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Impeach RFK Jr.? Critics Pan Congresswoman’s Plan to Launch Impeachment Bid

By Michael Nevradakis, Ph.D. | The Defender | September 25, 2025

Michigan Congresswoman Haley Stevens today said she will introduce articles of impeachment against U.S. Health Secretary Robert F. Kennedy Jr., claiming his leadership of the U.S. Department of Health and Human Services (HHS) has resulted in “health care chaos” and “reckless cuts.”

Stevens, a Democrat, first announced her intent in a post earlier today on X. She followed up with a statement citing four reasons why she seeks to impeach Kennedy.

Stevens alleged that Kennedy is “severely restricting access to vaccines and spreading absurd conspiracies,” including withdrawing “federal recommendations for COVID shots for pregnant women and healthy children” and promoting “wild and unfounded claims” about the risks of acetaminophen.

She also claimed that Kennedy has abdicated his duty as HHS secretary by “cutting funding for lifesaving research,” including cancer research and studies on sudden infant death syndrome (SIDS).

According to Stevens, Kennedy has failed to “carry out statutory duties of HHS” in administering the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention (CDC), and lied during his confirmation hearing before the U.S. Senate earlier this year.

Stevens also claimed Kennedy’s policies are “making our country less safe and making healthcare less affordable and accessible” and are reflective of his “contempt for science” and “the constant spreading of conspiracy theories.”

“Enough is enough — we need leaders who put science over chaos, facts over lies, and people over politics, which is why I am announcing today that I have begun drafting articles of impeachment against Secretary Kennedy,” Stevens stated.

A spokesperson for Stevens’ office told The Defender the articles of impeachment are being drafted and “will be introduced soon.”

Stevens has repeatedly advocated for Kennedy’s removal, including a call for Kennedy’s resignation earlier this month.

In a statement provided to The Defender, Andrew Nixon, communications director for the HHS said, “Secretary Kennedy remains focused on the work of improving Americans’ health and lowering costs, not on partisan political stunts.”

‘Founders did not want people removed from office over policy disagreements’

According to The Detroit News, it is “unlikely that Stevens’ call for impeachment will be successful, given Republican majorities in Congress.”

A simple majority in the U.S. House of Representatives and a two-thirds majority in the U.S. Senate after a trial are required for an impeachment effort to succeed. Republicans hold majorities in both chambers.

Sayer Ji, chairman of the Global Wellness Forum and founder of GreenMedInfo, said that, “with a Republican-controlled House, impeachment is a political non-starter,” but that the goal is “to generate headlines, stigmatize dissent, and chill debate — reputational warfare disguised as constitutional accountability.”

Attorney Rick Jaffe suggested Stevens’ effort may be an inappropriate use of the impeachment process and may set a “dangerous” precedent. He said:

“Those are the kinds of disputes the political process is supposed to resolve. If Congress thinks HHS policy is wrong, it holds hearings, passes oversight statutes or uses the purse. ‘Impeachment as policy veto’ is dangerous.

“Normalizing impeachment for contested scientific positions would chill executive-branch debate and weaponize impeachment as a routine tool. The Constitution reserves impeachment for treason, bribery or comparable abuses. If this standard becomes ‘I disagree with your science,’ every Secretary of HHS under either party will face perpetual impeachment threats. That destabilizes public health governance.”

The Detroit Free Press also called into question the legality of Stevens’ impeachment attempt, writing:

“Given that the Constitution limits impeachment to charges of ‘treason, bribery, or other high crimes and misdemeanors,’ with the presumption being the founders did not want people removed from office over policy disagreements, there almost certainly would be question as to the legality of an impeachment drive.”

Jaffe said that the impeachment push is unlikely to succeed but may further fuel the political divide in the U.S. He said:

“This, in all likelihood, will not remove Kennedy, since the votes aren’t there in the House, and there does not appear to be a path to two-thirds in the Senate. But it will harden lanes. Expect more hearings, subpoenas and media escalation aimed at discrediting HHS leadership.

“If Congress wants to change policy, it should legislate. If it wants accountability, it should investigate. Impeachment is a constitutional last resort, not a press release.”

Stevens eyeing Michigan’s open Senate seat next year

Ji and Jaffe noted that Stevens may also have a political motive in attempting to impeach Kennedy, as she will run for Michigan’s open Senate seat next year.

“Stevens herself is not acting in a vacuum,” Ji said. “This gambit delivers national visibility as a ‘defender of science.’ But her language mirrors pharma-aligned talking points so closely it reads like a continuation of the script.”

According to Jaffe, “Filing impeachment in a GOP-run House is a branding exercise. She gets the headline, tests a message with the primary electorate and positions herself as a ‘defender of science.’ Smart politics from the Democrats’ point of view. They want to keep that Senate seat.”

The Detroit Free Press reported that Stevens faces a Democratic primary along with two other major candidates for the open Senate seat. Her impeachment push “makes clear that Democrats intend to use disapproval of Kennedy with the voters against Republicans in next year’s midterm elections.”

According to The Daily Beast, recent moves by Kennedy and other public health officials have “raised concerns, including among some Republican lawmakers.” The Hill reported today that unnamed Republican senators “are growing increasingly uncomfortable with health actions being taken by the Trump administration.”

Stevens’ donors include Pfizer, medical organizations, health insurers

Data from Open Secrets shows that Stevens received $98,739 in donations from “health professionals” during the 2023-2024 donation cycle, making this one of the top five industries that donated to her.

She also received $17,756 from pharmaceutical and health products companies during the same period.

Open Secrets data also show that Stevens received a $1,500 donation from Pfizer last year — and donations from medical and health organizations including the American Medical Association and the American College of Emergency Physicians.

Stevens has also received donations from pharmacy chains including CVS Health and Target, major insurers including Blue Cross/Blue Shield of Michigan and UnitedHealth, and from BlackRock, Google, Mastercard, McDonald’s and Microsoft.

Are calls for impeachment part of ‘hybrid warfare’ aiming to oust RFK Jr.?

According to Ji, the effort to impeach Kennedy is part of a broader, coordinated attempt by multiple actors, including political figures, pharmaceutical companies and their lobbyists, and some legacy media outlets, to oppose Kennedy.

“Stevens’ announcement is not genuine ‘oversight’ — it is the next front in a coordinated influence operation,” which includes the recent Senate hearing in which Susan Monarez, Ph.D., operated and a series of op-eds published in prominent outlets, Ji said.

These efforts mirror proposals contained within a leaked document — purportedly the minutes of an April meeting of the Biotechnology Innovation Organization (BIO), a major pharmaceutical lobbying organization. BIO has denied the authenticity of the document.

In June, research scientist and author James Lyons-Weiler, Ph.D., first went public with the alleged minutes of an April meeting of BIO’s Vaccine Policy Steering Committee. He said the document was sent “anonymously by whistleblowers.”

According to the BIO document, John F. Crowley, president and CEO of BIO, allegedly participated in the meeting and proposed a “creative communication campaign” targeting legislators and influencers while isolating Kennedy.

Crowley also allegedly suggested that BIO spend $2 million on such lobbying efforts.

Participants in the BIO meeting, including current employees and board members of vaccine manufacturers, also allegedly said, “It is time to go to The Hill and lobby that it is time for RFK Jr to go … communicate what’s going on in business.”

‘Looks like a part of the coordinated action’ against Kennedy

Ji connected efforts targeting Kennedy to the U.K.-based Center for Countering Digital Hate (CCDH), a nongovernmental organization that, in 2021, included Kennedy on its “Disinformation Dozen” list of the 12 “leading online anti-vaxxers.”

According to documents leaked by a whistleblower last year, CCDH planned “black ops” against Kennedy. “Black ops” are defined as a “secret mission or campaign carried out by a military, governmental or other organization, typically one in which the organization conceals or denies its involvement.”

The leaked documents, containing minutes from internal CCDH staff meetings held between January and October 2024, revealed that CCDH planned these “black ops” in response to “Nervousness about the impact of him on the election.”

CCDH, currently under investigation by Congress, and its founder and CEO Imran Ahmed, maintain ties to members of the Democratic Party.

Ji said core components of this coordinated campaign include “congressional convergence” and the dissemination of a narrative opposing Kennedy in the media.

Last month, MedPageToday reported that doctors and “public health advocates” were calling for Kennedy’s impeachment. Later in August, USA Today published an op-ed titled, “RFK Jr. is an anti-vaccine kook destroying the CDC. Impeach him.”

Earlier this month, a Mother Jones op-ed stated, “Impeach RFK Jr.,” characterizing him as one of several “unqualified extremists” in Trump’s cabinet. On Sept. 15, Free Speech for People cited unnamed “constitutional law experts” in calling for Kennedy’s impeachment, accusing him of “abuses of power.”

