COVID-19
Trump Team names acting NIH Director, moving out senior officials who mislead the public
Paul D. Thacker
Trump Team Taps Dr. Matthew J. Memoli as Acting NIH Director, to Control Political Games and Push Aside Lawrence Tabak
“He took risk and stood up to Tony Fauci when no-one else on the inside of NIAID would.” – Dr Robert Malone
The Trump transition team has apparently tapped senior NIH researcher Matthew J. Memoli to serve as acting director to help calm the agency until the Senate confirms Stanford’s Jay Bhattacharya to run the NIH. Memoli won the NIH director’s award in 2021 for supervising a national study of undiagnosed COVID cases and runs a research team at the National Institutes of Allergy and Infectious Disease (NIAID) formerly headed by Tony Fauci, who Biden pardoned on his last day in office for any COVID-related offenses.
NIH Director Monica M. Bertagnolli stepped down from her position last week, after the Trump transition team advised her to resign, placing Deputy Director Lawrence A. Tabak as the agency’s top official. The new administration and congressional leaders view Tabak as dishonest and manipulative, and NIH insiders contacted for this story complain that Tabak helped Fauci mislead the public about grants Fauci provided to the Wuhan Institute of Virology, where some suspect the pandemic started.
“They didn’t take action on the COVID origins question,” an official inside the NIH Director’s office said. “And there’s a continued lack of transparency.”
The Trump administration sent a memo two days ago to federal health agencies telling them to halt external communications such as issuing documents, guidance or notices, until such documents can be approved by “a presidential appointee.” While all administrations control final approval of agency communications, federal employees immediately leaked the memo to reporters at the Washington Post and NPR.
Although the memo says nothing about halting private meetings, the NIH took the extraordinary step of then shutting down private study sections that review scientific grant approvals, a move that seems designed to harass the incoming administration.
“Researchers facing ‘a lot uncertainty, fear and panic’,” reads a breathless report from Science Magazine.
“The memo doesn’t say anything about private meetings, and they shut down these study sections to scare everyone into believing [research] studies will shut down and labs will shutter,” said an NIH official in the Director’s office. “This is a manipulation tactic by the NIH Director’s office to tar the new administration: ‘This is the fascism we expected.’”
Tabak’s demotion comes after Congress and independent reporters spent years trying to uncover how the pandemic started, only to meet obfuscation and “slow rolling” from Tabak. In one example, House congressional leaders demanded NIH explain funding Fauci provided to EcoHealth Alliance, a nonprofit that was run by Peter Daszak, and which funded gain-of-function virus research at the Wuhan Institute of Virology.
The NIH ignored Republican congressional requests for over a year. When Tabak eventually sent a response to Congress on October 20, 2021, he simultaneously leaked the letter to friendly science writers at the New York Times. The letter noted that EcoHealth had failed to report data and research as required by the NIH grant.
“It’s all smoke and mirrors with them at the NIH,” said a congressional investigator. “And then they get friendly media to carry their water.”
Congress sent the NIH a letter a month later demanding NIH explain changes they secretly made to an NIH webpage on October 20, 2021, the day before Tabak admitted that EcoHealth Alliance was out of compliance with NIH grant regulations. The webpage provided the definition for “gain of function research.” However, the NIH had changed the definiton to make it appear EcoHealth Alliance had not performed gain of function research.
Tabak’s name came up again in August last year when reporter Jimmy Tobias released a tranche of NIH emails he got from a public records request. Emails showed Tabak and other NIH officials conspiring to avoid answering questions about EcoHealth Alliance early in the pandemic, from the chairs of several House committees.
“We are going to draft a response to the letter that doesn’t actually answer the questions in the letter but rather presents a narrative of what happened at a high level…” wrote NIH associate director for legislative policy, Adrienne Hallett, in a July 2020 email. Copied in on the exchange is Lawrence Tabak. “The Committee may come back for other documents but I’m hoping to run out the clock.”
“Sounds like a good plan,” responded Francis Collins, then director of the NIH.
“Thanks so much Adrienne!” replied Michael Lauer, the NIH’s deputy director of extramural research. “I’ll draft something today.”
In the Biden administration’s final week, the U.S. Department of Health and Human Services (HHS) finally debarred EcoHealth Alliance and Peter Daszak “to protect the Federal Government’s business interests” after congressional investigators uncovered NIH wrongdoing.
Acting Director Memoli
While in his role as Acting Director, Memoli will likely continue his studies of respiratory viruses and their vaccines. In late 2021, Memoli led a debate inside the NIH on the ethics of the COVID vaccine mandates, putting him at odds with Fauci, who promoted the vaccines for the White House during a time when the media denigrated any COVID vaccine critic as an “anti-vaxxer.”
“I do vaccine trials. I, in fact, help create vaccines,” Memoli told the Wall Street Journal in 2021. Memoli said blanket vaccinations of people at low risk of severe disease with the COVID vaccines could hamper the development of more-robust population immunity from acquired infection. However, he supported COVID vaccination in the elderly, obese, and other high-risk. “Part of my career is to share my expert opinions, right or wrong.…I mean, if they all end up saying I’m wrong, that’s fine. I want to have the discussion.”
