Tag: vaccines

Sudden Deaths, Incapacitations Soar Among COVID-Jabbed Airline Pilots

“Something happened in 2021” that has jeopardized air travel safety, according to a disturbing report by Dr. Kevin Stillwagon, a retired airline pilot and immunology expert.

Mounting evidence points to the COVID-19 vaccinations that airlines, acting under pressure from the U.S. government, mandated or otherwise coerced their cockpit, cabin, and ground crews into taking.

Since 2021, there has been a marked increase in deaths of “younger” airline pilots while long-term disabilities for pilots have skyrocketed. All of this has been accompanied by an astronomical increase of near-miss incidents at the nation’s airports.

“Incapacitations of pilots are definitely increasing, especially in younger pilots,” Stillwagon said in a video discussion with Nicolas Hulscher, an epidemiologist and administrator at the McCullough Foundation.

“There was a 40% increase in pilots dying early – before mandatory retirement age of 65 – in 2021,” Stillwagon said.

“Starting in 2021, pilot long-term disabilities have tripled,” he noted. “Prior to 2021, there was only one near-miss at the Washington National Airport (DCA).  But after 2021, there were 28 near-misses per year.”

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FDA Suspends License For Chikungunya Vaccine After ‘Serious Adverse Events’

Federal regulators on Aug. 25 said they’ve suspended approval for a vaccine against chikungunya, a mosquito-borne virus.

Due to reports of serious adverse events following administration of the vaccine, the Food and Drug Administration’s Center for Biologics Evaluation and Research (CBER) “believes this vaccine is not safe and that continued administration to the public would pose a danger to health,” the FDA said in a statement.

France-based Valneva makes the vaccine, known as Ixchiq.

“As we determine potential next steps, and as the clear threat of chikungunya continues to escalate globally, Valneva remains fully committed to maintaining access to our vaccine as a global health tool for addressing and preventing outbreaks of this devastating illness,” Thomas Lingelbach, Valneva’s CEO, said in a statement.

Zachart Stieber reports for The Epoch Times that the FDA originally approved Ixchiq in 2023 to prevent disease caused by the chikungunya virus in adults deemed to have an increased risk of exposure. The Centers for Disease Control and Prevention in 2024 recommended the vaccine for people traveling to certain countries.

Health officials said in an alert in May that they were advising a pause in administering the vaccine to elderly adults due to reports that some of those vaccinated had been experiencing serious adverse events (SAEs), including neurologic and cardiac problems.

This included 38 SAE reports for 32 unique cases (7 U.S., 25 foreign), including 21 hospitalizations and three deaths.

After CBER Director Dr. Vinay Prasad resigned, the FDA, in early August, ended the recommended suspension, stating that an updated assessment of risks and benefits for Ixchiq showed the benefits still outweighed the risks for some people.

In the new announcement, regulators said that is no longer the case.

The latest risk-benefit assessment includes four new foreign reports that came to light since the FDA lifted the recommended pause, including a report of problems following vaccination in a 55-year-old male.

Prasad said in a memorandum dated Aug. 22 that of the 32 cases, five tested positive for the vaccine strain of the virus, making it nearly certain that the vaccine caused the problem.

“There are reasonable grounds to believe the risks of the vaccine outweigh its benefits, and that it poses a danger to health. Therefore, CBER is suspending approval,” Prasad said.

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Report: Trump Administration Planning to Phase Out COVID-19 Vaccine

The Trump administration is reportedly planning to phase out the COVID-19 vaccine, according to a report from the Daily Beast.

Dr. Aseem Malhotra, who is one of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.’s “closest associates,” told the outlet that while a decision to remove the COVID-19 vaccine from the market could come “within months,” it could occur “in a number of stages.” Malhotra also added that “those closest” to Kennedy have reportedly expressed that they “cannot understand” why the COVID-19 vaccine “continues to be prescribed.”

“It could [happen] in a number of stages, including learning more about the data,” Malhotra, who is a British cardiologist, told the outlet. “But given the increased talk of vaccine injuries in the past few weeks among the administration, it could also come with one clean decision.”

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‘Right This Wrong’: GRACE Act Would Strip Federal Funding From Schools That Ban Religious Exemptions

A member of the U.S. Congress has drafted legislation that would strip federal funding from schools that don’t allow parents to apply for religious exemptions from vaccination requirements for their children.

The GRACE Act, or Guaranteeing Religious Accommodation in Childhood Education Act, drafted by Rep. Greg Steube (R-Fla.), would target elementary and secondary schools, as well as local and state educational agencies.

The legislation would not require state authorities or educational institutions to offer religious exemptions, but it would deny federal funds to those entities if they maintain vaccine mandates that don’t include provisions for religious exemptions.

“The denial of religious exemptions to families and children is un-American and unconstitutional,” said Michael Kane, CHD’s director of advocacy and founder of Teachers for Choice. “CHD and I thank Rep. Steube for putting forth this important legislation to right this wrong that is a clear violation of the First Amendment.”

