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COVID-19

Florida Surgeon General’s Call to Halt Use of the Vaccines Sparks Debate

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Dr Joseph Ladapo, Florida’s Surgeon General at the microphone

From the Brownstone Institute

BY Maryanne DemasiMARYANNE DEMASI   

On January 3, 2024, Florida Surgeon General Joseph Ladapo called for a halt in the use of the mRNA Covid-19 vaccines after US health agencies failed to adequately address his concerns about DNA contamination in the products.

In a statement on X, Ladapo accused the FDA and CDC of always playing it “fast and loose” with Covid-19 safety, but their failure to test whether DNA fragments in the vaccine could integrate into a person’s genome was “intolerable.”

As I and others have pointed out on numerous occasions, the FDA’s own guidance on regulatory limits for residual DNA in vaccines states “there are several potential mechanisms by which residual DNA could be oncogenic [cause cancer], including the integration and expression of encoded oncogenes or insertional mutagenesis following DNA integration.”

In a letter, Ladapo had also asked the two agencies if they’d carried out any risk assessment regarding the presence of the “SV40 promoter” in the vaccines, which is thought to enhance DNA integration into host cells.

But the FDA’s top vaccine official Peter Marks responded to Ladapo’s demand for answers with intransigence and obfuscation.

Similar to how the FDA shut down my previous enquiries into this matter, the agency failed to provide Ladapo with any evidence that it had even conducted tests to address the risk of genomic integration.

In fact, Marks had the temerity to imply that ongoing discussion about this topic was perpetuating misinformation “which results in vaccine hesitancy that lowers vaccine uptake.”

Ladapo explained;

DNA integration poses a unique and elevated risk to human health and to the integrity of the human genome, including the risk that DNA integrated into sperm or egg gametes could be passed onto offspring of mRNA Covid-19 vaccine recipients. If the risks of DNA integration have not been assessed for mRNA Covid-19 vaccines, these vaccines are not appropriate for use in human beings.

He also recommended that providers concerned about health risks of Covid-19 should prioritise patient access to non-mRNA Covid-19 vaccines and treatment.

Quick to dismiss Ladapo’s concerns was Paul Offit, director of the Vaccine Education Centre at Children’s Hospital of Philadelphia, who serves on the FDA’s vaccine advisory committee.

Offit hit back in a video published on MedPage Today saying, “It is hard to believe that Dr Ladapo actually issued that statement…[DNA fragments] can’t possibly do harm. So scaring people unnecessarily like this has been hard to watch.”

Professor Paul Offit, Children’s Hospital of Philadelphia

Unfortunately, Offit’s video contains a series of erroneous statements that exposes his fundamental misunderstanding of the manufacturing and regulation of Covid vaccines.

For example, Offit says it’s unlikely that DNA fragments enter the cytoplasm of cells, or survive, once they’re inside.

“Our cytoplasm hates foreign DNA and it has a variety of mechanisms, including innate immunological mechanisms and enzymes, to destroy foreign DNA,” says Offit.

“That DNA, which would never survive the cytoplasm, would have to then cross the nuclear membrane into the nucleus, which would require a nuclear access signal that these DNA fragments don’t have…So the chance that DNA could affect your DNA is zero,” he adds.

But this statement is disingenuous on multiple fronts.

Offit talked about DNA fragments as if they were not encapsulated in lipid nanoparticles, which specifically ferry the genetic material into the cell cytoplasm. Indeed, without the lipid nanoparticles, the vaccines would never have made it to market.

A recent publication in Nature found that within hours, around 7% of cells are integrated when mixed with a transfection solution containing linear pieces of DNA.

Offit also said that DNA wouldn’t cross into the cell’s nucleus, but scientists have known that foreign DNA can be delivered into mammalian cells to modify a host cell’s genetic makeup in a process called “DNA transfection.”

It also ignores the fact that the DNA fragments contain the “SV40 promoter” which includes a nuclear targeting signal (NTS) to aid its entry into the nucleus.

A full critique of Offit’s commentary was recently published by Dr Robert Malone who pioneered some of the early work into mRNA technology.

Phillip Buckhaults, a cancer genomics expert, and professor at the University of South Carolina, has confirmed the presence of DNA fragments in the vaccines after replicating the work of McKernan et al.

Buckhaults has welcomed Ladapo’s announcement.

“I’m glad Dr Ladapo is taking a firm leadership stance to protect the people under his care. I think he is taking a lot of heat over genuinely looking out for others. I think he is acting in good faith and that is to be respected,” says Buckhaults.