“Far from independent analysis, this is narrative warfare — reputational framing masquerading as journalism, designed to normalize impeachment talk before it even reached Congress,” Ji said, calling this an example of “hybrid warfare — reputational, legislative and media-based.”

Jaffe called the string of op-eds calling for Kennedy’s impeachment “an unmistakable pile-on” that “looks like a part of the coordinated action” against Kennedy.

Stevens has a controversial congressional past. In March 2020, House leadership ruled Stevens was “out of order” following a speech that ran over time on a proposed COVID-19 relief package. The Detroit News described the speech, during which Stevens wore pink latex gloves, as a “yelling spree.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

September 28, 2025 Posted by | Progressive Hypocrite | , | Leave a comment

Pharma’s Coup Attempt: How Cartel Insiders Are Plotting to Oust Robert F. Kennedy, Jr.

By Paul Anthony Taylor | Dr. Rath Health Foundation | September 5, 2025

leaked memo from one of the pharma cartel’s most powerful trade groups has revealed a desperate plan to push Robert F. Kennedy, Jr. out of his role as United States Secretary of Health and Human Services (HHS). The document, apparently originating from a closed-door meeting of the Biotechnology Innovation Organization (BIO), shows that industry leaders are prepared to spend millions of dollars lobbying Congress and manipulating public opinion to force Kennedy from his job. At stake is not just U.S. government vaccine policy, but the deeper question of who actually runs public health in America – democratically elected officials, or the corporations that profit from disease.

The plan unveiled

The memo appears to come from BIO’s Vaccine Policy Steering Committee, a powerful body representing companies such as Pfizer, Merck, Novavax, and Vaxcyte. According to whistleblowers, the group met on April 3, 2025, to discuss the “threat” posed by Kennedy’s healthcare reform agenda. The summary leaves no doubt about its intentions. One line is especially blunt: “It is time to go to The Hill and lobby that it is time for RFK Jr. to go.”

The threat to the cartel is clear. Kennedy has insisted on long-term safety data for vaccines, full publication of trial results, and the restoration of manufacturer liability for injuries. These proposals would dramatically slow down the fast-track approvals and legal protections that have allowed vaccine makers to rake in billions while avoiding accountability. In the eyes of BIO, this is not just policy reform – it is a direct attack on its business model.

Fear of accountability

BIO’s real fear is not scientific debate but financial disruption. The memo quotes one executive from Vaxcyte warning that “investors have stated they are leaving until the next data read out,” citing uncertainty caused by Kennedy’s push for tighter regulation. Capital, in other words, is fleeing the vaccine sector. Instead of reassuring the public with stronger safety standards, BIO is working to reassure Wall Street by removing the man calling for reform.

This exposes the heart of the problem: the pharmaceutical industry has become so dependent on weak oversight and political protection that it views accountability itself as a threat. Rather than adapt to higher safety expectations, BIO would rather manipulate politics to preserve the old system.

Buying influence

The most revealing part of the plan is financial. BIO has committed $2 million to a new communications campaign titled ‘Why We Vaccinate.’ But this is no ordinary public health initiative. According to the memo, its goal is not education but “inspire and frighten” messaging designed to sway the “movable middle” of public opinion. Essentially, by tying vaccination to national security, economic productivity, and workforce resilience, the campaign seeks to use fear as a political weapon.

This is not science. It is psychology. Instead of engaging Kennedy’s arguments on their merits, BIO plans to drown out discussion with a flood of fear-based advertising and carefully managed surrogates. Among those mentioned as possible allies are Dr. Mehmet Oz and Senator Bill Cassidy. These figures are expected to provide a veneer of bipartisan legitimacy while avoiding any real debate about the substance of Kennedy’s proposals.

Controlling the narrative

Equally troubling is BIO’s strategy of redefining language itself. The leaked document reveals plans to replace words like “protect” and “defend” with softer-sounding terms such as “streamline,” “optimize,” and “enhance.” But behind the rebranding lies a cynical truth. As Robert W. Malone MD has pointed out, when BIO says “efficiency,” it means fewer safety checks. When it says “transparency,” it means PR-polished talking points, not the release of raw scientific data. When it says “resilience,” it means consumer obedience, not real safeguards.

This is not reform – it is narrative disingenuity that would not be out of place in George Orwell’s dystopian novel Nineteen Eighty-Four. BIO is attempting to control the vocabulary while ensuring that nothing actually changes. It is a form of deception that goes beyond lobbying, seeking to manipulate the very terms of debate so the public never realizes reform has been hollowed out.

The plot is already underway

The memo points to this month (September 2025) as a critical deadline. Congress is back in full session, budget negotiations are getting underway, and the media cycle is returning to full speed after the summer lull. BIO’s campaign is timed to seize this moment, flooding the airwaves with its ‘Why We Vaccinate’ messaging before Kennedy’s reform agenda gains traction.

September also marks the reopening of schools, a time when vaccine debates are most prominent in the public eye. By striking early, BIO hopes to dominate the narrative and silence Kennedy before he can rally broader public support. For the pharma industry, this is not about science but survival.

Significantly, therefore, in the past couple of days, we have already seen nine former leaders of the Centers for Disease Control and Prevention (CDC) speaking out against Kennedy, publishing an open letter in The New York Times that criticizes his policies.

Separately, and simultaneously, more than 1,000 current and former HHS employees are said to be calling for Kennedy to either resign or be fired. Their letter – which does not name the signatories but mentions vaccines eight times – accuses him of endangering the nation’s health. It is difficult not to see the hand of BIO behind these moves.

A threat to democracy

The implications of this plot go far beyond health policy. If corporations can secretly conspire to spend millions lobbying for the removal of a sitting government official, then democracy itself is in danger. Whether one agrees with Kennedy’s policies or not, it should not be the pharmaceutical lobby that decides who serves in public office. That decision belongs to the people and their elected representatives, not to an industry that stands to profit from the outcome.

This is why the BIO leak matters so much. It shines a light on the machinery of influence that usually operates in the shadows – closed-door meetings, carefully managed talking points, and money flowing into Washington to buy outcomes that serve shareholders instead of citizens.

Who decides about global health?

The BIO plot also has international implications, as it aligns with broader efforts to centralize health policy through global treaties and the algorithmic censorship of dissenting medical views. If left unchecked, this could lead to a future where drug companies, aided by international bodies, dictate not only U.S. policy but all global health decisions as well. The Kennedy reforms represent a direct challenge to that vision.

Ultimately, therefore, this story is not just about Robert F. Kennedy, Jr. It is about whether public health will be guided by the principles of science, safety, and consent – or by the profit motives of an industry that sees accountability as a threat. Seen in this light, BIO’s efforts to remove Kennedy are not a sign of power. They are an admittance of weakness.

Kennedy’s reforms may be inconvenient for Wall Street, but they reflect the public’s increasing demands for safety, consent, and honesty in medicine. The real question now is whether corporations will continue to dictate the rules – or whether the American people can successfully reclaim health policy for the public good.


Paul Anthony Taylor

Executive Director of the Dr. Rath Health Foundation and one of the coauthors of our explosive book, “The Nazi Roots of the ‘Brussels EU’”, Paul is also our expert on the Codex Alimentarius Commission and has had eye-witness experience, as an official observer delegate, at its meetings.

September 7, 2025 Posted by | Corruption, Science and Pseudo-Science | , , | Leave a comment

HHS Cancels mRNA Vaccine Development – ‘poses more risk than benefit’ says RFK Jr

By Jefferey Jaxen | August 5, 2025

A stunning announcement from HHS Secretary RFK Jr. has set the media ablaze.

“After reviewing the science and consulting top experts at NIH and FDA, HHS has determined that mRNA technology poses more risk than benefits than these respiratory viruses.”

The official HHS press release states:

“BARDA is terminating 22 mRNA vaccine development investments because the data show these vaccines fail to protect effectively against upper respiratory infections like COVID and flu. We’re shifting that funding toward safer, broader vaccine platforms that remain effective even as viruses mutate.”

The announcement wipes out nearly $500 million worth of Covid mRNA vaccine development projects, “we’re moving beyond the limitations of mRNA and investing in better solutions” stated Kennedy in the HHS press release.

Kennedy’s announcement comes after months of outside pressure to wind down the Covid mRNA vaccine platform in the U.S.

In May 2025, RFK Jr. removed COVID-19 vaccines from the list of routine immunizations for healthy pregnant women and children.

HHS and America now have pressing work at hand to undue the damage of the rushed and forced mRNA vaccine platform.

