Longevity & Life Extension

An FDA committee is meeting next week to review the first COVID vaccine. We must demand that full transparency is given to the American public. Action Alert!
Pfizer has applied for emergency use authorization (EUA) for its COVID-19 vaccine, and an FDA advisory committee will meet in an open session on December 10 to review Pfizer’s data; Moderna recently announced that it, too, has filed for an EUA. We’re being told by the manufacturers that both of these vaccines have above 90% efficacy and serious adverse events are low. That’s all well and good, but we cannot rely on the word of vaccine makers that their products are safe. We need the data, and so far, we are not even close to getting it. This is completely unacceptable. Please let us know what you think of this article in our comment section. Thank you.

On August 26, Children’s Health Defense (CHD) wrote a letter to Dr. Jerry Menikoff, Director of the Department of Health and Human Services’ Office of Human Research Protection (OHRP), asking for an investigation into serious safety concerns with the COVID-19 vaccine being developed by Moderna. Moderna’s version of the vaccine, championed by Dr. Anthony Fauci and funded with $500 million in taxpayer dollars through Dr. Fauci’s National Institute of Allergy and Infectious Diseases, contains polyethylene glycol (PEG), a molecule to which approximately 72% of the American population have antibodies and 8% have highly elevated levels of antibodies. People who have pre-existing PEG antibodies could experience life-threatening anaphylaxis if injected with PEG-containing substances such as the Moderna COVID vaccine. Additionally, antibodies to PEG can both decrease the effectiveness of the vaccine and increase the risk of side effects.

Recently, scientists published “new science” that claims to address the growing problem of drug-resistant bacteria known as Superbugs. Never mind that overuse of antibiotics (i.e., antilife) has caused the proliferation of these Superbugs. Scientists have found “an alternative way,” moving from antibiotics to anti-vitamins. And they are not using the term “alternative” to suggest anything natural. Scientists have to admit they’ve been duped by the microbes. Traditional antibiotics have targeted a bacteria’s protective cell wall and have subsequently been made obsolete in short order. That’s because in Nature, microbes have amazing abilities to acquire genes from each other, and from their environment” to show that they are highly adaptive in favor of life.

Package inserts are available online for all vaccines licensed in the U.S. In addition to containing bits of practical information for the clinicians who administer the vaccines, the inserts provide members of the public with one of their only opportunities to learn about a vaccine’s contraindications, warnings, precautions and—perhaps most importantly—potential adverse reactions. The inserts communicate the information about adverse reactions in two distinct sections: “Clinical trials experience” (Section 6.1) and “Data from postmarketing experience” from the U.S. or other countries (Section 6.2). In April, 2020, Children’s Health Defense summarized the postmarketing data for over three dozen vaccines given routinely to American infants, children and adolescents. That tally showed that vaccines touted for the prevention of 13 illnesses (Table 1) have been linked to at least 217 adverse medical outcomes reported post-licensure, including serious infections, autoimmune conditions, life-threatening allergies and death.

Eating dinner at 2 p.m., or skipping supper altogether, and fasting until the next morning, combats weight gain by reducing hunger, increasing fat burning and improving metabolic flexibility to burn both fat and carbs. Men and women who eat dinner two or more hours before bedtime have a 26 percent and 16 percent lower risk of prostate and breast cancer respectively than those who eat dinner closer to bedtime. #intermittentfasting

Join Robert F. Kennedy’s Children’s Health Defense for a live, virtual press conference on Thursday, July 30, 2020 at 3:30 p.m. ET/12:30 PT to discuss this exciting milestone in our landmark case against the Federal Communications Commission (FCC) – the submission of the evidentiary brief. To fulfill our commitment to stopping the harmful exposure of our children to 5G and wireless radiation, CHD has taken this giant step toward unprecedented litigation against the FCC and you are invited to learn more directly from our attorneys and petitioners.