MTG asks DOJ to drop charges against 'hero' doctor accused of destroying COVID vaccines, giving out fake vax records



Georgia Rep. Marjorie Taylor Greene and other Republican lawmakers expressed support this week for Dr. Michael Kirk Moore Jr., the Utah plastic surgeon presently on trial and facing more than 35 years in jail for allegedly destroying COVID-19 vaccines and handing out fraudulent fake vaccination records during the pandemic.

Moore, his neighbor Kristin Jackson Andersen, and two others were charged in 2023 with conspiracy to defraud the U.S. government; conspiracy to convert, sell, convey, and dispose of government property; and conversion, sale, conveyance, and disposal of government property as well as aiding and abetting.

According to the federal indictment, Moore — a member of a group seeking to "'liberate' the medical profession from government and industry conflicts of interest" — signed a Centers for Disease Control and Prevention COVID-19 Vaccination Program Provider Agreement in order to secure COVID-19 vaccines and vaccination record cards. He then ordered hundreds of doses of vaccines from the CDC.

Instead of administering the vaccines, Moore, 58, allegedly dumped around $28,000 worth of doses down the drain and handed out vaccination record cards in exchange for cash or donations to a charitable organization.

Between May 2021 and September 2022, the defendants also allegedly administered harmless "saline shots to minor children to trick them into thinking they had received a vaccine" at the request of their parents.

The Biden Department of Justice was evidently keen to throw Moore in jail; however, he has since become something of a folk hero for giving Americans a way to avoid experimental medicine at a time when vaccines were being foisted on the population.

'This man is a hero, not a criminal.'

Health Secretary Robert F. Kennedy Jr. noted in April that Moore "deserves a medal for his courage and his commitment to healing."

"He's one of the few surgeons who stood against the worst COVID-era mandates," said Texas surgeon Dr. Eithan Haim. "Which is why they're trying to send him to prison."

RELATED: What happened to RFK Jr.’s red line on risky vaccines?

 Photo illustration by Joe Raedle/Getty Images

As jury selection began for his 15-day trial on Monday, supporters rallied in support of Moore outside the Orrin G. Hatch U.S. Courthouse in Salt Lake City.

Among those who showed up were Utah House Speaker Mike Schultz (R) and Republican state Reps. Karianne Lisonbee and Trevor Lee, reported the Utah News Dispatch.

"The way those of us [who] stood up and pushed back were treated was wrong. We were treated like second-class citizens if we didn't get the shot, we didn’t get the vaccine," Schultz told the crowd. "Think about it for just a minute. You had to have a vaccine passport to walk down the streets and go into a shop, to go to a Jazz game, to go to a restaurant. That was unbelievable."

Rep. Marjorie Taylor Greene announced Tuesday that she was writing a letter to the Department of Justice asking that all charges be dropped against Moore — a move celebrated by Dr. Robert Malone, one of Robert F. Kennedy's new appointments to the CDC's Advisory Committee on Immunization Practices.

"This man is a hero, not a criminal," wrote Greene. "The Covid vaccine kills and injures people, but this brave doctor, who is a veteran by the way, is being prosecuted for helping people avoid tyrannical vaccine mandates under Democrats."

"Big Pharma was given billions of taxpayer's [sic] dollars for experimental covid vaccines and then the MrNA covid vaccines were forced on Americans, our military, and our children against their will," continued Greene. "Covid vaccines do not stop the spread of covid and are proven to cause life threatening myocarditis, miscarriages, strokes, blood clots, and many other issues that many Americans are angrily still dealing with today."

Kentucky Rep. Thomas Massie (R) echoed Greene, noting that Moore "should NOT be prosecuted for helping people avoid the tyrannical vax mandates, which were based on a corrupted FDA approval process."

RELATED: FDA slaps damning warnings on COVID-19 vaccines; highlights Biden administration's safety-risk gloss

 Photo by JOSEPH PREZIOSO/AFP via Getty Images

Utah Sen. Mike Lee (R), who has repeatedly suggested that Kirk be let off the hook, said on Thursday, "I'm both surprised and disappointed that Dr. Kirk Moore is still being prosecuted — potentially facing three decades in prison — considering all that we've learned about COVID, the vaccines, and the unjust mandates imposed by the Biden administration."

"I just did what was right," Dr. Moore said outside the courthouse, clearly overwhelmed by the support.

Blaze News has reached out to the DOJ for comment.

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FDA slaps damning warnings on COVID-19 vaccines; highlights Biden administration's safety-risk gloss



Federal health authorities rebuked Florida Surgeon General Dr. Joseph Ladapo for suggesting in 2022 that the benefit of COVID-19 vaccination among healthy young men was outweighed by the risk of heart conditions, myocarditis in particular.

Ladapo issued guidance that stated, "Based on currently available data, patients should be informed of the possible cardiac complications that can arise after receiving a mRNA COVID-19 vaccine."

“Our goal is not to get into like a fight or a tiff, because public health isn’t served well by this,” said Dr. Peter Marks, then-director of the U.S. Food and Drug Administration's Center for Biologics Evaluation and Research. "Our goal is to help get to … an acceptance that there are overall benefits of these vaccines, despite the fact that yes, it is true that there could be some side effects."

'Most of these patients had received a two-dose primary series of an mRNA COVID-19 vaccine prior to their diagnosis.'

Marks' former agency has since acknowledged that there is a greater risk of post-vaccination myocarditis than the so-called experts were first willing to publicly admit.