World-leading cancer researcher Dr. Patrick Soon-Shiong recently stated in an interview: “This non-infectious pandemic of cancer is sadly upon us” referring to how both the virus and the vaccine can awaken sleeping cancer cells in the body. A topic mainstream science is just now, after years of alternative researchers and journalists banging the drum, beginning to admit and study. The new study in the journal Nature chronicles how it is actually the immune system’s response to the lab created gain-of-function bioweapon (and the mRNA shot as we have pointed out) that down-regulates and allows for accelerated cancer progression.

Kennedy has signaled over the last month that he is now taking aim at the broken vaccine injury compensation in the United States.

America, and other countries that align with our mission, must now develop a Manhattan Project-level effort to reverse the many harms brought about by the lab-constructed virus and the shot we were falsely told would save us from it.

August 5, 2025 Posted by | Science and Pseudo-Science | , , | Leave a comment

U.S. Cancels Contracts Worth $766 Million for Moderna Bird Flu Vaccine After ‘Rigorous Review’

By Michael Nevradakis, Ph.D. | The Defender | May 29, 2025

The Trump administration cancelled two contracts totaling $766 million with Moderna for the development of its mRNA-1018 vaccine for the H5N1 strain of bird flu, citing safety and efficacy concerns identified during its clinical trials, the U.S. Department of Health and Human Services (HHS) has confirmed.

“After a rigorous review, we concluded that continued investment in Moderna’s H5N1 mRNA vaccine was not scientifically or ethically justifiable,” HHS Communications Director Andrew Nixon told The Defender.

“This is not simply about efficacy — it’s about safety, integrity and trust. The reality is that mRNA technology remains under-tested, and we are not going to spend taxpayer dollars repeating the mistakes of the last administration, which concealed legitimate safety concerns from the public,” Nixon said.

Moderna first revealed the cancellation of the two awards in a statement published Wednesday. Moderna also announced “positive interim data” from its Phase 1 and 2 clinical trials for mRNA-1018.

“While the termination of funding from HHS adds uncertainty, we are pleased by the robust immune response and safety profile observed in this interim analysis,” Moderna said in its statement.

Last year, HHS awarded Moderna $176 million for the late-stage development of the mRNA-1018 vaccine. In the final days of the Biden administration in January, HHS granted Moderna $590 million to accelerate the development of its bird flu vaccine and expand clinical studies for vaccines targeting five other flu virus subtypes.

‘A major policy shift away from dangerous mRNA injection programs’

Some scientists criticized the cancellation of the awards. Dr. Ashish Jha, dean of the Brown University School of Public Health and the Biden administration’s COVID-19 response coordinator, told CNN, “The attack on mRNA vaccines is beyond absurd” and that “we will come to regret this” if bird flu starts spreading between humans.

However, epidemiologist Nicolas Hulscher called the news “a very positive development” that “marks a major policy shift away from dangerous mRNA injection programs.”

Vermont-based lawyer and farmer John Klar called it a “sensible decision,” noting the seasonal nature of the virus and its waning virulence.

Dr. Clayton Baker, an internal medicine physician, called the contract cancellation “absolutely the right decision.”

“The mRNA gene therapy platform, as demonstrated by the multiple toxicities of the COVID-19 shots, is fundamentally unsafe and should be removed from use altogether,” Baker said.

Baker suggested that the timing of the January 2025 grant, just days before the start of President Donald Trump’s second term, was likely intended to “promote the bird flu panic that was perpetrated by the outgoing administration, in order to derail the new administration.”

HHS told Reuters earlier this year that it would review agreements the Biden administration made for vaccine production. In March, HHS denied rumors that it was considering cancelling funding for mRNA vaccine research.

In February, the U.S. Department of Agriculture announced a $1 billion plan to combat the spread of bird flu among chickens. The plan included a strategy to develop vaccines for chickens, but not for humans.

According to Reuters, Moderna “has been banking on revenue from newer mRNA shots, including its bird flu vaccine and experimental COVID-flu combination vaccine, to make up for waning post-pandemic demand for its COVID vaccine.” The company “plans to explore alternatives for late-stage development and manufacturing” of its bird flu vaccine.

News of the canceled contracts came just days after Moderna withdrew its application for U.S. Food and Drug Administration (FDA) approval of its mRNA-1083 combination flu and COVID-19 vaccine.

Last week, Reuters reported that Moderna’s decision to withdraw its application came amid “increased regulatory scrutiny of the vaccine approval process since Robert F. Kennedy Jr. took the top U.S. health job earlier this year.”

Markets did not immediately react to news of the grants’ cancellation. Moderna shares remained flat during after-hours trading Wednesday, but were up by over 2.6% by press time Thursday.

No human bird flu cases reported in three months

According to Reuters, bird flu has infected 70 people in the past year, mostly farm workers, but “has spread aggressively among cattle herds and poultry flocks.”

In January, a Louisiana man who was hospitalized with the first severe case of bird flu in the U.S. died — the first bird flu-related death in the U.S. and all of North America. However, the man, who was older than 65, had underlying medical conditions, and it remains unclear whether bird flu directly caused his death.

There have been no new human bird flu cases in three months, The Associated Press (AP) reported May 19.

Dr. Meryl Nass, an expert on biological warfare and founder of Door to Freedom, said, “H5N1 was a dangerous virus if you caught it from a chicken years ago.” But it has never spread person-to-person, and has “mutated to cause extremely mild disease in almost all humans that have caught it over the past five to 10 years.”

Nass said this makes a new bird flu vaccine for humans unnecessary. “There is absolutely no reason why the United States needs another bird flu vaccine, and there is even less reason to develop an mRNA vaccine because the platform itself is dangerous.”

Bird flu scare a ‘propaganda campaign’

Mainstream media outlets and many scientists continue to suggest that bird flu poses an imminent threat to humans, in what Dr. Richard Bartlett, an emergency room director, former Texas Department of Health and Human Services advisory council member, and expert on bird flu, called a “propaganda campaign.”

“The messaging has been that bird flu spread from penguins to sea lions, to a western Minnesota goat, to Texas dairy cattle and finally to a dairy farmer with red eyes. It’s been a two-year marketing campaign,” Bartlett said.

Bartlett said the messaging is intended to “manufacture the perception of a need for new mRNA products — despite the absence of long-term safety data.”

Last year, former FDA Commissioner Robert Califf warned that a potential bird flu pandemic could have a 25% mortality rate. Jeremy Farrar, Ph.D., then the World Health Organization’s chief scientist, warned that bird flu has an “extremely high” mortality rate for humans and could mutate to pass between humans.

In December 2024, Dr. Leana Wen, the former commissioner of the Baltimore City Health Department and a professor of public health at George Washington University, said the outgoing Biden administration had not done enough to address bird flu and criticized the lack of availability of a bird flu vaccine.

After the start of Trump’s second term and the implementation of funding cuts to government health agencies, mainstream media reports suggested the cuts were placing the public at risk of a worsening bird flu outbreak.

In February, Reuters reported the cuts “disrupted the U.S. response to bird flu as the outbreak worsens,” resulting in “anxiety among federal health staff that critical information about bird flu will not be disseminated in a timely manner or at all.”

In April, USA Today reported that cuts affecting the FDA’s Center for Veterinary Medicine “will hamper the FDA’s ability to respond to animal disease outbreaks, including bird flu, and protect public health.”

Also that month, virologists from 40 countries published a report in The Lancet urging the Trump administration to prepare for a bird flu pandemic, according to Gavi, the Vaccine Alliance.

The report was funded by the Bill & Melinda Gates Foundation, which in 1999 established Gavi. The Gates Foundation holds one of the four permanent seats on Gavi’s board and continues to heavily fund the organization.

According to the AP, “experts are puzzling over why reports of new human cases have stopped” in the last three months. The report suggests that infections potentially aren’t being detected, that immigrant farm workers may be afraid to be tested, and that efforts to find bird flu cases were “weakened by government cuts.”

Baker said such scenarios are unlikely to account for the lack of recent bird flu cases. “What does this say about the severity of the illness in humans? It says that the illness is either mild or entirely asymptomatic and that there’s no need for a vaccine for an asymptomatic condition.”

U.S. ‘poured a king’s ransom’ into bird flu vaccine development

Nass said that the FDA has already licensed three vaccines for H5N1 and that “there have been dozens of experimental bird flu vaccines that were never taken to licensure. The U.S. government “has already poured a king’s ransom” into funding these vaccines, even though bird flu has never spread between humans.

Baker said that instead of funding new bird flu vaccines, the U.S. government should “stop the gain-of-function style manipulation of bird flu into a bioweapon, which takes place at the Kawaoka lab at the University of Wisconsin and the Southeast Poultry Research Laboratory in Athens, Georgia, as well as at other labs.”

