have been privy to seeing where these messenger RNA [mRNA] vaccines go after vaccination,” Bridle said in an interview with Alex Pierson where he first disclosed the data. “Is it a safe assumption that it stays in the shoulder muscle? The short answer is: absolutely not. It’s very disconcerting.”

The Sars-CoV-2 has a spike protein on its surface. That spike protein is what allows it to infect our bodies, Bridle explained. “That is why we have been using the spike protein in our vaccines,” Bridle said. “The vaccines we’re using get the cells in our bodies to manufacture that protein. If we can mount an immune response against that protein, in theory we could prevent this virus from infecting the body. That is the theory behind the vaccine.”

“However, when studying the severe COVID-19, […] heart problems, lots of problems with the cardiovascular system, bleeding and clotting, are all associated with COVID-19,”  he added. “In doing that research, what has been discovered by the scientific community, the spike protein on its own is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.”

When the purified spike protein is injected into the blood of research animals, they experience damage to the cardiovascular system and the protein can cross the blood-brain barrier and cause damage to the brain, Bridle explained.

The biodistribution study obtained by Bridle shows the COVID spike protein gets into the blood where it circulates for several days post-vaccination and then accumulates in organs and tissues including the spleen, bone marrow, the liver, adrenal glands and in “quite high concentrations” in the ovaries.

“We have known for a long time that the spike protein is a pathogenic protein, Bridle said. “It is a toxin. It can cause damage in our body if it gets into circulation.”

A large number of studies have shown the most severe effects of SARS-CoV-2, the virus that causes COVID, such as blood clotting and bleeding, are due to the effects of the spike protein of the virus itself.

A recent study in Clinical and Infectious Diseases led by researchers at Brigham and Women’s Hospital and the Harvard Medical School measured longitudinal plasma samples collected from 13 recipients of the Moderna vaccine 1 and 29 days after the first dose and 1-28 days after the second dose.

Out of these individuals, 11 had detectable levels of SARS-CoV-2 protein in blood plasma as early as one day after the first vaccine dose, including three who had detectable levels of spike protein. A “subunit” protein called S1, part of the spike protein, was also detected.

Spike protein was detected an average of 15 days after the first injection, and one patient had spike protein detectable on day 29 — one day after a second vaccine dose — which disappeared two days later.

The results showed S1 antigen production after the initial vaccination can be detected by day one and is present beyond the injection site and the associated regional lymph nodes.

Assuming an average adult blood volume of approximately 5 liters, this corresponds to peak levels of approximately 0.3 micrograms of circulating free antigen for a vaccine designed only to express membrane-anchored antigen.

In a study published in Nature Neuroscience, lab animals injected with purified spike protein into their bloodstream developed cardiovascular problems. The spike protein also crossed the blood-brain barrier and caused damage to the brain.

It was a grave mistake to believe the spike protein would not escape into the blood circulation, according to Bridle. “Now, we have clear-cut evidence that the vaccines that make the cells in our deltoid muscles manufacture this protein — that the vaccine itself, plus the protein — gets into blood circulation,” he said.

Bridle said the scientific community has discovered the spike protein, on its own, is almost entirely responsible for the damage to the cardiovascular system, if it gets into circulation.

Once in circulation, the spike protein can attach to specific ACE2 receptors that are on blood platelets and the cells that line blood vessels, Bridle said. “When that happens it can do one of two things. It can either cause platelets to clump, and that can lead to clotting — that’s exactly why we’ve been seeing clotting disorders associated with these vaccines. It can also lead to bleeding,” he added.

Both clotting and bleeding are associated with vaccine-induced thrombotic thrombocytopenia (VITT). Bridle also said the spike protein in circulation would explain recently reported heart problems in vaccinated teens.

Stephanie Seneff, senior research scientists at Massachusetts Institute of Technology, said it is now clear vaccine content is being delivered to the spleen and the glands, including the ovaries and the adrenal glands, and is being shed into the medium and then eventually reaches the bloodstream causing systemic damage.

“ACE2 receptors are common in the heart and brain,” she added. “And this is how the spike protein causes cardiovascular and cognitive problems.”

Dr. J. Patrick Whelan, a pediatric rheumatologist, warned the U.S. Food and Drug Administration (FDA) in December mRNA vaccines could cause microvascular injury to the brain, heart, liver and kidneys in ways not assessed in safety trials.

In a public submission, Whelan sought to alert the FDA to the potential for vaccines designed to create immunity to the SARS-CoV-2 spike protein to instead cause injuries.

Whelan was concerned the mRNA vaccine technology utilized by Pfizer and Moderna had “the potential to cause microvascular injury (inflammation and small blood clots called microthrombi) to the brain, heart, liver and kidneys in ways that were not assessed in the safety trials.”

More Deaths Reported After J&J, AstraZeneca Vaccines, Plus Researchers Link AstraZeneca to Strokes in Young Adults

More Deaths Reported After J&J, AstraZeneca Vaccines, Plus Researchers Link AstraZeneca to Strokes in Young Adults

The AstraZeneca and Johnson & Johnson COVID vaccines came under scrutiny again this week as more reports of deaths — largely due to blood clot disorders — surfaced in Belgium, Canada and Greece, and a new report linked the AstraZeneca vaccine to strokes in young adults.

By Megan Redshaw

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The AstraZeneca and Johnson & Johnson (J&J) COVID vaccines came under scrutiny again this week as more reports of deaths — largely due to blood clot disorders — surfaced in Belgium, Canada and Greece.

Adding to the vaccine makers’ woes is a new report out of London from researchers who identified the first cases of strokes occurring in young adults who received the AstraZeneca vaccine, which was co-developed by the University of Oxford University in the UK.

Belgium suspends use of J&J vaccine

Belgium said Wednesday it was suspending vaccinations with J&J vaccine, for people under the age of 41, following the death of a woman from blood clots after she received the shot. This is the second time Belgium has paused the one-shot vaccine.

“The Inter-ministerial conference has decided to temporarily administer Janssen’s vaccine to the general population from the age of 41 years, pending a more detailed benefit-risk analysis by the EMA,” said a statement issued by Belgium’s federal health minister and seven regional counterparts.

The woman, who was under the age of 40, died May 21 after being admitted to the hospital with severe thrombosis and platelet deficiency, Reuters reported.

The government asked for urgent advice from the European Union’s drug regulator, the European Medicines Agency (EMA), before it would consider lifting the suspension.

The EMA said it is reviewing the death of the woman in Belgium, along with other reports of blood clots, with the Belgian and Slovenian medicines agencies, and has asked J&J to carry out a series of additional studies to help assess a possible link between the shot and rare blood clots.

J&J said April 20 it would resume the roll-out in the EU of its COVID vaccine, marketed under the company’s Janssen subsidiary — with a warning on its label — after several countries, including Belgium, first paused the vaccine amid concerns of its possible link to blood clotting disorders.

The EMA confirmed a “possible link,” but concluded the vaccine’s benefits outweighed the risks. The drug regulator’s safety committee (PRAC) said a warning should be added to the product label, but the blood clot-related disorders should be listed as “very rare” side effects of the vaccine.

On April 23, the Centers for Disease Control and Prevention (CDC) voted to resume the use of J&J’s vaccine without restrictions after the vaccine was paused to investigate reports of rare blood clots. The recommendation by the CDC’s advisory panel said the link between blood clots and J&J’s COVID vaccine was “plausible,” but concluded the vaccine’s benefits outweighed the risks and recommended use for persons 18 years of age and older in the U.S. under the FDA’s Emergency Use Authorization.

