https://thenewamerican.com/covid-vax-destroying-female-reproductive-systems-killing-kids-toxicologist-warns/ Video Here (Approx. 20 Min)
Covid Vax Destroying Female Reproductive Systems & Killing Kids, Toxicologist Warns
Podcast: Play in new window | Download (Duration: 20:38 — 28.5MB)
The experimental Covid injections forced on millions by the Biden administration are killing people and wreaking havoc on female reproductive organs and other body systems, warned toxicologist Dr. Janci Lindsey in this interview on Conversations That Matter with The New American magazine’s Alex Newman. Dr. Lindsey, who holds PhDs in biochemistry and molecular biology and serves as director of Toxicology and molecular biology for a toxicology firm, worked on Rockefeller-funded research into fertility regulating vaccines in the 1990s. Among other concerns, she warned that the shots are causing all sorts of toxic effects on the human body. Within the next 6 months, humanity should expect to see another “plandemic” to bring in more medical tyranny, she warned. Dr. Lindsey urged everyone to refuse to comply.
At 11:30 Dr. Lindsey discusses minocycline as a therapeutic to ameliorate COVID “vaccine” injury as well as glutathione, NAC, proper diet, and vitamin C. She also discussed how the spike protein hangs out in the lymph nodes and that ivermectin & HCQ may help this as well as the dangers blood clotting.
Breaking: FDA Panel Recommends Moderna Two-Dose COVID Vaccine for Kids Ages 6 to 17 Despite Serious Safety Concerns
The U.S. Food and Drug Administration’s vaccine advisory panel on Tuesday voted 22 – 0 to authorize Moderna’s COVID-19 vaccines for children ages 6 to 11 and 12 to 17 despite the lack of short- and long-term safety data and no evidence children are at risk of serious illness.
By Megan Redshaw
The U.S. Food and Drug Administration’s (FDA) vaccine advisory panel today voted unanimously to recommend Moderna’s COVID-19 vaccine for children ages 6 to 17 after determining the benefits of the vaccine outweigh the risks for use.
The Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted 22 to 0 to recommend Moderna’s two-dose vaccine for 6- to 11-year-olds at half the strength of the adult version, and 22 to 0 in favor of authorizing the shot for 12- to 17-year-olds at the same strength as adults.
The FDA’s vaccine advisors will meet again on Wednesday to discuss amending Emergency Use Authorization (EUA) for Moderna’s COVID-19 vaccine to include the “administration of the primary series to infants and children 6 months through 5 years of age.”
(See link for article)
FDA Rubberstamps the Moderna COVID-19 Vaccine for Kids Aged 6-17 Based on Insufficient Evidence
Yesterday, the vote was in 100% in favor of “approval” of the vaccine for kids 6 to 17. None of the votes were based on Science.
This article is dedicated to the parents of the children not yet harmed or killed by COVID-19 vaccines. We are trying to warn you that the FDA and CDC are whole-heartedly engaged in fraud.
Dr. Toby Rogers deserves credit for sitting through a grueling, “heart-braking” nine hours of FDA rubber-stamping COVID-19 vaccines based on clinically trivial endpoints. This rubber-stamp is based on data showing no serious cases of COVID19 in children (no hospitalizations). Here I review most of his interview with Steve Kirsch. (Link to video).
Under EUA rules, an emergency must be in place. Yesterday, I pointed out the vanishingly small number of cases since March 2020. (See link for Weiler’s point by point detailing of the FDA’s “political theatre.”
There was a public comment session during the meeting where many expressed serious concern over recommending a gene therapy injection to an age group that has almost a ZERO risk of experiencing severe illness or death from COVID.
Dr. Harvey Klein, orthopedic surgeon, mechanical engineer and yes, even a rocket scientist said he is appalled at the FDA’s arrogance in even “thinking of vaccinating healthy children with outdated, highly toxic COVID vaccines,” and that have a 99.998% recovery rate with no sequelae.
Pharmacologist, pharmacist, FDA and healthcare policy oversight fellow and FDA reform advocate at the Ethics and Public Policy Center in Washington, D.C., Dr. David Gortler states the FDA and the advisory panel have “maintained a highly non-scientific and casual attitude toward approving a vaccine whose short- and long-term effects on children are unclear.” After reminding the FDA of the need for parents to be informed of “vaccine” safety, he stated the FDA has failed to address genotoxicity, teratogenicity, oncogenicity of COVID-19 vaccines and cardiovascular risk following “vaccination”, potential fertility issues and clinical effects of spike proteins in donated or transfused blood. He ended by stating that four million doses must be administered to children 5 to 11 years of age to prevent a single ICU admission in the same age group.
This means that if you assume two doses per child, two MILLION children must risk potentially serious side-effects and/or death to prevent a single child from entering the ICU.
But the real clincher came from Kathy Dopp and Dr. Stephanie Seneff’s analysis which highlighted the following:
- Children under 18 are 51 more times more likely to die from the injection than they are to die from COVID if not “vaccinated.”
- The COVID injection actually increases a child’s risk of dying from COVID.
It was also pointed out that instead of breaking down the data per age group, the “vaccine” manufacturer lumped all the age groups together to “massage” the data. When each group is looked at separately, the shot fails in each category according to Dr. Toby Rogers. He also points out that Moderna created 20 adverse event tables allowing it to simply eliminate or hide data is didn’t like. Please also see this important paper written by Dr. Rogers on how the FDA is set to decide on Pfizer’s jab for kids based on unethical trial data that makes the data functionally useless for making decisions.
Again, it can not be over emphasized that science is now being done by press release and the very people doing the “science” are selling the products.
Lastly, despite the CDC’s narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department, 635 cases of myocarditis in the 5 to 17 age group have been confirmed. Imagine the numbers if the case definition were more realistic and accurate. Lyme/MSIDS patients should be well aware of the CDC’s shenanigans with “case definitions” by now.
It doesn’t take a rocket scientist to see something is rotten in Denmark.
Take a stand and tell the FDA to get their hands off our children.
- https://madisonarealymesupportgroup.com/2020/12/21/warning-3150-injuries-in-1st-week-of-covid-vaccines-among-american-healthcare-workers-pregnant-women-included/ Latest VAERS data. Over 4,000 fetal deaths after COVID shots plus many reports of adverse reactions in women including irregular menstrual cycles, excess bleeding, problems with milk flow, blood clots, and even death.