Tell the FDA: Stop the Genocide!
The government is getting ready to rubber stamp more Covid-19 vaccine emergency use authorizations for children. The vaccines offer no benefit to children and cause serious harm, including death.
Dr. Toby Rogers has the complete story on his Substack page, detailing the upcoming meetings in which the FDA is expected to approve the following:
a Pfizer Covid-19 vaccine for children under 5;
a Moderna Covid-19 vaccine for children 0 to 17
a “Future Framework” that will allow future Covid-19 vaccines to be approved without further clinical trials to demonstrate their safety or efficacy.
Please see Dr. Rogers’ excellent series of articles, for which he truly deserves a Pulitzer, beginning with this one:
The sole purpose of the Moderna and Pfizer mRNA shots in kids is to eliminate the control group. There are no health benefits, only harms (substack.com)
In it, he writes:
“The risk benefit document for Moderna is 190 pages single-spaced. It was released two business days before the June 14-15 VRBPAC meeting. A similar risk benefit assessment for Pfizer’s EUA application for kids under 5 will be released tomorrow (just 24 hours before the meeting). This guarantees that NONE of the members of the VRBPAC will have read either of these documents prior to the meeting — which is exactly what the cartel wants.”
Rogers, who DID read the Moderna report, conducted a thorough analysis. He found:
No actual health benefits of the Moderna vaccine for children. The risk from the virus is so low in children that there were no severe cases of Covid-19 in either the treatment or the control group. Moderna attempted to get around this problem by pointing to the presence of certain antibodies in the vaccinated. Meanwhile, no studies have shown that merely having these antibodies prevents Covid. Also, Moderna did not measure antibodies in the control group. It is entirely possible that children who didn’t get the vaccine had just as many of the same antibodies, all from natural infection.
Moderna tested the antibodies in the vaccine group two months after the second dose. We know from other studies that this is the period in which antibodies from the Covid-19 vaccine are at their peak. They quickly fade after two months and result in negative efficacy within six months, at which point vaccinated children are MORE likely to be infected with Covid-19 than their unvaccinated peers.
Serious adverse events were common. In the adolescent group, 25 percent of vaccine recipients suffered a reaction that was Grade 3 or higher. Adverse events in the other age groups were just as bad, although Moderna attempted to obscure — through muddled groupings — the frequency and severity of these events in the younger age groups.
Adverse events in the control group also were high in many, but not all, categories. Rogers rightly suspects that this is because Moderna rigged the placebo to make adverse events in both groups comparable. This is a common trick employed by the pharmaceutical industry. Rather than give the control group a harmless saline injection, companies inject the control group with an adjuvant or other known toxin from the vaccine that they are testing. Then they say, “Sure, adverse events in the vaccinated group are high. But look, they’re just as high in the placebo group. Therefore, the vaccine is just as safe as placebo.” In this case, the most likely suspect for the placebo is lipid nanoparticles, which spread throughout the body and can even cross the blood-brain barrier.
Moderna vaccinated the control group 53 days after Dose Two. Presumably this was done to prevent a case-control comparison of the frequency of heart attacks, myocarditis, strokes, blood clots, neurological disorders, shingles, and many other serious health complications that we know from adults can occur up to several months post-vaccination. It also prevents long-term studies of vaccine safety. For example, in my opinion, it is not just possible but likely that the Covid-19 vaccine will cause autism in a significant subset of the infants and toddlers who receive it. We already know that the spike protein in the lipid nanoparticles can cross the blood-brain barrier, resulting in psychosis and other neurological disorders in adults and children. A 53-day study of safety cannot monitor children for the onset of autism, since autism typically takes much longer to develop and diagnose.
The FDA and Moderna cited 26 studies showing that mRNA vaccines in general, and Moderna in particular, cause myocarditis. Then they pointed to a couple of rigged CDC-led studies claiming to show minimal risk of myocarditis from the shots and used that data to dismiss the data from the other 26 studies.
