COVID wasn’t the only virus. Arrogance infected public health.



America doesn’t have a science problem. It has a trust problem.

The collapse of trust didn’t happen in a vacuum. It happened because the people running our institutions — government agencies, public health bureaucracies, and elite media — chose fear over facts, power over principle, and silence over accountability.

Truth alone won’t restore trust. We need courage. We need accountability. And above all, we need to stop pretending that silence keeps the peace.

I’ve spent more than three decades in life sciences, investing in innovation and funding companies that bring real cures to market. Bureaucracy can slow progress. But during COVID-19, the damage went farther. It wasn’t just red tape. It was arrogance, censorship, and the collapse of debate inside institutions once devoted to transparency and truth.

We told Americans to “trust the experts,” then changed the story every few weeks. We locked down playgrounds while allowing political protests. We shut down small businesses while rewarding massive platforms. We punished skepticism, not misinformation. We arrested surfers, fired nurses, and drove policemen and military personnel out of their jobs for refusing a vaccine. Where were the “my body, my choice” voices then?

Now Americans don’t just question mandates — they question everything: the data, the motives, the science itself.

Who can blame them? Childhood vaccination rates are falling because public health failed. An entire generation lost precious developmental time in isolation. Families grieved alone. And the same bureaucrats behind those mandates persuaded us to blame COVID, when in fact it was their decisions that did much of the damage. No one has been questioned. No one has been punished. Not one county health official has been held accountable.

A recent Gallup poll showed trust in institutions like the CDC and FDA has collapsed by more than 30 points in just a few years. That trust won’t be restored by press conferences or new slogans. It will only be restored when real leaders tell the truth about what went wrong and take responsibility to make sure it doesn’t happen again.

Dr. Scott Atlas put it plainly: The lockdowns weren’t the result of the virus. They were the result of decisions — decisions made by people who ignored known data, silenced dissent, and wielded authority like a weapon. And they got it wrong. Pretending otherwise only guarantees the disaster repeats.

So where do we start if we want to rebuild trust?

End the illusion of absolute authority. The CDC, NIH, and FDA must return to their proper role: advisory. They don’t make laws. They don’t issue mandates. They provide information — period.

Impose term limits on public health leadership. No more 30-year bureaucratic dynasties. Power without turnover hardens into ideology.

Ban conflicts of interest. No royalty payments to government scientists from the very companies they regulate. No revolving door between regulators and pharma.

Demand transparency. Every agency meeting, vote, and decision should be public and immediate. If they work for us, we should know what they’re saying.

These aren’t partisan talking points. They’re common-sense reforms. The stakes are too high to shrug and “move on.” Parents who lost a year of their children’s development, the elderly who died alone, the small business owners who lost everything — they deserve accountability. This isn’t about public policy. It’s about principle.

RELATED: No perp walks, no peace

Eric Lee/Bloomberg via Getty Images

And here’s the deeper truth: Fixing this mess isn’t just government’s job. It’s up to us — the entrepreneurs, innovators, parents, doctors, investors, and voters — to become stewards of truth. Not because we crave power, but because we believe in clarity. Because we still believe in the ideals America was built on.

I came to the United States at 15 after fleeing war in Beirut. I’ve seen what happens when fear and control override freedom and reason. I’ve spent my life betting on better — on ideas, on people, and on this country.

Truth alone won’t restore trust. We need courage. We need accountability. And above all, we need to stop pretending that silence keeps the peace.

It doesn’t. It only postpones the next disaster.

RFK Jr pulls plug on mRNA jabs because they 'pose more risks than benefits'



Government officials, the establishment media, and pharmaceutical representatives advertised the experimental mRNA vaccines that were rushed to market during the pandemic as "safe and effective."

Those who correctly suggested otherwise were often attacked and censored, and many of those Americans who refused the jabs — the first-ever mRNA vaccines approved by the U.S. Food and Drug Administration — lost their jobs. Meanwhile, the liability-shielded manufacturers of the vaccines enjoyed record profits.