J&J has said no clear causal relationship has been established between its vaccine and blood clots.

Researchers identify strokes in young adults after AstraZeneca shot

The first cases of large-vessel arterial occlusion strokes in young adults linked to AstraZeneca’s vaccine were described in detail for the first time in a letter published online in the Journal of Neurology Neurosurgery & Psychiatry.

The three cases, one of which was fatal, occurred in two women and one man in their 30s or 40s who developed characteristics of vaccine-induced immune thrombotic thrombocytopenia (VITT), a reaction associated with the AstraZeneca vaccine.

“These are the first detailed reports of arterial stroke believed to be caused by VITT after the AstraZeneca COVID vaccine, although stroke has been mentioned previously in the VITT data,” senior author, Dr. David Werring, professor of clinical neurology at the Stroke Research Centre, University College London Queen Square Institute of Neurology, told Medscape Medical News.

“VITT has more commonly presented as CVST (cerebral venous sinus thrombosis) which is stroke caused by a venous thrombosis; these cases are showing that it can also cause stroke caused by an arterial thrombosis,” Werring explained.

Werring noted the reports do not add anything to the overall risk/benefit of the vaccine, as they are describing only three cases. “While VITT is very serious, the benefit of the vaccine still outweighs its risks,” he said.

The first case, a 35-year-old woman, experienced intermittent headaches on the right side and around her eyes for six days after vaccination. Five days later, she awoke feeling drowsy and with weakness to her left face, arm and leg.

Imaging revealed the woman had a blocked right middle cerebral artery with brain infarction and clots in the right portal vein. She underwent brain surgery to reduce the pressure in her skull, plasma removal and replacement, and treatment with anticoagulant and fondaparinux, but suffered brain stem death and subsequently died.

The second case, a 37-year-old woman, presented with headache, confusion, weakness in her left arm and loss of vision on the left side 12 days after vaccination with AstraZeneca. Imaging showed occlusion of both carotid arteries, as well as blood clots in her lungs and brain. She improved clinically with treatment.

The third case occurred in a 43-year-old man who presented 21 days after vaccination with problems speaking. Imaging showed a clot in the left middle cerebral artery. He was treated and remains stable.

The researchers said young patients presenting with ischaemic stroke after receiving AstraZeneca’s vaccine should urgently be evaluated for VITT.

Ontario man dies from ‘rare but real’ blood clot after first dose of AstraZeneca

An Ontario man in his 40s died after receiving his first dose of the AstraZeneca vaccine, public health officials confirmed Tuesday.

Dr. Barbara Yaffe, Ontario’s associate chief medical officer of health, said his death is being investigated, but the man suffered from VITT.

“While the investigation is ongoing and a final cause of death has yet to be officially determined, it has been confirmed that the individual did have VITT at the time of his death,” Yaffe said Tuesday. “The risks associated with this vaccine are [rare], but they are real.”

Chief Medical Officer Dr. David Williams restricted AstraZeneca vaccinations for people who have not yet received the first dose as of May 11, due to a higher-than-expected rate of blood clots.

Greece investigating four cases of blood clots after AstraZeneca shot

Α 63-year-old woman from Greece died of blood clots after vaccination with AstraZeneca. The case was one of four being investigated by the National Organization for Medicines (EOF) for a potential correlation between AstraZeneca’s vaccine and rare blood clots, according to the Greek City Times.

Also in Greece, a 44-year-old woman is in serious condition after experiencing VITT. Her case was the second incident found by EOF to be linked to the vaccine, according to the Greek Reporter.

A third blood clotting incident involved a 35-year-old man from Crete who suffered two blood clots after receiving AstraZeneca’s vaccine. The man was hospitalized after suffering a clot in his leg a few days after getting the jab. He suffered a second blood clot in his brain while hospitalized

As The Defender reported April 7, European regulators said they confirmed a “possible link” between AstraZeneca’s COVID vaccine and “very rare” blood clots, but concluded the benefits of the vaccine still outweigh the risks.

The EMA did not recommend restricting use of the vaccine based on age, gender or other risk factors, but did say cases of blood clotting after vaccination “should be” listed as a possible side effect, according to a statement issued by the agency’s safety committee.

The AstraZeneca vaccine is not yet authorized for use in the U.S.

Nobel Prize winner: Mass COVID vaccination an ‘Unacceptable Mistake’ that is ‘Creating the Variants’

Nobel Prize Winner: Mass Vaccination an "Unacceptable Mistake"

In every country, ‘the curve of vaccination is followed by the curve of deaths,’ the famous virologist said

 

As published on LifeSite News by Celeste McGovern

French virologist and Nobel Prize winner Luc Montagnier called mass vaccination against the coronavirus during the pandemic “unthinkable” and a historical blunder that is “creating the variants” and leading to deaths from the disease.

“It’s an enormous mistake, isn’t it? A scientific error as well as a medical error. It is an unacceptable mistake,” Montagnier said in an interview translated and published by the RAIR Foundation USA yesterday. “The history books will show that, because it is the vaccination that is creating the variants.”

 

Many epidemiologists know it and are “silent” about the problem known as “antibody-dependent enhancement,” Montagnier said.

“It is the antibodies produced by the virus that enable an infection to become stronger,” he said in an interview with Pierre Barnérias of Hold-Up Media earlier this month. 

Vaccination leading to variants

“It is clear that the new variants are created by antibody-mediated selection due to the vaccination.”

Vaccinating during a pandemic is “unthinkable” and is causing deaths, the winner of the 2008 Nobel Prize in Medicine for discovery

‘Deaths follow vaccination’

“The new variants are a production and result from the vaccination. You see it in each country, it’s the same: in every country deaths follow vaccination,” he said.

A video published last week on YouTube uses data from the Institute for Health Metrics and Evaluation at the University of Washington to illustrate the spikes in deaths in numerous countries across the globe after the introduction of COVID vaccination, confirming Montagnier’s observation.

The French interviewer pointed to data from the World Health Organization(WHO) showing that since the vaccines were introduced in January, new infections contamination have “exploded,” along with deaths, “notably among young people.”

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“Yes,” agreed Montagnier who is a professor at Shanghai Jiao Tong University. “With thrombosis, etc.”

Thrombosis – or blood clots — have been an unexpected problem linked to the new coronavirus vaccines and the cause of AstraZeneca’s vaccine being pulled in several countries. The head of Canada’s public health agency, Theresa Tam, told a press conference Tuesday that there are now 21 confirmed cases of vaccine-induced thrombotic thrombocytopenia, or VITT, including among three women who died from the blood-clotting disorder potentially linked to AstraZeneca’s vaccine and another 13 cases are under investigation. 

Breakthrough cases

Montagnier said that he is currently conducting research with those who have become infected with the coronavirus after getting the vaccine. The Centers for Disease Control and Prevention reported in April that it had received 5,800 reports of people who had “breakthrough” COVID after being vaccinated, including 396 people who required hospitalization and 74 patients who died. 

“I will show you that they are creating the variants that are resistant to the vaccine,” Montagnier said.

Coronavirus made in a lab

The famous French virologist created waves in April 2020 when he told a French television station that he believed SARS-CoV2, the new pandemic coronavirus, was man-made in a laboratory. The “presence of elements of HIV and germ of malaria in the genome of coronavirus is highly suspect and the characteristics of the virus could not have arisen naturally,” he said

Though he was ridiculed by French experts for having “a conspiracy vision that does not relate to the real science,” Montagnier published a paper in July 2020 supporting his claims that the novel coronavirus must have originated from human experimentation in a lab – a theory that has recently resurfaced and is currently considered the most likely origin of the virus.