Setting the Stage
I am asking all my readers to take a few minutes today to politely put FDA officials and their accomplices on notice that we are tracking the agency’s every move and that their day of reckoning is coming. When that day comes, ignorance will not be an acceptable defense. Those responsible for this genocide will face justice.
We have until 11:59 p.m. eastern time tonight to submit a formal comment via the Federal Register. Click here and look for the blue Comment button in the upper left-hand corner of the website.
I also strongly encourage my readers to write directly to the FDA political appointees, career staff, and committee members involved in this genocide. Their emails, courtesy of Dr. Rogers, are below. No need to separate the addresses and send your messages one by one. Simply cut and paste this entire list into the address line of your email and speak to the entire cabal at once:
firstname.lastname@example.org, email@example.com, DeanofPublicHealth@brown.edu, Aux7@cdc.gov, Peter.Marks@fda.hhs.gov, Hong.Yang@fda.hhs.gov, Richard.Forshee@fda.hhs.gov, Huilee.Wong@fda.hhs.gov, Leslie.Ball@fda.hhs.gov, Doran.Fink@fda.hhs.gov, CBERVRBPAC@fda.hhs.gov, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, Jportnoy@cmh.edu, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, RandyHawkins@cdrewu.edu, firstname.lastname@example.org, JYLee@uams.edu, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org, email@example.com, firstname.lastname@example.org
Also, please see the Children’s Health Defense 1-click call to action for a way to quickly alert your lawmakers to the genocide that is occurring under their watch.
Use the Comments section below to tell us what you’re telling them. Also, please share this post on your social media accounts to help us spread the word.
Here's my comment in the Federal Register:
I am horrified that the FDA is even considering authorizing the Covid-19 vaccine for children under five. The mRNA vaccines should all be pulled from the market, not expanded into new markets! Try as it might, the U.S. government cannot hide hundreds of thousands of critical injuries, affecting all vaccinated age groups, from these Covid-19 vaccines. Nor can it hide the fact that the vaccinal antibodies from these injections begin to wane after just two months, resulting in NEGATIVE EFFICACY for children within six months. In addition, we know that deaths from this virus represent fewer than one percent of all deaths in U.S. children since the start of the pandemic. The FDA and CDC are now going to waste billions of taxpayer dollars trying to chase fewer than one percent of child deaths. Meanwhile, the CDC continues to aggressively ignore most of the factors behind the other 99 percent of deaths. The U.S. would be far better off taking the money you're going to waste purchasing and promoting the Covid-19 vaccine for children and giving it to swim instructors. Drowning is a leading cause of death for young children in the U.S., causing far more deaths in this age group than Covid-19 ever could. Many people are now talking seriously about Nuremburg 2.0. I personally cannot wait for that day of reckoning to arrive. When it does, I hope and pray that every single VRBPAC member faces trial for crimes against humanity.
Here’s my comments to the Cabal:
To Whom It May Concern:
1. Do not force Covid-19 shots that failed clinical trials onto kids. According to the journal Nature Medicine, children and young people have a 99.995% recovery rate from this genetically altered virus. According to the CDC, the overwhelming majority of children already have natural immunity anyway. Never mind that the harms from Covid-19 shots in kids are nith short of catastrophic.
2. The FDA and CDC must pivot to therapeutics. About 20 off-the-shelf treatments are more effective than vaccines (if used for prophylaxis or early intervention). Get these safe and effective medicines to people who need them and let doctors be doctors again and treat patients based on their own best clinical judgment.
3. Any reformulated Covid-19 shots MUST go through proper HUMAN clinical trials and FDA review. That means:
• large (50,000+ person) double-blind randomized controlled trials with inert saline placebos conducted by an independent third party;
• safety and efficacy studies for two years prior to any application; monitor the treatment and control group for the rest of their lives to record non-specific effects;
• any future “vaccine” or other prophylaxis claiming to provide any level of conferred “immunity” to the subject must provide sterilizing immunity with greater than 90% efficacy and less than 0.1% Grade 3 Adverse Events; and
• proper monitoring for carcinogenesis, mutagenesis, and impairment of fertility.
Thank you for your consideration.