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NIH director who led agency during COVID abruptly resigns

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Dr. Lawrence A. Tabak, the No. 2 at the National Institutes of Health (NIH) who served as acting director during the COVID-19 pandemic, has abruptly resigned. His departure follows a broader shakeup at the Department of Health and Human Services (HHS) under President Donald Trump’s administration.

Key Details:

  • Tabak, 73, spent 25 years at the NIH, serving as the agency’s principal deputy director since 2010 and acting director during the COVID-19 pandemic.
  • He was heavily scrutinized by Republicans for his role in pandemic-related decision-making and congressional probes into the origins of COVID-19.
  • His resignation comes amid Trump’s restructuring of HHS, with potential firings and budget cuts within the agency.

Diving Deeper:

Dr. Lawrence A. Tabak, the longtime No. 2 at the National Institutes of Health (NIH), has abruptly resigned from government service, effective February 11, 2025. Tabak, who served as acting director of the NIH during key periods—including the COVID-19 pandemic—announced his departure in an internal email to staff earlier this week. His resignation letter did not provide an explanation for his decision to step down.

The timing of Tabak’s exit coincides with a significant shakeup at the Department of Health and Human Services (HHS), the NIH’s parent agency, under President Donald Trump’s leadership. Reports suggest that the administration is implementing budget cuts and potential mass firings within the agency, aligning with Trump’s broader efforts to overhaul Washington’s bureaucratic institutions.

Tabak was a key figure during the pandemic, frequently appearing alongside Dr. Anthony Fauci and former NIH Director Dr. Francis Collins in congressional hearings. Republican lawmakers repeatedly grilled him over the agency’s handling of COVID-19 policies, including controversial guidance on lockdowns, vaccine mandates, and research funding linked to the Wuhan Institute of Virology.

He also played a role in shaping the early COVID-19 origin narrative. GOP-led investigations revealed that Tabak was part of a confidential call with Fauci, Collins, and other prominent scientists in early 2020—an event that critics argue helped suppress the lab-leak theory. House Republicans have accused Tabak and his colleagues of slow-walking the release of documents related to gain-of-function research.

Under normal circumstances, Tabak would have likely resumed his role as acting director until a new NIH leader was confirmed. However, the Biden-era holdover was bypassed in favor of Dr. Matthew Memoli, a former researcher at the National Institute of Allergy and Infectious Diseases and a known critic of COVID-19 vaccine mandates.

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Freedom Convoy

Court Orders Bank Freezing Records in Freedom Convoy Case

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A Canadian court has ordered the release of documents that could shed light on how federal authorities and law enforcement worked together to freeze the bank accounts of a protester involved in the Freedom Convoy.
Both the RCMP and TD Bank are now required to provide records related to Evan Blackman, who took part in the 2022 demonstrations and had his accounts frozen despite not being convicted of any crime at the time.
The Justice Centre for Constitutional Freedoms (JCCF) announced the Ontario Court of Justice ruling. The organization is representing Blackman, whose legal team argues that the actions taken against him amounted to a serious abuse of power.
“The freezing of Mr. Blackman’s bank accounts was an extreme overreach on the part of the police and the federal government,” said his lawyer, Chris Fleury. “These records will hopefully reveal exactly how and why Mr. Blackman’s accounts [were] frozen.”
Blackman was arrested during the mass protests in Ottawa, which drew thousands of Canadians opposed to vaccine mandates and other pandemic-era restrictions.
Although he faced charges of mischief and obstructing police, those charges were dismissed in October due to a lack of evidence. Despite this, prosecutors have appealed, and a trial is set to begin on August 14.
At the height of the protests, TD Bank froze three of Blackman’s accounts following government orders issued under the Emergencies Act. Then-Prime Minister Justin Trudeau had invoked the act to grant his government broad powers to disrupt the protest movement, including the unprecedented use of financial institutions to penalize individuals for their support or participation.
In 2024, a Federal Court Justice ruled that Trudeau’s decision to invoke the act had not been justified.
Blackman’s legal team plans to use the newly released records to demonstrate the extent of government intrusion into personal freedoms.
According to the JCCF, this case may be the first in Canada where a criminal trial includes a Charter challenge over the freezing of personal bank accounts under emergency legislation.
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COVID-19

FDA requires new warning on mRNA COVID shots due to heart damage in young men

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From LifeSiteNews

By Doug Mainwaring

Pfizer and Moderna’s mRNA COVID shots must now include warnings that they cause ‘extremely high risk’ of heart inflammation and irreversible damage in males up to age 24.

The Trump administration’s Food and Drug Administration (FDA) announced it will now require updated safety warnings on mRNA COVID-19 shots to include the “extremely high risk” of myocarditis/pericarditis and the likelihood of  long-term, irreversible heart damage for teen boys and young men up to age 24.

The required safety updates apply to Comirnaty, the mRNA COVID shot manufactured by Pfizer Inc., and Spikevax, the mRNA COVID shot manufactured ModernaTX, Inc.

According to a press release, the FDA now requires each of those manufacturers to update the warning about the risks of myocarditis and pericarditis to include information about:

  1. the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
  2. the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 injection.

The FDA has also required the manufacturers to describe the new safety information in the adverse reactions section of the prescribing information and in the information for recipients and caregivers.

Additionally, the fact sheets for healthcare providers and for recipients and caregivers for Moderna COVID-19 shot and Pfizer-BioNTech COVID-19 shot, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax prescribing information and information for recipients and caregivers.

In a video published on social media, Dr. Vinay Prasad, director of the Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, explained the alarming reasons for the warning updates.

While heart problems arose in approximately 8 out of 1 million persons ages 6 months to 64 years following reception of the cited shots, that number more than triples to 27 per million for males ages 12 to 24.

Prasad noted that multiple studies have arrived at similar findings.

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