May 9, 2019

In response to a smear story yesterday appearing in Politico and headlined by the New York Times, Robert F. Kennedy, Jr. has issued the following statement: “I love my family. The Kennedys have a long and continuing history of involvement with the public health agencies. It is very difficult for any of us to accept that any of those officials would be less than candid about vaccine risks. I am not anti-vaccine. I want safe vaccines with robust safety testing. Not one of the 72 vaccine doses currently mandated for American children have ever been safety tested against an Inert placebo as is required for other drugs and medical devices. I don’t think we should be forcing pharmaceutical products on unwilling American citizens without understanding the downside risks.”

Mr. Kennedy is slated to visit Stowe, Vermont on May 11th, 2019.

There are many vested interested at play here, and the truth is very difficult to face, for sure. However, Bobby Kennedy did uncover a total lack of vaccine safety testing. This should be of concern to everyone – especially those who want to rely on vaccines.

If you are just getting started, here is an overview for you of the “Vaccine Safety Crisis”, with links to all the documents and references:

– The Informed Consent Action Network (ICAN) spent months researching the state of vaccine safety in the United States. The shocking result of this effort was presented to the heads of the National Institutes of Health with Robert F. Kennedy, Jr. in May of 2017. The information contained in that presentation has been distilled into an easy to read, thorough white paper that goes through many of the shortcomings and failures of the vaccine safety program.
> Read the Vaccine Safety White Paper here.

– In a letter dated October 12, 2017 to the US Department of Health and Human Services (HHS), ICAN outlined consumer concerns over its failure to fulfill its obligations to ensure vaccine safety under the National Childhood Vaccine Injury Act of 1986.
> Read the October 12, 2017 letter to HHS here.

– HHS responded three months later, but the HHS’s letter to ICAN only heightened the serious concerns previously raised regarding the safety of the childhood vaccine schedule. As a result, on December 31, 2018, ICAN sent another letter to HHS detailing the glaring gaps in safety studies which were used to gain FDA licensure for each vaccine product. As shocking as it sounds, no placebo-controlled studies had ever been carried out.
> Read the December 31, 2018 letter to HHS here.

Chart from 12/31/2018 letter to the US Department of Health and Human Services, from the Informed Consent Action Network.

Well folks, you know what happened next (measles hysteria!), with the MMR vaccine at the heart of the debate.

Now, a new Freedom of Information Act disclosure from the Federal Food and Drug Administration (FDA) has revealed that the MMR vaccine that industry/public health is seeking to mandate without exception was licensed based on clinical trials which in total had less than 1,000 participants and far more adverse reactions than previously acknowledged. The following are some of the key facts learned from the clinical trial reports produced by the FDA, which the agency relied upon to license the MMR:
* There were eight clinical trials that in total had less than 1,000 individuals, out of which only 342 children received the MMR vaccine
* The safety review period only tracked ‘adverse events’ for 42 days after injection
* More than half or a significant percent of all participants in each of the eight trials developed gastrointestinal symptoms and upper respiratory infections
* All adverse events were generically described as ‘other viruses’ and not considered in safety profile of licensure
* The control group received other vaccines for either rubella or measles and rubella, and none of the controls received a placebo (an inert substance such as a saline injection)

from: May 2, 2019: MMR Vaccine Licensing Called Into Question Following ICAN’s Latest FOIA Exposure of FDA Coverup.

> View MMR Licensure data at: https://icandecide.org/government/FDA-Production-FOIA.pdf.

We are deeply appreciative of the important work that Bobby Kennedy is doing. He is on the right side of history, speaking the truth.