The GRACE Act is a response to the “alarming erosion of civil rights” that occurred under the Biden administration, said Cait Corrigan, a former congressional candidate from New York and an advocate for medical freedom and religious liberty.

“This issue is one of religious freedom, individual liberty and parental rights, which I often describe as part of a broader response to years of increasing concern,” Corrigan said.

Steube’s office did not respond by deadline to The Defender’s request for comment on the legislation.

‘A matter of conscience, faith and the fundamental dignity of every family’

Corrigan said the proposed legislation is “not just an issue of policy” but “a matter of conscience, faith and the fundamental dignity of every family in this country.”

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ACIP Launches Sweeping Covid-19 Vaccine Review Under Retsef Levi

MIT professor Retsef Levi has been an outspoken voice on the CDC’s vaccine advisory committee (ACIP) since its dramatic overhaul in June.

He has pressed agency officials on uncomfortable questions, challenging the narrow surveillance windows used to track harms and insisting that delayed effects could not simply be ruled out.

He also raised concerns about the safety of RSV monoclonal antibodies after clinical trials showed a clear imbalance in infant deaths.

Now, Levi is no longer just a dissenter.

He has been appointed chair of the CDC’s new Covid-19 vaccine working group, and with today’s release of its Terms of Reference, the scale of his task has come into sharp focus.

Under the guidance of Levi and his colleagues, the ACIP working group now has a mandate unlike anything the committee has ever undertaken.

For the first time, federal advisers will investigate the unresolved issues that have dogged the vaccines since their rushed rollout in late 2020.

From DNA contamination in the manufacturing process to the persistence of spike protein and mRNA in the body, from immune class switching following repeated boosting to safety in pregnancy, cardiovascular risks, and long-term disability, the list of questions is as sweeping as it is sensitive. (full list below)

The Terms of Reference stretch far beyond the narrow remit that characterised ACIP’s early deliberations, when myocarditis was acknowledged as the only confirmed harm and most safety reviews stopped at 42 days.

Levi and his team are now tasked with probing long-term outcomes, mapping vaccine policies around the world, and assessing, to what extent, years of official reassurances about safety and efficacy hold up against emerging data.

It is a striking reversal for the CDC and the FDA.

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Yale’s Censored Vaccine Injury Research and the Urgent Need for Scientific Reform

One premier research group has bravely studied the vaccine-injured and provided many critical details about their multi-year illnesses.

•Unfortunately, despite their excellent research, medical journals have refused to publish their results, including the most recent study which showed clear differences exist between long COVID and COVID-19 vaccine injuries.

•Science is ultimately predicated upon the methods we use discern what is actually true (epistemology). As this subject has been neglected, our epistemological standards frequently result in existing dogmas and vested interests being reaffirmed while critically important data never reaches the public awareness (e.g., due to widespread medical journal censorship).

•During COVID-19, the severe abuses of the scientific community (which ultimately resulted from it having no accountability for failing to uphold its social responsibilities) broke the public trust in science, and allowed something previously inconceivable—MAHA to gain control of our corrupt scientific apparatus and have a mandate to reform it.

•NIH director Jay Bhattacharya has announced his commitment to fixing the scientific apparatus and has engaged in a variety of NIH initiatives and public discussions which are vital to allowing science to serve the people rather than vested-interests.

Yale’s medical school is widely considered to have one of the top autoimmunity research and treatment programs in America. As long COVID is considered to be immunological in nature, their researchers extensively studied it, and remarkably some of them then pivoted to also studying vaccine injuries (in part because the COVID vaccines rather than curing long COVID patients, sometimes made them much worse). A few days ago, they finished a new research paper on the subject, but like their previous ones, it was immediately summarily rejected by the “reputable” journals it was submitted to (including the one I feel was the most obligated to publish these findings). In this article, I aim to cover the importance of their most recent results and, more important, examine what their habitual censorship reveals about science in general.

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Same Excess Death Patterns in Multiple Data Sets after mRNA Vaccine Rollouts

This article is based on the painstaking and meticulous work of intrepid researcher and Substack writer csofand. I will refer to him as “the researcher,” as he prefers to remain anonymous.

I am also grateful for the assistance of citizen researcher/journalist Benjamin Marten, who generously shared his VAERS data queries and results with me.

Why am I writing about excess mortality associated with Covid mRNA vaccines?

Recently, I was talking to some friends about various Covid topics and casually mentioned deaths and disabilities associated with the mRNA vaccines, as documented by the company that made them. My friends, who are somewhat open to Covid skepticism but have not explored the subject very thoroughly, and are still ensconced in the corporate media bubble, were taken aback. “You mean people died from the vaccines?” they asked incredulously.

Which, for me, raised the question: How can we still be arguing about this?

I hope the information compiled here can help put an end to the question of whether or not Covid mRNA vaccines harm and kill people.

What Is “Excess Mortality”?

According to Wikipedia, excess mortality is an epidemiological term that means “the increase in the number of deaths during a time period and/or in a certain group, as compared to the expected value or statistical trend during a reference period (typically of five years) or in a reference population.”

