Late last month, the U.S. Food and Drug Administration (FDA) approved a monkeypox vaccine that is known to “shed from the vaccination site” and cause heart inflammation in about 1 in every 175 persons.
ACAM2000, made by Emergent BioSolutions, was developed to prevent monkeypox disease in individuals determined to be at high risk for mpox infection. But according to the FDA’s own medication guide for the product, the risks of the vaccine appear to outweigh the benefits.
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Sheila Matthews, co-founder of the national non-profit parent organization AbleChild, and activist Amy Miller with the Reform Pharma initiative of Children’s Health Defense, detailed the progress a bill that would help determine the link between Big Pharma drugs and mass shooters has made in the Tennessee General Assembly since its introduction.
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Activist Amy Miller with the newest initiative of Children’s Health Defense, Reform Pharma, and private citizen Bernadette Pajer explained how a recent bill filed in the Tennessee General Assembly would help determine the link between Big Pharma drugs and mass shooters.
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Activist Amy Miller with Reform Pharma, the newest initiative of Robert F. Kennedy Jr.’s non-profit organization Children’s Health Defense, said she is a “mama bear on a mission” to remove the “corruption of Big Pharma.”
“Children’s Health Defense has a new initiative called Reform Pharma, and that’s who we are. We’re systematically removing the corruption of Big Pharma. It’s a large project to tackle. They’ve been doing this for decades, you know, interweaving their so-called help and corruption into our education system, our government, just basically any part of your life, but we want to remove and basically separate pharma and state. It’s, it’s much needed,” Miller explained during Wednesday’s episode of The Tennessee Star Report with Michael Patrick Leahy.
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The Pentagon conducted “human experimentation without consent” by falsely advertising a COVID-19 vaccine under emergency use authorization as fully licensed, a “bait and switch” that killed a college student, according to a new lawsuit against Defense Secretary Lloyd Austin by the student’s estate.
George Watts was waiting for FDA approval of Pfizer’s Comirnaty to fulfill the COVID vaccine mandate at New York’s Corning Community College, which provided a 35-day grace period for compliance following Comirnaty’s Aug. 23, 2021, approval, the filing states.
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Robert F. Kennedy, Jr. announced his bid for the 2024 Democrat presidential nomination Wednesday by promising to end the “toxic” polarization in America that has grown so “dangerous,” he said, “than at any time since the Civil War.”
The lifelong Democrat, whose family was portrayed for decades, by an infatuated media, as American royalty, now appears to be an outlier in his party’s current far-left worldview, and is even attracting some conservatives.
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Data journalist and pollster Rich Baris posted to social media he predicts a “homeschool boom” following the news that the Centers for Disease Control and Prevention’s (CDC) vaccine advisory committee unanimously voted to add the COVID shot to the children and adolescent immunization schedule, a move that will likely lead many states to require COVID shots for school attendance.
Baris, also known as “The People’s Pundit,” tweeted Wednesday, “Parents will flip the F–k out, with good reason. Homeschool boom.”
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The Centers for Disease Control and Prevention (CDC) Advisory Committee on Immunization Practices (ACIP) may have scheduled in its meeting agenda for Wednesday and Thursday a vote on whether to recommend adding COVID-19 shots to the standard Child and Adolescent Immunization Schedule.
The agenda’s wording is ambiguous, as Children’s Health Defense (CHD) President and General Counsel Mary Holland noted.
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The Food and Drug Administration’s (FDA) vaccine advisory panel unanimously voted Wednesday to recommend the Moderna and Pfizer vaccines for infants and young children despite an abundance of calls from physicians, children’s health organizations, and members of Congress to refrain from approving the shots for a population that shows the least risk for serious disease from COVID.
The Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted, 21-0, in favor of recommending Emergency Use Authorization (EUA) for the Moderna and Pfizer mRNA COVID vaccines for infants, toddlers, and preschool-age children.
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As the White House anticipates approval of the Emergency Use Authorization (EUA) application for COVID vaccines for babies and young children, Dr. Jay Bhattacharya, professor of health policy at Stanford University, and a founding fellow at the Academy for Science and Freedom, says the claim that COVID is “a far greater threat to kids than the flu is” amounts to “scare-mongering.”
Bhattacharya responded in a column at the Wall Street Journal Sunday to White House COVID-19 Response Coordinator Dr. Ashish Jha’s recent tweet in which he made the claim “COVID is a far greater threat to kids than the flu is.”
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Pfizer and the Food and Drug Administration (FDA) said Friday they are delaying their plan for Pfizer’s Emergency Use Authorization (EUA) for its coronavirus vaccine for children under five years old due to insufficient data on the efficacy of a third dose.
Pfizer announced February 1 FDA had asked the drug company, and its partner BioNTech, to submit data on a COVID vaccine series for babies as young as six months old and young children up until age five.
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