BREAKING: Days before Trump Inauguration HHS fires doctor in charge of gain of function research project

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11 months ago

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Dr. Daszak will likely be protected by the DoD & CIA from additional penalties.

By John Leake

HHS Formally Debars EcoHealth Alliance, President Peter Daszak Fired.

On January 17, 2025—just three days before President Trump is to be sworn in—Congress issued a press release with the following statement:

Today, after an eight-month investigation, the U.S. Department of Health and Human Services (HHS) cut off all funding and formally debarred EcoHealth Alliance Inc. (EcoHealth) and its former President, Dr. Peter Daszak, for five years based on evidence uncovered by the Select Subcommittee on the Coronavirus Pandemic.

As far as I can tell, the New York Times did not report this story, though the New York Post did.

More interesting than the superficial news reporting is the HHS ACTION REFERRAL MEMORANDUM recommending that Dr. Peter Daszak be barred from participating in United States Federal Government procurement and nonprocurement programs.

The Memorandum also states:

Dr. Peter Daszak was the President and Chief Executive Officer of EHA from 2009 until his termination, effective January 6, 2025. Dr. Daszak was the Project Director (PD)/Principal Investigator (PI) for Grant Number 1R01AI110964-01.

I am not sure what to make of this document, which is written in such an arcane and convoluted style that it challenges the attention span of even the most focused reader.

I have been researching this story for four years, and I found the following paragraphs the most intriguing:

9. In a letter dated May 28, 2016, the NIAID contacted EHA concerning possible GoF research based on information submitted in its most recent Year 2 RPPR. The NIAID notified EHA that GoF research conducted under Grant Number 5R01AI110964-03 would be subject to the October 17, 2014, United States Federal Government funding pause, and that per the funding pause announcement, new United States Federal Government funding would not be released for GoF research projects that may be reasonably anticipated to confer attributes to influenza, MERS, or SARS viruses such that the virus would have enhanced pathogenicity and/or transmissibility in mammals via the respiratory route. In the letter, the NIAID requested that EHA provide a determination within 15 days of the date of the letter as to whether EHA’s research under Grant Number 5R01AI110964-03 did or did not include GoF work subject to the funding pause.

10. In a letter dated June 8, 2016, EHA provided a response to the NIAID’s May 28, 2016 letter. EHA explained that the goal of its proposed work was to construct MERS and MERS-like chimeric CoVs in order to understand the potential origins of MERSCoV in bats by studying bat MERS-like CoVs in detail. EHA stated that it believed it was highly unlikely that the proposed work would have any pathogenic potential, but that should any of these recombinants show evidence of enhanced virus growth greater than certain specified benchmarks involving log growth increases, or grow more efficiently in human airway epithelial cells, EHA would immediately: (1) stop all experiments with the mutant, (2) inform the NIAID Program Officer of these results, and (3) participate in decision-making trees to decide appropriate paths forward.

11. Based on the information provided by EHA, the NIAID concluded that the proposed work was not subject to the GoF research pause. In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.

Note that various statements in the above paragraphs are inconsistent with what Baric et al. state in their 2015 paper A SARS-like cluster of circulating bat coronavirus shows potential for human emergence—a research paper funded by the NIAID EcoHealth Grant “Understanding the Risk of Bat Coronavirus Emergence.”

As the authors state in the section on Biosafety and biosecurity:

Reported studies were initiated after the University of North Carolina Institutional Biosafety Committee approved the experimental protocol (Project Title: Generating infectious clones of bat SARS-like CoVs; Lab Safety Plan ID: 20145741; Schedule G ID: 12279). These studies were initiated before the US Government Deliberative Process Research Funding Pause on Selected Gain-of-Function Research Involving Influenza, MERS and SARS Viruses (http://www.phe.gov/s3/dualuse/Documents/gain-of-function.pdf). This paper has been reviewed by the funding agency, the NIH. Continuation of these studies was requested, and this has been approved by the NIH.

As I noted in my series of essays titled The Great SARS-CoV-2 Charade, one of the silliest lies told by Dr. Anthony Fauci has been his insistence that NIAID did not approve Gain-of-Function work by EcoHealth.

Fauci has repeatedly asserted this in a loud and vexed tone, as though he is outraged by the mere proposition. And yet, Ralph Baric and his colleagues—including Zhengli-Li Shi at the Wuhan Institute of Virology—plainly state in their 2015 paper that their Gain-of-Function experiments, performed in Baric’s UNC lab and Zhengli-Li Shi’s lab in Wuhan, were grandfathered in, given that they were funded before the 2014 Pause.

Another statement (in paragraph 11 of the recent HHS Action Referral Memo) that deserves special scrutiny is the following:

In a letter dated July 7, 2016, however, the NIAID informed EHA that should any of the MERS-like or SARS-like chimeras generated under the grant show evidence of enhanced virus growth greater than 1 log over the parental backbone strain, EHA must stop all experiments with these viruses and provide the NIAID Program Officer and Grants Management Specialist, and WIV Institutional Biosafety Committee, with the relevant data and information related to these unanticipated outcomes.

