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‘We need to ask these questions’: Experts accuse government, Pharma of covering up vaccine risks

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From LifeSiteNews

By Michael Nevradakis Ph. D., The Defender

Medical experts, political figures, journalists and whistleblowers today accused public health agencies and the mainstream media of censoring and covering up information relating to COVID-19 vaccine injuries and adverse events during a U.S. Senate roundtable discussion.

Sen. Ron Johnson hosted the discussion – “Federal Health Agencies and the COVID Cartel: What Are They Hiding?” – which his office said was intended to “expose the truth about how the COVID cartel – federal health agencies, Big Pharma, legacy media, and Big Tech – engaged in censorship and coverups.”

“It was heartening to hear these courageous experts willing to risk careers and reputations in order to tell the truth despite tremendous pressure to look the other way,” said Laura Bono, Children’s Health Defense (CHD) vice president.

Bono, who attended the roundtable, added:

We can’t ensure that the global devastation caused by the COVID crisis will never occur again unless we are able to analyze what happened and speak about it freely. We are immensely grateful to Senator Johnson for presenting this crucial discussion to the American public.

The discussion focused on six topics: COVID-19 vaccine issues, the history of vaccine injury cover-ups, the corruption of medical research and federal public health agencies, media censorship and propaganda, the COVID-19 response in other countries and the World Health Organization’s (WHO) proposed “pandemic agreement.”

Brian Hooker, Ph.D., CHD chief scientific officer, told The Defender he was “riveted listening to the panelists during the entire four-hour session.”

Hooker, co-author with Robert F. Kennedy Jr. of Vax-Unvax: Let the Science Speak, participated in the roundtable, highlighting the health risks posed by vaccines and the lack of adequate testing by federal health agencies.

HHS never submitted required vaccine safety report to Congress

In his testimony, Hooker said, “The CDC [Centers for Disease Control and Prevention] has never tested the cumulative effect of the vaccine schedule on childhood health outcomes.”

He referenced several scientific studies to support his testimony.

Vaccinated children were at least twice as likely to be diagnosed with developmental delays, ear infections and gastrointestinal disorders. The likelihood of an asthma diagnosis among the vaccinated group was four-and-a-half times higher than the unvaccinated group,” he said.

Hooker said unvaccinated children have shown “incidence rates between 4-20 times lower” than vaccinated children for autoimmune, neurodevelopmental and other disorders.

He also referred to the sharp rise in myocarditis diagnoses following COVID-19 vaccination.

“Myocarditis is a serious disorder and 76% of all cases following COVID-19 vaccination, as reported to the Vaccine Adverse Event Reporting System [VAERS], required emergency care and/or hospitalization,” he said. Yet, the “CDC significantly downplays myocarditis as a side effect of the vaccine.”

Further highlighting government inaction in studying and responding to vaccine injuries, Hooker said:

The 1986 National Childhood Vaccine Injury Act requires that the Department of Health and Human Services (HHS) report to Congress on the state of vaccine safety in the U.S. every two years.

Yet HHS has “never submitted a vaccine safety report to Congress,” he said.

Big Pharma ‘controls the levers of power,’ suppresses unprofitable treatments

Edward Dowd, a former BlackRock executive who has extensively studied the increase in excess deaths during and after the COVID-19 pandemic, also participated in the roundtable.

Dowd, author of Cause Unknown’: The Epidemic of Sudden Deaths in 2021 and 2022, said that government and WHO statements claiming the COVID-19 vaccines were “safe and effective” have “been proven false.”

“It has become clear that the U.S. government, along with the health regulators, do not desire an honest accounting of … policies that were imposed mostly under federal mandates,” he said, noting that this has resulted in high human costs.

Dowd told the panel:

The total excess deaths since the rollout of the vaccine in the U.S. is approximately 1.1 million for 2021, 2022 and 2023. We estimate the economic cost of productive working age people dying at $15.6 billion [and] estimate 28.4 million individuals are chronically absent, resulting in an estimated economic cost of $135 billion since 2021.

Jessica Rose, Ph.D., an immunologist and biochemist, told The Defender in advance that her testimony would focus on an “Analysis of the VAERS pharmacovigilance database in the context of the COVID-19 injectable products,” which “has revealed strong emergent safety signals – from myocarditis to death – that are not being acknowledged by the owners of the data.”

“This goes against standard operating procedures and begs the question: Why?” she said.

Rose also referred to recent revelations, later confirmed by Canadian public health authorities, about the contamination of COVID-19 mRNA vaccines.

“Is there a risk associated with DNA insertion in the context of the modified mRNA shots? Yes,” she said.

Dr. Pierre Kory, president and chief medical officer of the Frontline COVID-19 Critical Care Alliance, discussed the suppression of potentially effective treatments by public health agencies.

“We are only now beginning to understand that many long-established drugs may have other uses that we don’t even know about, effectively treating diseases we never imagined using them against,” he said. “So why on earth aren’t we systematically testing them for potential new uses?”