Months after telling both vaccine manufacturers to include new safety information regarding their respective drugs in the stated interest of "radical transparency," 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 FDA also required Pfizer and Moderna to describe the new safety information in the adverse reactions section of their vaccine information inserts.

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

 Photo illustration by Joe Raedle/Getty Images

For years, the fact sheets for the mRNA COVID-19 vaccines noted that reports of adverse events demonstrated increased risks of myocarditis and pericarditis, particularly following the second dose, and that the "observed risk is highest in males 12 through 17 years of age."

Now, the package inserts state that "the observed risk has been highest in males 12 years through 24 years of age" and:

Based on analyses of commercial health insurance claims data from inpatient and outpatient settings, the estimated unadjusted incidence of myocarditis and/or pericarditis during the period 1 through 7 days following administration of the 2023-2024 Formula of mRNA COVID-19 vaccines was approximately 8 cases per million doses in individuals 6 months through 64 years of age and approximately 27 cases per million doses in males 12 through 24 years of age.

The package inserts for both drugs also now state:

Follow-up information on cardiovascular outcomes in hospitalized patients who had been diagnosed with COVID-19 vaccine-associated myocarditis is available from a longitudinal retrospective observational study. Most of these patients had received a two-dose primary series of an mRNA COVID-19 vaccine prior to their diagnosis. In this study, at a median follow-up of approximately 5 months post-vaccination, persistence of abnormal cardiac magnetic resonance imaging (CMR) findings that are a marker for myocardial injury was common. The clinical and prognostic significance of these CMR findings is not known. Information is not yet available about potential long-term sequelae of myocarditis or pericarditis following administration of mRNA COVID-19 vaccines.

When discussing the updates, Dr. Vinay Prasad, director of the FDA's Center for Biologics Evaluation and Research, provided a refresher about the effort by the previous administration to downplay the risk of myocarditis.

Prasad, referring to congressional testimony given by Sen. Ron Johnson (R-Wis.) in May, noted that Centers for Disease Control and Prevention and the FDA officials were aware in early 2021 of a safety signal for the heart condition on the basis of Pentagon and Israeli data.

'The FDA's new Covid-19 philosophy represents a balance of regulatory flexibility and a commitment to gold-standard science.'

A day after health officials at the agencies acknowledged a safety signal, and after the CDC discussed whether to issue a Health Alert Network message on myocarditis, the Biden White House distributed talking points to top U.S. health officials de-emphasizing the risk.

On May 26, 2021, then-acting FDA Commissioner Janet Woodcock told then-CDC Director Rochelle Walensky that the "FDA does not concur with the issuance of the myocarditis HAN as written."

That day, both agencies reportedly decided to "nix the HAN" alert.

"The risk of myocarditis and pericarditis appears to be very low given the number of vaccine doses that have been administered," Woodcock stated the following month. "The benefits of COVID-19 vaccination continue to outweigh the risks, given the risk of COVID-19 diseases and related, potentially severe, complications."

The nixed alert could have made a difference.

After all, Prasad noted that "in August of 2021, in an FDA regulatory action, we document that based on the health insurance claims Optum dataset, the rate of post-vaccination myocarditis from the Pfizer-BioNTech vaccine was approaching 200 cases per million or approximately 1 in 5,000" among 16- and 17-year-old males.

RELATED: Democrats who locked down America during COVID now cry dictator over Trump's deportations

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FDA Commissioner Martin Makary and Prasad noted in a May article in the New England Journal of Medicine that "the FDA’s new Covid-19 philosophy represents a balance of regulatory flexibility and a commitment to gold-standard science. The FDA will approve vaccines for high-risk persons and, at the same time, demand robust, gold-standard data on persons at low risk."

Blaze News reached out to the FDA but did not immediately receive a response.

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



Health and Human Services Secretary Robert F. Kennedy Jr. last week canned all 17 members of the Advisory Committee on Immunization Practices — the federal panel whose vaccine recommendations become official policy at the Centers for Disease Control and Prevention and apply to the entire American population once adopted by the agency's director.

Kennedy accused the ACIP of "malevolent malpractice" and vowed to appoint "highly credentialed physicians and scientists who will make extremely consequential public health determinations by applying evidence-based decision-making with objectivity and common sense."

Among the eight individuals whom Kennedy has appointed to the committee are:

  • Dr. Martin Kulldorf, a former professor of medicine at Harvard University who risked his career by both swimming against the tide of establishment thinking during the pandemic and co-authoring the Great Barrington Declaration with now-National Institutes of Health Director Jay Battacharya;
  • Dr. Robert Malone, an early pioneer in messenger RNA technology who faced years of abuse for questioning the safety of mRNA vaccines and the severity of COVID-19; and
  • Dr. Cody Meissner, a professor of pediatrics at the Geisel School of Medicine at Dartmouth who ruffled feathers in 2021 by criticizing ruinous mask mandates for children.

The removal and replacement of members of the committee is a wish fulfilled for longtime critics of the ACIP and a nightmare realized for medical and pharmaceutical establishmentarians satisfied with the status quo.

Those in the establishmentarian camp now clutching pearls over Kennedy's actions appear eager to ignore or downplay the conflicts of interest, ideological bents, and questionable decisions that were apparently commonplace on the committee.

