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New Bill Aims to Remove COVID-19 Vaccine Manufacturer Liability Protections

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A new bill has been introduced that could potentially strip COVID-19 vaccine manufacturers of their existing liability protections. Proposed by Rep. Chip Roy (R-Texas) on March 5, the bill targets the Public Readiness and Emergency Preparedness Act (PREP Act), a legal framework that shields vaccine manufacturers from certain liabilities.

The bill’s primary objective is to enable Americans who have experienced adverse effects from COVID-19 vaccines to pursue legal action against the companies responsible for manufacturing them. If passed, this legislation would mark a substantial shift in the legal landscape surrounding vaccine injury claims.

At the core of the proposed bill is the retroactive removal of liability protections granted to COVID-19 vaccine manufacturers under the PREP Act. This Act, initiated by former Health Secretary Alex Azar during the Trump administration and subsequently extended by President Joe Biden, offers immunity to manufacturers and individuals involved in administering vaccines, with exceptions only for cases involving willful misconduct.

Rep. Chip Roy’s rationale for introducing the bill rests on principles of justice and accountability. He emphasizes the need to empower Americans who have suffered vaccine-related injuries and to challenge what he perceives as undue federal protection for vaccine manufacturers. Roy contends that many individuals were coerced into receiving the COVID-19 vaccine and subsequently faced adverse health effects with limited recourse for restitution.

Under the current framework, individuals with suspected or confirmed vaccine-related injuries can seek compensation through the Countermeasures Injury Compensation Program. However, the program’s track record reveals limited success for claimants, with just 11 individuals compensated as of January, and numerous claims rejected. Critics, including those involved in a lawsuit challenging the program’s constitutionality, characterize it as a “kangaroo court.”

The bill proposed by Rep. Roy explicitly states that it does not impede individuals’ ability to seek compensation through existing channels such as the Countermeasures Injury Compensation Program. This clarification aims to ensure that avenues for restitution remain accessible to affected individuals.

The response from pharmaceutical companies and industry representatives has been mixed. While Pfizer, Moderna, and trade groups like the Pharmaceutical Research and Manufacturers of America express concerns about jeopardizing vaccine development and public health response mechanisms, supporters of the bill, including Children’s Health Defense, advocate for increased accountability and transparency in vaccine injury cases.

With 19 co-sponsors already on board, including prominent figures like Rep. Lauren Boebert (R-Colo.) and Rep. Ralph Norman (R-S.C.), the bill reflects a growing sentiment among certain lawmakers and advocacy groups for greater scrutiny of COVID-19 vaccine manufacturer liabilities.

The introduction of this bill signifies a pivotal moment in the ongoing discourse surrounding COVID-19 vaccines, as debates unfold and stakeholders weigh in on the proposed legislation, its fate will likely shape the future trajectory of vaccine liability protections and individual rights in the context of public health emergencies. Only time will tell how this legislative effort will impact the landscape of vaccine accountability and the pursuit of justice for those affected by vaccine-related injuries.

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FEMA under investigation over discrimination against Trump supporters

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The Federal Emergency Management Agency (FEMA) is under fire as House Oversight Chair Rep. James Comer (R-Ky.) launches an investigation into allegations that the agency has discriminated against supporters of Donald Trump. Whistleblower reports suggest that anti-Trump bias has been rampant within FEMA for years, raising serious concerns about fairness in disaster relief efforts.

“[O]n the condition of anonymity, a FEMA official stated that the practice of avoiding ‘white or conservative-dominated’ areas is an ‘open secret at the agency that has been going on for years,’” Comer wrote in a letter to FEMA Administrator Deanne Criswell.

The investigation was sparked after FEMA terminated one of its hurricane response supervisors, who reportedly instructed workers to avoid “Trump houses.” The employee has publicly claimed she was following orders and adhering to a longstanding agency culture.

Comer, along with over two dozen Republican lawmakers, has demanded FEMA provide internal policies, spending data, and incident reports. Their request is bolstered by additional whistleblower accounts.

“Additionally, another whistleblower contacted the Committee during the hearing,” the lawmakers’ letter stated. “This individual informed the Committee that a FEMA contractor warned a disabled veteran’s family in Georgia to remove Trump campaign materials from their home because FEMA supervisors viewed Trump supporters as domestic terrorists.”

Rep. Greg Steube (R-Fla.) further criticized FEMA during a recent hearing, citing complaints from 35 of his constituents who alleged similar discrimination. The lawmakers also questioned FEMA’s recent emphasis on Diversity, Equity, and Inclusion (DEI) initiatives, which the agency named its top strategic goal in its latest report.

FEMA has also faced criticism over its spending priorities. “In the fiscal year of 2023, FEMA spent nearly a billion dollars, $789 million, to shelter illegals in the United States,” Rep. Marjorie Taylor Greene (R-Ga.) said at the hearing. “This past year it was $641 million, and this money is largely distributed through NGOs…and this was to house illegal aliens. Not Americans, who by the way all that money, that comes from Americans bank accounts when they write their checks to pay their taxes.”