Gain-of-function research increases the transmissibility or virulence of viruses and is often used in vaccine development. Earlier this month, Trump issued an executive order pausing gain-of-function research in the U.S. for 120 days while a new regulatory framework is developed. The order also ended U.S. funding for such research in some countries.

“Gain-of-function research produces human pathogens, the process is driven by fear in the media, and then proprietary vaccines are presented as the solution,” Baker said. “It needs to end.”

Recently, there have been growing calls among scientists for a moratorium or ban on mRNA vaccines, including a petition pending before the FDA.

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

May 29, 2025 Posted by | Aletho News | , , | Leave a comment

Using Medicalization to Suppress the Exercise of First Amendment Rights

By Adam Dick | Ron Paul Institute | March 19, 2025

A repugnant tactic of authoritarianism is categorizing people’s desire for or exercise of freedom as illness that government should suppress. An example of this was the deeming of dissidents in the Soviet Union as mentally ill to justify their detention and punishment.

In America, there has long been resistance against an effort to similarly have the United States government medicalize the exercise of gun rights as a means to circumvent the constitutional protection of the right to bear arms contained in the Second Amendment. In the 1990s this resistance led to congressional imposition of a spending prohibition against the Centers for Disease Control and Prevention (CDC) at the Department of Health and Human Services (HHS) advocating or promoting gun control.

The effort to prevent the US government from using medicalization to crack down on gun rights appears to have had a success in the new Trump administration with the removal from the HHS website of a guns and public health advisory from the preceding Biden administration. Abené Clayton reported Monday at the Guardian :

The Trump administration has removed former surgeon general Vivek Murthy’s advisory on gun violence as a public health issue from the US Department of Health and Human Services’ website. This move was made to comply with Donald Trump’s executive order to protect second amendment rights, a White House official told the Guardian.

The strange thing is that while the Trump administration appears to be taking action to cut off HHS threats to Second Amendment rights, HHS is helping lead Trump administration efforts to expand US government threats to First Amendment rights. Medicalization to restrict free speech, assembly, and petition is on the ascendancy at HHS as demonstrated by a March 3 announcement by HHS, the Department of Education (ED), and the General Services Administration (GSA) concerning the US government’s Task Force to Combat Anti-Semitism, created the month before, reviewing actions or inactions of Columbia University relative to “antisemitism” and potential penalties that may be imposed upon that university. This is all justified in the announcement by reference to a January 29 executive order of President Donald Trump that employs a peculiarly expanded definition of antisemitism incorporated into an executive order from Trump’s first term that includes positions against the Israel government in addition to the commonly understood definition that concerns positions against an ethnicity or religion.

“Anti-Semitism – like racism – is a spiritual and moral malady that sickens societies and kills people with lethalities comparable to history’s most deadly plagues,” declared HHS Secretary Robert F. Kennedy, Jr. in the announcement. That is medicalization in a nutshell: Your “bad thoughts” are a plague the government must stop to protect public health.

Four days later — on March 7, HHS, ED, and GSA were back with a new announcement that, due to review by the Joint Task Force to Combat Anti-Semitism, about 400 million dollars in US grants to Columbia University had been canceled, with more grant cancelations expected to follow. Then, on March 13 the HHS, ED, and GSA followed up with a letter to Columbia University using the denial of funding as leverage to demand the university crack down on free speech, assembly and petition, as well as change, and even hand to US government control over, a variety of university policies and procedures.

Meanwhile, the US government is making an example of Mahmoud Khalil who was involved in protests challenging US foreign policy and related to Israel at Columbia University. The US government has arrested and detained him, and is seeking his deportation, because Khalil apparently did nothing more than exercise First Amendment protected rights.

These actions against Columbia University are not one-off. A February 28 press release from the Department of Justice (DOJ) listed ten universities — Columbia University plus George Washington University; Harvard University; Johns Hopkins University; New York University; Northwestern University; the University of California, Los Angeles; the University of California, Berkeley; the University of Minnesota; and the University of Southern California — as subject to visits from the Task Force to Combat Anti-Semitism because their campuses “have experienced antisemitic incidents since October 2023.” Expect the list to keep growing.

Leo Terrell, described in the February DOJ press release as “[l]eading Task Force member and Senior Counsel to the Assistant Attorney General for Civil Rights,” made clear in an included quote that the Task Force to Combat Anti-Semitism means business. He stated:

The Task Force’s mandate is to bring the full force of the federal government to bear in our effort to eradicate Anti-Semitism, particularly in schools. These visits are just one of many steps this Administration is taking to deliver on that commitment.

It looks like we are witnessing the beginning of a major crackdown on First Amendment rights. The US government, however, will claim this development is nothing to worry about because the purpose is to make America healthy again.

March 19, 2025 Posted by | Civil Liberties, Full Spectrum Dominance | , , , , , | Leave a comment

HHS is Opposing Experimental Bird Flu ‘Vaccines’ for Poultry. USDA Seems Supportive.

By Adam Dick | Peace and Prosperity Blog | March 8, 2025

Last week, I wrote about experimental “vaccines” that the United States government has been working with pharmaceutical companies to develop — different ones for poultry and people. I asked if Department of Health and Human Services (HHS) Secretary Robert F. Kennedy, Jr. and Department of Agriculture (USDA) Secretary Brooke Rollins, both new to their jobs in February, would stand up against this and other aspects of “the US government’s bird flu scheme ramped up during the previous presidential administration.” Here is an update.

In a new interview at Fox Nation, Kennedy indicated that HHS opposes giving chickens the bird flu “vaccine.” Kennedy stated: “There’s no indication that those vaccines actually provide sterilizing immunity, and all three of my health agencies at NIH, CDC, and FDA — the acting heads of those agencies — have all recommended against the use of the bird flu vaccine.” This conclusion is supported, Kennedy stated, by the fact that “the vaccine could actually promote antigenic shift, which means your turning those birds into mutant factories, and that could actually accelerate the jump [of the bird flu] to human beings.”

The catch, though, is that the authority over this in regard to poultry raised in America largely resides in the USDA. Therefore, it is important what Rollins decides. So far, she seems to be “on the vaccine train” as was her predecessor in the Joe Biden administration. On February 26, Rollin released the USDA’s Five-Pronged Approach to Address Avian Flu that includes substantial boosting of giving a bird flu “vaccine” to poultry in its fourth of five sections. Here is that section:

Explore Pathways toward Vaccines, Therapeutics, and Other Strategies for Protecting Egg Laying Chickens to Reduce Instances of Depopulation

  • USDA will be hyper-focused on a targeted and thoughtful strategy for potential new generation vaccines, therapeutics, and other innovative solutions to minimize depopulation of egg laying chickens along with increased bio-surveillance and other innovative solutions targeted at egg laying chickens in and around outbreaks. Up to a $100 million investment will be available for innovation in this area.
  • Importantly, USDA will work with trading partners to limit impacts to export trade markets from potential vaccination. Additionally, USDA will work alongside the U.S. Department of Health and Human Services to ensure the public health and safety of any such approaches include considerations of tradeoffs between public health and infectious disease strategy.
  • USDA will solicit public input on solutions, and will involve Governors, State Departments of Agriculture, state veterinarians, and poultry and dairy farmers on vaccine and therapeutics strategy, logistics, and surveillance. USDA will immediately begin holding biweekly discussions on this and will also brief the public on its progress biweekly until further notice.

Will President Donald Trump step in to settle any disagreement between HHS and USDA on the matter?

Notably, the USDA report also indicated that USDA will continue to back the mass slaughter of poultry in the name of countering bird flu, stating that the Animal and Plant Health Inspection Service “will continue to indemnify producers whose flocks must be depopulated to control the further spread of HPAI.” HPAI is short for highly pathogenic avian influenza — bird flu.

As I wrote last week, Kennedy has in his early actions provided reason to expect that he would support ending US involvement in developing and promoting bird flu shots for people, something under the control of his department. He has yet to implement such a change.

March 8, 2025 Posted by | Science and Pseudo-Science | , , | Leave a comment

Kennedy Hits Pause on COVID Vaccine Project Worth Hundreds of Millions

By Brenda Baletti, Ph.D. | The Defender |February 26, 2025

Secretary of Health and Human Services (HHS) Robert F. Kennedy Jr. put the brakes on a multi-million contract with the American biotech company Vaxart to create a new COVID-19 vaccine, Fox News Digital reported.

Kennedy on Feb. 21 issued a 90-day stop-work order on the contract until HHS determines whether it is “prudent and safe” to continue. The order came just as the next phase of the company’s clinical trial, involving 10,000 participants, was set to start on Monday.

In this phase of the trial, the company is planning to test the efficacy of its vaccine against existing mRNA vaccines, bypassing a placebo-controlled assessment.