Lucrative questions, questionable decisions

The ACIP's members as of April 2025 were:

  • Helen Talbot, professor of medicine at Vanderbilt University School of Medicine;
  • Edwin Jose Asturias, professor of pediatrics and infection diseases at the University of Colorado School of Medicine;
  • Noel Brewer, professor in public health at UNC Gillings School of Global Public Health;
  • Oliver Brooks, interim chief executive officer at the National Foundation for Infectious Diseases;
  • Lin Chen, associate professor of medicine at Harvard Medical School;
  • Helen Chu, professor of medicine and epidemiology at the University of Washington;
  • Sybil Cineas, clinical associate professor of pediatrics and medicine at Warren Alpert Medical School of Brown University;
  • Denise Jamieson, vice president for medical affairs at the University of Iowa's Carver College of Medicine;
  • Mini Kamboj, professor of medicine at Weill Cornell Medical College;
  • George Kuchel, professor of medicine at University of Connecticut Health;
  • Jamie Loehr, family physician;
  • Karyn Lyons, chief of the immunization section at the Illinois Department of Public Health;
  • Yvonne Maldonado, professor of global health and infectious diseases at Stanford University;
  • Charlotte Moser, co-director of the Vaccine Education Center at Children's Hospital of Philadelphia;
  • Robert Schechter, chief of the California Department of Public Health Immunization branch;
  • Albert Shaw, professor of medicine at the Yale School of Medicine; and
  • Jane Zucker, adjunct professor at SUNY's department of community health services.

All 17 of the members were appointed by the Biden administration. Thirteen were appointed last year.

RELATED: RFK Jr. torches vaccine panel to make consequences count again

 Photo illustration by Joe Raedle/Getty Images

Data provided on OpenPaymentData.CMS.gov, a site managed by the U.S. Centers for Medicare and Medicaid Services, provides some insights into just how cozy some of the former members were with the organizations whose products they were tasked with scrutinizing.

The website indicates that between 2017 and 2023:

  • Asturias apparently collected around $54,000 from pharmaceutical companies, including $20,705 in what appear to be consulting fees. Among the companies that paid Asturias what appear to have been consulting fees were Pfizer and Merck Sharpe & Dohme LLC, a bio-pharmaceutical subsidiary of the company whose pneumococcal vaccine Capvaxive the committee voted to recommend in October. Asturias also appears to have received millions of dollars in research support from Big Pharma, including over $3.1 million from Pfizer and over $730,000 from the British pharmaceutical company GlaxoSmithKline LLC. The Colorado Sun reported that the research support was for Asturias to study RSV, pneumonia, and other diseases both in Guatemala and the United States.
  • Brooks apparentlyreceived over $18,000 in what appear to be consulting fees from the vaccine maker Sanofi Pasteur and thousands of dollars more from the company categorized as "compensation for services other than consulting, including serving as faculty or as a speaker at a venue other than a continuing education program."
  • Chen, a proponent of masking during the pandemic, apparently collected $55,111.07 from pharmaceutical companies. Like Asturias, she has collected thousands of dollars in consulting fees from Merck Sharpe & Dohme LLC but also plenty in consulting fees from the vaccine manufacturer Valneva, which the committee has since blessed with multiple recommendations. During Chen's directorship, Mount Auburn Hospital Travel Center received over $245,000 from the COVID-19 vaccine maker Moderna.
  • Chu apparently received over $6,000 in consulting fees from Merck Sharpe & Dohme and thousands more from the Illinois-headquartered pharmaceutical company AbbVie Inc. According to documentation from the Washington State Department of Health, Chu served as a co-investigator on studies funded by Pfizer, Novavax, and GlaxoSmithKline; has received research support from Gates Ventures, the Gates Foundation, Sanofi Pasteur, and Cepheid; and has served on advisory boards for Abbvie, Merck, Pfizer, Ellume, and the Gates Foundation.
  • Kuchel apparently received $10,720 in consulting fees from Big Pharma, the largest payment of which was from Johnson & Johnson's pharmaceutical company, Janssen Global. ACIP recommended the use of the Janssen COVID-19 vaccine last year.
  • Maldonado, who publicly emphasized the supposed need for children to get vaccinated for COVID-19, apparently received over $33,147 from pharmaceutical companies, including $27,577.71 in what appear to be consulting fees. Like Asturias and Chen, Maldonado received a sizeable consulting fee payment from Merck Sharp & Dohme in 2023. When broken down by general payments, Pfizer ranked number one for Maldonado. Prior to her appointment to the ACIP, the CDC indicated that Maldonado "served as Data and Safety Monitoring Board (DSMB) for Pfizer meningococcal vaccine trials and as a site PI for Pfizer pediatric COVID-19 and maternal RSV vaccines and AstraZenaca [sic] varicella zoster vaccine trials." She reportedly abstained form voting on the COVID-19, pneumococcal, and influenza vaccines.
  • Shaw, a member of Yale's Infectious Disease Diversity, Equity, and Antiracism Committee, apparently received $2,590 in consulting fees from Boehringer Ingelheim Pharmaceuticals.

According to the HPV IQ subpage on the University of North Carolina at Chapel Hill's Gillings School of Global Public Health website, Brewer "has received grants from and/or served on paid advisory boards for Pfizer, Merck, [GlaxoSmithKline LLC], FDA, CDC, and NIH."

The Defender reported in 2023 that Brewer — who suggested in 2023 that the "U.S. needs to get on an annual [COVID-19 vaccine] schedule, as we do for seasonal flu vaccination" — served on different paid Merck human papillomavirus boards since 2011 and served as a general consultant for the company for several years.

'They have a big job to do.'

Brewer reportedly received over $500,000 in grant funding to study HPV vaccine uptake from Merck and over $400,000 from Pfizer to "study how trainings might improve physician perceptions and recommendations of the HPV vaccine."

A Science investigation published in March downplayed the possible impact of Big Pharma ties among ACIP members, claiming that five of the 13 physicians on the committee prior to Kennedy's purge received no Big Pharma payments in the "several years before the service began" and that the various kinds of payments from drugmakers that eight other members received "averaged just over $4000 a year, nearly $3000 less than the average for all U.S. specialist physicians."

Blaze News reached out to Asturias, Brewer, Brooks, Chen, Chu, Maldonado, and Shaw for comment.

Brewer told Blaze News that his "last research grant from a pharmaceutical company ended nine years ago, in 2016," and the numbers provided above "are about right" and that "the actual numbers are higher by maybe $10K and change."

Brewer added, "I wish the new ACIP committee members well. They have a big job to do," then referred Blaze News to a recent article in Science, which notes that "the new panel members have been authors on about 78% fewer vaccine-related papers than the ousted members."

Ideological bent

Helen Chu joined Democratic Sen. Patty Murray (Wash.) to complain at a press conference on Thursday about the firings. Murray called the removal of Biden administration appointees a "dangerous, practically unthinkable step to undermine public health and vaccine confidence."

Chu, meanwhile, characterized the previous work of the ACIP as "transparent" and "unbiased."

Contrary to Chu's suggestion, biases ran deep on the panel in years past. While some of these biases may have been professional, others were ideological.

Noel Brewer, for instance, is a 2020 Biden donor whose social media history signals a possible DEI-lensed preoccupation with race.

'We must ask whether our own research, teaching, and service are intentionally antiracist.'

Brewer kicked off 2023 complaining that AI tools like ChatGPT sounded "straight, white and probably a few other things too." Months later, Brewer suggested that the lack of diversity in the authorship of certain textbooks was indicative of "white supremacy culture in academia." When discussing academic tenure and promotion decisions in September 2023, Brewer claimed that "fit, culture, and so on are tools of white supremacy."

Oliver Brooks — criticized in 2022 by Food and Drug Administration Commissioner Marty Makary for reportedly voting in favor of recommending that kids ages 5-11 receive COVID-19 vaccine booster shots without outcomes data — is a repeat donor to Democratic politicians including Los Angeles Mayor Karen Bass, Georgia Sen. Raphael Warnock, and failed presidential candidate Kamala Harris.

Like Brewer, his outlook appears tinged by identity politics.

Amid the Black Lives Matter riots in 2020, Brooks tried to provide an analogy to George Floyd's death in an editorial titled "Police Brutality and Blacks: An American Immune System Disorder" in the Journal of the National Medical Association in which he stated that the "country as a whole sets stereotypes as well as biases against black Americans which inevitably leads to social misinterpretation of the safety of Americans when a black person is present."

Brooks also noted, quoting another article, "We must ask whether our own research, teaching, and service are intentionally antiracist and challenge the institutions we work in to ask the same."

When Americans were protesting in 2020 in favor of reopening the country, Brooks framed the matter in identitarian terms on C-SPAN, noting, "If you look at those protesting to open up the environment — I prefer to use the term 'environment' as opposed to 'the economy' because it's not about money; it's about lives — most, I won't say all, most of the protesters are white or not inclusive of African-Americans or LatinX individuals."

Like some of her former colleagues on the panel, Sybil Cineas apparently has found it difficult to separate medicine from racial concerns or vice versa.

For instance, Cineas, listed as a member of the advisory group for Brown University's Office of Belonging, Equity, Diversity, and Inclusion, signed an open letter in 2021 to Tulane University's board of trustees, which complained of a "pervasive culture of White Supremacy" in the medical profession that "is perpetuated by the deeply hierarchical power structures of academic medicine."

The 'nuclear' decision

Kennedy noted in a June 9 op-ed that the point of "retiring" the committee members, including those "last-minute appointees of the Biden administration," was to help restore the public's trust "that unbiased science guides the recommendations from our health agencies."

"The committee has been plagued with persistent conflicts of interest and has become little more than a rubber stamp for any vaccine," wrote the health secretary. "It has never recommended against a vaccine — even those later withdrawn for safety reasons. It has failed to scrutinize vaccine products given to babies and pregnant women. To make matters worse, the groups that inform ACIP meet behind closed doors, violating the legal and ethical principle of transparency crucial to maintaining public trust."

'Most of ACIP's members have received substantial funding from pharmaceutical companies.'

When painting the committee as a succession of compromised members, Kennedy referred to a decades-old investigation that found a "web of close ties" between the CDC and the companies that make vaccines.

RELATED: CDC knew the COVID jab was dangerous — and pushed it anyway

 Photo by JOSEPH PREZIOSO/AFP via Getty Images

He also highlighted the revelation that four of the eight then-ACIP members who voted in 1997 to recommend routine vaccination of infants with the rotavirus vaccine had financial ties to the very pharmaceutical companies developing such vaccines. This was especially damning because the recommended vaccine was subsequently withdrawn on account of its ruinous and in some cases deadly side effects.

Although members are now barred from holding stocks or serving on advisory boards associated with vaccine makers, Kennedy indicated that "these conflicts of interest persist."

"Most of ACIP's members have received substantial funding from pharmaceutical companies, including those marketing vaccines," wrote the health secretary.