Health Secretary Robert F. Kennedy Jr., who has long understood that the mRNA vaccines "don't prevent transmission" and suggested in 2021 that the COVID-19 jab might be "the deadliest vaccine ever made," announced on Monday that the U.S. Department of Health and Human Services is winding down its mRNA vaccine development activities under the Biomedical Advanced Research and Development Authority.

'The vaccine paradoxically encourages new mutations.'

Blaze News senior editor Daniel Horowitz, author of "Rise of the Fourth Reich: Confronting COVID Fascism with a New Nuremberg Trial So This Never Happens Again," said in response to the announcement that "there have been concerns in the medical freedom movement that RFK has forgotten about the issue that brought him to the ball amidst his focus on healthy food. However, yesterday's cancellation of mRNA research contracts shows that he has steadily maintained his focus on the dangers of mRNA."

"Over the past few weeks, BARDA reviewed 22 mRNA vaccine development investments and began canceling them," said Kennedy.

"Most of these shots are for flu or COVID, but as the pandemic showed us, mRNA vaccines don't perform well against viruses that affect the upper respiratory tract."

Kennedy noted that mRNA "only codes for a small part of the viral proteins" and that all it takes for the vaccine to become useless is a single mutation.

"This dynamic drives a phenomenon called 'antigenic shift,' meaning that the vaccine paradoxically encourages new mutations and can actually prolong pandemics as the virus constantly mutates to escape the protective effects of the vaccine," said the health secretary.

After consulting with experts and reviewing the relevant science, HHS has concluded that "mRNA technology poses more risks than benefits for these respiratory viruses," said Kennedy.

HHS indicated that its wind-down of the mRNA regime includes axing the agency's contracts with Emory University and Tiba Biotech; the "de-scoping of mRNA-related work in existing contracts with Luminary Labs, ModeX, and Seqirus"; and canceling or rejecting pre-award solicitations, including proposals from Pfizer and Sanofi Pasteur.

'Those shots are very problematic yet have received new approval.'

HHS has further instructed Global Health Investment — its partner that managed BARDA Ventures — to cease all mRNA-based equity investments and indicated that no new mRNA projects will be greenlit. However, a handful of final-stage contracts will apparently be permitted to wrap up "to preserve prior taxpayer investment."

RELATED: How Big Pharma left its mark on woke CDC vax advisory panel — and what RFK Jr. did about it

Photo by JOSEPH PREZIOSO/AFP via Getty Images

When pressed for further comment, HHS referred Blaze News to its press release.

"Let me be absolutely clear: HHS supports safe, effective vaccines for every American who wants them," said Kennedy. "That’s why we're moving beyond the limitations of mRNA for respiratory viruses and investing in better solutions."

While celebrating the cancellations, Horowitz noted that the key test will be whether Kennedy goes after existing approval for the current mRNA shots both for COVID and RSV.

"Those shots are very problematic yet have received new approval," said Horowitz. "Moderna has received approval for its new COVID shots. Likewise, despite its children's RSV shot showing negative efficacy ... Moderna had its mRNA RSV shot for seniors approved."

Horowitz added, "It reflects what is likely a balancing act for Bobby — attempting to implement what he knows is right in the face of some mRNA lobbyists close to the president who want to see the shots continue. This is going to be a constant tug-of-war, but it's good to see that RFK hasn't given up on the fight."

HHS' about-face on mRNA technology comes just weeks after the FDA required Pfizer and Moderna to update the side-effect warnings on their mRNA vaccines.

The FDA indicated on June 25 that it required Pfizer and Moderna to note the estimated unadjusted incidence of heart conditions following administration of the 2023-2024 formula of the Comirnaty and Spikevax vaccines, as well as the longitudinal results of a 2024 study concerning cardiac manifestations and outcomes of vaccine-associated myocarditis in American youths.

The agency required both vaccine manufacturers to include this information in the adverse reactions section of the jab information inserts.

Like Blaze News? Bypass the censors, sign up for our newsletters, and get stories like this direct to your inbox. Sign up here!

