Please Comment to the FDA — Tell them “NO!” to Pfizer’s Covid Vaxx FOR CHILDREN 5 through 11 years of age!

Please Comment to the FDA — Tell them “NO!” to Pfizer’s Covid Vaxx FOR CHILDREN 5 through 11 years of age!

This is an URGENT ALERT re: the U.S. Food and Drug Administration (FDA) Public Comment process pertaining to VAXXING kids with Pfizer’s so-called “Covid Vaccine” — which is actually novel, experimental, and dangerous mRNA gene therapy. This is total criminal insanity, obviously.

On October 26th, Pfizer seeks to extend its “Emergency Use Authorization” to permit the use of its COVID so-called “vaccine” (mRNA gene therapy) … TO CHILDREN 5 through 11 years of age!

You may submit your comment here:
https://www.regulations.gov/document/FDA-2021-N-1088-0001

More information, and resources to inform your comments OPPOSING this Pfizer’s request, follow below.

Pfizer’s request to FDA will be considered at a public advisory committee meeting of the Vaccines and Related Biological Products Advisory Committee (VRBPAC).

Per FDA:
https://www.regulations.gov/document/FDA-2021-N-1088-0001

The [VRBPAC] meeting will be held on October 26, 2021, from 8:30 a.m. to 5 p.m. Eastern Time. Submit either electronic or written comments on this public meeting by October 25, 2021.

Comments received on or before October 21, 2021, will be provided to the committee. Comments received after October 21, 2021, and by October 25, 2021, will be taken into consideration by FDA.

Please, let’s get our comments in ASAP, so that they will be provided to the committee before they meet.

We need to generate MANY comments to the FDA, as soon as possible! Please pass this along to anyone in your group of influence that cares about the health of today’s kids and our future freedom and health.

TELL FDA: “NOT SO FAST!”

Regarding extending EUA of the Pfizer “vaccine” to children aged 5 through 11, we strongly agree with the comments of Dr. Elizabeth Mumper, as reported recently by Children’s Health Defense:

EXCERPT:

“It is distressing to hear that the Biden administration has already purchased 65 million doses of pediatric COVID vaccines,” said Dr. Elizabeth Mumper, pediatric physician and CEO of the Rimland Center for Integrative Medicine. “Vaccinating children is not the way out of the pandemic.”

In an email to The Defender, Mumper said she hopes the White House will consider the following data:

• 99.998% of patients under the age of 18 survive COVID
• COVID “vaccines” have not undergone adequate long-term safety studies
• According to the latest available data from the Vaccine Adverse Event Reporting System, as of Oct. 1, there have been a total of 21,298 reports of adverse events, including 1,284 rated as serious and 22 reported deaths (two of the 22 deaths were suicides) in the 12- to 17-year-old age group
• healthy adolescents given COVID “vaccines” have experienced blood clots, myocarditis, abnormal menses, neurologic symptoms and extreme fatigue
• most COVID cases are spread from adults to children — children are not a significant threat to the elderly and vulnerable

Remember, Mumper said, COVID injections do not diminish transmission, the vaccinated can catch and spread COVID and with children we should first do no harm.

END EXCERPT

Unfortunately, Sarasota for Vaccination Choice notes that, as of today (10/18/21), the FDA has posted fewer than 200 public comments about this Pfizer request.

As our friend “M” notes, in urging people to submit comments to the FDA on this fateful matter:

It’s hard to believe that we are where we are but now is not time to lay down. Our most precious are under attack. Please take some time to draft a comment to FDA Advisory Committee. There needs to be hundreds of thousands of comments opposing this. Please share with your friends and family.

… Empowerment to you, your family, our nation, and the world! We will WIN!

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Agenda: The meeting presentations will be heard, viewed, captioned, and recorded through an online teleconferencing platform. On October 26, 2021, the committee will meet in open session to discuss a request to amend Pfizer-BioNTech’s EUA for administration of their COVID-19 mRNA vaccine to children 5 through 11 years of age.

https://www.regulations.gov/document/FDA-2021-N-1088-0001

TO COMMENT, click on the blue “Comment” button near the top left, or GO HERE:

https://www.regulations.gov/commenton/FDA-2021-N-1088-0001

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Here is an example of a comment, submitted by Jim Morris, on October 15, 2021:

Please DO NOT approve this application. There is a serious safety design flaw in the vaccine that allows the spike proteins to migrate throughout the body which can result in a wide range of adverse effects. This vaccine has been shown to be UNSAFE and has resulted in a significant number of adverse events and deaths. Some of the worse side effects have involved the brain and heart where clotting can result in catastrophic negative outcomes. Before proceeding with this vaccine, an Independent Safety Review Board should be established for the purpose of tracking adverse events and compiling monthly SAFETY Reports. Given the known safety concerns, it’s unacceptable to approve this vaccine for 5-11 years old children. Approval of the application will certainly lead to mandates requiring vaccinations before these children can attend school. I am also contacting my representatives in the US House and Senate and asking them to act immediately through oversight investigations and legislation to prevent the FDA from allowing the uses of products without having stringent safety protocols in place. Please help keep our children safe by REJECTING this application.