 

To view the original article, please click here

 

 

 

Government Caught “Scrubbing” Covid-19 Vaccine Injuries and Deaths

Government caught "scrubbing" Covid-19 vaccine injuries and deaths

Dr. Peter McCullough, one of the world’s premiere medical doctors who specializes in treating the Wuhan coronavirus (Covid-19), told journalist Alex Newman during a recent interview that the United States government is lying about the true number of Chinese Virus vaccine reactions that are occurring. The government’s strategy, McCullough says, which is coordinated with the Bill & Melinda Gates Foundation and the World Health Organization (WHO), has resulted in tens of thousands of unnecessary deaths that are being ignored or swept under the rug. This is unprecedented because the government has pulled past drugs and vaccines from the market for far less. Between Dec. 14 and April 23, Donald Trump’s “Operation Warp Speed” jabs caused at least 3,544 deaths along with 12,619 serious injuries. Neither the Food and Drug Administration (FDA) nor the Centers for Disease Control and Prevention (CDC), however, are at all concerned. “A typical new drug at about five deaths, unexplained deaths, we get a black-box warning, your listeners would see it on TV, saying it may cause death,” McCullough stated. “And then at about 50 deaths, it’s pulled off the market.” Back in 1976 during the “swine flu” crisis, the U.S. attempted to jab some 55 million Americans but stopped the program after 500 cases of paralysis and 25 deaths were reported. Compare that to the Wuhan Flu shots of today, which are still being aggressively pushed despite untold thousands of injuries and deaths. “In the U.S. today [as of late March] we have approximately 77 million people vaccinated for COVID and we have 2,602 deaths reported, so it’s unprecedented how many deaths have accrued,” McCullough further explained. “Then on March 8 the CDC announced on their website with very little fanfare that they had reviewed about 1,600 deaths with unnamed FDA doctors and they indicated not a single death was related to the vaccine. he added. I think that was concerning in the academic community.”

Wuhan Flu shots are mass genocide

Had the CDC truly conducted such an investigation, McCullough says, it would have taken months to complete. Instead, the CDC rolled it out in a matter of days to declare all of the jabs “safe and effective” so the program would continue. “I have chaired and participated in dozens of data safety monitoring boards and sat on those committees and I can tell you that this type of work would have taken many months to review all the labs, the death certificates and all the circumstances of an event,” McCullough explained. “It is impossible for unnamed regulatory doctors without any experience with COVID-19 to opine that none of the deaths were related to the vaccine.” Another factor to consider is that only about 1-10 percent of all vaccine-related deaths even get logged into the CDC’s Vaccine Adverse Event Reporting System (VAERS). This suggests that many thousands more deaths are not even included in the official numbers. Even without this missing data, Chinese Virus injections are already proving to be far more dangerous than seasonal flu shots. Every year, 20-30 deaths from flu shots are reported to VAERS based on 195 million injections. Wuhan Flu shots, on the other hand, have already caused at least 2,602 deaths based on 77 million injections. “So the U.S. government has made a decision, along with the stakeholders – the CDC, NIH, FDA, Big Pharma, World Health Organization, Gates Foundation – they have made a commitment to mass vaccination as the solution to the COVID pandemic and we are really going to be witness to what’s going to happen in history,” McCullough warns. “We’re sitting on, right now, the biggest number of vaccine deaths, there’s been tens of thousands of hospitalizations, all attributable to the vaccine, and going strong.” More related news can be found at Pandemic.news

Sources for this article include: LeoHohmann.com NaturalNews.com

19,916 ‘eye disorders’ including blindness following COVID vaccine reported in Europe

19,916 ‘eye disorders’ including blindness following COVID vaccine reported in Europe

More than 10,000 reports of eye disorders after COVID shots in the U.K. alone

By Celeste McGovern

May 1, 2021 (LifeSiteNews) – Hundreds of cases of blindness are among the 19,916 reports of “eye disorders” to the World Health Organization’s European drug monitoring agency following injection of experimental COVID-19 vaccines

The nearly 20,000 eye disorders reported to VigiBase, a database for the WHO maintained by the Uppsala Monitoring Centre(UMC) in Uppsalla, Sweden, include:

  • Eye pain (4616)
  • Blurred vision  (3839)
  • Photophobia or light intolerance (1808)
  • Visual impairment (1625)
  • Eye swelling (1162)
  • Ocular hyperaemia or red eyes (788)
  • Eye irritation (768)
  • Itchy eyes or eye pruritus (731)
  • Watery eyes or increased lacrimation (653)
  • Double vision or diplopia (559)
  • Eye strain or asthenopia (459)
  • Dry eye (400)
  • Swelling around the eye or periorbital swelling (366)
  • Swelling of eyelid (360)
  • Flashes of light in the field of vision or photopsia (358)
  • Blindness (303)
  • Eyelid oedema (298)
  • Eye or ocular discomfort (273)
  • Conjunctival haemorrhage or breakage of a small eye vessel (236)
  • Blepharospasm or abnormal contraction of an eye muscle(223)
  • Vitreous floaters (192)
  • Periorbital oedema (171)
  • Eye haemorrhage (169)

More than half of the eye disorders (10, 667) were also reported to the U.K.’s Yellow Card adverse event reporting system. These would have followed injection primarily of AstraZeneca’s and Pfizer’s COVID-19 vaccines but included eight reports of eye disorders among the 228 reports concerning Moderna’s vaccine, of which only 100,000 first doses had been administered by April 21.

Eye disorders were not reported in the clinical trials for vaccines which have been granted Emergency Use Authorization (EUA) only. The U.S. Food and Drug Administration’s fact sheet for those administering Pfizer’s experimental vaccine does not mention eye side effects. It does state, however, that “Additional adverse reactions, some of which may be serious, may become apparent with more widespread use of the Pfizer-BioNTech COVID-19 Vaccine.”

VAERS reports

VigiBase and Yellow Card reports do not offer details of the patients’ experiences of adverse side-effects. However, those in the U.S. Vaccine Adverse Event Reporting System (VAERS) system include some reporting on the patient, his or her age, and the general case presentation.

One VAERS report describes a 33-year-old pilot from Mississippi who took Pfizer’s vaccine and developed vision problems among numerous other symptoms.

“I noticed a headache in the very top of my head within an hour of getting the vaccine,” he reported. “I thought it was normal because everyone I know said they got a headache from it. Over the next few hours, the pain moved down the back of my neck and became a burning sensation at the bottom of my skull.”

“Two days after receiving the vaccine I flew my plane and immediately noticed something was wrong with me,” the report continues. “I was having a very hard time focusing. Approximately 2 hours into my flying I felt sudden and extreme pressure in my head and nearly blacked out. I immediately landed and stopped flying.”

The pilot experienced the same thing two days later when he tried flying again. The burning in his neck intensified and was accompanied by dizziness, nausea, disorientation, confusion, uncontrollable shaking, and tingling in his toes and fingers.

The patient was diagnosed with vertigo and prescribed a medication which provided “no relief,” according to the VAERS account. He underwent extensive testing including balance, eye, and hearing tests, CT and MRI scans, and he was informed that an allergic reaction to the Pfizer COVID vaccine had increased the pressure in his spinal cord and brain stem.

“That pressure causes my vision problems and ultimately ruptured my left inner ear breaking off several crystals in the process,” the report states.  “I cannot fly with this condition. I’m currently taking Diamox to reduce the pressure in my spinal cord and brain stem.”