‘Disease X’ coming? WHO’s ‘replicon’ plan looks like doom



On Monday, May 5, President Trump signed an executive order banning “dangerous gain-of-function biological research in the United States and around the world.” This directive added muscle to his previous decision to withdraw from the World Health Organization. However, the United States remains vulnerable to international control.

Let’s review the history.

Until President Trump severs all remaining ties between the United States and the WHO, the public health of all Americans remains under threat of global government control.

On January 30, 2020, Tedros Ghebreyesus, director general of the World Health Organization, announced a “public health emergency of international concern.” With these magic words, Tedros put into force the WHO's International Health Regulations that supercharged the WHO into a one-world government health agency with the legal authority to declare pandemic sovereignty over all member nations, including the United States.

Tedros (as he is known) was born in Ethiopia and is not a medical doctor. Still, he is a Marxist and member of the Tigray People’s Liberation Front, a group the Ethiopian government has classified as a terrorist organization. So Tedros, by extension, is not only a Marxist, but he’s also a terrorist. Tedros handled the COVID-19 response by running cover for the Chinese Communist Party, denying resolutely that the virus leaked from the Wuhan Institute of Virology, and setting the stage for medical martial law and planet depopulation.

On January 20, 2025, President Trump finally withdrew the United States from the World Health Organization. Under terms of the WHO constitution, however, America’s involvement will not end officially until January 23, 2026.

Enter the Pentagon’s Defense Health Agency. The DHA monitors vaccine creation and “communicable” diseases and determines disease origination. The DHA uses the CDC for guidance, and its Influenza Division “provides ... leadership for the detection ... and control of influenza in the United States and around the world.” More importantly, the DHA still maintains “a vital partnership” with the WHO in a collaboration that includes "expanding military biodefense vaccine manufacturing."

This could become especially alarming if the world faces “Disease X.”

“Disease X” is the generic term the WHO uses to refer to an anticipated but unspecified future pandemic. That future may be now. Our research suggests that “Disease X” has already been weaponized and released in the form of a gain-of-function-enhanced version of COVID-19 that is more contagious and possibly more lethal than its predecessor.

A new “vaccine” to combat the next pandemic includes a “replicon” that continues to reproduce the active ingredient of the virus spike protein throughout a patient's body, even after the patient is dead. Replicon is a self-amplifying mRNA technology that copies itself and crosses between species. There is no known antidote that can stop the replicon from propagating the pathogenic COVID-19 spike protein.

RELATED: WHO director is upset ‘conspiracy theories’ may derail his global pandemic treaty

Photo by FABRICE COFFRINI/AFP via Getty Images

A more contagious and fast-acting version of COVID-19 propelled through the body by a replicon vaccine could well become a highly lethal nightmare pandemic concoction. In 2024, scientists in Japan developed the world’s first replicon vaccine, brand-named “Kostaive.”

Knowing that the United States remains tied to the WHO until next January and that the DHA maintains a “partnership” with the organization, what assurance do we have that our military would not bow to the WHO if the WHO defied the U.S. commander in chief by declaring a “Disease X global health emergency” that required forced replicon vaccination?

Until President Trump issues an executive order severing all remaining ties between the NIH, the CDC, and the DHA and the World Health Organization, the public health of all Americans remains under threat of global government control.

Ghebreyesus is, in our view, the most powerful and potentially dangerous person on the planet. With his connections and self-professed infallibility, what possibly could go wrong?

Editor’s note: This article has been adapted from “Disease X and Medical Martial Law: Defeating the Globalist Plan to Depopulate the World and Enslave the Remnant” (Post Hill Press).

The Best Way For Trump To Stick It To WHO Is To Stick With It

Trump should mold the WHO into an organization that serves countries and their populations — not profit — and replace it if he can't.

Francis Collins’ Latest Book Doubles Down On His Massive Abuses Of Power

Collins frets about the politicization of science, but largely conflates science with his own political agenda.

Latest Covid Shots Released Without Safety Data Under 4.5-Year-Old ‘Emergency’

HHS and the FDA should be leading the world in health care policy, not being over one year behind the curve.