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** BACKGROUND TO THIS FDA MEETING… for your public comments to FDA **

White House Tells Governors to Get Ready to Vaccinate Young Kids, Even Though FDA Hasn’t Approved It. Pediatrician Says, Not so Fast.
https://childrenshealthdefense.org/defender/white-house-governors-prepare-vaccinate-young-kids-fda-not-approved
The White House on Tuesday told states to prepare to vaccinate children as young as 5 by early November, even though the U.S. Food and Drug Administration hasn’t yet authorized Pfizer’s COVID vaccine for children under 12, and despite safety concerns expressed by scientists and pediatricians.

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13 reasons why you should not allow your child to get the Covid-19 Vaccine – The Expose
https://theexpose.uk/2021/09/14/13-reasons-why-you-should-not-allow-your-child-to-get-the-covid-19-vaccine/

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Why Children Should Not Receive the COVID Shot
https://www.lewrockwell.com/2021/06/joseph-mercola/why-children-should-not-receive-the-covid-shot/

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JANCI CHUNN LINDSAY, PH.D: WE COULD POTENTIALLY STERILIZE AN ENTIRE GENERATION:
Dr. Chunn Lindsay is a molecular biologist and toxicologist. In a public comment to the CDC in April, Dr. Janci Chunn Lindsay, called to immediately halt Covid vaccine production and distribution. Citing fertility, blood-clotting concerns (coagulopathy), and immune escape, Dr. Lindsay explained to the committee the scientific evidence showing that the coronavirus vaccines are not safe.

See:
https://www.jennifermargulis.net/halt-covid-vaccine-research-scientist-urges-cdc/

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INFORMED CONSENT: Before delivering your child to a so-called ‘school-based vaccination clinic’
https://sarasotavaccinationchoice.wordpress.com/2021/09/12/informed-consent-before-delivering-your-child-to-a-so-called-school-based-vaccination-clinic/

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For more articles about myocarditis in young people who’ve received the covid jab, see:
https://childrenshealthdefense.org/?s=myocarditis&type=defender

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Young males are six times more likely to suffer from heart problems after being jabbed than be hospitalised from coronavirus, study finds
https://www.telegraph.co.uk/news/2021/09/09/teenage-boys-risk-vaccines-covid/

Read the study, here:
https://www.medrxiv.org/content/10.1101/2021.08.30.21262866v1

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The Conspiracy Theorists Were Right; It IS a “Poison-Death Shot”
https://www.lewrockwell.com/2021/09/no_author/the-conspiracy-theorists-were-right-it-is-a-poison-death-shot/
By Mike Whitney, The Unz Review, September 18, 2021

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‘Serious Violations and Manipulations of Trial Protocol’: How Pfizer Obtained FDA Emergency Authorization for Children
https://www.greenmedinfo.com/blog/serious-violations-and-manipulations-trial-protocol-how-pfizer-obtained-fda-emerg

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Studies Confirm Pfizer Vaccine Immunity Wanes at 2 Months, as Pharma Giant Seeks FDA Approval for Kids 5 to 11
https://childrenshealthdefense.org/defender/pfizer-vaccine-immunity-fda-kids-5-to-11/
A study from Israel covering 4,800 healthcare workers showed antibody levels waned rapidly after two doses of Pfizer’s COVID vaccine. Meanwhile, Pfizer today officially asked the U.S. Food and Drug Administration to authorize its vaccine for children 5 to 11 years old.

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MORE:

VRBPAC Meeting on Pfizer Data on Its COVID-19 Vaccine for Children 5-11

(From the FDA News Release titled “FDA to Hold Advisory Committee Meetings to Discuss Emergency Use Authorization for Booster Doses and COVID-19 Vaccines for Younger Children”)
https://www.fda.gov/news-events/press-announcements/fda-hold-advisory-committee-meetings-discuss-emergency-use-authorization-booster-doses-and-covid-19

EXCERPT:

VRBPAC Meeting on Pfizer Data on Its COVID-19 Vaccine for Children 5-11

The FDA anticipates receiving a request from Pfizer to amend its emergency use authorization to allow the use of its COVID-19 vaccine in children 5 through 11 years of age. In anticipation of the request, the FDA is moving forward with scheduling an advisory committee meeting on Oct. 26 to inform the agency’s decision-making.

“We know from our vast experience with other pediatric vaccines that children are not small adults, and we will conduct a comprehensive evaluation of clinical trial data submitted in support of the safety and effectiveness of the vaccine used in a younger pediatric population, which may need a different dosage or formulation from that used in an older pediatric population or adults,” said Acting FDA Commissioner Janet Woodcock, M.D.

The FDA intends to make background materials for both VRBPAC meetings available to the public, including the meeting agendas and committee rosters, no later than two business days before each meeting.

The FDA intends to livestream the VRBPAC meetings on the agency’s YouTube page (Oct. 14 meeting linkExternal Link Disclaimer; Oct. 15 meeting linkExternal Link Disclaimer; Oct. 26 meeting linkExternal Link Disclaimer), which will be viewable on the agency’s FacebookExternal Link Disclaimer and TwitterExternal Link Disclaimer channels; the meetings will also be webcast from the FDA website.