Trump transition team members say they may be replacing other senior NIH officials, such as Renate Myles, who runs the agency’s communications department and coordinates activities across all the NIH’s 27 institutes and centers. Myles is known in the NIH Director’s office as a loyal foot soldier to Fauci and someone who helped to spread the media myth that it was a “conspiracy theory” to question if the pandemic started in Wuhan lab that Fauci funded.
“They politicized the issue but then attributed the politicization to Republicans or anyone who questioned them—anyone but themselves,” said the NIH official.
The DisInformation Chronicle is a community-supported publication. To receive new posts and support this work, consider becoming a free or paid subscriber.
COVID-19
Trump DOJ seeks to quash Pfizer whistleblower’s lawsuit over COVID shots
From LifeSiteNews
The Justice Department attorney did not mention the Trump FDA’s recent admission linking the COVID shots to at least 10 child deaths so far.
The Trump Department of Justice (DOJ) is attempting to dismiss a whistleblower case against Pfizer over its COVID-19 shots, even as the Trump Food & Drug Administration (FDA) is beginning to admit their culpability in children’ s deaths.
As previously covered by LifeSiteNews, in 2021 the BMJ published a report on insider information from a former regional director of the medical research company Ventavia, which Pfizer hired in 2020 to conduct research for the company’s mRNA-based COVID-19 shot.
The regional director, Brook Jackson, sent BMJ “dozens of internal company documents, photos, audio recordings, and emails,” which “revealed a host of poor clinical trial research practices occurring at Ventavia that could impact data integrity and patient safety […] We also discovered that, despite receiving a direct complaint about these problems over a year ago, the FDA did not inspect Ventavia’s trial sites.”
According to the report, Ventavia “falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial.” Overwhelmed by numerous problems with the trial data, Jackson filed an official complaint with the FDA.
Jackson was fired the same day, and Ventavia later claimed that Jackson did not work on the Pfizer COVID-19 shot trial; but Jackson produced documents proving she had been invited to the Pfizer trial team and given access codes to software relating to the trial. Jackson filed a lawsuit against Pfizer for violating the federal False Claims Act and other regulations in January 2021, which was sealed until February 2022. That case has been ongoing ever since.
Last August, U.S. District Judge Michael Truncale dismissed most of Jackson’s claims with prejudice, meaning they could not be refiled. Jackson challenged the decision, but the Trump DOJ has argued in court to uphold it, Just the News reports, with DOJ attorney Nicole Smith arguing that the case concerns preserving the government’s unfettered power to dismiss whistleblower cases.
The rationale echoes a recurring trend in DOJ strategy that Politico described in May as “preserving executive power and preventing courts from second-guessing agency decisions,” even in cases that involve “backing policies favored by Democrats.”
Jackson’s attorney Warner Mendenhall responded that the administration “really sort of made our case for us” in effectively admitting that DOJ is taking the Fair Claims Act’s “good cause” standard for state intervention to mean “mere desire to dismiss,” which infringes on his client’s “First Amendment right to access the courts, to vindicate what she learned.”
Mendenhall added that in a refiled case, Jackson “may be able to bring a very different case along the same lines, but with the additional information” to prove fraud, whereas rejection would send the message that “if fraud involves government complicity, don’t bother reporting it.”
That additional information would presumably include the FDA’s recent admission that at least 10 children the agency has reviewed so far “died after and because of receiving COVID-19 vaccination.”
“The truth is we do not know if we saved lives on balance,” admitted FDA Chief Medical Officer Vinay Prasad in a recent leaked email. “It is horrifying to consider that the U.S. vaccine regulation, including our actions, may have harmed more children than we saved. This requires humility and introspection.”
The COVID shots have been highly controversial ever since the first Trump administration’s Operation Warp Speed initiative prepared and released them in a fraction of the time any previous vaccine had ever been developed and tested. As LifeSiteNews has extensively covered, a large body of evidence has steadily accumulated over the past five years indicating that the COVID jabs failed to prevent transmission and, more importantly, carried severe risks of their own.
Ever since, many have intently watched and hotly debated what President Donald Trump would do about the situation upon his return to office. Though he never backed mandates like former President Joe Biden did, for years Trump refused to disavow the shots to the chagrin of his base, seeing Operation Warp Speed as one of his crowning achievements. At the same time, during his latest run he embraced the “Make America Healthy Again” movement and its suspicion of the medical establishment more broadly.
So far, Trump’s second administration has rolled back several recommendations for the shots but not yet pulled them from the market, despite hiring several vocal critics of the COVID establishment and putting the Department of Health & Human Services under the leadership of America’s most prominent anti-vaccine advocate, Robert F. Kennedy Jr. Most recently, the administration has settled on leaving the current jabs optional but not supporting work to develop successors.
