COVID-19
Dr. McCullough praises RFK Jr., urges him to pull COVID shots from the market
From LifeSiteNews
By Frank Wright
“I am behind what’s happening right now,” he said, of the likely inclusion of RFK Jr. and other “disruptors” such as Elon Musk and Vivek Ramaswamy in the new administration. “I think the whole nation feels that we are finally getting back on track.”
In a video published November 15, prominent mRNA “vaccine” critic Dr. Peter McCullough responds to the Make America Healthy Again manifesto promised by the incoming Trump administration.
Welcoming the “tremendous … team selection” behind Robert F. Kennedy Jr., who has been nominated to lead the Department of Health and Human Services, McCullough also pressed the need for deep reform of a “corrupt” system.
“The pandemic has called for a sweep of corruption out of [U.S. government] agencies,” he said, warning viewers that “we don’t want health to be as political as other areas.”
Robert F. Kennedy Jr. has been described as a “vaccine skeptic” and charged with being unsuitable for the leadership of the U.S.’s main health agency.
“He is really just a person without a health background who’s already caused great damage in health in the country,” Georges C. Benjamin, former executive director of the American Public Health Association, told the BBC.
The incumbent administration, by contrast, considers the transvestite Richard Levine as unquestionably qualified to be assistant secretary of health.
Levine was described as “a dangerous man spewing potentially deadly information” in support of “the idea that children can change their sex.”
Jennifer Bilek, the leading critic of the “transgender” cult of “synthetic sexual identities,” says Levine is a “quack” who was placed in his influential position by the powerful “Big Pharma” lobby.
Levine, who calls himself “Rachel,” is described by Bilek as “a man dressed as a woman who wants your kid to do what he did.”
His tenure is a case in point of the deep corruption which McCullough says must be swept out by the new administration. McCullough also mentions the growing evidence that so-called “transgender care” is “increasing mortality” – ending lives, despite its supporters claims that puberty blockers and mutilation saves them.
“This is gone now,” said McCullough, citing President Trump’s statement that Medicare and Medicaid will no longer fund “transgender care.”
“We are not going to have children subjected to this,” said McCullough. He concludes by saying that not only should the public be protected from the harmful dominance of health by Big Pharma, but “protecting children from ‘transgender health’” is also a laudable priority for the new administration.
McCullough, who is the chief scientific officer at the Wellness Company and world-leading expert on internal medicine, cardiovascular diseases, and clinical lipidology, stresses the need for leadership of Health and Human Services which can bridge the political divide in America – rather than reinforce it.
“For Health and Human Services – which is Medicare, Medicaid, NIH, CDC, FDA – we want somebody who is going to be able to work with both political leanings,” he said.
He says the new health leadership must work for the American people – and their health – against the vested interests of “Big Pharma.”
McCullough believes the “disruptive force” of RFK Jr. will play a “big role” in restoring the confidence of the American public in its discredited institutions.
“I am behind what’s happening right now,” he said, of the likely inclusion of RFK Jr. and other “disruptors” such as Elon Musk and Vivek Ramaswamy in the new administration.
“I think the whole nation feels that we are finally getting back on track.”
McCullough puts the issue of the COVID-19 “vaccines” at the top of his list of priorities for RFK Jr.’s health leadership.
He reminds viewers that the “current ones on the market are not FDA-licensed,” explaining that “Biden ended the COVID-19 emergency years ago,” and so there is no public health reason to promote them.
“Nobody in America thinks we have an emergency,” he said, and “COVID-19 is like the common cold, so the vaccine boosters are not clinically indicated.”
Aside from being “medically unnecessary,” McCullough restates the so-called “vaccines” have had “great safety concerns, with injuries, disabilities and deaths.”
He notes that “sadly, the people who are in a sense forced to take them are sadly children – in order to fulfill the vaccine schedule and go to school.”
He called for the new government to “convene a safety review,” with “Pfizer, Moderna and Novavax at the table” with academics and former U.S. health agency leaders. What would be the message?
“They are coming off the market” is what McCullough says should be said about the experimental injections.
“I think America would be overjoyed,” he explained, if these so-called vaccines were taken off the market “for the reasons I have outlined.”
McCullough goes on to say that the issue is not restricted to the novel mRNA treatments, in demanding the removal of legislation which protects all scheduled vaccines from claims of injury.
This, he says, would compel vaccine manufacturers to have to “stand behind their products,” echoing RFK Jr.’s own claim that what he wants to see is the transparent and scientific review of all scheduled vaccines.
McCullough also notes that with the precursor supply chain for U.S. medicines captured by China, a Trump administration could repatriate drug manufacture to the U.S., providing a verifiable and secure provenance for American prescription drugs in future.
His endorsement of Kennedy marks the redemption arc of a man still labeled by U.S. and U.K. regime media as a “crank” for his criticism of the corruption of U.S. healthcare – and the dangers this represents to the American public.