Scientists acknowledge COVID vaccines and containment protocols may have boosted excess mortality



Dutch researchers indicated in a new peer-reviewed study that COVID-19 vaccines and governmental containment policies may have boosted excess mortality in the West.

The study, published Monday in the peer-reviewed journal BMJ Public Health, explored excess all-cause deaths in 47 Western countries from 2020 to 2022. It indicated that during this period, there were 3,098,456 excess deaths: 87% of the countries under review suffered excess mortality in 2020; 89% in 2021; and 91% in 2022.

The researchers made clear that excess mortality "includes not only deaths from SARS-CoV-2 infection but also deaths related to the indirect effects of the health strategies to address the virus spread and infection."

What caught the researchers' attention was not only the persistence of high excess mortality following the pandemic but that "the highest number of excess deaths [1,256,942] was recorded" in 2021 — the year containment measures were coupled with experimental vaccination.

In 2020, when Western citizens largely only had to contend with the virus, government-limited mobility rights and shuttered schools, churches, workplaces, restaurants, and parks, there were 1,033,122 excess deaths.

In 2022, when most containment protocols had been lifted and uptake of COVID-19 vaccines was in fast decline, researchers indicated there were 808,392 excess deaths.

'This is unprecedented and raises serious concerns.'

These massive figures reflect the difference in the number of reported deaths in a country in a given year and the expected number of deaths under normal conditions. For a baseline, the Dutch researchers used Ariel Karlinsky and Dmitry Kobak's linear regression estimate model, which draws on "historical death data in a country from 2015 until 2019 and accounts for seasonal variation in mortality and year-to-year trends due to changing population structure or socioeconomic factors."

"Excess mortality has remained high in the Western World for three consecutive years, despite the implementation of COVID-19 containment measures and COVID-19 vaccines," wrote the researchers. "This is unprecedented and raises serious concerns."

"During the pandemic, it was emphasized by politicians and the media on a daily basis that every COVID-19 death mattered and every life deserved protection through containment measures and COVID-19 vaccines," continued the researchers. "In the aftermath of the pandemic, the same morale should apply."

The Dutch researchers noted at the outset of their study that while experimental COVID-19 vaccines and draconian containment measures may have been effective in protecting segments of the population — particularly those with comorbidities and the elderly — they nevertheless had "detrimental effects that cause inferior outcomes as well."

"Although COVID-19 vaccines were provided to guard civilians from suffering morbidity and mortality by the COVID-19 virus, suspected adverse events have been documented as well," wrote the researchers.

The secondary analysis of the placebo-controlled, phase III randomized clinical trials of mRNA COVID-19 vaccines showed that the Pfizer trial had a 36% higher risk of serious adverse events in the vaccine group. The risk difference was 18.0 per 10000 vaccinated (95% CI 1.2 to 34.9), and the risk ratio was 1.36 (95% CI 1.02 to 1.83). The Moderna trial had a 6% higher risk of serious adverse events among vaccine recipients. The risk difference was 7.1 per 10,000 vaccinated (95% CI −23.2 to 37.4), and the risk ratio was 1.06 (95% CI 0.84 to 1.33).39. By definition, these serious adverse events lead to either death, are life-threatening, require inpatient (prolongation of) hospitalization, cause persistent/significant disability/incapacity, concern a congenital anomaly/birth defect or include a medically important event according to medical judgement.

Previous comparisons of established flu vaccines to the novel mRNA vaccines — which the Dutch researchers indicated have been classed in multiple French studies as "gene therapy products requiring long-term stringent adverse events monitoring" — have revealed the latter to carry a far higher risk of serious adverse reactions.

'Both medical professionals and citizens have reported serious injuries and deaths following vaccination.'

COVID-19 vaccines have also been linked to various ailments, including heart disease, blood clots, hemorrhages, gut issues, thromboses, myocarditis, pericarditis, and autoimmune diseases. A number of these linkages have been well-demonstrated and even admitted by pharmaceutical giants, as in the case of AstraZeneca.