'Ending the conflict of interest is the first critical step to restoring unbiased, science-based analysis of safety and efficacy of vaccines.'

The health secretary emphasized that the "malpractice" impacts Americans nationwide, in part due to the committee's "stubborn unwillingness to demand adequate safety trials before recommending new vaccines for our children."

Kennedy claimed that "a compliant American child receives between 69 and 92 routine vaccines (depending on brand/dictated dosage) from conception to 18 years of age."

"ACIP has recommended each of these additional jabs without requiring placebo-controlled trials for any of them," said Kennedy. "This means that no one can scientifically ascertain whether these products are averting more problems than they are causing."

Peter Hotez, a cable news vaccine promoter and the founding dean of the National School of Tropical Medicine at Baylor College of Medicine, was among the medical establishmentarians to recently contest this claim about placebo-controlled trials, saying, "That's simply not true."

'The pharmaceutical companies have been running a regulatory capture scam.'

Kennedy claimed in response that such protesters were wrong — and made sure to bring receipts.

— (@)  
 

The health secretary also indicated on Friday that the ACIP will "institute bias policies recommending that ACIP panelists recuse themselves from decisions in which their current or former clients have a financial interest."

Mixed reception

Blaze News senior editor Daniel Horowitz said, "This is a nuclear bomb on the biomedical security state."

"The heart of the problem with vaccine safety stems from the fact that the pharmaceutical companies have been running a regulatory capture scam," continued Horowitz. "They place scientists and doctors on their payroll and then insert those individuals into government advisory positions. Ending the conflict of interest is the first critical step to restoring unbiased, science-based analysis of safety and efficacy of vaccines."

RELATED: Who is bankrolling the anti-MAHA movement? 

 Photo by Tasos Katopodis/Getty Images

Children's Health Defense, which was chaired by Kennedy from 2015 to 2023, similarly celebrated the news.

Mary Holland, president and CEO of CHD, told Blaze News in a statement that Kennedy's announcement "marks a pivotal advancement in the radical transparency he promised the country."

"Children's Health Defense has long highlighted the conflicts of interest involving the ACIP committee. It is unbelievable that ACIP members were allowed to participate in deliberations regarding a product in which they might have a financial stake," said Holland. "No wonder the committee consistently approved every vaccine for use, including those that were proven unsafe and subsequently removed shortly after approval. Ending this practice represents a significant step forward in restoring the public’s trust in our health agencies."

Of course, Kennedy's actions did not please everyone.

'I've never seen anything this damaging to public health happen in my lifetime.'

Massachusetts Sen. Elizabeth Warren, one of the Democratic lawmakers who has received a fortune in donations from the pharmaceutical industry, called the firing of the ACIP members "a public health disaster."

Paul Offit, director of the Vaccine Education Center at Children's Hospital of Philadelphia, was among the many who concern-mongered last year about the impact that Kennedy could have if afforded power and access in the Trump administration.

Last week, Offit wrote, "RFK Jr. will do everything he can to make sure that all vaccines are no longer mandated and to make vaccines less available, less affordable and more feared. This is only the beginning."

One of the dismissed ACIP members complained to CNN, "I've never seen anything this damaging to public health happen in my lifetime."

RELATED: HHS scraps COVID vaccine schedule for children and pregnant women: 'It's common sense, and it's good science'

 

  Rebecca Noble/Getty Images

The ex-member, whose name was not disclosed, added, "I'm shocked. It's pretty brazen. This will fundamentally destabilize vaccination in America."

Bruce Scott, the president of the American Medical Association, similarly expressed distress last week, claiming that the action undermines public trust "and upends a transparent process that has saved countless lives."

Tina Tan, president of the Infectious Diseases Society of America, claimed that Kennedy's "allegations about the integrity of CDC’s Advisory Committee on Immunization Practices are completely unfounded."

BlazeTV host Steve Deace, considering the action within the broader context of the MAHA movement, told "Blaze News: The Mandate" last week that President Donald Trump's decision to make Kennedy the health secretary "might be the closest we're ever going to get in America to a tribunal on what happened during that time [the pandemic]."

The firings at the ACIP are "the closest thing to real consequences — people losing their jobs — that we have seen," added Deace.

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HHS indicated in a statement that it will convene its next meeting June 25 through June 27 at the CDC headquarters in Atlanta.

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‘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).

Soldier discharged under Biden after refusing COVID vax finally gets justice, thanks to Trump



Mark Bashaw, a former lieutenant in the U.S. Army, finally has a measure of justice after he was criminally convicted and discharged for refusing to abide by COVID-related protocols implemented under President Joe Biden.

In August 2021, then-Secretary of Defense Lloyd Austin imposed a COVID vaccine mandate for members of the military, claiming the shots were critical for maintaining healthy, ready armed forces. Those like Bashaw who refused were required either to work from home or to subject themselves to COVID testing before going into the office, where they would have to wear a mask.

Bashaw — the company commander of the Army Public Health Center in Aberdeen Proving Ground, Maryland — refused to abide by those directives. As a result, he was convicted by a court martial in 2022 of failing to obey lawful orders.

In a 2023 social media post, he claimed he had been court-martialed because he "refused to participate with lies." Following his conviction, he was involuntarily discharged.

Some 8,000 service members were similarly discharged from the military for refusing the shot. However, Bashaw is believed to have been the first to be court-martialed for failing to adhere to the COVID protocols issued by Austin, The Hill reported.