Lambasted as an “anti-vaxxer” for refusing Dr. Anthony Fauci’s advice to “stick with the science” on vaccines, RFK Jr. was described by a former director of the CDC as “more science-oriented than a lot of his critics,” as what Kennedy is seeking is an evidence based review of vaccine safety.
Kennedy’s former campaign manager Dennis Kucinich said, “[RFK Jr.’s] position is to protect the people, to put people above profit.”
Kucinich explained, “Kennedy is not opposed to vaccines, he’s for vaccine safety. He’s concerned about the health effects of pesticides, about GMOs, which are now populating our agriculture.”
Kennedy warned in a tweet of June 2021 about a published link between myocarditis and pericarditis and the Pfizer and ModeRNA “vaccines.”
In 2023, he followed up with an an extensive list of injury concerns for the same injections, which included Bell’s palsy, blood clotting, and death.
A video from November 10, 2024, saw him explain his position on vaccines to NewsNation.
“I think most people don’t know what my stance is on vaccines. I’ve never been anti-vaccine. And I’ve said that hundreds and hundreds of times, but it doesn’t matter, because that is a way of silencing me,” he said.
RFK Jr. went on to explain how and why he was silenced and stigmatized – a method familiar to any “vaccine skeptic”: “Using that pejorative to describe me is a way of silencing or marginalizing me.”
He said his position was simple – and universally popular.
“I think virtually every American would agree with my stance on vaccines, which is that vaccines should be tested like other medicines.”
Donald Trump’s election victory has delivered a mandate for change, strongly desired by the public, which McCullough welcomes for its potential to safeguard the American people, and their children, from an industry captive to profit and protected by censorship and propaganda.
Brownstone Institute
The Deplorable Ethics of a Preemptive Pardon for Fauci
From the Brownstone Institute
Anthony “I represent science” Fauci can now stand beside Richard “I am not a crook” Nixon in the history books as someone who received the poison pill of a preemptive pardon.
While Nixon was pardoned for specific charges related to Watergate, the exact crimes for which Fauci was pardoned are not specified. Rather, the pardon specifies:
Baseless and politically motivated investigations wreak havoc on the lives, safety, and financial security of targeted individuals and their families. Even when individuals have done nothing wrong – and in fact have done the right things – and will ultimately be exonerated, the mere fact of being investigated and prosecuted can irreparably damage reputations and finances.
In other words, the dying breath of the Biden administration appears to be pardoning Fauci for crimes he didn’t commit, which would seem to make a pardon null and void. The pardon goes further than simply granting clemency for crimes. Clemency usually alleviates the punishment associated with a crime, but here Biden attempts to alleviate the burden of investigations and prosecutions, the likes of which our justice system uses to uncover crimes.
It’s one thing to pardon someone who has been subjected to a fair trial and convicted, to say they have already paid their dues. Gerald Ford, in his pardon of Richard Nixon, admitted that Nixon had already paid the high cost of resigning from the highest office in the land. Nixon’s resignation came as the final chapter of prolonged investigations into his illegal and unpresidential conduct during Watergate, and those investigations provided us the truth we needed to know that Nixon was a crook and move on content that his ignominious reputation was carve d into stone for all of history.
Fauci, meanwhile, has evaded investigations on matters far more serious than Watergate. In 2017, DARPA organized a grant call – the PREEMPT call – aiming to preempt pathogen spillover from wildlife to people. In 2018 a newly formed collaborative group of scientists from the US, Singapore, and Wuhan wrote a grant – the DEFUSE grant – proposing to modify a bat sarbecovirus in Wuhan in a very unusual way. DARPA did not fund the team because their work was too risky for the Department of Defense, but in 2019 Fauci’s NIAID funded this exact set of scientists who never wrote a paper together prior or since. In late 2019, SARS-CoV-2 emerged in Wuhan with the precise modifications proposed in the DEFUSE grant submitted to PREEMPT.
It’s reasonable to be concerned that this line of research funded by Fauci’s NIAID may have caused the pandemic. In fact, if we’re sharp-penciled and honest with our probabilities, it’s likely beyond reasonable doubt that SARS-CoV-2 emerged as a consequence of research proposed in DEFUSE. What we don’t know, however, is whether the research proceeded with US involvement or not.
Congress used its constitutionally-granted investigation and oversight responsibilities to investigate and oversee NIAID in search of answers. In the process of these investigations, they found endless pages of emails with unjustified redactions, evidence that Fauci’s FOIA lady could “make emails disappear,” Fauci’s right-hand-man David Morens aided the DEFUSE authors as they navigated disciplinary measures at NIH and NIAID, and there were significant concerns that NIAID sought to obstruct investigations and destroy federal records.
Such obstructive actions did not inspire confidence in the innocence of Anthony Fauci or the US scientists he funded in 2019. On the contrary, Fauci testified twice under oath saying NIAID did not fund gain-of-function research of concern in Wuhan…but then we discovered a 2018 progress report of research NIAID funded in Wuhan revealing research they funded had enhanced the transmissibility of a bat SARS-related coronavirus 10,000 times higher than the wild virus. That is, indisputably, gain-of-function research of concern. Fauci thus lied to the American public and perjured himself in his testimony to Congress, and Senator Rand Paul (R-KY) has referred Fauci’s perjury charges to the Department of Justice.