“While it is crucial that the Department [of] Health and Human Services (HHS) support pandemic preparedness, four years of the Biden administration’s failed oversight have made it necessary to review agreements for vaccine production, including Vaxart’s,” Kennedy told Fox News Digital.

“I look forward to working with Vaxart and medical experts to ensure this work produces safe, effective, and fiscal-minded vaccine technology,” he said.

Fox News Digital reported that the trial is only paused, not terminated. HHS will decide whether to resume development of the vaccine within the next 90 days.

The development of Vaxart’s new COVID-19 vaccine was part of the Biden administration’s $4.7 billion Project NextGen initiative, launched in 2023 to develop innovative vaccines — like oral pills and nasal sprays — that are easier to administer and provide improved protection against the SARS-CoV-2 virus.

Project NextGen is the successor to the Trump administration’s “Operation Warp Speed,” launched in March 2020 to expedite the development of COVID-19 vaccines.

Similar to Operation Warp Speed, Project NextGen — with funding from the Bill & Melinda Gates Foundation and the Rockefeller Foundation — encourages public-private partnerships.

Vaxart announced in June 2024 that it had been awarded up to $453 million to fund the Phase 2b trials of its pill vaccine under a contract from the Biomedical Advanced Research and Development Authority (BARDA). BARDA operates under the Administration for Strategic Preparedness and Response (ASPR), a department of HHS.

The company was developing a COVID-19 vaccine that can be taken orally. The paused trial was designed to compare the efficacy of Vaxart’s oral vaccine to an approved mRNA vaccine.

Of the $453 million approved, $240 million had already been authorized for the preliminary study, according to Fox Digital. The company had been recently authorized to bill the remaining balance of the contract for the clinical trials, but that billing is now on hold.

Vaxart can still bill the federal government for the costs of monitoring those people who participated in earlier phases of the trial.

The company said in an email statement to The Defender that it did not know the nature of the stop work order, but was informed it would be in effect for 90 days. The spokesperson said the trial hadn’t had any impediments to date and they “remain excited” to move forward.

“We recognize and appreciate the importance of oversight, transparency, and fiscal responsibility in government-funded biomedical research, and we are committed to working collaboratively with Secretary Kennedy, HHS, BARDA and other members of President Trump’s administration as they evaluate the data supporting the 10,000-participant portion of the Phase 2b study and determine how the study should move forward,” the spokesperson said.

Children’s Health Defense (CHD) Senior Research Scientist Karl Jablonowski said taxpayers have paid more than enough to vaccine makers, who don’t have the public’s best interests in mind.

He said:

“The U.S. taxpayers have already paid for our pandemic. Big Pharma has made out like bandits. They are using the Biden administration’s $4.7 billion Project NextGen initiative funds to expand their patent portfolio — for the betterment of profit.

“They are not beholden to the 340 million Americans footing the bill, they are beholden to the 227 million publicly traded shares of their company.”

The pause comes less than two weeks after Kennedy was sworn in as HHS secretary. During the nomination process, he came under fire from mainstream media and Democratic politicians for his so-called “anti-vaccine views.”

Kennedy and the organization he founded, CHD, were vocal critics of the COVID-19 vaccine and were censored on social media for dissenting views.

The Center for Countering Digital Hate targeted him for censorship as one of the “Disinformation Dozen” who raised questions about the government’s COVID-19 vaccine narrative.

Kennedy has repeatedly said he is not “anti-vaccine,” but wants vaccines to be subjected to rigorous safety testing and pledged to investigate the childhood immunization schedule as part of his work at HHS.

In 2023, the CDC added COVID-19 vaccines to the childhood immunization schedule, even though they were shown to provide little or no benefit to children.

Biden administration was funding new nasal and oral COVID vaccines

When BARDA funded Vaxart, it also granted funding to CyanVac’s (up to $40 million) and Castlevax’s ($34 million) intranasal vaccines.

Each company’s Phase 2b trials were set to recruit 10,000 volunteers to compare the safety and efficacy of the investigational vaccine against the existing mRNA vaccines.

ASPR Assistant Secretary Dawn O’Connell said in a news release at the time that the new vaccines “may … be easier to administer through intranasal or oral delivery.” The announcement suggests the delivery methods have the “potential to improve vaccine access.”

Jablonowski said oral vaccines, like the one being developed by Vaxart, “have generally not been terribly effective in creating and sustaining an immune response,” with the exception of the oral polio vaccine. That vaccine, which is a liquid, not a pill, has been plagued with safety issues, causing polio outbreaks in many countries.

When the funding was awarded, Vaxart CEO Steven Lo celebrated it in a press release. “Vaccine delivery has relied primarily on injection for more than 150 years. This funding from BARDA will assist us in determining whether we can bring a transformational, next-generation approach to global vaccination.”

Vaxart’s pill, VXA-CoV2-1, uses an adenovirus vector to infect epithelial cells in the lower small intestine. The vaccine delivers the genetic material to create the spike protein. The company boasts that a special coating allows the oral pill to survive the low pH in the stomach.

Adenovirus vaccines reportedly cannot make you sick, and cannot replicate or be integrated into the host body’s DNA.

However, Jablonowski said, “Two adenovirus-based COVID vaccines have already been pulled from the market because they were remarkably unsafe, yet passed initial — and clearly insufficient — safety standards.”

Johnson & Johnson’s (J&J) and AstraZeneca’s COVID-19 vaccines also used adenovirus vectors.

The use of J&J’s vaccine was paused in April 2021 after reports of thrombosis with thrombocytopenia syndrome (TTS), a severe blood clotting disorder. In July 2021, the FDA warned about the risk of Guillain-Barré syndrome with the J&J vaccine, after approximately 100 cases were reported among 12.5 million vaccine recipients.

With existing doses of the J&J vaccine having expired in May 2023, the vaccine is no longer in use.

The AstraZeneca COVID-19 vaccine also caused blood clots, resulting in temporary pauses in its use in several countries. It was removed from the market in May 2024.

In addition to its COVID-19 vaccine, Vaxart is also developing oral vaccines for norovirus and bird flu, with initial trials for the norovirus vaccine beginning this year.

Related stories in The Defender 

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

February 26, 2025 Posted by | Corruption | , , , , | 1 Comment

RFK Jr. Wins Crucial Vote, Moves One Step Closer to Top HHS Post

By Michael Nevradakis, Ph.D. | The Defender | February 4, 2025

The Senate Finance Committee today narrowly advanced Robert F. Kennedy Jr.’s nomination to lead the U.S. Department of Health and Human Services (HHS) to the full Senate for a confirmation vote.

The 14-13 vote along party lines came after Kennedy secured the vote of Sen. Bill Cassidy (R-La.), chair of the Senate Health, Education, Labor, and Pensions Committee that oversees HHS. Cassidy was the lone Republican considered to be a possible hold-out.

The Senate is expected to vote on Kennedy’s confirmation later this week or early next week, ABC News reported. The nomination “is likely to succeed absent any last-minute vote switches,” The Associated Press reported.

Kennedy, founder and former chairman of Children’s Health Defense (CHD), can be confirmed even if up to three Republican senators and all Democrats vote against him in the full Senate.

If confirmed, Kennedy will oversee a $1.7 trillion budget and 90,000 employees. HHS oversees 13 public health agencies, including the Centers for Disease Control and Prevention (CDC), the U.S. Food and Drug Administration (FDA) and the National Institutes of Health (NIH).

During today’s committee meeting, Sen. Thom Tillis (R-N.C.) said, “It is time to put a disruptor” like Kennedy at the helm of the HHS. “I hope he goes wild,” Tillis said.

Shares of vaccine manufacturers and packaged food companies, including Pfizer, Moderna, BioNTech, Novavax, Kraft Heinz, General Mills, Mondelez and Hershey, dropped after today’s vote, Reuters reported.

CHD CEO Mary Holland welcomed today’s outcome. She said:

“CHD is delighted that the Finance Committee is sending RFK Jr.’s nomination to the full Senate. Given the 2024 presidential results, this seems only fitting. ‘Make America Healthy Again’ has become a worldwide rallying cry, and CHD is proud to be a foundational part of this movement.”

In a statement, Dr. Joseph Varon, president and chief medical officer of the Independent Medical Alliance, also welcomed today’s vote. He said:

“Americans demand a frank conversation about the state of our government healthcare agencies, and we’re very grateful for the Senators who responded by voting to move RFK Jr.’s nomination to the full Senate.

“RFK Jr. has been asking the tough questions, and he’s been unmoved in the face of big-corporate money campaigns against him.”

In a statement before the vote, Sen. Mike Crapo (R-Idaho), chair of the committee, said that if confirmed, Kennedy “will have the opportunity to deliver much-needed change to our nation’s healthcare system.”