The Dutch researchers indicated that some of the risks these experimental vaccines carry were realized overtime outside of clinical trials: "Both medical professionals and citizens have reported serious injuries and deaths following vaccination to various official databases in the Western World, such as VAERS in the USA, EudraVigilance in the European Union and Yellow Card Scheme in the UK."

The researchers framed the dangers posed by the vaccines as even more troubling given the understanding that the threat posed by the virus was overblown.

The pre-vaccination infection fatality rate for persons over 60 was reportedly 0.03% and the rate was 0.07% for those over 70. It posed virtually no threat to people ages 19 and younger, who alternatively faced an infection fatality rate of 0.0003%.

Gordon Wishart, chief medical officer at Check4Cancer, told the Telegraph, "The authors are correct to point out that many vaccine-related serious adverse events may have been unreported, and point to the fact that the simultaneous onset of excess mortality and Covid vaccination in Germany is worthy of further investigation on its own."

Just as the vaccines were nowhere near as "safe and effective" as promised, the supposed health safety protocols appear to have had an inverse effect.

The study acknowledged that it is challenging to differentiate between the various causes of excess mortality, particularly because national mortality registries "not only vary in quality and thoroughness but may also not accurately document the cause of death," and there was a lack of consensus in the medical community on whether to label deaths of persons infected with COVID-19 but not caused by the disease as COVID-19 fatalities.

However, they appeared confident enough to assert that "indirect effects of containment measures have likely altered the scale and nature of disease burden for numerous causes of death since the pandemic," citing a study that indicated there was a "substantial increase" in American deaths attributed to non-COVID causes in the first two years of the pandemic.

American heart disease deaths were apparently 6% above baseline in 2020 and 2021. Diabetes deaths were 17% over baseline in 2020 and 13% over in 2021. Alzheimers disease mortality was up 19% in 2020 and 15% in 2021. Alcohol-related deaths were 28% over baseline in 2020 and up 33% in 2021. Drug-related deaths were 33% over baseline in 2020 and up 54% in 2022.

The study noted that "lockdowns, school closures, physical distancing, travel restructions, business closures, stay-at-home orders, curfews, and quarantine measures with contract tracing" had numerous adverse indirect effects such as "economic damage, limited access to education, food insecurity, child abuse, limited access to healthcare, disrupted health programmes and mental health challenges" that increased morbidity and mortality from other causes.

The researchers concluded by recommending policymakers and government officials to "thoroughly investigate underlying causes of persistent excess mortality and evaluate their health crisis policies."

Like Blaze News? Bypass the censors, sign up for our newsletters, and get stories like this direct to your inbox. Sign up here!

FDA approves new Moderna mRNA vaccine without bothering with independent advisers



The U.S. Food and Drug Administration has approved Moderna's mRNA-1345 vaccine, which allegedly protects adults aged 60 and older from respiratory syncytial virus infection-caused lower respiratory tract disease.

The agency's breakthrough therapy designation approval for the drug, which will be marketed as mResvia, is only the second Moderna drug the FDA has approved. More significantly, it is the first mRNA vaccine to have been approved to address a disease other than COVID-19.

'We did not refer your application to the Vaccines and Related Biological Products Advisory Committee.'

Even though that amounts to a big step, it appears the regulator was keen to jump past additional levels of scrutiny.

The FDA noted in its Friday approval letter, "We did not refer your application to the Vaccines and Related Biological Products Advisory Committee because our review of information submitted in your [biologics license application], including the clinical study design and trial results, did not raise concerns or controversial issues that would have benefited from an advisory committee discussion."

The advisory committee's job is to review and evaluate data concerning the "safety, effectiveness, and appropriate use of vaccines and related biological products," then provide independent expert advice to the agency.

According to the pharmaceutical company, the approval was based on "positive data from the Phase 3 clinical trial ConquerRSV, a global study conducted in approximately 37,000 adults ages 60 or older in 22 countries."