What was NIAID trying to preempt with their obstruction of Congressional investigations? What is Biden trying to preempt with his pardon of Fauci? Why do we not have the 2019 NIAID progress report from the PI’s who submitted DEFUSE to PREEMPT and later received funding from NIAID?
It is deplorable for Biden to preemptively pardon Fauci on his last day in office, with so little known about the research NIAID funded in 2019 and voters so clearly eager to learn more. With Nixon’s preemptive pardon, the truth of his wrongdoing was known and all that was left was punishment. With Fauci’s preemptive pardon, the truth is not yet known, NIAID officials in Fauci’s orbit violated federal records laws in their effort to avoid the truth from being known, and Biden didn’t preemptively pardon Fauci to grant clemency and alleviate punishment, but to stop investigations and prosecutions the likes of which could uncover the truth.
I’m not a Constitutional scholar prepared to argue the legality of this maneuver, but I am an ethical human being, a scientist who contributed another grant to the PREEMPT call, and a scientist who helped uncover some of the evidence consistent with a lab origin and quantify the likelihood of a lab origin from research proposed in the DEFUSE grant. Any ethical human being knows that we need to know what caused the pandemic, and to deprive the citizenry of such information from open investigations of NIAID research in 2019 would be to deprive us of critical information we need to self-govern and elect people who manage scientific risks in ways we see fit. As a scientist, there are critical questions about bioattribution that require testing, and the way to test our hypotheses is to uncover the redacted and withheld documents from Fauci’s NIAID in 2019.
The Biden administration’s dying breath was to pardon Anthony Fauci not for the convictions for crimes he didn’t commit (?) but to avoid investigations that could be a reputational and financial burden for Anthony Fauci. A pardon to preempt an investigation is not a pardon; it is obstruction. The Biden administration’s dying breath is to obstruct our pursuit of truth and reconciliation on the ultimate cause of 1 million Americans’ dying breaths.
To remind everyone what we still need to know, it helps to look through the peephole of what we’ve already found to inspire curiosity about what else we’d find if only the peephole could be widened. Below is one of the precious few emails investigative journalists pursuing FOIAs against NIAID have managed to obtain from the critical period when SARS-CoV-2 is believed to have emerged. The email connects DEFUSE PI’s Peter Daszak (EcoHealth Alliance), Ralph Baric (UNC), Linfa Wang (Duke-NUS), Ben Hu (Wuhan Institute of Virology), Shi ZhengLi (Wuhan Institute of Virology) and others in October 2019. The subject line “NIAID SARS-CoV Call – October 30/31” connects these authors to NIAID.
It is approximately in that time range – October/November 2019 – when SARS-CoV-2 is hypothesized to have entered the human population in Wuhan. When it emerged, SARS-CoV-2 was unique among sarbecoviruses in having a furin cleavage site, as proposed by these authors in their 2019 DEFUSE grant. Of all the places the furin cleavage site could be, the furin cleavage site of SARS-CoV-2 was in the S1/S2 junction of the Spike protein, precisely as proposed by these authors.
In order to insert a furin cleavage site in a SARS-CoV, however, the researchers would’ve needed to build a reverse genetic system, i.e. a DNA copy of the virus. SARS-CoV-2 is unique among coronaviruses in having exactly the fingerprint we would expect from reverse genetic systems. There is an unusual even spacing in the cutting/pasting sites for the enzymes BsaI and BsmBI and an anomalous hot-spot of silent mutations in precisely these sites, exactly as researchers at the Wuhan Institute of Virology have done for other coronavirus reverse genetic systems. The odds of such an extreme synthetic-looking pattern occurring in nature are, conservatively, about 1 in 50 billion.
The virus did not emerge in Bangkok, Hanoi, Bago, Kunming, Guangdong, or any of the myriad other places with similar animal trade networks and greater contact rates between people and sarbecovirus reservoirs. No. The virus emerged in Wuhan, the exact place and time one would expect from DEFUSE.
With all the evidence pointing the hounds towards NIAID, it is essential for global health security that we further investigate the research NIAID funded in 2019. It is imperative for our constitutional democracy, for our ability to self-govern, that we learn the truth. The only way to learn the truth is to investigate NIAID, the agency Fauci led for 38 years, the agency that funded gain-of-function research of concern, the agency named in the October 2019 call by DEFUSE PI’s, the agency that funded this exact group in 2019.
A preemptive pardon prior to the discovery of truth is a fancy name for obstruction of justice. The Biden administration’s dying breath must be challenged, and we must allow Congress and the incoming administration to investigate the possibility that Anthony Fauci’s NIAID-supported research caused the Covid-19 pandemic.
Republished from the author’s Substack
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.
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