Below is the letter I just finished crafting. It likely needs tweaking. I intend to mail, fax, and email this letter to each of the 23 names (including FDA voting members) presented on the Children's Health Defense website. Refer to the other post I made for details about the call for Americans to voice their objections to vaccinating our 6 month to 4 year olds. We have until February 15, 2022. https://greatawakening.win/p/141YNJQAdR/urgent-stop-fda-approval-of-pfiz/c/

Thank you in advance for the feedback.

Dear (FDA member's name)

Like many Americans I am deeply troubled and alarmed by the FDA’s continued support of an experimental vaccine without long-term studies? Doesn’t your approval process typically take five to 15 years? If any FDA member has ties to a vaccine manufacturer (past or present), wouldn’t that be a clear conflict of interest? Also, why did Pfizer recently request their data be withheld for 75 years (also very troubling)? According to the CDC, children 0-18 years of age have a 99.997% recovery rate. Yet, the FDA swiftly moved forward with approving the experimental vaccine for children 5-18 years of age (the damage already being revealed) and now you are set to vote on the most innocent and fragile group among us, our babies and toddlers.

As you are already aware, kids, including babies and toddlers, are simply not super spreaders nor are they high risk for COVID-19. According your data, out of 73 million children in the United States, as of December, 2021, approximately 700 reportedly died from COVID-19 and most of these children had serious comorbid health conditions (CDC). Furthermore, numbers of COVID-19 associated hospital admissions for children have been inflated, with more children being hospitalized “with” COVID and not “because” of COVID (Fauci). Studies have already shown children experience more serious and debilitating reactions from the vaccines than from the virus (e.g., Myocarditis). The January 14, 2022, data report from your FDA/CDC Vaccine Adverse Events Reporting System shows over one million COVID-19 adverse-event reports have been filed; of these, approximately 35,000 were for children ages 5-18. And we know VAERS is underreported (the latest study released by Columbia University, 2021, further supports this finding) and vaccine deaths and injuries are significantly higher.

Many Americans know your FDA approved Pfizer vaccine, Comirnaty, is not in circulation in the United States and children and adults are still being given the Emergency Use Authorization (EUA) vaccines. Both the EUA Pfizer vaccine and Comirnaty (as well as Moderna) are based on experimental mRNA technology that was never marketed in vaccines prior to the pandemic. Dr. Robert Malone, the primary inventor of the mRNA biotechnology, continues to speak out about the dangers of this vaccine, especially for children, and recently released a warning statement. Other distinguished and renowned practitioners have voiced their concerns as well. I encourage you to review the panel discussion held by Senator Ron Johnson several weeks ago that included several distinguished and renowned members from the medical community.

Your clinicaltrials.gov website shows the Pfizer trials for children began in March of 2021 and will not be completed until June, 2024. So in essence, children are participating in an experiment with different children receiving different vaccine batch formulas. Data findings from the Pfizer clinical trial for the “6 months – 4 years” age group show the vaccine for this group is ineffective. To suggest that a third dose would be necessary is utterly unethical and immoral. As such, for you to move forward with approval for this age group would be A CLEAR VIOLATION OF THE NUREMBERG CODE.

Like many Americans, my family has spent of a lot of time researching the origin of COVID-19; patent dates; vaccine efficacy studies; financial beneficiaries of the pandemic; NIH, FDA and media ties to Pfizer; and your VAERS data. However, the most compelling information is found in testimonies from medical professionals and vaccine-injured patients, many of whom have been censored or cancelled. There are tens of thousands of healthcare practitioners, scientists, and researchers around the world warning against vaccinating children with this experimental gene therapy. In fact several countries, the most recent being Sweden, have withdrawn the COVID-19 vaccine for children.

In recent months the global narrative has changed in regards to the waning efficacy of the experimental COVID-19 vaccines, the role of natural immunity, transmissibility of the virus among both the vaccinated and unvaccinated, hospitalizations of those “with” and “because of” COVID-19, adverse reactions associated with the vaccines, ineffectiveness of masks and lockdowns, lack of validity and reliability of the COVID-19 tests (e.g., PCR test), alternative therapeutics such as Ivermectin and Hydroxychloroquine, and of course, the vaccine mandates. Finally, isn’t informed consent a basic tenet of medical experimentation and treatment? So why would the FDA even consider approving this vaccine for anyone, let alone our babies? The trust in our medical institutions, including the CDC and the FDA, has been violated and the resulting damage incalculable. The citizens are waking up. We are watching. We are standing up for our children as well as medical freedom. And we are taking note of those individuals who violate the Nuremberg and Helsinki codes. DO NOT APPROVE THE COVID-19 VACCINE FOR 0 – 4 YEAR OLDS.

Concerned American Citizen,