Administrator Criswell responded by pledging to request an Inspector General investigation into the discrimination claims. While she does not believe the fired employee’s actions reflect a systemic problem, Criswell admitted FEMA has revisited homes that were allegedly skipped and vowed to prevent future incidents.

“The Committee is in the process of investigating these claims,” the Oversight letter stated. “If they are true, they would corroborate concerns that political discrimination extends beyond [the fired FEMA employee]. Furthermore, they suggest an apparent culture, whether sanctioned or not, within FEMA to politically discriminate against disaster survivors, specifically those who support President-elect Donald Trump.”

As the investigation unfolds, lawmakers are pressing for accountability and a reassessment of FEMA’s operational priorities. Whether the claims point to isolated incidents or a larger cultural issue remains to be seen.

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Doctor Fails to Publish $10 Million Taxpayer-Funded Study Exposing Puberty Blockers

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A $10 million study on the mental health effects of puberty blockers in transgender youth has become a focal point in the ongoing debate over gender-affirming care in the United States. Dr. Johanna Olson-Kennedy, a prominent advocate for transgender rights and the study’s lead researcher, has chosen to withhold the results, citing concerns that the findings could be used against gender-affirming care for children. This decision has sparked criticism from both fellow researchers and opponents of puberty blockers, who argue that withholding the study is contrary to scientific standards.

The National Institutes of Health (NIH)-funded study, which began in 2015, tracked 95 children, with an average starting age of 11, as they received puberty blockers—medications designed to delay the onset of physical changes during puberty. After two years, the study found that the mental health of the children had not improved as a result of the treatment. Olson-Kennedy explained in an interview with The New York Times that the participants’ mental health was relatively stable before and after treatment, attributing the lack of significant change to the children being “in really good shape” mentally from the outset.

However, this finding contradicts earlier data gathered by the study, which indicated that roughly 25% of participants experienced symptoms of depression or suicidal thoughts before starting treatment. The decision not to publish has raised questions about scientific transparency and integrity, particularly in a field where public opinion is sharply divided and access to reliable data is critical.

Critics argue that withholding research results due to concerns over their potential misuse sets a dangerous precedent. Amy Tishelman, a clinical and research psychologist who was involved in the study, told The New York Times that while she understands the fear of data being “weaponized,” the results should be made public. “No change isn’t necessarily a negative finding—there could be a preventative aspect to it,” she said, emphasizing the need for further investigation.

Erica Anderson, a clinical psychologist and expert on transgender youth, expressed her dismay, calling the decision “shocking” and “disturbing.” She argued that it is the responsibility of researchers to share their findings, regardless of the potential backlash, noting that “it’s not her prerogative to decide based on the results that she will or won’t publish them.”

Olson-Kennedy’s decision is rooted in concerns about how the study’s results could be used in legal battles against gender-affirming care for minors. She noted that critics might leverage the findings in court cases to challenge the use of puberty blockers, especially as more than 20 states have passed bans or restrictions on such treatments in recent years. Olson-Kennedy emphasized the need for a careful and thorough analysis before releasing the study, saying, “It has to be exactly on point, clear and concise. And that takes time.”

This delay has drawn criticism from those who believe that research should be released without bias, with the aim of fostering informed debate. Opponents of withholding the data argue that the results could contribute to a more nuanced understanding of the effects of puberty blockers and help inform future medical decisions.

The controversy around the study comes amid a broader international reevaluation of puberty blockers and gender-affirming care. England’s National Health Service (NHS) recently limited the use of puberty blockers for minors, following a review that found the evidence for their benefits was limited. Similarly, Finland’s leading pediatric gender medicine expert, Dr. Riittakerttu Kaltiala, has advised caution, stating that a majority of gender-questioning children eventually come to accept their bodies without the need for medical intervention.

In contrast, the 2011 Dutch study, which has served as a cornerstone for advocating puberty blockers, found that the treatment led to improved mental health and reduced emotional distress in transgender youth. The differing outcomes between the Dutch research and Olson-Kennedy’s study underscore the complexities of this evolving field.

With the scientific and medical community divided over the best approach to treating gender dysphoria in children, many stress the need for open access to research findings. Transparency in studies like Olson-Kennedy’s is seen as crucial for developing an evidence-based understanding of how best to support transgender youth. “We’re craving information about these medical treatments for gender-questioning youth,” Anderson said, adding that releasing such data helps ensure that the care provided is rooted in the best available science.

While Olson-Kennedy’s concerns about the potential misuse of the study’s findings are understandable, critics argue that the decision to withhold the data undermines the values of scientific integrity and public trust. As debates about gender-affirming care continue to unfold across the country, the need for clarity, honesty, and evidence has never been more pressing.

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