TV News LIES

A federal judge on Monday blocked Health and Human Services (HHS) Secretary Robert F. Kennedy Jr.’s changes to vaccine policy, including the reduction of the recommended childhood immunizations and his remaking of a key vaccine advisory panel.

U.S. District Judge Brian E. Murphy, a Biden appointee, granted a motion by the American Academy of Pediatrics for a preliminary injunction against the reduced childhood immunization schedule earlier this year, along with the remaking of the Advisory Committee on Immunization Practices (ACIP) for the Centers for Disease Control and Prevention, invalidating all votes made by the committee since.

Murphy found that the reconstitution of the ACIP last year failed to abide by the Federal Advisory Committee Act. He also found that the CDC bypassing the ACIP when changing the childhood immunization schedule was both a “technical, procedural failure” and “an abandonment of the technical knowledge and expertise embodied by that committee.”

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New guidelines for managing cholesterol call for more aggressive prevention and earlier treatment, including a recommendation that all adults be tested once for lipoprotein(a), a genetic risk marker for heart disease.

The American Heart Association and the American College of Cardiology released the updated guidelines Friday, which aim to expand the tools doctors use to assess cardiovascular risk. Cardiovascular disease is the leading cause of death for men and women in the United States.

New guidelines for managing cholesterol call for more aggressive prevention and earlier treatment, including a recommendation that all adults be tested once for lipoprotein(a), a genetic risk marker for heart disease.

"We know 80% or more of cardiovascular disease is preventable and elevated LDL cholesterol, sometimes referred to as 'bad' cholesterol, is a major part of that risk," wrote Dr. Roger Blumenthal, a cardiologist at Johns Hopkins in Baltimore who chaired the guideline writing committee, in a statement.

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by Nicolas Hulscher, MPH

I had the honor of speaking at the Massive Epidemic of Vaccine Injury (MEVI) Round Table hosted by the MAHA Institute in Washington, D.C. The event was a major success, with panelists presenting extensive scientific evidence to the media and public demonstrating that vaccines are, in fact, a significant contributor to America’s disastrous chronic disease epidemic—where nearly 60% of Americans now suffer from at least one chronic disease.

The attached video is a compilation of my segments from the Round Table. Below is a summary of my discussion, along with the key studies and data supporting the points I presented.

My work in this field began while studying epidemiology at the University of Michigan School of Public Health. During my time as a student, I was able to secure an internship with Dr. Peter McCullough to conduct a systematic review of autopsy findings following COVID-19 vaccination.

When I began researching deaths following COVID-19 vaccination, professors warned me that pursuing this topic would end my career. Thankfully, I did not listen to them and proceeded anyway.

The study ultimately examined 325 autopsy cases worldwide in which individuals died shortly after receiving COVID-19 injections.

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The U.S. Food and Drug Administration (FDA) has issued a warning to Novo Nordisk over its alleged failure to report adverse side effects, including death, in patients who took its GLP-1 medications, popularly known as Ozempic and Wegovy.

The FDA wrote in a March 5 letter that it observed “serious violations” of reporting requirements during an inspection at a Novo facility in early 2025.

The letter cited three deaths among patients using semaglutide, the active ingredient in several of its weight-loss medications, which it said were not properly investigated or reported. One of those cases involved suicide, according to the FDA.

The agency accused Novo of violating procedures that required the company to perform follow-ups in cases where death occurred. The FDA also said the company failed to report adverse reactions to the medication within the required 15-day timeframe.

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More than 100 substances widely used in common US foods, supplements and beverages underwent no health and safety review by the US Food and Drug Administration, a new analysis of federal records finds.

The review of FDA records by the Environmental Working Group (EWG) non-profit reveals that diverse products across the food pyramid, such as Capri Sun drinks, Kettle and Fire organic broth, Acme smoked fish, and Quaker Oats snack bars, use a range of substances that have not undergone review by regulators.

Companies are using the generally recognized as safe (GRAS) rule that was developed in 1958 to allow ingredients such as salt or white vinegar to be used without a burdensome and needless review process.

But companies are increasingly exploiting the rule and sending potentially dangerous new chemicals or substances into the food system without scrutiny, EWG found. Some of these have caused health problems. In 2022, food made with the GRAS ingredient tara flour was believed to have caused over 300 illnesses and 113 hospitalizations.

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Last month, Justin and Amy Miller packed their vehicles with three kids, two dogs, a pet bearded dragon, and whatever belongings they could fit, then drove 2,000 miles from Wisconsin to British Columbia to leave President Trump's America.

The Millers resettled on Vancouver Island, their scenic refuge accessible only by ferry or plane. Justin went to work in the emergency room at Nanaimo Regional General Hospital, where he became one of at least 20 U.S.-trained nurses hired since April.

Trump, some of the nurses said, was why they left.

"There are so many like-minded people out there," said Justin, who now works elbow to elbow with Americans in Canada. "You aren't trapped. You don't have to stay. Health care workers are welcomed with open arms around the world."

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