Kory told the panel:

The ugly truth is it’s not profitable. Big Pharma makes money on complicated new drugs, and it controls the levers of power. Nearly half of FDA’s [U.S. Food and Drug Administration] budget is bankrolled by the drug industry, and its tentacles are deep in academia, medicine and other regulatory agencies like the NIH [National Institutes of Health].

He cited ivermectin and hydroxychloroquine as examples of treatments that were suppressed during the pandemic despite evidence they were effective.

 

Johnson: Those who ask questions ‘vilified,’ ‘ridiculed’

In an interview with The Gateway Pundit Sunday, Johnson discussed adverse events related to the COVID-19 vaccines, the discovery by embalmers of “strange white fibrous clots” in bodies of the deceased since the vaccine rollout began in late 2020 and efforts to suppress ivermectin and hydroxychloroquine as COVID-19 treatments.

Referring to the clotting phenomenon, Johnson said, “What’s unfortunate is the medical establishment in general, and certainly, our federal health agencies, are discouraging autopsies. So, the only evidence we’re getting of this is from embalmers that are having a difficult time getting embalming fluid into [the] cadavers.”

Johnson suggested that Big Pharma and government health agencies promoted mRNA vaccines because of a profit motive.

He said:

They’ve had this mRNA platform. It never succeeded in animals, but they knew how profitable a platform it could be. They’ve already found out how profitable vaccines are because there’s no worry of liability. You just get those things on the childhood vaccine schedule, and you just start printing money.

Nobody can question the efficacy. Nobody can question the safety of them. So, vaccines are highly profitable for pharmaceutical companies, so they’re going to push them. And of course, they’ve got their individuals in government that push them right along with them.

Again, our health agencies have been completely captured by Big Pharma.

Johnson also questioned the addition of an increasing number of vaccines to the childhood vaccination schedule in the U.S.

“With the number [of vaccines] we administer to children now, gee, what could go wrong?” he said. “Every time you inject a child with a vaccine, you’re messing with their immune system. Is that why autoimmune diseases are up?”

“We need to ask these questions,” Johnson said. “My problem is we’re just not even able to ask questions, and those who ask questions, those who put forward evidence are immediately ostracized, criticized, vilified, ridiculed – and that’s not science.”

Johnson also implied that some of his congressional colleagues have sustained injuries related to the COVID-19 vaccines but are not speaking out.

“My guess is they understand how people that do question this stuff are ridiculed and vilified. And they just don’t want to put up with the hassle,” he said.

Johnson also spoke out against pharmaceutical company advertising, suggesting it should be subject to a government ban.

“Pass a law,” he said. “We are one of the very few countries that allow that.”

Johnson said that while he is “a free-market guy” who usually “would not be on the side of imposing that kind of government restriction on business,” he said that having seen how Big Pharma “spends the billions and how they use that to capture the narrative and destroy anybody who questions the narrative,” he believes “that’s got to stop.”

Participants at the roundtable included:

Several of the participants – and Sen. Johnson – previously spoke at this past weekend’s International Crisis Summit in Washington, D.C., which Malone organized. Rep. Greene recently spoke in support of vaccine injury victims at a U.S. House of Representatives vaccine safety hearing.

Watch Sen. Johnson’s roundtable discussion here:

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

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COVID-19

Pfizer reportedly withheld presence of cancer-linked DNA in COVID jabs from FDA, Health Canada

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From LifeSiteNews

By Clare Marie Merkowsky

According to information released by the Epoch Times, Pfizer purposefully failed to advise drug regulators, including Health Canada, the U.S. FDA and the European Medicines Agency, that the cancer-linked SV40 DNA enhancer was present in their experimental COVID shot.

Pharmaceutical giant Pfizer reportedly “chose not to” inform Health Canada, the U.S. Food and Drug Administration and other regulatory agencies that the cancer-linked Polyomavirus Simian Virus 40 (SV40) DNA sequence was in their widely distributed COVID-19 vaccine.  

According to information released April 23 by the Epoch Times, Pfizer purposefully failed to advise drug regulators, including Health Canada, the U.S. Food and Drugs Administration, and the European Medicines Agency, that SV40 was present in their experimental COVID shot.   

“I understand that there have been internal discussions at CBER [Center for Biologics Evaluation and Research] regarding the presents [sic] of an SV40 enhancer/promoter sequence, noting that its presence is unrelated to the purpose of the Pfizer’s plasmid as a transcription template for their mRNA COVID-19 vaccine,” Dr. Dean Smith, a senior scientific evaluator in Health Canada’s Vaccine Quality Division, wrote in an email to a colleague at the FDA about SV40. 

The August email was obtained by an access to information request by the Epoch Times.  

“Pfizer has communicated to us recently, that they apparently chose not to mention this information to EMA, FDA or HC at the time of their initial or subsequent submissions,” he added. 

Smith noted that Kevin McKernan, a microbiologist and former researcher and team leader for the MIT Human Genome project, and Dr. Phillip J. Buckhaults, who is a professor of cancer genomics as well as the director of the Cancer Genetics Lab at the University of South Carolina, had raised in a public manner earlier this year how SV40 was present in the jabs. 