More than 1,200 reports to VAERS include “eye pain” among the listed symptoms. One report filed by a 50-year-old physician from Wisconsin for himself said he experienced “severe sweating; fever; weakness” and the “worst headache of my life” following receiving a second dose of Pfizer’s Wuhan coronavirus vaccine in January.  The doctor said he experienced “searing eye pain for the last 2 months” and “daily headaches” – events described as a “disability” and “permanent damage.”

One 26-year-old student in California received Johnson & Johnson’s vaccine on April 9 and reported experiencing “typical” post-vaccine symptoms of nausea, muscle aches, chills, fatigue which “dissipated.” On the fifth day following the shot, however, she went for a light walk in the morning and “completely lost vision in both eyes.” She also described her “excruciating headache behind eyes” as the “worst headache of my life.” At a hospital emergency ward she was given morphine which she reported did not help the pain and a head CT scan ruled out a clotting event. Her report filed six days later, said: “I’m terrified because I know something is very wrong.”

‘Frightening, stressful, and uncertain’

Michelle Jorgenson, 31, of Arizona got her first dose of Moderna’s vaccine in mid-January, and second dose mid-February and developed blurred vision along with symptoms of headaches, “brain fog” and fatigue. She’s undergone CT and MRI scans and doctors don’t know what’s causing her problems,” she said.

“It’s frightening, stressful, and uncertain. I’m 31, and I have never in my life had double vision before,” she says.

Jorgenson said illness is affecting her ability to both work and drive. “I’m not currently driving at all, as it is just not safe.”

She has cut her at-home work schedule from 40 hours per week to about 25 hours per week, “but that’s also a struggle, because of the double vision, headache, brain fog, and fatigue.”

“I don’t know what the doctors can do from here,” she said.

Bleeding and clotting disorders

Numerous vision problems are associated with hemorrhaging and blood clotting incidents:

  • A 25-year-old from Massachusetts began experiencing symptoms on the day of receiving her first dose of Moderna’s vaccine in January and an MRI revealed “inflammation, and brain bleed and swelling,” according to the VAERS reportfiled by a healthcare professional.
  • An 83 year-old from Indiana who had Moderna’s vaccine and went blind in her left eye the same day. “Went to emergency room at Hospital Was told I have Blood clot in my eye causing the blindness and Ophthamologist says it will probably be permanent,” her report states.
  • A 50-year-old woman from Oklahoma with no prior health conditions experienced a central retinal vein occlusion (CRVO) 2 and ½ hours after receiving a second dose of Pfizer’s COVID-19 vaccine resulted in loss of sight to her right eye, according to another VAERS report. “I am currently prescribed baby aspirin and will have to get injections in my eye when macular edema occurs, an expected occurrence with a blood clot in the retinal vein.”
  • “Within 12 hours of receiving the 2nd dose of the Moderna vaccine, I experienced an occipital cerebral infarction in the left occipital lobe,” states the VAERS report of a 73-year-old Florida man. “As a result, I have a loss of peripheral vision in the right upper quadrant.”
  • Another VAERS report describes a 68-year-old California man’s four-day hospitalization and numerous interventions after his first dose of Pfizer’s vaccine: “Permanent loss of vision in right eye three weeks after receiving first COVID 19 vaccination. Diagnosed with Branch Retina Artery Occlusion (BRAO) clotting of the retinal artery.”

Previous coronavirus

Pennsylvania immunologist Hooman Noorchashm has warned about the potential for vaccinating the 20% to 30% of people who have already had a recent or underlying COVID infection may lead to catastrophic events. That may be the reason why a 52-year-old man from Michigan who was diagnosed with COVID-19 on December 13, 2020 who then received a series of shots on December 22 and January 10, 2021 was diagnosed one day after his second shot with opthalmic artery thrombus causing vision loss in his left eye.

Allergic eye disorders

Some eye disorders happened in the context of severe allergic or “anaphylactic” or “anaphylactoid” events for which there are 915 VAERS report. More than 60 reports refer to “anaphylaxis” and eye symptoms in the same event, as in the case of a 55-year-old asthmatic woman with food allergies who had a reaction to Pfizer’s second dose of COVID vaccine and according a VAERS report was put “under the care of an eye doctor for her severe double vision, eye crossing, and eye drooping.”

Shingles

Some eye pain reports are in association with herpes – or shingles — infection, which has already been raised as a potential elevated risk factor following COVID vaccination. According to a report on one 30-year-old woman, her “severe right side eye pain” and “vesicular rash with severe pain above right eyelid” developed after she got her Johnson & Johnson one-shot in January. She was diagnosed with Zoster Ophthalmicus of Right Eye and treated in urgent care. After her rash crusted she still had residual severe neuropathic pain at the time of the report nine days later.

Uveitis

In Great Britain, 35 reports of uveitis – an inflammation of the middle layer of the eye – following coronavirus vaccination were generated by April 21, about four months following the vaccines rollout in December.

This may seem a small number except that one 2016 study that looked for cases of “vaccine-associated” uveitis found 289 reports over 26 years of data from three databases – which works out to about 11 cases per year for all vaccinations. In which case, reports for uveitis are many fold higher than what one would expect to see from vaccination.

“The nature of Yellow Card reporting means that reported events are not always proven side effects,” according to the government website that catalogues the reports. “Some events may have happened anyway, regardless of vaccination.”

While public health officials have frequently stated that vaccine adverse events are only “one or two in a million” shots, the Medicines and Healthcare products Regulatory Agency (MHRA) for Britain states that for the Pfizer/BioNTech and AstraZeneca vaccines, the overall reporting rate is “around 3 to 6 Yellow Cards per 1,000 doses administered.”

As well, because both the U.S. VAERS the U.K. Yellow Card are passive collections systems, they tend to capture only a fraction of adverse events. A Harvard Pilgrim Healthcare study found that less than one percent of vaccine adverse events are reported to VAERS.

Asked about the high numbers of reported adverse eye events, a spokesperson for the MHRA, which oversees Yellow Card reports, said in an emailed statement: “We continually review Yellow Card data, as well as other data sources, to determine if reports may indicate any previously unrecognised risks.”

The statement added that the agency applies “statistical techniques” which compare events to what would be expected generally in the population.  

“Everything has to be looked at on a case by case basis, and there is no set trigger to determine whether something may be linked to a vaccine,” the MHRA statement said. “All reports are kept under review taking into account the information available and whether there are other plausible explanations.”

Among the 12,140 adverse events reported to Canada’s coronavirus vaccine adverse event reporting system by April 23, there is not a single account of an eye disorder— which, given the extraordinarily high numbers in other countries, raises questions about Canada’s reporting process.

COVID-Vaccinated Can ‘Shed’ Spike Protein, Harming Unvaccinated

America’s Frontline Doctors: COVID-vaccinated can ‘shed’ spike protein, harming unvaccinated

As these experimental vaccines create ‘spike proteins,’ vaccinated individuals ‘can shed some of these particles to close contacts’ causing disease in them, including in children.

By Patrick Delaney

 

LOS ANGELES, California, May 3, 2021 (LifeSiteNews) — In their latest issue brief, America’s Frontline Doctors (AFLDS) warned how spike proteins resulting from experimental COVID-19 gene therapy vaccines have the capacity to 1.) pass through the “blood-brain barrier” causing neurological damage, 2.) be “shed” by the vaccinated, bringing about sickness in unvaccinated children and adults, and 3.) cause irregular vaginal bleeding in women.

