Moderna Rep Admits Everyone Is Part of Huge Experiment by Dr. Joseph Mercola
In the featured video, which aired June 22, 2021, independent reporter Stew Peters plays an audio recording1 made by a young woman who suddenly developed Guillain-Barre syndrome after her Moderna injection. Her neurologist believes her condition is the direct result of the COVID shot.
While the neurologist filed an adverse event report with the U.S. Vaccine Adverse Events Reporting System (VAERS), the woman decided to report it to Moderna as well. The Moderna rep does not appear the least surprised by the injury, and appears to admit he’s received similar reports before.
Everyone Who Gets the Jab Is Part of the Safety Trial
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During that call, the Moderna representative reads her the following disclaimer:
“The Moderna COVID-19 vaccine has not been approved or licensed by the Food and Drug Administration, but it has been authorized for emergency use by the FDA under an emergency use authorization to prevent coronavirus disease 2019, for use in individuals 18 years of age and older.
There is no FDA-approved vaccine to prevent COVID-19. The EUA for the Moderna COVID-19 vaccine is in effect for the duration of the COVID-19 EUA declaration, justifying emergency use of the product unless that declaration is terminated or the authorization is revoked sooner.”
The rep also points out that all clinical trial phases are still ongoing, and that long-term protective efficacy against COVID-19 is unknown. When the patient asks whether everyone who gets the COVID shot — even if they did not specifically sign up to be a trial participant — is in fact part of the clinical trial, he replies, with a chuckle, “pretty much, yeah.”
So, in a nutshell, while vaccine makers, health authorities, mainstream media, social media platforms like Facebook and public advertisements tell you the vaccine has undergone rigorous testing, has been “approved” and is safe and effective, none of those claims are true.
The shots have received emergency use authorization only, which is completely different from regular FDA approval and licensing. They don’t know how effective the shot is, or how long the effects last, and they don’t know if it’s safe, because the trials have not been completed. In fact, the public vaccination campaign is a big part of those trials, whether people realize it or not.
Children Are Being Coerced into Medical Experimentation
This makes the push to inject children and teens all the more disturbing. Vaccine manufacturers have received EUA for children as young as 12,2 and parents are now being told their children “must” participate in what is a medical experiment.
People are being told it’s their social “duty” to participate in a medical experiment. People are told they have to participate in a medical experiment or lose their job or educational prospects. What’s happening here is no different than being told you “must” participate in a new cancer drug trial in order to keep your job or attend school. It’s completely absurd, unethical and illegal.3,4,5
When people do get the shot, they are not informed that they’re taking part in a medical experiment and they’re not asked to sign a consent form (as this particular requirement is waived under EUA rules). While consent forms are waived under an EUA, providing truthful information about potential side effects is not.
It’s really important to realize that coercing people to participate in medical experimentation violates long-established research ethics rules. If you wanted to perform a medical study and decided to lure participants with free ice cream or a free Playstation, the ethics committee would shut down your project.
The problem here is that the COVID-19 injection trials have no oversight boards. There’s no Data Safety Monitoring Board, no Clinical Event Committee and no Clinical Ethics Committee. This despite the fact that such oversight is standard practice for all human research. If such committees do exist, they’ve not been announced and no standard reports have been published.
Myocarditis Update
Peters also addresses an increasingly common side effect, namely myocarditis, i.e., heart inflammation. Animal research performed by Masonic Medical Research Institute researchers in collaboration with the Boston Children’s Hospital was posted on the preprint server bioRxiv, June 20, 2021.6