Professor Phillip Buckhaults, University of South Carolina

He also believes that Ladapo’s stance on the mRNA vaccines is “based on solid scientific reasoning” because the long-term genomic safety has not been demonstrated for fragments of DNA that are encapsulated in lipid nanoparticles.

However, rather than completely halting the vaccines, Buckhaults says he would err on the side of caution and still “recommend the vaccine to select populations who are at high risk for death from [Covid-19].”

Buckhaults hopes that Ladapo can use his authority to compel the FDA to request an extra “cheap and easy step” in the processing of the vaccines to remove the vast majority of DNA from upcoming batches.

“Then we would not even need to have this argument about DNA anymore. The risk of the DNA would be essentially gone and the crisis in confidence in leadership would be addressed,” he says.

Buckhaults has testified before a South Carolina Senate hearing about his alarm over the “very real hazard” that these fragments of foreign DNA can insert themselves into a person’s genome and become a “permanent fixture of the cell.”

He has also discussed with me at length the potential harms to people’s health caused by DNA contamination in the mRNA vaccines. Last year, Buckhaults notified the FDA of his concerns via email but never received a response.


Supplementary information: reading:

FDA shuts down enquiries about DNA contamination in [Covid] vaccines

EXCLUSIVE: An interview with Buckhaults about DNA contamination in [Covid] vaccines

Republished from the author’s Substack

Author

  • Maryanne Demasi

    Maryanne Demasi, 2023 Brownstone Fellow, is an investigative medical reporter with a PhD in rheumatology, who writes for online media and top tiered medical journals. For over a decade, she produced TV documentaries for the Australian Broadcasting Corporation (ABC) and has worked as a speechwriter and political advisor for the South Australian Science Minister.

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COVID-19

Trudeau gov’t has paid out over $500k to employees denied COVID vaccine mandate exemptions

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From LifeSiteNews

By Clare Marie Merkowsky

The Department of Health paid $177,991, the Department of Foreign affairs paid $88,223, the Correctional Service of Canada paid $65,694, and Statistics Canada paid $33,240

Federal managers have paid out over $500,000 in settlements to employees that were suspended under the Trudeau government’s COVID vaccine mandate. 

According to information obtained April 24 by Blacklock’s Reporter, records have revealed that Canadian federal managers have paid a total of $509,746 in damages and compensation to employees who were denied vaccine mandate exemptions. 

“What are the total expenditures on compensation, severance packages and settlements to employees who were impacted by the government’s requirement during the COVID-19 pandemic that federal public servants provide proof of vaccination?” Conservative MP Ted Falk had questioned. 

According to the official numbers released by Blacklock’s, the Department of Health paid $177,991, the Department of Foreign affairs paid $88,223, the Correctional Service of Canada paid $65,694, and Statistics Canada paid $33,240. 

The Department of National Defence further revealed that it compensated three employees with “damages under the Canadian Human Rights Act on grounds of discrimination based on religion.”  

Beginning November 2021, Prime Minister Justin Trudeau’s government mandated that a total of 275,983 employees from the RCMP, military and main federal departments provide proof of vaccination as a condition of employment.    

Those who failed to do so risked dismissal or suspension without pay. While there were provisions for medical and religious exemptions, these were rarely granted. According to internal information, at the time of the mandates 95 percent of employees had already received the COVID vaccine.  

When the federal mandate was lifted in June 2022, 2,560 employees had been suspended without pay for refusing to show proof of vaccination.    

Indeed, implementing the vaccine mandate for federal employees has proved costly for Canadian taxpayers as Trudeau budgeted $198 million to enforce the COVID jabs on federal employees.  

“Treasury Board officials told us it was for rapid testing purchases and distribution,” Conservative MP Kelly McCauley (Edmonton West) told the House of Commons in 2021.  

“The Treasury Board website shows there are about 3,400 unvaccinated employees,” he added. “That works out to about $24,000 per employee for rapid testing.” 

Additionally, the Trudeau government will likely have to pay out even more former employees due to ongoing lawsuits over the mandates.  

In October, LifeSiteNews reported on how over 700 vaccine-free Canadians negatively affected by federal COVID jab dictates have banded together to file a multimillion-dollar class-action lawsuit against the Trudeau government.  

Similarly, Canadian taxpayers have already paid over $6 million via Canada’s Vaccine Injury Program (VISP) to those injured by COVID injections, with some 2,000 claims remaining to be settled. 

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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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