Released last week and titled “Identifying Post-vaccination Complications & Their Causes: an Analysis of Covid-19 Patient Data,” the stated purpose of the document is “to provide additional information for concerned citizens, health experts, and policymakers about adverse events and other post-vaccination issues resulting from the three experimental COVID-19 vaccines currently administered under EUA (emergency use authorization)” by the U.S. Food and Drug Administration (FDA).

The non-profit organization highlighted the thousands of adverse events which are related to these “vaccines” and captured by the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS). “Yet these complications have received a fraction of the attention paid to J&J’s blood-clotting controversy,” they lamented with dismay, asking, “Why?”

In taking a closer look at this data, AFLDS presents “some major categories of concern as-yet publicly unaddressed by either the FDA or CDC,” asserting that failure of these regulators “to consider these and other ‘known unknowns’ is a dereliction of basic medical research.”

They breakout their general categories of concern as shown below:

First, there are significant fears regarding the wide distribution of these new vaccines, which employ a new technology and remain only experimental without full approval from the FDA. Instead of employing an attenuated antigen response – as happens with conventional vaccines – these experimental agents introduce something called a “spike protein” into one’s system.

“It takes years to be sure something new is safe,” the AFLDS document confirms. “No one knows definitively the long-term health implications for the body and brain, especially among the young, related to this spike protein. In addition, if documented problems with the protein do arise, there will never be any way to reverse the adverse effects in those already vaccinated.”

Second, unlike conventional vaccines, these spike proteins, along with “lipid nanoparticles” have the capacity to pass through the “blood-brain barrier” which provides special protection for these sensitive areas of the body.

“There simply has not been enough time to know what brain problems and how often a brain problem will develop from that,” the document warns.

Risks from such penetration include “chronic inflammation and thrombosis (clotting) in the neurological system, contributing to tremors, chronic lethargy, stroke, Bell’s Palsy and ALS-type symptoms. The lipid nanoparticles can potentially fuse with brain cells, resulting in delayed neuro-degenerative disease. And the mRNA-induced spike protein can bind to brain tissue 10 to 20 times stronger than the spike proteins that are (naturally) part of the original virus.”

Third, as these experimental vaccines produce many trillions of spike proteins in their recipients, these vaccinated individuals “can shed some of these (spike protein) particles to close contacts,” causing disease in them.

In an email correspondence with LifeSiteNews, Dr. Simone Gold, the founder of AFLDS, directed this writer to an April 29 tweet where she posted a document from Pfizer’s experimental trials in which the pharmaceutical giant “acknowledges this mechanism” of potential shedding, she wrote. 

As the document states, one can be “exposed to [the] study intervention due to environmental exposure,” including “by inhalation or skin contact” with someone involved in the study, or with another who has been exposed in the same way.

And this, according to AFLDS, can be dangerous. As the issues brief continues, “the spike proteins are pathogenic (‘disease causing’) just like the full virus.” Furthermore, these “spike proteins bind more tightly than the fully intact virus” and thus cases around the world of “pericarditis, shingles, pneumonia, blood clots in the extremities and brain, Bell’s Palsy, vaginal bleeding and miscarriages have been reported in persons who are near persons who have been vaccinated.” Such shedding also “appears to be causing wide variety of autoimmune disease (where the body attacks its own tissue) in some persons.”

In addition, other more serious dangers to even the unvaccinated are possible due to the fact that these “spike proteins can cross the blood brain barrier, unlike traditional vaccines.”

Fourth, such shedding leaves children vulnerable if they are in proximity to parents and teachers who have received these experimental vaccines. While the threat of COVID-19 to the young is rightly described as “irrelevant,” including a 99.997% survival rate for those under 20 years of age, AFLDS is concerned some children may become symptomatic due to such proximity to the vaccinated. At such point there is a danger that “public health bureaucrats” might use such cases to “speculate that a child’s illness is related to a SARS-CoV-2 ‘variant,’” when it is a result of contact with vaccinated adults.

“Our other concern is that children could develop long-term chronic autoimmune disease including neurological problems due to the fact that children have decades ahead of them and trillions of the spike proteins mentioned above.”

Fifth, “AFLDS is aware of thousands of reports involving vaginal bleeding, post-menopausal vaginal bleeding, and miscarriages following COVID-19 vaccination as well as anecdotal reports of similar adverse events among those in close contact with the vaccinated.” While at this point the independent physicians organization “cannot comment definitively on the close contacts” other than to mention they “have heard reports of this worldwide,” the many reported incidents of post-vaccination vaginal bleeding establishes a clear “connection between the vaccine and irregular bleeding.”

“Despite this clear-cut evidence, menstrual-cycle changes were not listed among the FDA’s common side effects in its phase-three clinical participants. Women’s reproductive health needs to be taken seriously rather than waved away by agenda-driven public health officials,” the brief reads.

Finally, acknowledging the “irrepressible economic incentive among pharmaceutical companies” to market unnecessary and dangerous childhood COVID vaccinesboosters, and the like, AFLDS insists “Public health experts should stop and assess data on possible vaccine side effects and related post-vaccination questions before it is too late.”

 

EXCLUSIVE – Former Pfizer VP “Government is Lying to You”

EXCLUSIVE - Former Pfizer VP: ‘Your government is lying to you in a way that could lead to your death.’

Dr. Mike Yeadon

‘Look out the window, and think, “why is my government lying to me about something so fundamental?” Because, I think the answer is, they are going to kill you using this method. They’re going to kill you and your family.’

Published on LifeSite News By Patrick Delaney

Dr. Michael Yeadon, Pfizer’s former Vice President and Chief Scientist for Allergy & Respiratory who spent 32 years in the industry leading new medicines research and retired from the pharmaceutical giant with “the most senior research position” in his field, spoke with LifeSiteNews.

He addressed the “demonstrably false” propaganda from governments in response to COVID-19, including the “lie” of dangerous variants, the totalitarian potential for “vaccine passports,” and the strong possibility we are dealing with a “conspiracy” which could lead to something far beyond the carnage experienced in the wars and massacres of the 20th century.

His main points included:

1. There is “no possibility” current variants of COVID-19 will escape immunity. It is “just a lie.”

2. Yet, governments around the world are repeating this lie, indicating that we are witnessing not just “convergent opportunism,” but a “conspiracy.” Meanwhile media outlets and Big Tech platforms are committed to the same propaganda and the censorship of the truth.

3. Pharmaceutical companies have already begun to develop unneeded “top-up” (“booster”) vaccines for the “variants.” The companies are planning to manufacture billions of vials, in addition to the current experimental COVID-19 “vaccine” campaign.

4. Regulatory agencies like the U.S. Food and Drug Administration and the European Medicines Agency, have announced that since these “top-up” vaccines will be so similar to the prior injections which were approved for emergency use authorization, drug companies will not be required to “perform any clinical safety studies.”

5. Thus, this virtually means that design and implementation of repeated and coerced mRNA vaccines “go from the computer screen of a pharmaceutical company into the arms of hundreds of millions of people, [injecting] some superfluous genetic sequence for which there is absolutely no need or justification.”

6. Why are they doing this? Since no benign reason is apparent, the use of vaccine passports along with a “banking reset” could issue in a totalitarianism unlike the world has ever seen. Recalling the evil of Stalin, Mao, and Hitler, “mass depopulation” remains a logical outcome.

7. The fact that this at least could be true means everyone must “fight like crazy to make sure that system never forms.”

Dr. Yeadon began identifying himself as merely a “boring guy” who went “to work for a big drug company … listening to the main national broadcast and reading the broad sheet newspapers.”