Cassidy, Kennedy agree to ‘unprecedently close collaborative relationship’

During last week’s hearing in the Senate Finance Committee, Cassidy said he was “struggling” with some of Kennedy’s positions regarding vaccines.

“I’ve had very intense conversations with Bobby and the White House over the weekend and even this morning,” Cassidy posted on X earlier today. “I want to thank VP JD [Vance] specifically for his honest counsel. With the serious commitments I’ve received from the administration and the opportunity to make progress on the issues we agree on like healthy foods and a pro-American agenda, I will vote yes.”

Following today’s vote, Cassidy delivered remarks on the Senate floor, revealing the content of those discussions and the agreement he made with Kennedy to secure his vote.

He said Kennedy committed to a strong public health role for Congress and to meeting or speaking with Cassidy multiple times per month. They also agreed that Cassidy will participate in the hiring process for HHS and the public health agencies it oversees.

“He and I will have an unprecedently close collaborative relationship,” Cassidy said, noting that the hiring decisions that will follow “will allow us to represent all sides of those folks who have contacted me over this past weekend.”

Kennedy also agreed to maintain statements on the CDC website that vaccines do not cause autism and to maintain the recommendations of the CDC’s Advisory Committee on Immunization Practices.

Cassidy said he would also reject any attempt to remove the public’s access to “life-saving vaccines” without “iron-clad, causational scientific evidence” indicating otherwise. He also said he would carefully monitor any attempt to “wrongfully sow public confusion” about vaccines.

Cassidy conceded that “many mothers do need reassurance that the vaccine their child is receiving is necessary, effective, and most of all, safe” and expressed his support for Kennedy’s positions on toxic foods and reforming the NIH.

“These commitments, and my expectation that we can have a great working relationship to Make America Healthy Again, is the basis of my support,” Cassidy said, noting that institutions like NIH and FDA require “reform.”

During last week’s confirmation hearings, Kennedy emphasized his “Make America Healthy Again” agenda and said he would work to tackle the chronic disease epidemic in the U.S.

Kennedy also said he would implement “radical transparency” in HHS. He also voiced support for vaccines — if backed by “good science.”

Related articles in The Defender

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

February 4, 2025 Posted by | Civil Liberties, Corruption | , , , , , | 8 Comments

Johnson Subpoenas HHS for COVID Vaccine Safety Records, Fauci Emails

By Suzanne Burdick, Ph.D. | The Defender | February 3, 2025

Sen. Ron Johnson (R-Wis.) last week subpoenaed the U.S. Department of Health and Human Services (HHS) for COVID-19 vaccine safety records and communications about the COVID-19 pandemic, including a subset of Dr. Anthony Fauci’s emails.

HHS is required to produce the requested data and communications by Feb. 18. Johnson told The Defender it’s imperative that HHS comply promptly.

Johnson said:

“The federal government is supposed to serve the American people. Our taxes pay the bureaucrats’ salaries and fund their activities and studies. The results belong to the public and should be made available to us in a timely and transparent manner.

“Bureaucrats who withhold information only raise suspicion and reduce the credibility and integrity of their agencies.”

This was the first subpoena Johnson issued after being named chairman of the Permanent Subcommittee on Investigations on Jan. 21.

During the Biden administration, Johnson wrote more than 70 congressional oversight letters to HHS officials and its health agencies requesting information on COVID-19 vaccine adverse events and related communications, according to a Jan. 29 press release.

Biden HHS officials “either completely ignored or inadequately addressed” the requests.

Johnson said in a statement:

“In the waning days of the Biden administration and after years of obstructing my oversight efforts, I warned HHS officials that when I become chairman of the Permanent Subcommittee on Investigations, I will subpoena records and data on the COVID-19 pandemic that have been inappropriately withheld from Congress and the American people for far too long.”

The subpoena requires HHS to hand over:

  1. Previously withheld or heavily redacted communications about the pandemic, including Fauci’s emails, including but not limited to the approximately 50 pages of his emails that were withheld from Johnson’s office since September 2021.
  2. Safety surveillance data on the COVID-19 vaccines, including proportional reporting ratios and empirical Bayesian data mining.
  3. Unredacted records previously released through Freedom of Information Act (FOIA) requests regarding the government’s awareness of myocarditis and pericarditis cases in post-vaccinated individuals.
  4. Data and records relating to COVID-19 vaccine lots associated with higher rates of adverse events.
  5. Order forms and receipts showing government researchers purchasing DNA sequences from a biotechnology company.
  6. All communications relating to HHS’ receipt of and response (or lack thereof) to Johnson’s oversight letters between January 2021 and the present.

Risa Evans, an attorney for Children’s Health Defense (CHD), applauded Johnson’s efforts.

CHD has filed multiple FOIA requests to obtain records from HHS agencies including the U.S. Food and Drug Administration (FDA), the Centers for Disease Control and Prevention (CDC) and the National Institutes of Health (NIH) relating to the agencies’ monitoring of COVID-19 vaccine safety and injuries.

“The agencies have responded to our FOIA requests with delays, denials and redactions,” Evans said, “and we’ve been forced to sue to obtain records that, in truth, should be made public as a matter of course.”

Evans called the agencies’ lack of transparency “unconscionable — especially given the federal government’s relentless promotion of COVID-19 vaccination, coupled with claims that safety is being vigilantly monitored by the agencies and denials that the shots cause harm.”

Karl Jablonowski, Ph.D., senior research scientist at CHD, said:

“Time is washing away the knowledge of how the government’s monitoring of COVID-19 vaccine safety went wrong, and the fingerprints of the wrongdoers. Promptly responding to Senator Johnson’s subpoena may preserve enough knowledge to ensure the betrayal never happens again.”

FDA partially responds to CHD’s FOIA request

Some documents referenced in Johnson’s subpoena have already been released, Evans said. For example, on Jan. 10, the FDA posted emails about its safety surveillance of COVID-19 vaccines using empirical Bayesian data mining.

Empirical Bayesian data mining is a method of analyzing vaccine injury reports, Jablonowski said.

The FDA provided the emails to CHD and posted them on the agency’s website one day after the agency objected to a motion filed by CHD in federal court about a 2023 FOIA lawsuit. CHD sued the FDA after it failed to respond to CHD’s FOIA request for the documents.

Other groups and individuals — including Johnson, The Epoch Times and the Informed Action Consent Network — had also FOIAed the FDA for the same safety surveillance data.

On Jan. 10, the FDA sent CHD a letter explaining that it was posting the emails as a “partial reply” to CHD’s FOIA request.

In its FOIA request, CHD had asked for “records of any Empirical Bayesian data mining” that the FDA conducted and “records of any sharing or discussion of results and signals with the CDC.” The emails posted by the FDA showed some of those records.

However, CHD in its FOIA request also asked for records related to “consultations by FDA and/or CBER [the FDA’s Center for Biologics Evaluation and Research] with VAERS [Vaccine Adverse Event Reporting System] staff within the CDC’s Immunization Safety Office in connection with any signal that was detected.”

“The FDA still hasn’t responded to other key parts of our request,” Evans said. “In particular, it hasn’t provided records of the follow-up investigation the agency said it would conduct if it detected potential safety signals.”

Emails reveal FDA failed to detect safety signals

The emails released by the FDA revealed that in the first 18 months of the COVID-19 vaccine rollout, the FDA’s monitoring of VAERS showed consistent alerts for serious adverse events, including death, for the Janssen (Johnson & Johnson) vaccine.

VAERS, co-managed by CDC and FDA, is a “passive” monitoring system that accepts reports of adverse events experienced after vaccination.

Meanwhile, the FDA’s monitoring found almost no safety signals for the Moderna and Pfizer shots, failing to detect signals even for widely recognized risks like myocarditis, pericarditis and anaphylaxis.

According to Jablonowski’s analysis of the emails, the FDA and CDC were never sufficiently looking for safety signals, despite all the “posturing” the agencies did around the COVID-19 vaccines’ safety.

The FDA and CDC’s “willful ignorance” of the adverse events following COVID-19 vaccination is an “epic betrayal,” Jablonowski said.

Related articles in The Defender

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

February 3, 2025 Posted by | Civil Liberties, Deception | , , , , | Leave a comment

Sen. Johnson Threatens Legal Action Unless HHS Turns Over Unredacted Emails on COVID Vaccine Safety

By Brenda Baletti, Ph.D. | The Defender |November 22, 2024

Sen. Ron Johnson (R-Wis.) on Tuesday demanded public health agencies provide complete and unredacted documents about the development and safety of the COVID-19 vaccines, after learning of extensive redactions in documents released in response to multiple Freedom of Information Act (FOIA) requests.

