Tag: coronavirus

How to Ban Gain-of-Function in America: Repeal or Amend the 1989 ‘Biological Weapons Anti-Terrorism Act’

The Act enshrined into U.S. law the 1975 Biological Weapons Convention Treaty, an international agreement ratified by America and over 100 other nations.

The Biological Weapons Convention Treaty was created in response to the global recognition of the catastrophic potential of bioweapons, exemplified by their development during World War II and subsequent programs by nations such as the United States, the Soviet Union, and Japan.

These agreements sought to prevent the escalation of biological warfare in a post-nuclear age.

Countries that have not signed the treaty include Israel, Chad, Comoros, Djibouti, Eritrea, and Kiribati.

Article I of the international Treaty says that State Parties cannot “develop, produce, stockpile or otherwise acquire or retain microbial or other biological agents, or toxins whatever their origin or method of production.”

The treaty effectively prohibits the production of chemical, bacteriological, or biological weapons (bioweapons) in signatory nations.

Gain-of-function experiments by definition enhance the transmissibility or virulence of a potentially pandemic pathogen, making the product of such experimentation something that could be used as a biological weapon.

For example, the virus that caused the COVID-19 pandemic, SARS-CoV-2, was the result of gain-of-function research, as affirmed by the FBI, Department of Energy, various U.S. intelligence authorities, and the Select Subcommittee on the Coronavirus Pandemic under the House of Representatives Committee On Oversight and Accountability.

Over 1 million Americans were killed by COVID, according to the U.S. Centers for Disease Control and Prevention (CDC).

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How They Faked a Pandemic

In examining how the global response to COVID-19 unfolded, one cannot overlook the pivotal role of PCR testing. The very tool used to justify lockdowns, mandates, and “vaccines” was fundamentally flawed. Even the test’s inventor, Kary Mullis, warned that it was never meant to diagnose infectious diseases. Instead, it was weaponized to generate fear and compliance, creating what some call a “pandemic of PCR tests,” not an actual pandemic of disease.

PCR tests work by amplifying genetic material, doubling it with each cycle. With enough cycles—beyond the recommended 27—they can detect virtually anything. During the COVID-19 response, countries like Canada ran up to 43 cycles, yielding an overwhelming number of false positives. According to data from Germany’s Robert Koch Institute, these tests produced up to 86% false positives, leading to the illusion of widespread infection.

If we strip away the hysteria and false positives, the picture becomes clear: COVID-19 never approached the lethality or spread required to justify the measures taken. Respiratory infection peaks during 2019 and 2023 ranked higher in severity than the worst peaks attributed to COVID-19. What we faced was not a pandemic of disease but a carefully orchestrated narrative designed to justify unprecedented measures.

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VICTORY: Dr William Bay wins doctors’ right to criticise covid gene-vaccines

Friday marked the biggest victory yet for doctors against political persecution after the Queensland Supreme Court issued a scorching judgement against Australia’s medical regulators on Friday.

Queensland GP William Anicha Bay celebrated outside court after successfully overturning a politically motivated medical ban put on him for protesting against the covid gene-vaccines on safety grounds.

The Court did not enter into any debate about the safety of the controversial products but ruled only on whether the regulators’ decision or conduct was free from error.

The Medical Board of Australia suspended Dr Bay’s registration on August 17, 2022, less than three weeks after he accosted the Australian Medical Association (AMA) National Conference and asked the delegates to stop forcing the jabs on people in response to an infection where “there is only a 0.27 percent fatality rate”.

Dr Bay apologised for interrupting proceedings before saying the covid “vaccines” were killing people.

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What the declared pandemic was and was not

We need to be political, in the sense of influencing people on all sides

We are not going to fix the world with science, and we are not in charge.

We cannot prevent future elite assaults of this kind. We can only delay and dampen the next round by punishing those responsible, to the best of our abilities.

Responsibility for punishment is mostly individual, because virtually all the institutions are captured. Effectiveness of individual punishment relies in part on a sufficiently accurate perception of reality, which is a continuous challenge.

The need for and benefit from people defending themselves are the intrinsic societal reasons for free speech. (See many related essays here.)

Free speech (with or without permission) exists so that we can punish with words, images, disclosures, logic… and , yes, ridicule and humiliation; and so we can catalyze individual resistance and organizations of opposition. Free speech is not solely so that one can express impactless creativity and have human connection. It is a vital balancing structural mechanism in our social dominance hierarchies. (See many related essays here.)

Establishment collaborators, enablers and planners must be exposed and destabilized. The false self-image they adopt and project should be challenged. This is often the only way we can influence those agents away from their compliant and harmful behaviours.

People know this instinctively, which is why we vote to punish, rather than to reward.

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Will Congress Thwart RFK Jr.’s Data Audit and Recall of the COVID-19 Shots?

Congress’s December 4, 2024, Coronavirus Pandemic Report has inspired hope for justice in prosecuting US federal agencies and individuals who engaged in egregious acts of willful injury against Americans and global citizens (i.e. Dr. Anthony Fauci), while frequently citing 18 U.S.C 1001 (that it’s a crime to lie to Congress).