Continuing, he said: “But in the last year I have realized that my government and its advisers are lying in the faces of the British people about everything to do with this coronavirus. Absolutely everything. It’s a fallacy this idea of asymptomatic transmission and that you don’t have symptoms, but you are a source of a virus. That lockdowns work, that masks have a protective value obviously for you or someone else, and that variants are scary things and we even need to close international borders in case some of these nasty foreign variants get in.

“Or, by the way, on top of the current list of gene-based vaccines that we have miraculously made, there will be some ‘top-up’ vaccines to cope with the immune escape variants.

“Everything I have told you, every single one of those things is demonstrably false. But our entire national policy is based on these all being broadly right, but they are all wrong.”

‘Conspiracy’ and not just ‘convergent opportunism’

“But what I would like to do is talk about immune escape because I think that’s probably going to be the end game for this whole event, which I think is probably a conspiracy. Last year I thought it was what I called ‘convergent opportunism,’ that is a bunch of different stakeholder groups have managed to pounce on a world in chaos to push us in a particular direction. So it looked like it was kind of linked, but I was prepared to say it was just convergence.”

“I [now] think that’s naïve. There is no question in my mind that very significant powerbrokers around the world have either planned to take advantage of the next pandemic or created the pandemic. One of those two things is true because the reason it must be true is that dozens and dozens of governments are all saying the same lies and doing the same inefficacious things that demonstrably cost lives.

“And they are talking the same sort of future script which is, ‘We don’t want you to move around because of these pesky varmints, these “variants”’— which I call ‘samiants’ by the way, because they are pretty much the same — but they’re all saying this and they are all saying ‘don’t worry, there will be “top-up” vaccines that will cope with the potential escapees.’ They’re all saying this when it is obviously nonsense.”

Possible end game: vaccine ‘passports’ tied to spending allowances, thorough control

“I think the end game is going to be, ‘everyone receives a vaccine’… Everyone on the planet is going to find themselves persuaded, cajoled, not quite mandated, hemmed-in to take a jab.

“When they do that every single individual on the planet will have a name, or unique digital ID and a health status flag which will be ‘vaccinated,’ or not … and whoever possesses that, sort of single database, operable centrally, applicable everywhere to control, to provide as it were, a privilege, you can either cross this particular threshold or conduct this particular transaction or not depending on [what] the controllers of that one human population database decide. And I think that’s what this is all about because once you’ve got that, we become playthings and the world can be as the controllers of that database want it. “For example, you might find that after a banking reset that you can only spend through using an app that actually feeds off this [database], your ID, your name, [and] your health status flag.”

“And, yes, certainly crossing an international border is the most obvious use for these vaccine passports, as they are called, but I’ve heard talk of them already that they could be necessary for you to get into public spaces, enclosed public spaces. I expect that if they wanted to, you would not be able to leave your house in the future without the appropriate privilege on your app.

“But even if that’s not [the] true [intent of the vaccine campaign], it doesn’t matter, the fact that it could be true means everyone [reading] this should fight like crazy to make sure that [vaccine passport] system never forms.”

“[With such a system], here is an example of what they could make you do, and I think this is what they’re going to make [people] do.

“You could invent a story that is about a virus and its variations, its mutations over time. You could invent the story and make sure you embed it through the captive media, make sure that no one can counter it by censoring alternative sources, then people are now familiar with this idea that this virus mutates, which it does, and that it produces variants, which is true [as well], which could escape your immune system, and that’s a lie.

“But, nevertheless, we’re going to tell you it’s true, and then when we tell you that it’s true and we say ‘but we’ve got the cure, here’s a top-up vaccine,’ you’ll get a message, based on this one global, this one ID system: ‘Bing!’ it will come up and

say ‘Dr. Yeadon, time for your top-up vaccine. And, by the way,’ it will say ‘your existing immune privileges remain valid for four weeks. But if you don’t get your top-up vaccine in that time, you will unfortunately detrimentally be an “out person,” and you don’t want that, do you?’ So, that’s how it’ll work, and people will just walk up and they’ll get their top-up vaccine.”

Gov’t lies, Big Pharma moves forward, medicine regulators get out of the way, and possible ‘mass-depopulation’

“But I will take you through this, Patrick, because I am qualified to comment. I don’t know what Vanden Bossche is about. There was no possibility at all, based on all of the variants that are in the public domain, 4000 or so of them, none of them are going to escape immunity [i.e. become more dangerous].

“Nevertheless, politicians and health advisers (to loads of governments) are saying that they are. They’re lying. Well, why would you do that?

“Here’s the other thing, in parallel, pharmaceutical companies have said, several of them, it will be quite easy for us to adjust our gene-based vaccines, and we can hasten them through development, and we can help you.

“And here’s the real scary part, global medicines regulators like [the U.S. Food and Drug Administration] FDA, the Japanese medicines agency, the European Medicines Agency, have gotten together and announced … since top-up vaccines will be considered so similar to the ones that we have already approved for emergency use authorization, we are not going to require the drug companies to perform any clinical safety studies.

“So, you’ve got on the one hand, governments and their advisers that are lying to you that variants are different enough from the current virus that, even if you’re immune from natural exposure or vaccination, you’re a risk and you need to come and get this top-up vaccine. So, I think neither of those are true. So why is the drug company making the top-up vaccines? And [with] the regulators having got out of the way — and if Yeadon is right, and I’m sure I am or I wouldn’t be telling you this — you go from the computer screen of a pharmaceutical company into the arms of hundreds of millions of people, some superfluous genetic sequence for which there is absolutely no need or justification.

“And if you wanted to introduce a characteristic which could be harmful and could even be lethal, and you can even tune it to say ‘let’s put it in some gene that will cause liver injury over a nine-month period,’ or, cause your kidneys to fail but not until you encounter this kind of organism [that would be quite

possible]. Biotechnology provides you with limitless ways, frankly, to injure or kill billions of people.

“And since I can’t think of a benign explanation for any of the steps: variants, top-up vaccines, no regulatory studies… it’s not only that I cannot think of a benign explanation, the steps described, and the scenario described, and the necessary sort of resolution to this false problem is going to allow what I just described: unknown, and unnecessary gene sequences injected into the arms of potentially billions of people for no reason.

“I’m very worried … that pathway will be used for mass depopulation, because I can’t think of any benign explanation.”

‘Absurdly impossible’ variants will escape immunity, ‘just a lie’

“If I can show you that one major thing that governments around the world are telling the people is a lie, you should take my 32 years of experienced opinion that says, most of it, if not all of it, is a lie.”

“The most different variant is only 0.3% different from the original sequence as emailed out of Wuhan in … January 2020. 0.3% [is] the one [variant] that is the most different on the planet so far. And now another way of saying it is, ‘all of the variants are not less than 99.7% identical to each other.’

“Now, you might be thinking, ‘hmm, .3%, is that enough [to escape immunity and become more dangerous]?’ The answer is no. Get away, ya know, get out of here …

“The human immune system is a thing of wonder. What it does is when it faces a new pathogen like this, you’ve got professional cells, they’re called professional antigen-presenting cells —they’re kind of rough tough things that tend not to succumb to viruses. And their job is to grab foreign things in the near environment and tear them limb from limb [inside the cell]. They really cut them up into hundreds of pieces. And then they present these pieces on the surfaces of their cell to other bits of your immune system, and amazingly, because of the variability that God and nature gave you, huge variability to recognize foreign things, and your body ends up using 15 to 20 different specific motifs that it spots about this virus. They’re called epitopes, basically they’re just like little photographs of the details about this virus. That’s what they do. And that is what is called your repertoire, your immune repertoire is like 20 different accurate photographs, close-ups, of different bits of this virus.