Nearly 20,000 of the trial participants were based in the United States. There are at least 11 other studies under way examining the impact of the novel drug on other demographics.

The company claimed in a Feb. 29 overview of its trial data that the vaccine "continued to be efficacious through median 8.6 months follow-up" and was shown to prevent severe RSV disease "base on analysis of shortness of breath and medically attended RSV-[lower respiratory tract disease]."

The vaccine's efficacy is allegedly 83.7%. Reuters noted, however, that the label indicates the shot is only 79% effective at preventing at least two symptoms of RSV, such as fever and cough.

While the overview insisted that the vaccine was relatively effective and safe, it nevertheless highlighted a number of "systemic reactions" reported within seven days of vaccination, such as headache, fatigue, myalgia, arthralgia, and chills, besides customary injection site pain.

A Moderna-funded study published in the New England Journal of Medicine similarly alleged that a single dose of the vaccine "resulted in no evident safety concerns."

Despite similarly having been presented as a safe vaccine, Moderna's COVID-19 vaccine was linked in various studies, including in an FDA-funded study, to an increased risk of myocarditis and pericarditis, particularly in men ages 18-25.

Extra to heart inflammation, the Global COVID Vaccine Safety Project — a Global Vaccine Data Network initiative supported by both the CDC and the Department of Health and Human Services — revealed in a February study in the esteemed journal Vaccine that "Bell's palsy had an increased [observed to expected] ratio after a first dose of [Pfizer's] BNT162b2 and [Moderna's] mRNA-1273."

The study also noted that "there were also increased OE ratios for febrile seizures following a first and second dose of mRNA-1273 ... and for generalized seizures following first mRNA-1273 dose and fourth BNT162b2 dose."

Blaze News previously reported that the University of Auckland, which hosts the Global Vaccine Data Network, noted that there were safety signals for "acute disseminated encephalomyelitis (inflammation and swelling in the brain and spinal cord) after viral vector and mRNA vaccines."

Despite outstanding concerns about its only other approved vaccine, Moderna appears confident in its product and has evidently secured the FDA's confidence as well. Its next stop is the Centers for Disease Control and Prevention, whose Advisory Committee on Immunization Practices will review the vaccine during its June 26-27 meeting.

Analysts estimate Moderna will do roughly $340 million in RSV vaccine sales this year and possibly $830.5 million in 2025, reported Reuters.

Like Blaze News? Bypass the censors, sign up for our newsletters, and get stories like this direct to your inbox. Sign up here!

This One Abortion Story Changed Medicine Forever, But Pro-Lifers Hardly Talk About It

The growing use of aborted fetal cell lines in medical research has been largely ignored by Catholics and the pro-life movement.

Study claims harms of COVID-19 vaccines 'profoundly outweighed' benefits; calls for moratorium on mRNA shots



A new peer-reviewed study in a Springer Nature Group journal has painted a damning picture of the global COVID-19 vaccination campaign along with the novel mRNA products at its core — vaccines millions of Americans were compelled to take if they wanted to keep their jobs, eat in public, stay in school, remain in uniform, or visit their loved ones.

According to the study, published on Jan. 24 in the PubMed-listed open access journal Cureus, standards were dropped, corners were cut, and red flags were missed in the testing, authorization, and ultimate deployment of the COVID-19 vaccines. The result: a product with an "unacceptable harm-to-reward ratio."

Impurities

Extra to hinting at possible ulterior motives driving the decision to rush out the vaccines in a fraction of the time conventionally figured appropriate, epidemiologist M. Nathaniel Mead and his co-authors — including Texas cardiologist Peter McCullough — wrote that the vaccines "evaluated in the trials were not the same products eventually distributed worldwide."

Whereas the mRNA products from "clinical batches" in the registration trials were ostensibly free of process-related impurities, the doses made with "a method much more suitable for mass production known as Process 2 ... showed significantly reduced mRNA integrity," claimed the researchers.

"All of the COVID-19 mRNA products released to the public were produced via Process 2 and have been shown to have varying degrees of DNA contamination," said the study. "The failure of regulatory authorities to heretofore disclose process-related impurities (e.g., SV40) has further increased concerns regarding safety and quality control oversight of mRNA vaccine manufacturing processes."