In a letter sent Tuesday to the U.S. Department of Health and Human Services (HHS), U.S. Food and Drug Administration (FDA) and Centers for Disease Control and Prevention (CDC), Johnson said the redactions make the documents nearly impossible to comprehend and obscure the public’s understanding of issues like myocarditis and pericarditis linked to vaccines.

He also called out the agencies for not responding to his own requests for COVID-19 vaccine safety information. He wrote:

“The lack of transparency from your agencies during the Biden presidency has been appalling. Your agencies’ refusal to provide complete and unredacted responses and documents to my numerous oversight letters on the development and safety of the COVID-19 vaccines has hindered Congressional oversight and has jeopardized the public’s health.”

Johnson, an outspoken critic of the government’s handling of COVID-19-related information, sent over 60 public letters requesting more transparency on virus origins, early treatment and vaccine safety.

“What is clear from these excessive redactions, however, is a concerted effort to obscure Congress’ and the public’s understanding of your agencies’ detection of and response to COVID-19 vaccine adverse events such as myocarditis and pericarditis,” he wrote.

Johnson’s latest request demands the agencies preserve and release unredacted documents, specifically three documents he said comprised “only a small fraction” of the documents on myocarditis and pericarditis that the agencies “continue to conceal.”

Johnson gave the agencies until Dec. 3 to respond, warning that if the agencies don’t comply, he would take further action, including issuing subpoenas once he becomes chairman of the Permanent Subcommittee on Investigations in the next Congress.

CDC delayed telling public about link between vaccines and myocarditis

Children’s Health Defense (CHD) scientists Karl Jablonowski, Ph.D., and Brian Hooker, Ph.D., in 2022 published a study showing the CDC delayed reporting the incidence of myocarditis to the general public for three months after the first statistically significant signal appeared in the Vaccine Adverse Event Reporting System (VAERS) database.

CHD, attorney Ed Berkovich, The Epoch Times and others submitted FOIA requests seeking more information about what the public health agencies knew and when.

In his letter, Johnson cited responses to those FOIA requests as examples of how the agencies obstructed attempts by the public to hold them accountable.

For example, heavily redacted documents indicate that then-CDC Director Rochelle Walensky had received Pfizer documents regarding myocarditis and pericarditis by May 22, 2021. However, the Pfizer report provided via FOIA was completely redacted except for the cover page, making it impossible to decipher what Walensky learned and when.

Johnson included the FOIA documents in his letter so the public could see the extent of the redactions.

The documents showed that after receiving the FOIA data, Walensky and other CDC officials considered whether to issue a public warning about the risk of myocarditis from vaccination. They drafted a Health Alert Network (HAN) for the website, which is how they communicate “urgent public health incidents” with public information officers, practitioners, clinicians and local public health officials.

The draft alert sent to Walensky was redacted when the CDC produced documents in response to a FOIA request. A partially unredacted email to either a Moderna or Pfizer employee indicated that the agency was debating the pros and cons of issuing a HAN, but didn’t “want to appear alarmist.”

The agency never issued the alert. Instead, the CDC said on its website that there were “increased cases of myocarditis and pericarditis” reported but the CDC continues to recommend the vaccine for everyone ages 12 and up.

Johnson requested all documents about the alert, but the CDC has not provided them.

In Johnson’s third example, the Biden White House sent top public health officials 17 pages of talking points for a “tough QA” on COVID-19. In the FOIA documents, all the topics are redacted, making it impossible to know what the White House was communicating.

“Ultimately, despite your agencies’ awareness of the risks associated with the COVID-19 vaccines, the main talking point from these and other public health officials was uniform and entirely deceptive: the vaccines are safe and effective,” Johnson wrote.

Pattern of stonewalling and evading by government health agencies

Risa Evans, staff attorney at CHD, told The Defender that over the last several years, CHD has filed several FOIA requests with the FDA, CDC and National Institutes of Health seeking records connected with post-authorization safety monitoring of COVID-19 shots.

“We have found that obtaining these records is a challenge, due to a mix of denials, redactions and delays by the agencies,” she said.

When the agencies failed to respond to FOIA requests for records related to safety signals, CHD filed multiple FOIA lawsuits seeking the requested documents.

In one case the FDA requested at least 18 months to fulfill the request — after it had already delayed 14 months.

“The agencies’ failure to respond to our requests in a timely and open fashion is particularly ironic in light of recent statements by Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, calling for more transparency as a way of combating vaccine ‘hesitancy,’” Evans said.

The FDA also famously attempted to delay documents related to the licensing of Pfizer’s Comirnaty COVID-19 vaccine for 75 years.

The U.S. House Select Subcommittee on the Coronavirus Pandemic also investigated Dr. David M. Morens, a 25-year veteran of the National Institute of Allergy and Infectious Diseases and adviser to Dr. Anthony Fauci, after it was revealed he used his personal email address to evade FOIA requests for communications related to the origins of COVID-19.

Emails made public during that investigation also showed that Morens connected Fauci to Kaiser Health News reporter Arthur Allen through a “secret back channel.”

Jablonowski, who was among the first to detail the deception around myocarditis, told The Defender if the public health agencies aren’t compelled to be transparent, they can’t be held accountable.

He said the FDA and the CDC, “are not transparent in matters of myocarditis resulting from the COVID-19 vaccines. They are opaque, hidden behind redactions, and not accountable to the American people or members of Congress.”

“This is a rot in our government, and it spreads well beyond the confines of myocarditis, the CDC and the FDA,” he added. “How far beyond? We won’t know until we broadly investigate the actions and actors.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

November 23, 2024 Posted by | Deception | , , | Leave a comment

Trump names RFK Jr. to cabinet position

RT | November 14, 2024

US President-elect Donald Trump will nominate Robert F. Kennedy Jr. to be his Secretary of Health and Human Services (HHS), declaring that the former Democrat will ensure that “everybody will be protected from harmful chemicals [and] pollutants.”

Trump announced his choice in a social media post on Thursday evening. “For too long, Americans have been crushed by the industrial food complex and drug companies who have engaged in deception, misinformation, and disinformation when it comes to public health,” he wrote.

“HHS will play a big role in helping ensure that everybody will be protected from harmful chemicals, pollutants, pesticides, pharmaceutical products, and food additives that have contributed to the overwhelming health crisis in this country,” he continued. “Mr. Kennedy will restore these agencies to the traditions of gold standard scientific research… to Make America Great and Healthy Again!”

The New York Post claimed the previous day that some of Trump’s closest advisers were pushing for Kennedy to be given an advisory position, but that the former Democrat was “stubborn” in demanding control of HHS.

If confirmed, Kennedy would oversee the Centers for Disease Control and Prevention (CDC), Food and Drug Administration (FDA), National Institutes of Health (NIH), and other sub-agencies. Kennedy has been vocally critical of all of these agencies, and vowed to enact sweeping reforms if placed in charge of them.

A long-time vaccine skeptic and proponent of organic agriculture, Kennedy has promised to “get processed food out of school lunch immediately,” to recommend that fluoride be removed from the water supply, and to crack down on the use of chemical pesticides and herbicides in farming.

Kennedy announced last October that he would run for the presidency as an independent candidate, ending his bid to challenge President Joe Biden in the Democratic Party’s primary elections. He suspended his campaign and endorsed Trump in August, citing Trump’s support for free speech, his promise to end the Ukraine conflict, and his willingness to tackle what Kennedy called “the chronic disease epidemic” afflicting American children.

https://twitter.com/MidwesternDoc/status/1854781830693581049

November 14, 2024 Posted by | Science and Pseudo-Science | , , , , | Leave a comment

CDC Stands by Water Fluoridation After Report Linking Fluoride to Lower IQs in Kids Finally Published

By Brenda Baletti, Ph.D. | The Defender | August 22, 2024

The National Toxicology Program (NTP) on Wednesday published a controversial report linking fluoride exposure to neurotoxic effects in children, after public health officials tried for years to block its publication and water down its conclusions.

The report, which analyzed published studies on fluoride’s neurotoxicity, concluded with “moderate confidence” that higher levels of fluoride exposure in drinking water are consistently linked to lower IQs in kids.

It’s the first government publication to concede what fluoride researchers have long reported: that the chemical added to the drinking water of hundreds of millions of people in the U.S. and celebrated as one of the 10 greatest health achievements of the 20th century carries a serious risk of neurological damage, particularly for pregnant women and young children.

“The NTP monograph provides more than sufficient evidence against the deliberate exposure of humans to fluoride through intentional fluoridation of drinking water,” said risk analysis scientist Kathleen Thiessen, Ph.D., who was not involved with the study but co-authored the 2006 National Resource Council study on fluoride toxicity.

