"Moderna Rep Admits Everyone Is Part of Huge Experiment"
by Dr. Joseph Mercola
Except: "In the featured video, which aired June 22, 2021, independent reporter Stew Peters plays an audio recording 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. Please view the video on Rumble, Google Blogger will not permit it to be embedded:
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: 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, 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.
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.
The SARS-CoV-2 spike protein subunit directly damages the heart and causes myocarditis by triggering an exaggerated immune response - a cytokine storm - in the heart cells.
The study, “Selectively Expressing SARS-CoV-2 Spike Protein S1 Subunit in Cardiomyocytes Induces Cardiac Hypertrophy in Mice,”7 found that the spike protein itself (without the rest of the virus) “directly impairs endothelial function.” As it turns out, the S1 subunit of the SARS-CoV-2 spike protein activates NF-kB, a protein that controls not only the transcription of DNA but also cellular survival, cytokine production and secondary inflammation.
This disease process does not involve the ACE2 receptor but rather the toll-like receptor 4 (TLR4), which is responsible for the detection of pathogens and the initiation of innate immune responses. In summary, the research showed spike protein subunit “caused heart dysfunction, induced hypertrophic remodeling and elicited cardiac inflammation.”
“Since CoV-2-S does not interact with murine ACE2, our study presents a novel ACE2-independent pathological role of CoV-2-S [SARS-CoV-2], and suggests that the circulating CoV-2-S1 [CoV-2-spike protein subunit 1] is a TLR4-recognizable alarmin that may harm the CMs [cardiomyocytes, i.e., heart cells] by triggering their innate immune responses,” the authors state.
In short, the SARS-CoV-2 spike protein subunit directly damages the heart and causes myocarditis by triggering an exaggerated immune response - a cytokine storm - in the heart cells. Importantly, hypertrophic remodeling means this is a permanent reshaping and damage of the heart, which refutes claims that the hundreds of myocarditis cases reported to VAERS are of little concern and that their hearts will eventually heal. I believe those assumptions will be found to be wrong, and that many of them may be left with permanently damaged hearts.
‘They Knew What They Were Doing’: As noted by Jane Ruby, Ph.D., on the Stew Peters Show, this research should have been done before these injections were put out into the public domain. Instead of conducting rigorous animal trials, vaccine makers are using the public as guinea pigs in one of the biggest experiments in human history, making tens of billions of dollars in profits while enjoying absolute immunity from any damage their experimental jabs cause.
By falsely labeling these gene modification tools as vaccines (because gene therapy does not qualify as a pandemic treatment that can be granted immunity against liability), they’ve been given the green light to conduct human experimentation without remuneration, informed consent or liability under the guise of a public health emergency.
There’s no way these gene therapies in any rational society would have been released to be tested on this many human subjects, including pregnant women and children, were it not for this sinister misrepresentation.
Here’s the most disturbing part, though: It appears these COVID injections may have been designed to cause this kind of cell damage on purpose. Why? Because the researchers also tested the natural spike protein subunit of another coronavirus called NL63. This virus was chosen because it, like SARS-CoV-2, uses the ACE2 receptor for entry into the human cell. The NL63 spike protein did not, however, trigger this kind of heart damage. “They knew what they were doing when they engineered this mRNA to make this particular spike protein,” Ruby says."
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