On Wednesday, President Donald Trump issued Bashaw a full and unconditional pardon.

Bashaw's conviction did not result in any jail sentence, but it did give him a criminal record. Trump's pardon wipes his record clean.

Bashaw celebrated the news of his pardon on social media: "I just received a Presidential Pardon from President Donald J. Trump. I am humbled, grateful, and ready to continue fighting for truth and justice in this great nation. Thank you, Mr. President @realDonaldTrump and to your incredible team."

After thanking others, including former U.S. Attorney for D.C. Ed Martin, Bashaw's post added: "Time for accountability!" It also included an image that described COVID as a "plandemic."

RELATED: Ed Martin floats names of 'gatekeepers' in Biden autopen controversy; Trump accuses exploiters of 'TREASON'

  Photo by Craig Hudson For The Washington Post via Getty Images

Blaze News senior editor Daniel Horowitz applauded Bashaw's courage despite his "unfathomable" suffering "under the Biden-controlled DOD."

"It’s easy to be a hero now that COVID tyranny has been universally repudiated and it no longer costs anything to take a stand. Yet, Bashaw risked his entire career and even time in the brig for standing up for the rule of law and the medical ethics of public health," Horowitz told Blaze News.

Horowitz also thanked Trump for making good use of his pardon powers: "Well played, Mr. President."

BlazeTV host Steve Deace, who has long railed against the COVID shots, was likewise pleased to hear that Trump intervened in Bashaw's case.

"This is another commendable act of penance by President Trump for the mistakes of his first administration during the scamdemic, which set the stage for the outright tyranny imposed by whoever was making decisions for Biden the last four years. His language at times certainly has its bravado, but President Trump is really showing great humility in unraveling the original COVID narrative his first term succumbed to," Deace said in a statement to Blaze News.

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Biden admin covered up potentially deadly COVID vaccine side effects for months: Senate report



A Senate report claims that President Joe Biden's administration was aware for months about heart issues stemming from COVID-19 vaccines and purposely withheld the information from the public.

A report from the Senate Permanent Subcommittee on Investigations said government officials knew as early as February 2021 about the harmful side effects but waited until June to inform the public of the inherent dangers.

'The federal government was very well aware of the myocarditis signal, particularly in young men.'

The report revealed that U.S. health officials "knew about the risks" the vaccines carried related to myocarditis, inflammation of heart muscle, and pericarditis, inflammation of the fibrous sac surrounding the heart, but "downplayed the health concern" and "delayed informing the public about the risk."

RELATED: HHS scrapping COVID jab recommendations for pregnant moms and kids: Report

  

The report, first obtained by the Daily Wire, showed that the U.S. government ignored warnings from several sources.

In February 2021, U.S. entities were notified of adverse effects by the Israeli Ministry of Health, as the country rolled out vaccines faster than America did. Still, CDC officials declined to make public the "large reports of myocarditis, particularly in young people, following the administration of the Pfizer vaccine."

It is unclear whether the Israeli government made an effort to notify the public, either.

That same month, a CDC official who co-led the Vaccine Safety Technical Work Group emailed her colleagues about 19,536 vaccine adverse event reports (through the Vaccine Adverse Event Reporting System) that included 980 deaths after vaccination.

"Where known, the cause of death was often cardiovascular," the report read.

Senator Ron Johnson (R-Wis.) told the Daily Wire that the Biden administration did not want to increase "vaccine hesitancy" by reporting the side effects openly.

"But in being concerned about that, they violated the inviolable principle of informed consent," Johnson told the outlet. “The federal government was very well aware of the myocarditis signal, particularly in young men, as early as February [2021]."

RELATED: New documentary reveals heartbreaking COVID vaccine stories they kept secret

  

In May 2021, the CDC omitted information from its "clinical considerations" on its website that advised doctors to restrict patients with myocarditis from "rigorous activity like competitive sports for at least 3 months."

The report also said that in June 2021, the White House distributed talking points to U.S. health officials "downplaying the risk of myocarditis."

"The depths of depravity of this cover-up keep getting deeper. They knew about vaccine side effects early on but withheld that information as they continued to push emergency use authorization even as young people were dying," BlazeTV's Matt Kibbe said about the report.

Kibbe added, "This scandal is ultimately about self-dealing between government bureaucrats and pharmaceutical companies, who all had financial incentives to bury the truth and keep pushing the vaccines."

Blaze News reached out to the National Institutes of Health and Health and Human Services for comment but did not immediately receive a response.

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HHS scrapping COVID jab recommendations for pregnant moms and kids: Report



The Department of Health and Human Services is reportedly preparing to scrap its recommendation that pregnant women and kids get the COVID-19 vaccines. Individuals said to be familiar with the matter told the Wall Street Journal that the announcement is imminent and will coincide with the Centers for Disease Control and Prevention kicking off a new vaccine approval framework.

While the relevant agencies apparently did not respond to the Journal's requests for comment, U.S. Food and Drug Commissioner Dr. Marty Makary provided a fairly strong indication this week that the change was coming.

Makary told Turning Point USA CEO Charlie Kirk that he would "love to see the evidence to show that giving young, healthy children another COVID-19 shot — you know, a sixth COVID booster — would help them, but that evidence does not exist, and so we're not going to rubber-stamp things at the FDA."

"I don't think you're going to see a push at the CDC to be pushing COVID shots in young, healthy children," continued Makary, adding that he expected an announcement on that front in the coming weeks.