Thiessen told The Defender, “A conclusion of ‘moderate confidence’ of neurotoxic effects, especially on unborn and newborn children, ought to mean an immediate elimination of water fluoridation and minimization of fluoride exposure to the population.”

The report reviewed existing studies that assessed the relationship between fluoride exposure and neurodevelopmental effects in children and adults from across the world, including places where fluoride occurs naturally in groundwater and places like the U.S., Canada and Mexico, where it is intentionally added to drinking water or food.

The authors concluded that exposure to drinking water containing more than 1.5 milligrams per liter (mg/L) is consistently associated with lower IQ in children. That’s only twice the amount the Centers for Disease Control and Prevention (CDC) recommends be added to drinking water in the U.S. to prevent tooth decay.

Most environmental toxins regulated by the U.S. Environmental Protection Agency (EPA) are more strictly controlled. Typically, human exposure is banned at 30 times the level of their known toxic effects. None of the chemicals regulated under the Toxic Substances Control Act are permitted at a margin of less than 10.

The researchers found that almost all of the high-quality studies identified — 18 out of 19 — found a link between fluoride exposure and lower IQ in children. And 8 of 9 high-quality studies that looked at neurodevelopmental links other than IQ also found a link.

They said they were less confident that there was a consistent link between low levels of fluoride exposure in water and neurodevelopmental issues, and that more research is needed in that area. However, they also noted that water is not the only source of fluoride exposure.

“Additional exposures to fluoride from other sources would increase total fluoride exposure,” the report stated. “The moderate confidence conclusions may also be relevant to people living in optimally fluoridated areas of the United States depending on the extent of their additional exposures to fluoride from sources other than drinking water.”

Thiessen said pregnant women are often exposed to higher levels of fluoride because they drink much more water than others. And formula-fed infants are also at particularly high risk.

“While fluoridation of drinking water is the main source of fluoride intake for millions of people in the U.S., and probably the easiest to eliminate, it is not the only source of fluoride exposure, with toothpaste and tea probably being next in importance,” she said.

Fluoride advocates like the American Dental Association (ADA), the American Academy of Pediatrics (AAP) and the CDC argue that adding fluoride to water is an important public health practice because it prevents tooth decay by exposing teeth to low levels of fluoride throughout the day and strengthening teeth.

Federal health officials have been recommending water fluoridation for more than five decades. However, in the last several years as the NTP report has moved closer to publication, support for the practice has appeared to wane among some public health officials.

The U.S. surgeon general in 2015 officially lowered the recommended dosage for water fluoridation from 0.7-1.2 mg/L to 0.7 mg/L after considering adverse health effects. And in 2020, out of concern for the forthcoming findings in the NTP report, the U.S. surgeon general’s office declined to make a public statement endorsing the practice.

A spokesperson for the CDC told The Defender in a statement that the agency continues to support water fluoridation at current recommended levels.

“These recommendations are based on current scientific evidence and prioritize the safety, security, and health of all individuals,” the agency said. “Continued research is needed to better understand the health risks and benefits associated with low fluoride exposures.”

The spokesperson also said, “While concerns have been raised about potential risks associated with high fluoride exposure, it is important to note that these concerns are primarily based on studies conducted in countries with higher fluoride exposure than in the United States.”

However, some of the highest quality studies to date have been done in Canada and Mexico, where exposure levels were the same as exposure levels in parts of the U.S. And a paper published in JAMA Network Open in May found that children born to women exposed during pregnancy to fluoridated drinking water in Los Angeles were more likely to have neurobehavioural problems.

The ADA, AAP and EPA did not respond to The Defender’s request for comment.

The long road to publication

For more than two decades, researchers have drawn a link between fluoride exposure and neurodevelopmental issues. In 2006, the National Research Council of the National Academies of Science released a report on fluoride toxicity that identified serious health issues associated with fluoride exposure and called for further research.

The NTP, part of the U.S. Department of Health and Human Services (HHS) responsible for producing scientific research meant to inform policymaking, in 2016 began working on its review of fluoride’s neurotoxicity in humans.

After six years and multiple rounds of peer review, the NTP finalized its report in May 2022 — but public health officials within multiple agencies across HHS blocked its publication, according to emails obtained via a Freedom of Information Act request.

The NTP was compelled to send the report out for another round of peer review. Each round of peer review compelled the NTP to walk back some of its conclusions in what critics called an attempt to “delay it, to water it down.”

Former NTP director Dr. Brian Berridge told The Defender the report received unprecedented scrutiny because of challenges to the report by biased stakeholders. He said he believed it was an outcome of public health agencies’ desires to protect the practices they already have in place.

A draft version of the report was made public in March of 2023 under court order.

The order came as part of a lawsuit filed in 2017 by Food & Water Watch, Fluoride Action Network, Moms Against Fluoridation and other advocacy groups and individuals suing the EPA in a bid to force the agency to prohibit water fluoridation in the U.S. due to fluoride’s toxic effects on children’s developing brains.

After initial hearings in June 2020, presiding Judge Edward Chen placed the trial on hold pending the release of the report. After plaintiffs introduced evidence of agency attempts to suppress the report, Judge Chen ordered its release in draft form and the trial continued in January and February of this year.

The report, along with four major fluoride studies using birth cohorts — where researchers collect epidemiological data during pregnancy and then from children over their lifetimes to study a variety of health outcomes tied to environmental exposures — was key evidence in the trial.

The trial concluded on Feb. 13, and Judge Chen has not yet issued a decision.

The report finalized yesterday consists of one part of the NTP’s research. The other part, a meta-analysis, is forthcoming in a peer-reviewed journal.

NTP Director Rick Woychik said in a statement to The Defender that the delay in the report’s publication was due to an attempt to “get the science right” because “fluoride is such an important topic to the public and to public health officials.”

Woychik emphasized that water fluoridation “has been a successful public health initiative.”

Michael Connett, attorney for the plaintiffs in the case against the EPA, said the final version of the report, “confirms and actually further strengthens the NTP’s prior conclusions,” because the finalized version includes a supplemental review of more recent literature published between 2020 and 2023, which also finds a consistent link between fluoride exposure and adverse neurodevelopmental effects.

Connett added:

“Here you have an expert body of the US government confirming that fluoride is a neurotoxicant. That by itself is a very significant conclusion and should really prompt the question among policymakers and the public as to whether we really want to be adding a neurotoxicant to our water supply while questions remain about the precise doses that caused this effect.”

‘We didn’t sign up to add a neurotoxicant to our water’

The number of scientists and health professionals opposed to fluoridation has increased over the last several decades. Thiessen said the final publication of the monograph — and the forthcoming meta-analysis — provides important evidence for their position and might signal a change in the status quo public health position on fluoride.

“One hopes that it will help convince many more professionals that one of the 20th century’s top 10 public health achievements has in fact been terribly misguided from the beginning.”

The lawsuit brought public attention to the debate over water fluoridation ongoing among scientists working in public health for years, with many mainstream outlets addressing an issue that had often been disregarded as a conspiracy theory.

Connett said the government report ought to raise public concern and get more people asking questions about fluoridation. He said:

“This isn’t what people signed up for when we started adding fluoride to the water. We didn’t sign up to add a neurotoxicant to our water. We signed up for something that could help our teeth. Now that we know that it can affect their brain, we really need to go back to square one.”

Fluoride Action Network board member Rick North told The Defender that awareness about issues with water fluoridation has been growing for years.

“Fluoridation is a house of cards and it’s going to fall. It’s only a matter of when. The NTP report just made it sooner.” He said he hopes the final release of the report means a decision in the case against the EPA will come soon.

“For more than four years, Judge Edward Chen has waited for the final NTP report. Now he’s got it — even more scientific backing that fluoridation is an unreasonable risk to human health,” he said.

Stuart Cooper, Fluoride Action Network executive director, said the publication of the report was historic. “This report, along with the large body of published science, makes it abundantly clear that the question isn’t whether fluoridation is safe, but instead how many children have been needlessly harmed,” he said.

The report sometimes makes contradictory statements, Kim Blokker, a board member of Moms Against Fluoridation, told The Defender, showing the influence of the public health agencies on the reporting. “Do not be fooled by this attempt to muddy the waters of this otherwise definitive report, which contains more than enough evidence to prove the shockingly detrimental effects of fluoride exposure in young children.”

Kristie Lavelle, another board member of Moms Against Fluoridation, told The Defender they were happy to see the report finally published. “The time has come for fluoride to lose its status as a protected pollutant and to be treated the same as other recognized toxins such as lead and arsenic.”

With the publication of the report, she said, “We are one step closer to creating a world where clean water, air and food, and consequently vibrant health are the norm for our children and grandchildren.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

August 22, 2024 Posted by | Science and Pseudo-Science, Timeless or most popular | , , | Leave a comment