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COVID-19

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

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9 minute read

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

US House COVID report vindicates lab leak theory but tries to defend ‘success’ of the jabs

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From LifeSiteNews

By Calvin Freiburger

“the federal government supported dangerous gain-of-function research in Wuhan, China without adequate transparency or oversight, and that former White House COVID adviser and National Institute of Allergy & Infectious Diseases (NIAID) director Dr. Anthony Fauci “played semantics with the definition of gain-of-function research” to deny it

The U.S. House Oversight & Accountability Committee’s Select Subcommittee on the Coronavirus Pandemic has released its long-awaited After Action Review on COVID-19 and the government response, which affirms the verdict that COVID most likely originated in a lab through gain-of-function research and broadly condemns the lockdowns of personal freedom and economic activity but attempts to walk a far finer and sometimes contradictory line on the COVID vaccines.

Worked on for almost two years, the 520-page report is billed as the “single most thorough review of the pandemic conducted to date,” according to a press release from the committee.

“This work will help the United States, and the world, predict the next pandemic, prepare for the next pandemic, protect ourselves from the next pandemic, and hopefully prevent the next pandemic. Members of the 119th Congress should continue and build off this work, there is more information to find and honest actions to be taken,” said Republican Rep. Brad Wenstrup of Ohio, the chairman of the subcommittee. “The COVID-19 pandemic highlighted a distrust in leadership. Trust is earned. Accountability, transparency, honesty, and integrity will regain this trust. A future pandemic requires a whole of America response managed by those without personal benefit or bias. We can always do better, and for the sake of future generations of Americans, we must. It can be done.”

The report concludes that COVID most likely “emerged as the result of a laboratory or research related accident,” that the federal government supported dangerous gain-of-function research (that entails intentionally strengthening viruses to better study their potential effects) in Wuhan, China without adequate transparency or oversight, and that former White House COVID adviser and National Institute of Allergy & Infectious Diseases (NIAID) director Dr. Anthony Fauci “played semantics with the definition of gain-of-function research” to deny it, as well as prompting creation of the controversial “Proximal Origins” paper to attempt to discredit the lab-leak theory.

It further found that officials within NIAID actively attempted to flout Freedom of Information Act (FOIA) requests for documents on the matter, such as by intentionally misspelling various names and terms so they would be harder to find in word searches.

The report goes on to conclude that the enormous sums of money the government doled out in the name of COVID relief was rife with waste and abuse, including more than $191 billion in unemployment fraud, $64 billion worth of fraud in the Paycheck Protection Program, and the loss of $200 billion due to the Small Business Administration failing to implement proper oversight and controls.

Meanwhile, the infamous “social distancing” guidance for people to stand at least six feet apart was based on “no scientific trials or studies,” but despite admitting as much, Fauci declined to push back because, in his words, it was “not appropriate to be publicly challenging a sister organization.” Face masks were similarly unsupported by the science and ultimately proven to be ineffective at limiting COVID’s spread, and widespread lockdowns of businesses and public gatherings caused significant harm to the economy, to physical and mental health, and to children’s education and social development far outweighing whatever good they may have done.

On the subject of the controversial COVID vaccines, however, the report is far more deferential. It acknowledges that the shots “had adverse events that must be thoroughly investigated,” and discusses various shortcomings in the government’s reporting systems for adverse vaccine events but still concludes that, overall, the vaccines were “largely safe and effective,” and credits them with saving “millions” of lives.

Operation Warp Speed, the Trump administration initiative to develop vaccines for COVID in a fraction of the time vaccines usually take, “was a tremendous success,” the subcommittee says, and the resulting vaccines “undoubtedly saved millions of lives by diminishing likelihood of severe disease and death.” It even faults President Joe Biden and Vice President Kamala Harris, who were running against Donald Trump for the White House at the time, for “question(ing) the safety and efficacy of COVID-19 vaccinations” before they were released.