Florida Surgeon General Joseph Ladapo noted the detection of "Simian Virus 40 (SV40) promoter/enhancer DNA" in the vaccines in a Dec. 6 letter to the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention.

Peter Marks, director of the U.S. Food and Drug Administration's Center for Biologics Evaluation and Research, said in reply, "No SV40 proteins are encoded for or are present in the vaccines," and emphasized that the shots were safe and effective.

The European Medicines Agency, which regulates vaccines in the EU, indicated that "non-functional" fragments of SV40's DNA sequence are used in the manufacture of the COVID-19 vaccine, reported the Associated Press.

Pfizer indicated the SV40 sequence is commonly used in developing vaccines.

Regardless of whether elements of SV40 were specifically of any consequence, Mead and his coauthors underscored that the mRNA vaccines were not as advertised.

Harms and unintended consequences

"Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group," wrote Mead and the other researchers. "Numerous SAEs were identified following the Emergency Use Authorization (EUA), including death, cancer, cardiac events, and various autoimmune, hematological, reproductive, and neurological disorders."

According to the study's authors, many of these serious SAEs "have often been wrongly ascribed to COVID-19 rather than to the COVID-19 mRNA vaccinations."

"Misattributions of SAEs to COVID-19 often may be due to the amplification of adverse effects when mRNA injections are followed by SARS-CoV-2 subvariant infection," said the study. "Injuries from the mRNA products overlap with both [post-acute COVID-19 syndrome] and severe acute COVID-19 illness, often obscuring the vaccines' etiologic contributions."

The study suggested not only that the vaccines are likely responsible for a host of devastating side effects that have been conveniently blamed on the virus but also that boosters have actually had a paradoxical impact.

"Multiple booster injections appear to cause immune dysfunction, thereby paradoxically contributing to heightened susceptibility to COVID-19 infections with successive doses," wrote the researchers.

The researchers suggested further that the vaccines are perpetuating the emergence of new variants.

"Mass mRNA inoculations result in the natural selection of highly infectious immune-evading SARS coronavirus variants that successfully bypass vaccine-induced immunity, leading to a dramatic rise in the prevalence of these variants," said the study.

On the basis of their review, the researchers concluded that for most adults under the age of 50, "the perceived benefits of the mRNA boosters are profoundly outweighed by their potential disabling and life-threatening harms. Potential harms to older adults appear to be excessive as well."

In addition to calling for COVID-19 vaccines to be removed from the childhood immunization schedule along with the suspension of boosters, the researchers urged "governments to endorse and enforce a global moratorium on these modified mRNA products until all relevant questions pertaining to causality, residual DNA, and aberrant protein production are answered."

Regarding possible conflicts of interests, the authors indicated that no financial support was afforded them by any organization for the study.

Stephanie Seneff, one of the authors, nevertheless declared a grant from Quanta Computer Inc., a Taiwan-based computer manufacturer. Entrepreneur Steve Kirsch, another author, noted that he is the founder of the Vaccine Safety Research Foundation but "receives no income from this entity." McCullough, who supervised the study, highlighted his employment and stock options from the Wellness Company.

McCullough was involved in another troubling study that was recently published.

His peer-reviewed study published last month in the pharmacotherapy journal Therapeutic Advances in Drug Safety stressed that "COVID-19 vaccination is strongly associated with a serious adverse safety signal of myocarditis, particularly in children and young adults resulting in hospitalization and death."

"COVID-19 vaccines induce an uncontrolled expression of potentially lethal SARS-CoV-2 spike protein within human cells, have a close temporal relationship of events, and are internally and externally consistent with emerging sources of clinical and peer-reviewed data supporting the conclusion that COVID-19 vaccines are deterministic for myocarditis, including fatal cases," claimed the study.

Like Blaze News? Bypass the censors, sign up for our newsletters, and get stories like this direct to your inbox. Sign up here!