Sources told the Journal that it would only be a matter of days.

At the time of publication, the CDC was still recommending that everyone ages 6 months and older get a COVID-19 vaccine.

'Connected to serious adverse events, including myocarditis and pericarditis, failed pregnancies, and deaths.'

The agency states on its website that getting the shot is especially important for individuals who have survived this long without one, geriatrics, pregnant women, those planning to conceive, and breastfeeding mothers. The agency urges parents to get their children 6 months to 4 years of age loaded up with two doses of the Moderna vaccine or three doses of the Pfizer vaccine if they were starting fresh.

As of April 26, 14.4% of pregnant women had received a 2024-25 COVID-19 vaccine and 13% of children 6 months to 17 years of age were up to date, CDC data shows.

RELATED: Jab first, ask questions never: Vaccine truths your doctor won't tell you

 EKIN KIZILKAYA/iStock/Getty Images Plus

The CDC stuck with its recommendations until now despite credible warnings from Florida Surgeon General Dr. Joseph Ladapo and other experts; troubling scientific studies demonstrating the vaccines were not as safe and effective as advertised; glaring evidence that kids and teens were at low risk for COVID and could go without; and damning state-leveled allegations that one of the primary vaccine manufacturers sat on evidence that its COVID-19 vaccine "was connected to serious adverse events, including myocarditis and pericarditis, failed pregnancies, and deaths."

Just last month, a preprint study backed by the Florida Department of Health suggested that adults in the Sunshine State who received the Pfizer vaccine had "significantly higher risk of 12-month all-cause, cardiovascular, COVID-19, and non-COVID-19 mortality" than those who received the Moderna shot.

A study conducted by the Global COVID Vaccine Safety Project — a Global Vaccine Data Network initiative supported by both the CDC and the HHS — and published last year in the journal Vaccine detailed troubling links between the AstraZeneca, Moderna, and Pfizer vaccines and medical conditions such as Guillain-Barré syndrome, brain and spinal cord inflammation, Bell's palsy, and convulsions.

Another peer-reviewed study published last year in the pharmacotherapy journal Therapeutic Advances in Drug Safety indicated 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," said the study.

'The current risks of serious adverse events or deaths outweigh the benefits.'

Texas cardiologist Peter McCullough, a leading critic of the vaccines, said in a statement Thursday, "Two presidents, three HHS Secretaries, three FDA Commissioners, and nearly five years into the disastrous COVID-19 vaccine debacle, women and children receive long overdue yet welcome news. After record vaccine injuries, disabilities, and death, America is wondering will any of these leaders be held accountable?"

Dropping the recommendations appears to be a half measure, given that HHS Secretary Robert F. Kennedy Jr. previously fought to revoke authorization of COVID-19 vaccines altogether.

RELATED: Mandates, masks, and mayhem: Never again!

 Photographer: Al Drago/Bloomberg via Getty Images

In a petition he filed with the FDA on May 16, 2021, Kennedy said the agency should revoke all emergency use authorizations and refrain from approving future EUAs for any COVID vaccine for all demographic groups "because the current risks of serious adverse events or deaths outweigh the benefits, and because existing, approved drugs provide highly effective prophylaxis and treatment against COVID, mooting the EUAs."

Kennedy noted further that the agency should specifically spare children and pregnant women from the novel vaccines.

Kennedy's warnings and requests evidently fell on deaf ears.

In its final weeks, the Biden HHS extended liability protection to COVID-19 vaccine manufacturers and administrators through Dec. 31, 2029, precluding vaccine recipients who reportedly end up injured or their surviving family members from holding those responsible to account. This was the latest of several such extensions.

The reports of the HHS dropping the vaccine recommendations and other moves made in recent months by the Trump administration have elements of the medical establishment clutching pearls.

Paul Offit, director of the Vaccine Education Center at Children's Hospital of Philadelphia, told the New York Times, "I think that we are in the midst of watching the vaccine infrastructure being torn down bit by bit."

"I think everything is a target," said Tara Smith, an epidemiologist at Kent State University College of Public Health.

"Overturning the recommendation means that insurance companies will no longer have to cover these vaccines," Dorit Reiss, a law professor at UC Law San Francisco, complained to the health publication Stat.

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Johnson & Johnson worried about losses from China tariffs despite projecting $700 million in profits



Johnson & Johnson's CEO said President Trump's tariffs on pharmaceuticals could cause a problem for drug supply chains.

During an investor call, CEO Joaquin Duato told his colleagues that they should work with the Trump administration to address supply chain vulnerabilities that could arise as a result of tariffs.

The remarks were seemingly an effective call for the Trump administration to ease tariffs on raw ingredients and drugs from China, the country the president has hit hardest in his new economic plan.

At the same time, however, Johnson & Johnson reported strong first-quarter revenues that even surpassed Wall Street estimates, Reuters stated.

According to the report, the pharmaceutical giant detailed plans to raise U.S. investments by 25% in the next four years — with some commitments already made — which would total more than $55 million.

Sales for 2025 were forecast to be around $700 million, and an upcoming nasal spray that allegedly treats depression is expected to generate sales between $3 billion and $3.5 billion annually by 2028. The company's chief financial officer reportedly claimed that a $400 million loss, as a result of tariffs, had been worked into the profit margin calculations.

Following a third failed bankruptcy attempt, the company is still facing over 90,000 lawsuits from families who alleged that talc-based Johnson & Johnson products were contaminated with asbestos and caused ovarian cancer after prolonged use.