The Congressional report also ignited controversy amongst many members of the medical freedom movement. The major point of controversy comes from one bullet point on page-2 of Chairman Brad Wenstrup’s opening letter for the 557-page Subcommittee report.

“Operation Warp Speed was a tremendous success and a model to build upon in the future. The vaccines, which are now probably better characterized as therapeutics, undoubtedly saved millions of lives by diminishing likelihood of severe disease and death.”

This statement, combined with Trump’s and RFK Jr.’s recent Mar-a-lago meeting with the CEO’s of Pfizer, Eli Lilly, and PhRMA, are causing many health freedom leaders to contemplate if every current and even future government official of our federal, legislative and judicial branches under Trump is inevitably a “deep state operative.” Some medical freedom influencers continue to assert that we are simply watching more “good cop, bad cop theatre.”

A key question naysayers raise is, “Why would House Representative Wenstrup make a key point in the Coronavirus Pandemic Report be, ‘The COVID-19 vaccines undoubtedly saved millions of lives,’ unless everyone involved in the government, including Congress, were deep state operatives?”

Because Naysayers and Their Followers Only Read the 1st Two Pages of the 557-Page Report

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Justice Thomas Revives Emergency Injunction in Case to Halt Doctor Investigations Over COVID-19 Criticism

The US Supreme Court is set to once again consider a request to issue an injunction in the Stockton v. Ferguson case, that would prevent the Washington Medical Commission from investigating and sanctioning – effectively, censoring doctors because of their criticism of Covid policies.

The application was originally submitted as part of a lawsuit brought by basketball legend John Stockton, several dozen doctors affected by this censorship, and Robert F. Kennedy Jr.’s Children’s Health Defense (CHD), only to be rejected on November 20 by Justice Elena Kagan.

Two days later, the plaintiffs filed the injunction application again, addressing it at Justice Clarence Thomas, who then decided to schedule a Supreme Court private judicial conference for January 10, 2025.

We obtained a copy of the application for you here.

The justices will decide whether to approve the injunction or deny it, while another possible outcome is that oral arguments will be scheduled, with the case proceeding in that way.

The Washington Medical Commission is investigating the doctors, treating their publicly expressed opinions regarding the controversial measures as “potentially dangerous misinformation” that the state has the right to regulate (a 2018 Supreme Court ruling, however, says that this is not the case).

The doctors, meanwhile, argue that the First Amendment speech protections apply to them as well, regardless of their status as licensed medical professionals, including when their views clash with “medical orthodoxy.”

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Pfizer Accused of Hiding Deaths in COVID-19 Vaccine Trials, Including ‘Subject 11141050’ in Kansas, Team Research Alleges

A team of researchers analyzing Pfizer’s clinical trial data has accused the pharmaceutical giant of concealing deaths during its COVID-19 vaccine trials.

Among the allegations is the failure to disclose the death of a Kansas participant who was part of the BNT162b2 vaccine trial. The death reportedly occurred 41 days after the participant received their second vaccine dose.

The accusations stem from a detailed report led by Dr. Jeyanthi Kunadhasan, an anesthetist and perioperative physician, and a member of the DailyClout research team.

The team alleges that Pfizer’s reporting practices during the critical juncture leading to the FDA’s Emergency Use Authorization (EUA) for the vaccine were flawed, with significant delays in documenting serious adverse events, including deaths.

“The Polack paper disclosed six deaths — two in the BNT162b2 arm, and four in the Placebo arm. In the journal article and the EUA approval documentation[9], the six deaths covered the period of July 27, 2020, through November 14, 2020,” Dr. Kunadhasan wrote in a letter sent to Kansas Attorney General Kris Kobach, who filed a lawsuit against Pfizer.

“This letter will demonstrate that Pfizer-BioNTech possessed records showing that eight deaths, four in the BNT162b2 arm and four in the Placebo arm, should have been disclosed by Pfizer to the FDA.  In addition, the two undisclosed deaths presented a cardiac event signal in the clinical trial’s BNT162b2 recipients. One of the undisclosed deaths in the vaccinated arm of the trial occurred in Kansas,” she added.

Subject 11141050, a 63-year-old Kansas woman, participated in Pfizer’s clinical trial at a research site in Newton, Kansas.

Despite her pre-existing conditions, including hypertension and depression, she met the trial’s inclusion criteria and received her second vaccine dose on September 8, 2020. She passed away on October 19, 2020, with the cause of death determined to be sudden cardiac arrest.

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Revealed: The Hidden Pfizer Report That Shows Heart Conditions in the Vaccinated Getting Worse Over Time

I told you here about Pfizer’s abstract of its Interim Report 5, showing at least 23-40% higher risk of some heart-related conditions in the vaccinated, but that the MHRA, the U.K. medicines regulator, was withholding publication of the full report. As I said at the time : “In summary, if, as I suspect, MHRA is worried by the results in Pfizer’s ‘Interim Report 5’ then no wonder it is sitting on it.”