Again, it’s tough to interpret this statement, given that Baric et al. had, by the own admission, already generated chimeras that “replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV.”

Let’s review what Baric et al. state in their Abstract about the functionality of the chimeric virus (named SHCOI4-MA15) they claimed to have generated. Using humanized mice (genetically modified to have primary human airway cells) as their experimental animals, the authors state:

Using the SARS-CoV reverse genetics system², we generated and characterized a chimeric virus expressing the spike of bat coronavirus SHC014 in a mouse-adapted SARS-CoV backbone.

The results indicate that group 2b viruses encoding the SHC014 spike in a wild-type backbone can efficiently use multiple orthologs of the SARS receptor human angiotensin converting enzyme II (ACE2), replicate efficiently in primary human airway cells and achieve in vitro titers equivalent to epidemic strains of SARS-CoV. Additionally, in vivo experiments demonstrate replication of the chimeric virus in mouse lung with notable pathogenesis.

To this day, no legal authority that I am aware of has investigated the question: What became of the the chimeras SHC014-MA15 and WIV1-MA15? The latter chimera was documented by Baric et al. in their March 2016 paper titled SARS-like WIV1-CoV poised for human emergence—a chimera “that replaced the SARS spike with the WIV1 spike within the mouse-adapted backbone.”

What did the Wuhan Institute of Virology do with these chimeras? Did its researchers continue to modify and experiment with these chimeras?

Another exceedingly silly claim made by U.S. government officials—including members of Congress—is that the true origin of SARS-CoV-2 is likely to remain a mystery, given that the Chinese government and military will almost certainly never agree to perform a full and transparent investigation of their Wuhan Institute of Virology.

What did the U.S. government expect when it agreed to share cutting edge American biotechnology with the Wuhan Institute of Virology, which has long been known to be run by the Chinese military?

One grows weary of our U.S. government officials evading responsibility by pretending to be imbeciles or by revealing themselves to be true imbeciles.

If you found this post informative, please consider becoming a paid subscriber to our Substack. Penetrating the smoke and mirror show performed by the abominable U.S. government requires a great deal of time and effort.

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COVID-19

The dangers of mRNA vaccines explained by Dr. John Campbell

Published on November 30, 2025

Todayville

From the YouTube channel of Dr John Campbell

There aren’t many people as good at explaining complex medical situations at Dr. John Campbell. That’s probably because this British Health Researcher spent his career teaching medicine to nurses.

Over the last number of years, Campbell has garnered an audience of millions of regular people who want to understand various aspects of the world of medical treatment.

In this important video Campbell explains how the new mRNA platform of vaccines can cause very serious health outcomes.

Dr. Campbell’s notes for this video:

Excess Deaths in the United Kingdom: Midazolam and Euthanasia in the COVID-19 Pandemic https://www.researchgate.net/publicat… Macro-data during the COVID-19 pandemic in the United Kingdom (UK) are shown to have significant data anomalies and inconsistencies with existing explanations. This paper shows that the UK spike in deaths, wrongly attributed to COVID-19 in April 2020, was not due to SARS-CoV-2 virus, which was largely absent, but was due to the widespread use of Midazolam injections, which were statistically very highly correlated (coefficient over 90%) with excess deaths in all regions of England during 2020. Importantly, excess deaths remained elevated following mass vaccination in 2021, but were statistically uncorrelated to COVID injections, while remaining significantly correlated to Midazolam injections. The widespread and persistent use of Midazolam in UK suggests a possible policy of systemic euthanasia. Unlike Australia, where assessing the statistical impact of COVID injections on excess deaths is relatively straightforward, UK excess deaths were closely associated with the use of Midazolam and other medical intervention. The iatrogenic pandemic in the UK was caused by euthanasia deaths from Midazolam and also, likely caused by COVID injections, but their relative impacts are difficult to measure from the data, due to causal proximity of euthanasia. Global investigations of COVID-19 epidemiology, based only on the relative impacts of COVID disease and vaccination, may be inaccurate, due to the neglect of significant confounding factors in some countries. Graphs April 2020, 98.8% increase 43,796 January 2021, 29.2% increase 16,546 Therefore covid is very dangerous, This interpretation, which is disputable, justified politically the declaration of emergency and all public health measures, including masking, lockdowns, etc. Excess deaths and erroneous conclusions 2020, 76,000 2021, 54,000 2022, 45,000 This evidence of “vaccine effectiveness” was illusory, due to incorrect attribution of the 2020 death spike. PS Despite advances in modern information technology, the accuracy of data collection has not advanced in the United Kingdom for over 150 years, because the same problems of erroneous data entry found then are still found now in the COVID pandemic, not only in the UK but all over the world. We have independently discovered the same UK data problem and solution for assessing COVID-19 vaccination as Alfred Russel Wallace had 150 years ago in investigating the consequences of Vaccination Acts starting in 1840 on smallpox: The Alfred Russel Wallace as used by Wilson Sy “Having thus cleared away the mass of doubtful or erroneous statistics, depending on comparisons of the vaccinated and unvaccinated in limited areas or selected groups of patients, we turn to the only really important evidence, those ‘masses of national experience’…” https://archive.org/details/b21356336… Alfred Russel Wallace, 1880s–1890s 1840 Vaccination Act Provided free smallpox vaccination to the poor Banned variolation Vaccination compulsory in 1853, 1867 Why his interest? C 1885 The Leicester Anti-Vaccination demonstrations (1885) Growing public resistance to compulsory vaccination Wallace’s increasing involvement in social reform and statistical arguments Statistical critique of vaccination Government data on: Smallpox mortality trends before and after compulsory vaccination Case mortality rates Vaccination vs. sanitation effects Mortality trends before and after each Act, 1853 and 1867 “Forty-Five Years of Registration Statistics, Proving Vaccination to Be Both Useless and Dangerous” (1885) “Vaccination a Delusion; Its Penal Enforcement a Crime” (1898) Contributions to the Royal Commission on Vaccination (1890–1896) Wallace argued: Declining smallpox mortality was due to improved sanitation, not vaccination Official statistics were misinterpreted or biased Compulsory vaccination was unjust Re-vaccination did not reliably prevent outbreaks These views were strongly disputed, then and now. Wallace had a strong distrust of medical authority He and believed in: Statistical reasoning Social reform Opposition to coercive government measures The primacy of environmental and sanitary conditions in health