“Now, if a tiny piece of the virus changes, like the .3% I’ve just described, if you are reinfected by that variant, your professional cells tear into that virus and cut it

into pieces, present them again, and lo and behold, most of the pieces that you have already seen and recognized, are still there in the variants.

“There is absolutely no chance that all of them will fail to be recognized and that is what is required for immune escape, to escape your immunity. It must present to you as a new pathogen. It must be sufficiently different that, when it is cut up by your professional checker cells, it won’t find mostly the same thing it has seen before. And that is just absurdly impossible when you have only varied .3%, so it is 99.7% (similar). “You can go and check that by looking at papers by a person called Alison Tarke. There is also Shane Crotty, and all of the other co-authors.

“And before them, coming from my theoretical understanding of multi-locus immunity, which is what I just badly tried to describe, to what actually happens … If your [immune system] is presented with something that contains even half of those similar pieces, there is no way your body will say, ‘that’s a new pathogen.’

“And, so, the idea that 0.3% could even have a chance of getting around immunity is just a lie. It’s not [even] like an opinion difference.

“I don’t think 3% would be enough. That’s 10 times more variation than has occurred in 16 months [with this virus]. I don’t even think 30% difference would be enough. So, I’m saying that 100 times more variation than has actually happened, would still leave me putting a big bet on the human immune system not being fooled that these are new pathogens.

“I’ve chatted this over with several professors of immunology and they agreed with me, it’s like, ‘why are you asking me this?’

“So, I think that what I’ve just said is that governments and their advisors in multiple countries are lying about variants. That’s a massive thing! You should check it out. Your readers should check it out. If it’s true, don’t you think it’s terrifying?! It was when I realized it.

“So, they’re lying about variants, and then, of course, since [the variants] are not really different, you do not need a ‘top-up’ vaccine. Now you should be getting the hairs on the back of your neck up, because they are making them right now!” “They are making billions of vials of it. And they will be available by the end of the year.

“And I think they’ll require people to first, be on the vaccine passport one-world database, and then it will roll up into the top-ups, and if it takes a bit longer it will take a bit longer.

“But this is not going away. It won’t go away until enough people, if they ever do, say ‘you’re a bunch of frauds and we are taking our freedoms back, so you can just stop doing this.’

“Because one person shouting into the wilderness and all of the other academics looking the other way, will have us just going down this pipe maybe a week later than if I hadn’t said anything, but we’re still going down to hell.

“So, that’s why I’m frightened.

“The variants aren’t different. I call them ‘samiants’… they’re pretty much the same. They’re not different. Therefore, you don’t need a top-up vaccine, so don’t go near any of them.”

‘Why is my government lying to me?’ Because ‘they are going to kill you.’

“[And if you recognize that our governments are involved in a major verifiable lie], don’t just turn your computer off and go to supper. Stop. Look out the window, and think, ‘why is my government lying to me about something so fundamental?’ Because, I think the answer is, they are going to kill you using this method. They’re going to kill you and your family.

“The eugenicists have got hold of the levers of power and this is a really artful way of getting you to line-up and receive some unspecified thing that will damage you. I have no idea what it will actually be, but it won’t be a vaccine because you don’t need one. And it won’t kill you on the end of the needle because you would spot that.

“It could be something that will produce normal pathology, it will be at various times between vaccination and the event, it will be plausibly deniable because there will be something else going on in the world at that time, in the context of which your demise, or that of your children will look normal.

“That’s what I would do if I wanted to get rid of 90 or 95% of the world’s population. And I think that’s what they’re doing.”

“Now I don’t know [for certain] that they’re going to use that [system] to kill you, but I can’t think of a benign reason, and with that power they certainly could harm you, or control you, so you should object [and strenuously oppose it].”

People can’t deal with this level of evil, but Soviets, Hitler, Mao show its possibility

“It’s become absolutely clear to me, even when I talk to intelligent people, friends, acquaintances … and they can tell I’m telling them something important, but they get to the point [where I say] ‘your government is lying to you in a way that could lead to your death and that of your children,’ and they can’t begin to engage with it. And I think maybe 10% of them understand what I said, and 90% of those blank their understanding of it because it is too difficult. And my concern is, we are going to lose this, because people will not deal with the possibility that anyone is so evil…

“But I remind you of what happened in Russia in the 20th Century, what happened in 1933 to 1945, what happened in, you know, Southeast Asia in some of the most awful times in the post-war era. And, what happened in China with Mao and so on.

“We’ve only got to look back two or three generations. All around us there are people who are as bad as the people doing this. They’re all around us. So, I say to folks, the only thing that really marks this one out, is its scale.

“But actually, this is probably less bloody, it’s less personal, isn’t it? The people who are steering this … it’s going to be much easier for them. They don’t have to shoot anyone in the face. They don’t have to beat someone to death with a baseball bat, or freeze them, starve them, make them work until they die. All of those things did happen two or three generations back and our grandparents or great grandparents were either victims of this, or they were actually members of it, or at least they witnessed it from overseas. That’s how close we are.

“And all I’m saying is, some shifts like that are happening again, but now they are using molecular biology.

“And the people going along with it, I think they would probably say, ‘I was only following orders,’ which we have heard before.

“But I know, because I have talked to lots of people, and some of them have said ‘I don’t want to believe that you are right, so I’m going to just put it away because if it is true, I can’t handle it.’ And I think … all you need to do is find a good

reason to tell people, ‘Don’t take the vaccine unless you’re a medical risk of dying from the virus!’ That seems to me a pretty good line!”

Towards a solution – ‘We need God’

“I’m a scientist, and I can tell you, talking to non-scientists, using science as a tool, will not work. It will fail.

“So, we need philosophers, people who understand logic, religion, something like that, [they have] got to wrestle with this, and start talking in a language people will understand. Because if we leave it with scientists, people like me, even though I’m well-intentioned, I’m a gabbling alien as far as most people in the street are concerned. They won’t believe the government will lie to them, they don’t believe the government would ever do anything that will harm them, but they are [doing such things].”

Finally, in an email correspondence, Dr. Yeadon concluded, “I have latest taken to signing off with ‘May God save us’, because I think we need God now more than at any time since WW2.”

 

To view the original Article 

Pfizer and Moderna’s “95% effective” vaccines—we need more details and the raw data

Pfizer and Moderna’s “95% effective” vaccines—we need more details and the raw data

In An Article Published in the British Medical Journal on January 4th 2021, Peter Doshi examines what the preliminary data suggests in the ongoing Vaccine Trials and examines some of the potential flaws in the study.

On 5 February 2021 we published a clarification to this piece. It is available here. 

Five weeks ago, when I raised questions about the results of Pfizer’s and Moderna’s covid-19 vaccine trials, all that was in the public domain were the study protocols and a few press releases. Today, two journal publicationsand around 400 pages of summary data are available in the form of multiple reports presented by and to theFDA prior to the agency’s emergency authorization of each company’s mRNA vaccine. While some of the additional details are reassuring, some are not. Here I outline new concerns about the trustworthiness and meaningfulness of the reported efficacy results.

“Suspected covid-19”

All attention has focused on the dramatic efficacy results: Pfizer reported 170 PCR confirmed covid-19 cases, split 8 to 162 between vaccine and placebo groups. But these numbers were dwarfed by a category of disease called “suspected covid-19”—those with symptomatic covid-19 that were not PCR confirmed. According to FDA’s report on Pfizer’s vaccine, there were “3410 total cases of suspected, but unconfirmed covid-19 in the overall study population, 1594 occurred in the vaccine group vs. 1816 in the placebo group.”

