COVID-19
BREAKING: Days before Trump Inauguration HHS fires doctor in charge of gain of function research project

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.
2025 Federal Election
Before the Vote: Ask Who’s Defending Our Health

From the World Council for Health Canada
The health of Canadians has been compromised by government-mandated COVID-19 injections. The upcoming federal election is an opportunity to demand change and accountability. As you decide which candidate or party is most committed to defending the health of yourself and your family, please consider the following:
The Injections Were Never What They Claimed
The Canadian government successfully mandated the COVID-19 injections by labeling them “safe and effective vaccines.” These products are still being promoted and administered across the country. However, the truth is:
- They are not vaccines: Click Here
- They are not safe: Click Here
- They do not prevent infection or transmission.
- Evidence shows they increase the risk of COVID-19 disease and death: Click Here
These Products Contain Multiple Mechanisms of Harm
- They cause injury through multiple biological mechanisms: Click Here
- They have surpassed all vaccines in recorded history—for all infections, for all of the past thirty years combined—in causing deaths and injuries: Click Here
- They are chemically contaminated and adulterated with DNA: Click Here
- In Pfizer’s case, fraud is evident: the DNA contamination includes genetic engineering tools derived from the SV40 virus, associated with cancer risks: Click Here
This Election, We Must Demand Accountability
Insist that to have your vote, candidates must:
- Denounce the COVID-19 “vaccines.”
- Support a full halt to their manufacturing and administration.
- Uphold informed consent, scientific integrity, and bodily autonomy.
Your voice is important. Use it to reject censorship, harm, and medical coercion.
COVID-19
The Pandemic Justice Phase Begins as Criminal Investigations Commence

Nicolas Hulscher, MPH
Hulscher interviews the two attorneys who filed criminal referrals in 7 states—triggering active criminal investigations into top COVID officials for murder, terrorism, and racketeering.
In this explosive episode of Focal Points, I sit down with two fearless attorneys from Vires Law Group—Rachel Rodriguez and Mimi Miller—who are leading a historic legal effort to hold top public health officials accountable for their actions during the COVID-19 pandemic.
Rachel, founder of the Vires Law Group in South Florida, entered the fight through early litigation against mask and vaccine mandates. Mimi, a former criminal prosecutor, joined Rachel in 2023. Together, they’ve now filed seven criminal referral requests to Attorneys General across the U.S. accusing Fauci and top COVID officials of serious crimes such as murder, racketeering, fraud, abuse, and terrorism. These efforts have already resulted in two active criminal investigations:
In this interview, we dive deep into the criminal referrals:
The Accused
Dr. Anthony Fauci – Former Director, NIAID
Dr. Cliff Lane – Deputy Director, NIAID
Dr. Francis Collins – Former Director, NIH
Dr. Deborah Birx – Former White House COVID Response Coordinator
Dr. Rochelle Walensky – Former Director, CDC
Dr. Stephen Hahn – Former Commissioner, FDA
Dr. Janet Woodcock – Principal Deputy Commissioner, FDA
Dr. Peter Hotez – Dean, National School of Tropical Medicine, Baylor College of Medicine
Dr. Robert Redfield – Former Director, CDC
Dr. Peter Daszak – President, EcoHealth Alliance
Dr. Ralph Baric – Professor, University of North Carolina
Dr. Rick Bright – Former Director, BARDA
Administrators of various hospital systems and care facilities.
Applicable Crimes
The Vires Law Group is seeking state criminal investigations into the aforementioned individuals. The charges outlined include:
Terrorism
Under many state laws, terrorism includes committing crimes to coerce or influence government policy or civilian behavior. The attorneys argue that public fear was deliberately manufactured to increase uptake of vaccines, drive compliance, and suppress dissent—via manipulated death counts, relentless fear-based media messaging, and denial of early treatment.
Murder & Involuntary Manslaughter
Patients were knowingly given lethal treatments such as remdesivir—despite it being pulled from an Ebola study for causing over 50% mortality. Families were denied the right to refuse treatment, and ventilators were used despite overwhelming evidence of fatal outcomes.
Aggravated Assault & Lack of Informed Consent
Patients were subjected to medical procedures—ventilators, remdesivir, and even COVID-19 vaccines—against their will or without informed consent. This constitutes unlawful bodily harm under most state statutes.
Racketeering (RICO)
The team alleges this was a coordinated scheme for profit—fueled by CARES Act incentives and PREP Act immunity—where hospital administrations financially benefited by complying with federal protocols at the expense of patient lives.
Abuse of Vulnerable Adults
Victims were elderly or incapacitated, often denied food, water, vitamins, and family visitation—all while being isolated and coerced into fatal treatment pathways.
Scope & Strategy
While the larger COVID response is under scrutiny, the petitions focus specifically on hospital homicides—where the legal case is strongest and where witnesses (survivors and next-of-kin) are actively seeking justice.
By targeting state-level criminal codes, the team bypasses federal hurdles and builds strategic, streamlined cases with clearly defined jurisdiction and causality.
The goal: create a roadmap for local prosecutors to pursue charges, without being overwhelmed or confused by federal overlap or civil legal complexities.
Victims, Whistleblowers & Ongoing Investigations
Two states have already opened active criminal investigations—though confidentiality laws prevent disclosure of details.
Over 200 victim cases are already included across the seven petitions, with many more expected to be added. These include next-of-kin statements, medical records, and evidence of systemic wrongdoing.
Former nurses, doctors, and hospital staff have come forward, risking their licenses and careers to expose the abuse, forced protocols, and fatal policies they witnessed firsthand.
Epidemiologist and Foundation Administrator, McCullough Foundation
Please consider following both the McCullough Foundation and my personal account on X (formerly Twitter) for further content.
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