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Health Officials Allegedly Concealed Myocarditis Risks Associated with COVID Vaccines

Emerging Concerns: Senate Report on Myocarditis Risks Linked to COVID-19 Vaccines

A new Senate report has stirred significant discussion around the potential risks associated with COVID-19 vaccinations, particularly myocarditis—a type of heart inflammation. This report, spearheaded by Senator Ron Johnson, reveals that U.S. health officials were aware of these risks but allegedly chose to downplay them and delay informing the public.

The Inquiry Background

Senator Johnson, representing Wisconsin and serving as the chairman of the Senate Permanent Subcommittee on Investigations, has been leading a thorough investigation into the safety and efficacy of COVID-19 vaccines. Earlier this year, he exercised his authority by subpoenaing the Department of Health and Human Services (HHS) for records pertaining to vaccine safety data and communications regarding the pandemic.

Key Findings of the Interim Report

The interim report, a detailed 55-page document, surfaced findings that indicate federal health officials "withheld crucial health information" from both the Senate subcommittee and the general populace. Since 2021, Johnson has sent numerous oversight letters regarding these issues, many of which he claims were either ignored or inadequately addressed.

The report points specifically to evidence that U.S. health agencies, including HHS, the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA), were aware of myocarditis cases following mRNA COVID-19 vaccinations. The alarming aspect of this report is the assertion that these officials delayed issuing vital warnings about these risks.

Initial Discussions and Decisions

According to records from May 2021, there was internal dialogue among health officials about whether to formally notify the public concerning myocarditis. Initial plans involved disseminating this warning as a Health Alert Network message—a critical method used by the CDC to communicate urgent public health information to various stakeholders, including public health agencies and clinicians.

However, the report claims that the CDC and FDA ultimately opted against issuing a formal Health Alert Notification. Instead, they published only “clinical considerations” about myocarditis on the CDC’s website, a less direct method of alerting the public.

Evidence of Downplayed Risks

Senator Johnson’s report compiles documents that show U.S. health officials were not only aware of the myocarditis risks but also actively engaged in discussions about "safety signals" from mRNA vaccines as early as April 2021. They received notable communications from the Israeli Ministry of Health, which reported increased myocarditis cases, especially among younger individuals post-vaccination.

Several records highlight discussions among officials ranging from the CDC to representatives from vaccine manufacturers like Moderna and Pfizer, suggesting that risks were indeed acknowledged within professional circles.

The Response Timeline

Despite accumulating evidence, the report criticizes the Biden administration for waiting until late June 2021 to officially change the vaccine labeling for both Moderna and Pfizer products concerning the "suggested increased risks" of myocarditis and pericarditis. The delay in public communication is particularly troubling to Johnson, as officials were reportedly aware of the potential dangers yet chose not to alert healthcare providers and the community immediately.

Alarm Over Death Reports and Adverse Events

The implications of the report extend beyond myocarditis. As of April 25, 2025, the Vaccine Adverse Event Reporting System (VAERS) reported over 38,000 deaths associated with COVID-19 vaccines, with a staggering number of adverse events totaling over 1.6 million worldwide. Comparisons made in the report raise eyebrows, especially considering that only 2,663 deaths were reported from flu vaccines over a 35-year span.

This ratio of adverse events from COVID-19 vaccinations raises questions about the transparency and reliability of the safety data provided to the public by health officials.

Calls for Transparency

Senator Johnson’s findings prompted a clarion call for greater transparency and accountability from the Biden administration regarding its COVID-19 vaccine policies. The report emphasizes that taxpayers fund federal health departments and agencies, and thus, the information generated by these entities should be accessible to the American public.

In light of these findings, the report calls for a full revelation of the Biden administration’s handling of vaccine safety information, advocating for an unfiltered look into how public health risks were managed—or mismanaged—during the pandemic.

As the Permanent Subcommittee on Investigations continues to sift through more documents, there is a promise of future transparency, allowing Americans to grasp the full picture regarding COVID-19 vaccine safety and public health.

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