While Health Canada originally told Canadians it was unaware of the SV40 enhancer’s presence, the agency has since confirmed the presence of the monkey-linked DNA sequence known to cause cancer when it was used in old polio vaccines. 

SV40 is used to enhance gene transcription when the shots are made. It has been linked to the spread of turbo cancers in those who have been exposed to the virus via contaminated injections.   

According to a 2002 study published in the Lancet, there is evidence that links the older polio vaccines, which were filed with SV40 contaminants, to certain forms of cancer.  

The authors of the 2002 study claim that the SV40-contaminated polio vaccine may have caused up to half of the 55,000 cases of non-Hodgkin’s lymphoma diagnosed each year.  

SV40, according to the late vaccine developer Dr. Maurice Hilleman, was put in the polio vaccine and then put into wide circulation by Big Pharma company Merck inadvertently. 

Unfortunately, this is not the first evidence that Pfizer hid the presence of SV40 from drug regulators.  

According to Dr. Janci Lindsay, who works as the director of toxicology and molecular biology for Toxicology Support Services, Pfizer did not disclose the presence of SV40 “promoters” to both Health Canada and the U.S. Food and Drug Administration, as well as the European Medicines Agency.  

She said, as reported in The Epoch Times, that the drug company “hid them.” 

“So it’s not just the fact that they’re there, it’s the fact that they were purposefully hidden from the regulators,” she noted. 

The news of Pfizer’s purposeful withholding of information comes as adverse effects from the first round of COVID shots have resulted in a growing number of Canadians who have filed for financial compensation over alleged injuries from the jabs, via Canada’s Vaccine Injury Program (VISP). 

Thus far, some VISP has already paid over $6 million to those injured by COVID injections, with some 2,000 claims remaining to be settled. 

Additionally, a recent study done by researchers with Canada-based Correlation Research in the Public Interest showed that 17 countries have found a “definite causal link” between peaks in all-cause mortality and the fast rollouts of the COVID shots as well as boosters. 

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COVID-19

WHO Official Admits the Truth About Passports

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From the Brownstone Institute

BY Paul ThackerPAUL THACKER

The World Health Organization’s Dr. Hanna Nohynek testified in court that she advised her government that vaccine passports were not needed but was ignored, despite explaining that the Covid vaccines did not stop virus transmission and the passports gave a false sense of security. The stunning revelations came to light in a Helsinki courtroom where Finnish citizen Mika Vauhkala is suing after he was denied entry to a café for not having a vaccine passport.

Dr. Nohynek is chief physician at the Finnish Institute for Health and Welfare and serves as the WHO’s chair of Strategic Group of Experts on immunization. Testifying yesterday, she stated that the Finnish Institute for Health knew by the summer of 2021 that the Covid-19 vaccines did not stop virus transmission

During that same 2021 time period, the WHO said it was working to “create an international trusted framework” for safe travel while EU members states began rolling out Covid passports. The EU Digital COVID Certificate Regulation passed in July 2021 and more than 2.3 billion certificates were later issued. Visitors to France were banned if they did not have a valid vaccine passport which citizens had to carry to buy food at stores or to use public transport.

But Dr. Nohynek testified yesterday that her institute advised the Finnish government in late 2021 that Covid passports no longer made sense, yet certificates continued to be required. Finnish journalist Ike Novikoff reported the news yesterday after leaving the Helsinki courtroom where Dr. Nohynek spoke.

Dr. Nohynek’s admission that the government ignored scientific advice to terminate vaccine passports proved shocking as she is widely embraced in global medical circles. Besides chairing the WHO’s strategic advisory group on immunizations, Dr. Nohynek is one of Finland’s top vaccine advisors and serves on the boards of Vaccines Together and the International Vaccine Institute.

The EU’s digital Covid-19 certification helped establish the WHO Global Digital Health Certification Network in July 2023. “By using European best practices we contribute to digital health standards and interoperability globally—to the benefit of those most in need,” stated one EU official.

Finnish citizen Mika Vauhkala created a website discussing his case against Finland’s government where he writes that he launched his lawsuit “to defend basic rights” after he was denied breakfast in December 2021 at a Helsinki café because he did not have a Covid passport even though he was healthy. “The constitution of Finland guarantees that any citizen should not be discriminated against based on health conditions among other things,” Vauhkala states on his website.

Vauhkala’s lawsuit continued today in Helsinki district court where British cardiologist Dr. Aseem Malhotra will testify that, during the Covid pandemic, some authorities and medical professionals supported unethical, coercive, and misinformed policies such as vaccine mandates and vaccine passports, which undermined informed patient consent and evidence-based medical practice.

You can read Dr. Malhotra’s testimony here.

Republished from the author’s Substack

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  • Paul Thacker

    Paul D. Thacker is an Investigative Reporter; Former Investigator United States Senate; Former Fellow Safra Ethics Center, Harvard University

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