COVID-19

FDA says COVID shots ‘killed’ at least 10 children, promises new vaccine safeguards

Published on November 30, 2025

Todayville

From LifeSiteNews

By Emily Mangiaracina

“This is a profound revelation. For the first time, the US FDA will acknowledge that COVID-19 vaccines have killed American children”

At least 10 children have died because of the COVID shots, according to a recently publicized email from Trump Food and Drug Administration (FDA) officials.

“At least 10 children have died after and because of receiving COVID-19 vaccination,” FDA Chief Medical Officer Vinay Prasad wrote on Friday in an email to staff, obtained by The Daily Caller.

“This is a profound revelation. For the first time, the US FDA will acknowledge that COVID-19 vaccines have killed American children,” Prasad said in the memo.

The finding corroborates that of the Centers for Disease Control and Prevention (CDC), which recently linked at least 25 pediatric deaths to the COVID shot, via information from the Vaccine Adverse Event Reporting System (VAERS). Both counts likely significantly underestimate the real number of pediatric deaths from the shots, considering that studies have found vaccine injuries have been seriously underreported to VAERS.

In his Friday memo, Prasad ripped the Biden administration for pressuring the injection of these experimental mRNA shots into children.

“Healthy young children who faced tremendously low risk of death were coerced, at the behest of the Biden administration, via school and work mandates, to receive a vaccine that could result in death,” wrote Prasad.

“In many cases, such mandates were harmful. It is difficult to read cases where kids aged 7 to 16 may be dead as a result of covid vaccines.”

The disturbing admission by the Trump administration’s health agency highlights the silence of the Biden administration about these deaths and raises further questions about its integrity or lack thereof.

“Why did it take until 2025 to perform this analysis, and take necessary further actions? Deaths were reported between 2021 and 2024, and ignored for years,” wrote Prasad. He acknowledged that the vaccines potentially killed more children on balance, considering that they had virtually no risk of dying from COVID.

The Center for Biologics Evaluation and Research (CBER) will reportedly strengthen its safety protocols for vaccines, including by requiring more clinical trials as opposed to relying on antibody laboratory studies, modifying the annual flu vaccine release, and examining the effect of administering multiple vaccines in one round.

This year, the CDC removed COVID shots from its recommended “vaccines” for healthy children. A CDC panel had voted in 2022 to add the COVID shots to the childhood immunization schedule despite their experimental nature and the fact that they were produced in a fraction of the time ordinarily required to bring a vaccine to market.

The push for COVID shots for children was spearheaded at least in part by CBER Director Peter Marks, who pushed for full approval of the COVID shots even for the young and healthy and laid the foundation for COVID shot mandates.

A large, growing body of evidence shows that the mRNA shots were dangerous to human health in a wide variety of ways and caused deaths at a rate far exceeding usual safety standards for vaccines. As Dr. Mary Talley Bowden, an ear, nose and throat specialist in Houston, Texas, explained to Tucker Carlson in April:

Normally, the FDA will put a black box warning on a medication if there have been five deaths. They will pull it off the market if there have been 50. Well, according to VAERS, (the) Vaccine Adverse Event Reporting System – and it’s vastly under-reported, which I have seen firsthand – there have been 38,000 deaths from these COVID shots.

That number has since increased, according to VAERS, which now reports 38,773 deaths, 221,257 hospitalizations, 22,362 heart attacks, and 29,012 cases of myocarditis and pericarditis due to the COVID shot as of August 29, among other ailments.