The Citizen Petition is quite long, but it is a detailed criticism of the Covid vaccines themselves and the improper processes FDA has used to authorize their use. It shows that the standards required to issue an EUA were not met, and shows that the standards for licensing these vaccines are unmet.
A Citizen Petition is a legal document to which the FDA must respond. I am a coauthor, with colleagues who worked with me on the anthrax vaccine mandates, and Children’s Health Defense attorneys. We hope many thousands of people will read our petition, to be better informed about how the laws have been ignored, how much information on the vaccines and their side effects has been hidden, and how what we do know is frightening. We need everyone who cares about this issue to provide a comment to the FDA.
Here is how you can do this. You must go to the government website and download the Petition before you can read it. Click on the pdf logo where it says “Petition from Scientific Advisory Board…” To enter a comment, there is a blue button on the same page that takes you to the comment site. We have over 11,000 comments entered already, in just 3 days
I am finding it hard to write about a document that means a lot to me. It may provide a stepping stone to clarity about Covid, the vaccines, the falsehoods that have been promulgated by federal agencies. It may save us from the tyranny of forced injections containing what Moderna’s Chief Medical Officer Tal Zaks called, “the software of life.”
The FDA is obliged to respond to all the points we have made.
Here is a summary written by Children’s Health Defense of what the Petition is about:
Children’s Health Defense Petition:
Your help is crucial.
On May 16, Robert F. Kennedy, Jr. and Meryl Nass, MD, on behalf of Children’s Health Defense (CHD), took a landmark step in the COVID crisis that has irrevocably changed billions of lives around the globe by filing a Citizen Petition with the U.S. Food and Drug Administration (FDA) to withdraw COVID-19 vaccines from the market.
Your comment now on the FDA petition is vital in preventing further injuries and deaths from these experimental medical products. Let your voice be heard!
The actions of the FDA affect global health policy. This filing allows all of us—not just those in the United States, but people from around the world—to speak directly to the U.S. government by commenting on the petition.
Specifically, the petition calls upon the FDA to:
· Revoke the Emergency Use Authorizations (EUAs) for COVID vaccines
· Refrain from licensing COVID vaccines
· Disallow the participation of minors in COVID vaccine trials
· Immediately revoke all EUAs permitting vaccination of minors
· Revoke its tacit approval of pregnant women receiving COVID vaccines
· Immediately amend its existing guidance for the use of chloroquine drugs, ivermectin, and any other safe and effective drugs against COVID.
The FDA petition was imperative as our government health agencies continue to ignore the astonishing numbers of deaths and injuries being reported to the U.S. Health and Human Services (HHS) Vaccine Adverse Events Reporting System (VAERS). Updated each Friday, yesterday’s data release reports 227,805 adverse events and 4201 deaths following vaccination with COVID-19 vaccines from December 14, 2020 through May 14, 2021. Alarmingly, a 2010 HHS study found that less than 1% of adverse events are ever reported to VAERS. Despite this, government agencies at local, state and national levels continue to promote uptake of these vaccines. These agencies are joined by mainstream media, celebrities, and even the White House in calling for people of all ages to just “get the shot” despite the very real risk of injury and death.
All COVID-19 vaccines currently being administered were rushed through the Emergency Use Authorization (EUA) process even as doctors around the world are citing viable treatment options for COVID that are inexpensive and readily available. EUA status is intended for use only when effective treatment options can’t be found. Clearly, this is not the case with COVID.
We are asking you to comment on the FDA petition now and urge the government not to mandate or license COVID vaccines. Please forward this email to all of your friends and relatives so they can comment too. If some of them are still undecided regarding the safety of COVID vaccines, please share this crucial information with them:
- The Warnings Are Clear: Vaccinating Kids for COVID Is a Dangerous Gamble
- What Does a “Safe and Effective” Vaccine Look Like?
- COVID Vaccine Secrets Resources
We need to immediately stop the push for mandates, especially those aimed at children. The experimental COVID vaccines are already being recommended for 12-15-year-olds. It is only a matter of time before they recommend or mandate this vaccine for even younger children—including infants.
Please add your comment to the FDA petition now.
Below is a Defender article about the Petition. We hope to garner as many comments as possible. The number (and quality) of comments can make a huge difference in terms of the actions FDA takes. Please, at least give the document a glance.
Amid growing safety concerns, Robert F. Kennedy, Jr. and Dr. Meryl Nass, on behalf of Children’s Health Defense (CHD), filed a Citizen Petition with the U.S. Food and Drug Administration (FDA) asking the agency to immediately revoke the Emergency Use Authorizations (EUAs) for COVID vaccines and to refrain from licensing them.
Millions Against Medical Mandates (MAMM), a coalition of health freedom organizations and individuals, joins CHD and other vaccine safety and health freedom groups in inviting the public, including healthcare workers, parents and military members, to submit comments on the petition.
CHD compiled and submitted 72 references supporting the request for revocation and restraint. To read the full petition text, download it from the FDA website or read the full petition here — then submit your comments using this form.
According to the most recent Centers for Disease Control and Prevention’s Vaccine Adverse Event Reporting System data, there have been 192,954 reported adverse events following COVID vaccination, including 4,057 deaths between Dec. 14, 2020 and May 7, 2021.
These numbers stand in stark contrast to those reported following the aborted 1976 swine flu vaccine campaign that ended abruptly following approximately 30 reported deaths and 400 cases of Guillain–Barré syndrome.
Citing the extremely low risk to children from COVID, the petition calls on the FDA to immediately refrain from allowing minors to participate in COVID vaccine trials and to immediately revoke all EUAs permitting vaccination of children under 18.
“It’s time for the FDA to make a dramatic course correction before more deaths and injuries occur,” said Maureen McDonnell, MAMM founder.
The petition also urges the FDA to revoke its tacit approval for pregnant women to receive COVID vaccines.
The law stipulates that to grant EUA status, no other effective intervention may exist. The petition calls upon the FDA to immediately amend its existing guidance for the use of chloroquine drugs, ivermectin and any other safe and effective drugs against COVID.
“It’s time for the FDA to make effective COVID treatments available and to revoke the vaccine EUAs,” said CHD President and General Counsel Mary Holland. “It’s shocking that the FDA has ignored the unprecedented reports of injuries and deaths for five months.”
CHD and MAMM are asking the FDA to take these seven actions: