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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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Freedom Convoy

Court Orders Bank Freezing Records in Freedom Convoy Case

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A Canadian court has ordered the release of documents that could shed light on how federal authorities and law enforcement worked together to freeze the bank accounts of a protester involved in the Freedom Convoy.
Both the RCMP and TD Bank are now required to provide records related to Evan Blackman, who took part in the 2022 demonstrations and had his accounts frozen despite not being convicted of any crime at the time.
The Justice Centre for Constitutional Freedoms (JCCF) announced the Ontario Court of Justice ruling. The organization is representing Blackman, whose legal team argues that the actions taken against him amounted to a serious abuse of power.
“The freezing of Mr. Blackman’s bank accounts was an extreme overreach on the part of the police and the federal government,” said his lawyer, Chris Fleury. “These records will hopefully reveal exactly how and why Mr. Blackman’s accounts [were] frozen.”
Blackman was arrested during the mass protests in Ottawa, which drew thousands of Canadians opposed to vaccine mandates and other pandemic-era restrictions.
Although he faced charges of mischief and obstructing police, those charges were dismissed in October due to a lack of evidence. Despite this, prosecutors have appealed, and a trial is set to begin on August 14.
At the height of the protests, TD Bank froze three of Blackman’s accounts following government orders issued under the Emergencies Act. Then-Prime Minister Justin Trudeau had invoked the act to grant his government broad powers to disrupt the protest movement, including the unprecedented use of financial institutions to penalize individuals for their support or participation.
In 2024, a Federal Court Justice ruled that Trudeau’s decision to invoke the act had not been justified.
Blackman’s legal team plans to use the newly released records to demonstrate the extent of government intrusion into personal freedoms.
According to the JCCF, this case may be the first in Canada where a criminal trial includes a Charter challenge over the freezing of personal bank accounts under emergency legislation.
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COVID-19

FDA requires new warning on mRNA COVID shots due to heart damage in young men

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From LifeSiteNews

By Doug Mainwaring

Pfizer and Moderna’s mRNA COVID shots must now include warnings that they cause ‘extremely high risk’ of heart inflammation and irreversible damage in males up to age 24.

The Trump administration’s Food and Drug Administration (FDA) announced it will now require updated safety warnings on mRNA COVID-19 shots to include the “extremely high risk” of myocarditis/pericarditis and the likelihood of  long-term, irreversible heart damage for teen boys and young men up to age 24.

The required safety updates apply to Comirnaty, the mRNA COVID shot manufactured by Pfizer Inc., and Spikevax, the mRNA COVID shot manufactured ModernaTX, Inc.

According to a press release, the FDA now requires each of those manufacturers to update the warning about the risks of myocarditis and pericarditis to include information about:

  1. the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
  2. the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 injection.

The FDA has also required the manufacturers to describe the new safety information in the adverse reactions section of the prescribing information and in the information for recipients and caregivers.

Additionally, the fact sheets for healthcare providers and for recipients and caregivers for Moderna COVID-19 shot and Pfizer-BioNTech COVID-19 shot, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax prescribing information and information for recipients and caregivers.

In a video published on social media, Dr. Vinay Prasad, director of the Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, explained the alarming reasons for the warning updates.

While heart problems arose in approximately 8 out of 1 million persons ages 6 months to 64 years following reception of the cited shots, that number more than triples to 27 per million for males ages 12 to 24.

Prasad noted that multiple studies have arrived at similar findings.

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