Simply put, it means more deaths than expected based on previous trends and future projections. As it relates to Covid-19, starting very early in 2020, a major topic of concern became how much excess mortality was caused by the disease (whether or not the disease actually caused a lot of excess mortality is a separate issue). After 2020, with near universal exposure to the novel coronavirus, and the rollout of a global vaccination campaign, excess mortality was expected to go back down. Instead, it increased.

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The Case of the Damning FDA Memos

On July 21, 2025, the Informed Consent Action Network (ICAN) announced that it had secured the release of over 600,000 pages of Emergency Use Authorization (EUA) data used by the US Food and Drug Administration (FDA) to authorize and approve Pfizer-BioNTech’s COVID-19 vaccine (BNT162b2), following a successful lawsuit, culminating in a late 2024 court ruling.

These documents, now publicly available on ICAN’s website, are part of a broader release of over 1.6 million pages, including data from the vaccine’s licensure in August 2021 and the earlier EUA in December 2020.

This report builds on my prior investigative work analyzing thousands of FDA documents released following the Public Health and Medical Professionals for Transparency (PHMPT) lawsuit, which focused on the biological product file submitted by Pfizer for the full approval of its COVID-19 vaccine in August 2021.

I was one of the initial researchers to uncover and analyse the damning data hidden within Pfizer’s Pregnancy & Lactation Cumulative Review, Interim-Narrative-Sensitive document (3000+ pages), and Cumulative Analysis of Post-Authorization Adverse Event Reports document, among others.

Both ICAN and PHMPT’s lawsuits sought to make public the FDA’s data on the Pfizer-BioNTech’s COVID-19 shot, asserting that transparency is critical for public trust and independent analysis, given the global administration of billions of doses of this experimental gene-based product that was mandated in several countries.

My preliminary review of ICAN’s EUA data reveals several irregularities, outlined below with references to key documents and downloadable sources. This report focuses on four critical issues: manufacturing oversight gaps, missing Bell’s palsy data, clinical trial site deficiencies, and the exclusion of unconfirmed COVID-19 cases.

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AAP Received Tens of Millions in Federal Funding to Push Vaccines and Combat ‘Misinformation’

The American Academy of Pediatrics (AAP), which is suing U.S. Health Secretary Robert F. Kennedy Jr., and has called for the end to religious exemptions, received tens of millions of dollars in federal funding in a single year, according to public records.

AAP, which represents 67,000 pediatricians in the U.S., received $34,974,759 in government grants during the 2023 fiscal year, according to the organization’s most recent tax disclosure. The grants are itemized in the AAP’s single audit report for 2023-2024.

Documents show some of the money was used to advance childhood vaccination in the U.S. and abroad, target medical “misinformation” and “disinformation” online, develop a Regional Pediatric Pandemic Network, and highlight telehealth for children.

However, not all of the money could be tracked through public records.

The federal grants are in addition to financial contributions the AAP receives from several major pharmaceutical companies, including Eli Lilly, GSK, Merck, Moderna and Sanofi.

Sayer Ji, founder of GreenMedInfo and co-founder of Stand for Health Freedom, said the joint funding that the AAP receives from taxpayers and Big Pharma “reflects a troubling alignment between its policy positions and the interests of its largest funders — both federal agencies and pharmaceutical corporations.”

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American Academy Of Pediatrics Pushes COVID-19 Vax For All Infants

In stark contrast to reality, the American Academy of Pediatrics (AAP) – which is heavily funded by pharmaceutical companies, recommended on Tuesday that young children, including infants, receive the COVID-19 vaccine despite the fact that children are minimally impacted by the virus, the fact that the vaccine doesn’t prevent one from contracting it, and that it largely only helps the elderly and medically fragile from severe cases.

According to the organization, all children ages 6-23 months should receive the COVID-19 vaccine – regardless of whether they have natural immunity from prior infection, unless they have a contraindication such as a history of severe allergic reaction to a vaccine ingredient. 

While the recommendation is universal, the group said in a statement that their recommendation stems from infants and other children who are “at high risk for severe COVID-19.”

As the Epoch Times notes further, the organization pointed, in part, to a paper it published that found that among children hospitalized for COVID-19 from fall 2022 to spring 2024, the majority of those younger than 2 had no underlying conditions.

Of note, the paper cited surveyed 2,490 children who were hospitalized with COVID-19, effectively a rounding error. 

A spokesman for the Department of Health and Human Services, the CDC’s parent agency, told The Epoch Times in an email that the AAP, which receives funding from vaccine manufacturers, should strengthen its conflict-of-interest safeguards.

“By bypassing the CDC’s advisory process and freelancing its own recommendations, while smearing those who demand accountability, the AAP is putting commercial interests ahead of public health and politics above America’s children,” Andrew Nixon, the spokesman, said.

The CDC used to recommend that all children, except for those younger than 6 months, receive a COVID-19 vaccine.

In May, under orders from Health Secretary Robert F. Kennedy Jr., the CDC stopped recommending the vaccine for healthy children and pregnant women.

The CDC’s schedule currently states that children with moderately or severely compromised immune systems should receive a vaccine, even if they’ve been vaccinated before.

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