Well, MHRA is still sitting on the report but I’ve managed to obtain a copy. It looks like I was right – the detailed results in the full report are even more worrying than the Hazard Ratios in the abstract which I reported last time.

To recap: this is a report of a Post Authorisation Safety Study (PASS) of Pfizer’s Covid vaccine. National regulators routinely require pharmaceutical manufacturers to conduct PASS studies as a condition of authorisation of most new medicines. The regulators provide data to the manufacturer covering millions of patients registered in national healthcare systems. The manufacturer then conducts analysis, matched for things like age and sex, to determine whether the medicine has increased the risk of specified health conditions.

Let’s dive straight in. Below are some heart-related cumulative incidence graphs from Pfizer’s full ‘Interim Report 5’. You will immediately notice that the incidence for each type of condition is significantly greater in the Covid vaccinated (bad) – but we already knew that from the Hazard Ratios in the abstract. What’s worse is that the curves diverge over time, i.e., the relative incidence between vaccinated and unvaccinated increases over the time period of the data in the report (December 8th 2020 – March 21st 2022). I wonder what happened subsequently.

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FDA must disclose more COVID-19 vaccine records, US judge rules

A federal judge has ordered the U.S. Food and Drug Administration to publicly disclose more information underpinning its authorization of COVID-19 vaccines, after failing to persuade the court to end the public records lawsuit.

In a ruling, opens new tab on Friday, U.S. District Judge Mark Pittman in Fort Worth, Texas, ordered the agency to produce its “emergency use authorization” file to a group of scientists who wanted to see licensing information that the FDA relied on to approve the Pfizer-BioNTech coronavirus vaccine.

“The COVID-19 pandemic is long passed and so has any legitimate reason for concealing from the American people the information relied upon by the government in approving the Pfizer vaccine,” wrote Pittman, appointed in 2019 by then-President Donald Trump.

The lawsuit, filed in late 2021, attracted attention after the FDA said it could take decades to process and disclose records to Public Health and Medical Professionals for Transparency, the group that brought the case.

The FDA declined to comment.

Attorney Aaron Siri, representing the Public Health and Medical Professionals for Transparency, welcomed Pittman’s order.

“The FDA clearly lacks confidence in the review that it conducted to license Pfizer’s COVID-19 vaccine because it is doing everything possible to prevent independent scientists from conducting an independent review,” Siri said.

He said the agency was “hiding from the court and the plaintiff one million pages of clinical trial documents from the COVID-19 vaccine clinical trials.”

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Leading doctors sign HOPE Accord calling for the suspension of all covid mRNA “vaccines”

Thousands of doctors and healthcare professionals have signed a petition calling for the immediate suspension of all covid-19 mRNA products because they are contributing to an alarming rise in disability and in excess deaths. 

The online petition, known as the HOPE accord makes 5 calls for the international community concerning the covid mRNA vaccines that were given emergency use authorisation stating that “a growing body of evidence suggests that they are contributing to an alarming rise in disability and in excess deaths.”

The petition calls for “independent investigations to be properly resourced to allow a comprehensive re-evaluation of all covid-19 products. There must be a full exploration of mechanisms of harm to provide insight into their effect on the human body both short and long term.”

There are additional calls for immediate recognition and support for the vaccine injured. “The vaccine injured must be recognised and every effort be made to understand their conditions. Support should include readily accessible multidisciplinary clinics offering investigation and treatment as well as appropriate compensation for all those who have been harmed.” 

It also states, “The medical profession must lead by admitting we lost our way. By drawing attention to these medical and ethical issues surrounding the covid-19 response, we hope to validate and amplify the call to ensure the relevant facts and ensure vital lessons are learned. An honest and thorough investigation is needed, addressing the root cause that has led us to this place, including institutional groupthink, conflicts of interest and the suppression of scientific debate.” 

An open letter to the General Medical Council of the UK written by Consultant Cardiologist Dr Aseem Malhotra and copies in several leaders in health also refer to the petition of which he is a co-founder.  They include the chief medical officer, Sir Chris Whitty, the Chief scientific adviser to the British government, Patrick Valance and the secretary of state for health, Wes Streeting. 

Dr. Malhotra says that given the level of evidence of unprecedented harm, their position to not suspend the covid mRNA products is now untenable. Re-analysis of Pfizer and Moderna’s original randomised controlled trials on the covid mRNA products by independent experts that included the associate editor of The BMJ revealed a greater risk of serious harm from the vaccine than being hospitalised with covid. This rate of serious harm is 1 in 800 at two months suggesting harms are likely much greater as it does not take into consideration medium to long-term harms that include heart attacks, strokes and cancer. Conversely, the level of benefit in the highest risk group, those over 90, according to UKHSA data for 2024 is 1 in 7,000 to prevent a covid hospitalisation. In other words, at least eight times greater risk of harm than benefit in this group.

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