“COVID-19 vaccines were tremendously important in reducing the severity of COVID-19 symptoms and were extremely effective in doing so,” the report claims. “However, the Biden Administration oversold the power of these vaccines. On more than one occasion, President Biden himself overstated the vaccine’s ability to prevent infection and transmission. These false statements likely contributed to Americans’ confusion about COVID-19 vaccines and reduced overall vaccine confidence.”

The subcommittee report largely reiterates and aligns with a wealth of previous findings on the failures of lockdowns and forced masking, as well as the origins of COVID-19. On the subject of the vaccines, however, it neglects a large body of evidence of far more widespread harm.

The federal Vaccine Adverse Event Reporting System (VAERS) reports 38,068 deaths, 218,646 hospitalizations, 22,002 heart attacks, and 28,706 myocarditis and pericarditis cases as of October 25, among other ailments. U.S. Centers for Disease Control & Prevention (CDC) researchers have recognized a “high verification rate of reports of myocarditis to VAERS after mRNA-based COVID-19 vaccination,” leading to the conclusion that “under-reporting is more likely” than over-reporting.

An analysis of 99 million people across eight countries published February in the journal Vaccine “observed significantly higher risks of myocarditis following the first, second and third doses” of mRNA-based COVID vaccines, as well as signs of increased risk of “pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis,” and other “potential safety signals that require further investigation.” In April, the CDC was forced to release by court order 780,000 previously undisclosed reports of serious adverse reactions, and a study out of Japan found “statistically significant increases” in cancer deaths after third doses of mRNA-based COVID-19 vaccines and offered several theories for a causal link.

In Florida, an ongoing grand jury investigation into the vaccines’ manufacturers is slated to release a report on the safety and effectiveness of the COVID vaccines, and a lawsuit by the state of Kansas has been filed accusing Pfizer of misrepresentation for calling the shots “safe and effective.” The findings of both efforts are highly anticipated.

All eyes are currently on returning President Trump, and whose health team, which will be helmed by prominent vaccine critic Robert F. Kennedy, Jr. as his nominee for Secretary of Health & Human Services, has given mixed signals as to the prospects of reconsidering the shots for which he has long taken credit, and has nominated both critics and defenders of establishment COVID measures for a number of administration roles.

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COVID-19

Just 12% of Albertans have taken latest COVID shot, data show

Published on

From LifeSiteNews

By Anthony Murdoch

Official data from the Alberta government as of early December show that just 11.9% of Albertans, 557,702 people, have gotten the latest COVID shot, down from 16.9% last year.

Official data shows that Canadians in the province of Alberta are overwhelmingly shunning the reformulated COVID jab approved by Health Canada, with nearly 90 percent of residents overall choosing not to get the shots. 

Official data from the Alberta government as of early December show that just 11.9 percent of Albertans, 557,702 people, have gotten the latest COVID shot. At the same time last year, 16.9 percent of Albertans, or 855,343, chose to get a shot.  

The COVID jab uptake rate amongst kids aged 6 months to 19 years sits at just 3.76 percent. For those aged 20 to 50, the rate is only 5.6 percent. 

The jab uptake rate rises significantly for those aged 50 and over, topping out at 50.4 percent for those over 90, with the overall jab rate for those aged 65 and over being 36.2 percent. 

In all cases, the majority of the COVID jabs administered were done so in pharmacies.  

In September, Health Canada approved Moderna’s new mRNA COVID-19 jab for all Canadians over six months of age. 

The approval of the shots comes despite the fact that the nation’s very own Vaccine Injury Support Program (VISP) has had to pay out $14 million to those injured by the shots, a sizable figure considering most claims are still unpaid.

As reported by LifeSiteNews, a recent report claims that at least one federal Canadian MP told a constituent not to speak badly of reported delays in the VISP as well as the bungling of the program in general. 

The mRNA-based shots themselves have been linked to a multitude of negative and often severe side effects, especially in children. LifeSiteNews has published an extensive amount of research on the dangers of the experimental jabs, which include heart damage and blood clots.

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