With 20 times more suspected than confirmed cases, this category of disease cannot be ignored simply because there was no positive PCR test result. Indeed this makes it all the more urgent to understand. A rough estimate of vaccine efficacy against developing covid-19 symptoms, with or without a positive PCR test result, would be a relative risk reduction of 19% (see footnote)—far below the 50% effectiveness threshold for authorization set by regulators. Even after removing cases occurring within 7 days of vaccination (409 on Pfizer’s vaccine vs. 287 on placebo), which should include the majority of symptoms due to short-term vaccine reactogenicity, vaccine efficacy remains low: 29% (see footnote).

If many or most of these suspected cases were in people who had a false negative PCR test result, this would dramatically decrease vaccine efficacy. But considering that influenza-like illnesses have always had myriadcauses—rhinoviruses, influenza viruses, other coronaviruses, adenoviruses, respiratory syncytial virus, etc.—some or many of the suspected covid-19 cases may be due to a different causative agent.

But why should etiology matter? If those experiencing “suspected covid-19” had essentially the same clinical course as confirmed covid-19, then “suspected plus confirmed covid-19” may be a more clinically meaningful endpoint than just confirmed covid-19.

However, if confirmed covid-19 is on average more severe than suspected covid-19, we must still keep in mind that at the end of the day, it is not average clinical severity that matters, it’s the incidence of severe disease that affects hospital admissions. With 20 times more suspected covid-19 than confirmed covid-19, and trials not designed to assess whether the vaccines can interrupt viral transmission, an analysis of severe disease irrespective of etiologic agent—namely, rates of hospitalizations, ICU cases, and deaths amongst trial participants—seems warranted, and is the only way to assess the vaccines’ real ability to take the edge off the pandemic.

There is a clear need for data to answer these questions, but Pfizer’s 92-page report didn’t mention the 3410 “suspected covid-19” cases. Nor did its publication in the New England Journal of Medicine. Nor did any of the reports on Moderna’s vaccine. The only source that appears to have reported it is FDA’s review of Pfizer’s vaccine.

The 371 individuals excluded from Pfizer vaccine efficacy analysis

Another reason we need more data is to analyse an unexplained detail found in a table of FDA’s review of Pfizer’s vaccine: 371 individuals excluded from the efficacy analysis for “important protocol deviations on or prior to 7 days after Dose 2.”  What is concerning is the imbalance between randomized groups in the number of these excluded individuals: 311 from the vaccine group vs 60 on placebo. (In contrast, in Moderna’s trial, there were just 36 participants excluded from the efficacy analysis for “major protocol deviation”—12 vaccine group vs 24 placebo group.)

What were these protocol deviations in Pfizer’s study, and why were there five times more participants excluded in the vaccine group?  The FDA report doesn’t say, and these exclusions are difficult to even spot in Pfizer’s report and journal publication.

Fever and pain medications, unblinding, and primary event adjudication committees

Last month I expressed concern about the potential confounding role of pain and fever medications to treat symptoms. I posited that such drugs could mask symptoms, leading to underdetection of covid-19 cases, possibly in greater numbers in people who received the vaccine in an effort to prevent or treat adverse events. However, it seems their potential to confound results was fairly limited: although the results indicate that these medicines were taken around 34 times more often in vaccine versus placebo recipients (at least for Pfizer’s vaccine—Moderna did not report as clearly), their use was presumably concentrated in the first week after vaccine use, taken to relieve post-injection local and systemic adverse events. But the cumulative incidencecurves suggest a fairly constant rate of confirmed covid-19 cases over time, with symptom onset dates extending well beyond a week after dosing.

That said, the higher rate of medication use in the vaccine arm provides further reason to worry about unofficial unblinding. Given the vaccines’ reactogenicity, it’s hard to imagine participants and investigators could not make educated guesses about which group they were in.  The primary endpoint in the trials is relatively subjective making unblinding an important concern. Yet neither FDA nor the companies seem to have formally probed the reliability of the blinding procedure, and its effects on the reported outcomes.

Nor do we know enough about the processes of the primary event adjudication committees that counted covid-19 cases. Were they blinded to antibody data and information on patients’ symptoms in the first week after vaccination?  What criteria did they employ, and why, with a primary event consisting of a patient-reported outcome (covid-19 symptoms) and PCR test result, was such a committee even necessary? It’s also important to understand who was on these committees. While Moderna has named its four-member adjudication committee—all university-affiliated physicians—Pfizer’s protocol says three Pfizer employees did the work. Yes, Pfizer staff members.

Vaccine efficacy in people who already had covid?

Individuals with a known history of SARS-CoV-2 infection or previous diagnosis of Covid-19 were excluded from Moderna’s and Pfizer’s trials. But still 1125 (3.0%) and 675 (2.2%) of participants in Pfizer’s and Moderna’s trials, respectively, were deemed to be positive for SARS-CoV-2 at baseline.

Vaccine safety and efficacy in these recipients has not received much attention, but as increasingly large portions of many countries’ populations may be “post-Covid,” these data seem important—and all the more so as the US CDC recommends offering vaccine “regardless of history of prior symptomatic or asymptomatic SARS-CoV-2 infection.” This follows on from the agency’s conclusions, regarding Pfizer’s vaccine, that it had ≥92% efficacy and “no specific safety concerns” in people with previous SARS-CoV-2 infection.

By my count, Pfizer apparently reported 8 cases of confirmed, symptomatic Covid-19 in people positive for SARS-CoV-2 at baseline (1 in the vaccine group, 7 in the placebo group, using the differences between Tables 9 and 10) and Moderna, 1 case (placebo group; Table 12).

But with only around four to 31 reinfections documented globally, how, in trials of tens of thousands, with median follow-up of two months, could there be nine confirmed covid-19 cases among those with SARS-CoV-2 infection at baseline? Is this representative of meaningful vaccine efficacy, as CDC seems to have endorsed? Or could it be something else, like prevention of covid-19 symptoms, possibly by the vaccine or by the use of medicines which suppress symptoms, and nothing to do with reinfection?

We need the raw data

Addressing the many open questions about these trials requires access to the raw trial data. But no company seems to have shared data with any third party at this point.

Pfizer says it is making data available “upon request, and subject to review.” This stops far short of making data publicly available, but at least leaves the door open. How open is unclear, since the study protocol says Pfizer will only start making data available 24 months after study completion.

Moderna’s data sharing statement states data “may be available upon request once the trial is complete.” This translates to sometime in mid-to-late 2022, as follow-up is planned for 2 years.

Things may be no different for the Oxford/AstraZeneca vaccine which has pledged patient-level data “when the trial is complete.” And the ClinicalTrials.gov entry for the Russian Sputnik V vaccine says there are no plans to share individual participant data.

The European Medicines Agency and Health Canada, however, may share data for any authorized vaccines much earlier.  EMA has already pledged to publish the data submitted by Pfizer on its website “in due course,” as has Health Canada.

Peter Doshi, associate editor, The BMJ

Competing interests: I have been pursuing the public release of vaccine trial protocols, and have co-signed open letters calling for independence and transparency in covid-19 vaccine related decision making.

Spanish translation of this article

Footnote

Calculations in this article are as follows:  19% = 1 – (8+1594)/(162+1816); 29% = 1 – (8 + 1594 – 409)/(162 + 1816 – 287). I ignored denominators as they are similar between groups.

 

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