In a July interview, FDA Commissioner Marty Makary asked for patience from those unsatisfied by the administration’s handling of the shots, insisting more time was needed for comprehensive trials to get more definitive data.
COVID-19
University of Colorado will pay $10 million to staff, students for trying to force them to take COVID shots
From LifeSiteNews
The University of Colorado Anschutz School of Medicine caused ‘life-altering damage’ to Catholics and other religious groups by denying them exemptions to its COVID shot mandate, and now the school must pay a hefty settlement.
The University of Colorado’s Anschutz School of Medicine must pay more than $10.3 million to 18 plaintiffs it attempted to force into taking COVID-19 shots despite religious objections, in a settlement announced by the religious liberty law firm the Thomas More Society.
As previously covered by LifeSiteNews, in April 2021, the University of Colorado (UC) announced its requirement that all staff and students receive COVID jabs, leaving specific policy details to individual campuses. On September 1, 2021, it enforced an updated policy stating that “religious exemption may be submitted based on a person’s religious belief whose teachings are opposed to all immunizations,” but required not only a written explanation why one’s “sincerely held religious belief, practice of observance prevents them” from taking the jabs, but also whether they “had an influenza or other vaccine in the past.”
On September 24, the policy was revised to stating that “religious accommodation may be granted based on an employee’s religious beliefs,” but “will not be granted if the accommodation would unduly burden the health and safety of other Individuals, patients, or the campus community.”
In practice, the school denied religious exemptions to Catholic, Buddhist, Eastern Orthodox, Evangelical, Protestant, and other applicants, most represented by Thomas More in a lawsuit contending that administrators “rejected any application for a religious exemption unless an applicant could convince the Administration that her religion ‘teaches (them) and all other adherents that immunizations are forbidden under all circumstances.’”
The UC system dropped the mandate in May 2023, but the harm had been done to those denied exemptions while it was in effect, including unpaid leave, eventual firing, being forced into remote work, and pay cuts.
In May 2024, a three-judge panel of the U.S. Tenth Circuit Court of Appeals rebuked the school for denying the accommodations. Writing for the majority, Judge Allison Eid found that a “government employer may not punish some employees, but not others, for the same activity, due only to differences in the employee’s religious beliefs.”
Now, Thomas More announces that year-long settlement negotiations have finally secured the aforementioned hefty settlement for their clients, covering damages, tuition costs, and attorney’s fees. It also ensured the UC will agree to allow and consider religious accommodation requests on an equal basis to medical exemption requests and abstain from probing the validity of applicants’ religious beliefs in the future.
“No amount of compensation or course-correction can make up for the life-altering damage Chancellor Elliman and Anschutz inflicted on the plaintiffs and so many others throughout this case, who felt forced to succumb to a manifestly irrational mandate,” declared senior Thomas More attorney Michael McHale. “At great, and sometimes career-ending, costs, our heroic clients fought for the First Amendment freedoms of all Americans who were put to the unconscionable choice of their livelihoods or their faith during what Justice Gorsuch has rightly declared one of ‘the greatest intrusion[s] on civil liberties in the peacetime history of this country.’ We are confident our clients’ long-overdue victory indeed confirms, despite the tyrannical efforts of many, that our shared constitutional right to religious liberty endures.”
On top of the numerous serious adverse medical events that have been linked to the COVID shots and their demonstrated ineffectiveness at reducing symptoms or transmission of the virus, many religious and pro-life Americans also object to the shots on moral grounds, due to the ethics of how they were developed.
According to a detailed overview by the pro-life Charlotte Lozier Institute, Pfizer, Moderna, and Johnson & Johnson all used fetal cells derived from aborted babies during their COVID shots’ testing phase; and Johnson & Johnson also used the cells during the design and development and production phases. The American Association for the Advancement of Science’s journal Science and even the left-wing “fact-checking” outlet Snopes have also admitted the shots’ abortion connection, which gives many a moral aversion to associating with them.
Catholic World Report notes that similarly large sums have been won in other high-profile lawsuits against COVID shot mandates, including $10.3 million to more than 500 NorthShore University HealthSystem employees in 2022 and $12.7 million to a Catholic Michigander fired by Blue Cross Blue Shield in 2024.
-
Bruce Dowbiggin1 day agoWayne Gretzky’s Terrible, Awful Week.. And Soccer/ Football.
-
espionage14 hours agoWestern Campuses Help Build China’s Digital Dragnet With U.S. Tax Funds, Study Warns
-
Focal Points5 hours agoCommon Vaccines Linked to 38-50% Increased Risk of Dementia and Alzheimer’s
-
Opinion23 hours agoThe day the ‘King of rock ‘n’ roll saved the Arizona memorial
-
Agriculture24 hours agoCanada’s air quality among the best in the world
-
Business12 hours agoCanada invests $34 million in Chinese drones now considered to be ‘high security risks’
-
Economy13 hours agoAffordable housing out of reach everywhere in Canada
-
Health3 hours agoThe Data That Doesn’t Exist




