Hundreds of thousands of vaccine-injured children are the casualties of a federal system tainted with dangerous and unlawful behavior. National health agencies have been downplaying their failure to protect our children, as the unhealthiest state in America has the best vaccination rate, and every day children and babies die or develop chronic illness from vaccines marketed as safe. Shameful deception, fraud, and corporate interference now characterizes our government sponsored health programs and policy, while harmful exposures to toxic ingredients in food, water, and vaccines have been given free rein to poison our most vulnerable populations. Below you will read about a recent lawsuit won by Robert Kennedy Jr. and his team against HHS, finding HHS had neglected to follow to NVICA requirements for improving vaccine safety. Corruption within the CDC continues to be exposed as well, with an entire group of top CDC scientists admitting the breakdown of ethics and safety within their agency walls. Senior CDC scientist William Thompson has come forward to admit a Watergate-level cover-up, admitting he and his CDC colleagues manipulated scientific data to suppress public knowledge that the MMR can cause autism, meanwhile the Department of Justice also has blood on its hands, suppressing damning expert testimony from the Vaccine Injury Compensation Program.
With the global vaccine market now at tens of billions of dollars, vaccine safety should be of utmost concern to the Centers for Disease Control (CDC). But instead, rather than testing and monitoring the health effects of vaccines and patient injuries truthfully to the American public and making critical and necessary corrections in the program, […]
Informed Consent Action Network, Plaintiff, -against- United States food and drug administration Defendant. WHEREAS, plaintiff Informed Consent Action Network (“ICAN”) requested the following records from defendant United States Food & Drug Administration (“FDA”) pursuant to the Freedom of Information Act (“FOIA”): “A copy of the report for each clinical trial relied upon by the FDA when approving for use by pregnant women any influenza vaccine currently approved by the FDA.” WHEREAS, after ICAN appealed, the FDA responded, in relevant part, as follows: These requests sought the clinical trials relied upon by the FDA prior to approving any currently licensed influenza or Tdap vaccine for use in pregnant women as an indicated use. … We have no records responsive to your requests. THEREFORE, pursuant to F.R.C.P. 41(a)(1)(A)(i) of the Federal Rules of Civil Procedure, plaintiff ICAN by its undersigned counsel, hereby gives notice that the above captioned action is voluntarily dismissed, without prejudice against the defendant FDA.
This is the transcript from the 2001 closed-door meeting of the Immunization Safety Review Committee of the Institute of Medicine (IOM). Recently renamed the National Academy of Medicine, the IOM is a branch of the National Academy of Sciences. Importantly, it helps us understand how the IOM process worked when the committee was looking at […]
The National Vaccine Injury Compensation Program (NVICP) was created in 1986 as a no-fault alternative to the traditional legal system for resolving vaccine injury petitions. According to the US Health and Human Services, it was created after lawsuits against vaccine companies and health care providers threatened to cause vaccine shortages and reduce U.S. vaccination rates, […]
RFK, Jr. Proves HHS is in Violation of the “Mandate for Safer Childhood Vaccines” as Stipulated in the Vaccine Injury Compensation Act
When Congress granted economic immunity to pharmaceutical companies in 1986 for vaccine injury, Congress recognized it eviscerated the economic incentive for pharmaceutical companies to create safe vaccines or make existing ones safer. Congress therefore placed the responsibility and burden for vaccine safety directly and virtually entirely on the shoulders and in the hands of the […]
Thank you to CHD’s Coalition Partner, ICAN, for writing this comprehensive letter to the Department of Health and Human Services (HHS) on December 31, 2018. The letter is a brilliant summary of the science questioning the safety of aluminum adjuvants and an exposé of the pervasive corruption that characterizes HHS’s vaccine clinical trials. In the […]
The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation’s food supply, cosmetics, and products that emit radiation. More specifically, within the FDA is the Center for Biologics Evaluation […]