The Lawsuit Information Center reported that a bankruptcy court rejected Johnson & Johnson's $9 billion settlement proposal. Divided equally among 90,000 cases, that figure would equate to $100,000 per lawsuit.

At least 3,500 claimants are from the United Kingdom, making this case one of the largest class-action suits in English and Welsh history. While the majority of claimants are women, some men are included in those claims that also said the company's powder products contained asbestos and caused cancer.

According to the Guardian, the number of lawsuits has nearly doubled since November 2024.

'[Duato] oversaw the company’s rapid response to the COVID-19 pandemic.'

As for CEO Duato, the executive is coming off one of the most lucrative years of his career after his income increased to $28.4 million in 2023, versus $13.1 million in his first year as CEO in 2022, per Fierce Pharma.

Duato is a dual citizen of the U.S. and Spain and got his start at Johnson & Johnson subsidiary Janssen Pharmaceuticals. In 2021, BioSpace reported that Duato sat on the board of directors for UNICEF USA, while Fox Business noted he is the executive sponsor of Johnson & Johnson's African Ancestry Leadership Council.

Duato was also praised by his company for his work during COVID-19:

"[Duato] oversaw the company’s rapid response to the COVID-19 pandemic and led coordination of global initiatives to safeguard the health of employees and ensure business and supply chain continuity," a company release said.

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Fauci's wife, vax-peddling buddies get the boot at NIH



Health and Human Services Secretary Robert F. Kennedy Jr. indicated last week that his department would downsize its workforce from 82,000 to 62,000 employees as part of a broader overhaul intended to maximize efficiency and save taxpayers money. Senior officials at the National Institutes of Health, a subordinate agency, were evidently not immune to this shake-up.

Insiders told Politico that Christine Grady, the wife of former National Institute of Allergy and Infectious Diseases Director Anthony Fauci, was ousted Tuesday from her role as senior investigator at the NIH Clinical Center's Department of Bioethics. Kennedy allegedly signed off on the termination of Grady, who spearheaded research into the ethics of the U.S. pandemic response.

Fauci allies Clifford Lane, deputy director for clinical research and special projects at NIAID, and Emily Erbelding, director of the NIAID division of microbiology and infectious diseases, were reportedly also given the boot.

Several institute directors, including Fauci ally Jeanne Marrazzo — the NIAID director who claimed during the pandemic that "wearing a mask is very effective" and told people not to gather in groups, including at "gyms, bars and churches" — were among the officials linked to the government's development and rollout of the COVID-19 vaccines who were offered reassignments.

'What we've been doing isn't working.'

A copy of the agency's email to directors obtained by Nature states, "HHS proposes to reassign you as part of a broader effort to strengthen the Department and more effectively promote the health of the American people."

The letter offered the Washington, D.C., and Atlanta area-based directors the option of working in Alaska, Montana, and Oklahoma — supposedly an inducement to quit — noting, "This underserved community deserves the highest quality of service, and HHS needs individuals like you to deliver that service."

Whether they were fired or effectively resigned rather than transfer to distant outposts is unclear.

As the old guard were marched out of the NIH on what coincidentally was Dr. Jay Bhattacharya's first day in office as the director of the agency, Kennedy noted on X, "This is a difficult moment for all of us at HHS. Our hearts go out to those who have lost their jobs."

Despite characterizing the terminations as difficult, Kennedy underscored that they were necessary.

"The reality is clear: What we've been doing isn't working. Despite spending $1.9 trillion in annual costs, Americans are getting sicker every year. In the past four years alone, the agency’s budget has grown by 38% — yet outcomes continue to decline," wrote the health secretary. "We must shift course. HHS needs to be recalibrated to emphasize prevention, not just sick care. These changes will not affect Medicare, Medicaid, or other essential health services.

'This will go down as one of the darkest days in modern scientific history.'

Bhattacharya said in an email to staff that the terminations would "have a profound impact on key N.I.H. administrative functions, including communications, legislative affairs, procurement and human resources" and thanked the "scientists and staff whose work has contributed to lifesaving breakthroughs in biology and medicine."

Although a long time coming, the layoffs caught some workers off guard and enraged certain health establishmentarians.

Jessica Henry, formerly a digital communications specialist at the NIH's National Institute of Dental and Craniofacial Research, told the New York Times that she learned after showing up to at work in Maryland on Tuesday that she had been canned with her entire team of communications and health education specialists.

"I also just feel so confused, and honestly kind of angry, because we hear a lot about how the administration wants to increase transparency," said the former theater teacher. "They want accountability to the American people for how their tax dollars are being spent. And from what I can tell, they just fired all of us who do that."

Michael Osterholm, director of the University of Minnesota’s Center for Infectious Disease Research and Policy, bemoaned the layoffs, telling Nature, "This will go down as one of the darkest days in modern scientific history in my 50 years in the business. These are going to be huge losses to the research and public health community."

"These are going to be huge losses to the research community," added Osterholm.

Monica Bertagnolli, former NIH director under Joe Biden, told Nature the treatment of the directors was "frankly unconscionable," adding, "These are all outstanding leaders, who were let go without accounting for the harm that could be done with the loss of research productivity and the loss of programs delivering lifesaving treatments."

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Trump And RFK Should Accelerate Inexpensive Treatments For Long Covid And Other Diseases

Generic drugs can combat an array of chronic diseases, but only if the Trump administration creates a structured, interdisciplinary study of these drugs.