January 11, 2022, the Health and Human Services Committee of the Maine legislature held a public hearing on LD867 “An Act to Prohibit Mandatory COVID-19 Vaccinations for 5 Years to Allow for Safety Testing and Investigations Into Reproductive Harm”
Dr. Meryl Nass, an internist with a special interest in vaccine-induced illnesses and expertise in anthrax and bioterrorism, testified in favor of the bill
All currently available COVID shots in the U.S. are experimental. None is licensed. Comirnaty, which has received full license, is not available in the U.S., and won’t be made available as long as doses of the Emergency Use Authorized Pfizer shot, BNT162b2, remain
Since the COVID shots are experimental, U.S. law requires potential recipients to have the right to refuse. Experimental drugs also cannot be mandated, and potential recipients must give written informed consent. Informed consent cannot be given when reports of side effects are censored and not disclosed
Some foundational safety studies are just now starting and won’t be completed until 2027
January 11, 2022, the Health and Human Services Committee of the Maine legislature held a public hearing on LD8671 “An Act to Prohibit Mandatory COVID-19 Vaccinations for 5 Years to Allow for Safety Testing and Investigations Into Reproductive Harm.”
The American Cancer Society is vehemently opposed to this rational bill.2 In some twisted, incomprehensible logic, the ACS claims that banning mandatory COVID jabs would “place the health of cancer patients at greater risk.” How, one might ask, could that happen, considering the jabbed are just as likely to contract and spread the virus?
Getting the shot in no way, shape or form protects anyone around you. So, what could it be? One can only wonder if the ACS’ opposition has anything to do with their “long-standing partnership”3 with vaccine maker Pfizer, which in 2020 alone helped the ACS hand out $3.7 million in grants4 — but which also happens to produce one of the COVID mRNA injections?
If vaccine mandates are upheld, ACS’ partner, Pfizer, has lots to gain. But if mandates are banned, they could have plenty to lose. Among those who testified in favor of the bill was Dr. Meryl Nass, an internist with a special interest in vaccine-induced illnesses and expertise in anthrax and bioterrorism.
In her testimony, Nass presented several key reasons for why we need to prevent COVID jab mandates until there’s adequate safety data. Nass’ testimony is posted on her blog, anthraxvaccine.blogspot.com.5 Here, I’ll provide a summary review of her key points.
In short, it comes down to liability. The two products are not interchangeable (as confirmed in federal court8) because they are not identical in terms of liability under U.S. law. (The liability issue differs from country to country, which is likely why Comirnaty is available in Europe but not the U.S. Everything discussed here applies only to the U.S.)
Indeed, a federal district court judge in November 2021 rejected the U.S. Department of Defense’s claim that Pfizer’s EUA shot, BNT162b2, is interchangeable with the licensed Comirnaty.9 Why would Pfizer give up blanket immunity by withdrawing the remaining EUA lots and replacing them with a product they can be sued for by people who are injured?
The Pfizer-BioNTech EUA product, BNT162b2,10 has very limited financial liability for injuries and deaths, thanks to it being under EUA. This liability shield extends to the manufacturer, distributors, administrators, program planners and just about everyone else involved in the making, distribution and administering of this product.
Comirnaty, on the other hand, as a fully licensed product, does not enjoy this broad liability shield. It is subject to ordinary liability claims. Strangely enough, the FDA extended the EUA for BNT162b2 on the very same day it granted full license to Comirnaty, and Pfizer has no plan to make Comirnaty available in the United States as long as BNT162b2 doses are still available.11
Why didn’t the FDA pull the EUA for BNT162b2 once it licensed Comirnaty? They’re supposed to be identical products, so why the two wildly diverging and contradictory lines of approval?
By law, an EUA can only be granted when there are no other drugs available, so once a COVID shot was licensed, all EUA “vaccines” should actually have been pulled. As stated by the Children’s Health Defense in its lawsuit against the FDA and acting commissioner Janet Woodcock:12
“The black letter law is clear. There can be no biologic license approved to a medical product for diagnosing, preventing or treating COVID-19 if there is also still an Emergency Use Authorization for the same medical product serving the same purpose.”
I recently discussed this issue with Alix Mayer from Children’s Health Defense. If you are interested in more details please review the video below.
“More evidence is needed on the use of the different COVID-19 vaccines in children to be able to make general recommendations on vaccinating children against COVID-19 … Vaccine trials for children are ongoing and WHO will update its recommendations when the evidence or epidemiological situation warrants a change in policy,” the WHO states on its website.16
“If the World Health Organization believes there is insufficient evidence to support general vaccination of normal children, why would this committee and the Maine Legislature think otherwise?” Nass asks.
“The board reported that it had received two complaints concerning Nass, who is an internist in Ellsworth, Maine, and an active member of the anti-vaccine group Children’s Health Defense … The complaints alleged that Nass had spread misinformation about COVID-19.
Nass has reportedly been critical of vaccine effectiveness and supported the use of ivermectin and hydroxychloroquine to treat COVID-19, despite insufficient evidence that they are effective in fighting the virus. The board is also looking to conduct a psychological evaluation of Nass …”
It’s hard to believe that this action is anything but a bullying tactic intended to shut her up, because she knows her stuff and she’s not afraid to share the unvarnished truth. In its order, the State of Maine Board of Licensure in Medicine claims that:18
“… the continued ability of Dr. Nass to practice as a physician in the State of Maine constitutes an immediate jeopardy to the health and physical safety of the public who might receive her medical services, and that it is necessary to immediately suspend her ability to practice medicine in order to adequately respond to this risk.”
In a January 13, 2022, Substack post, Steve Kirsch commented on the Maine medical board’s decision:19
“Dr. Nass is guilty of prescribing FDA-approved drugs that have been shown in dozens of trials to be beneficial in treating COVID20… Here’s the interesting thing: had she prescribed nothing for these patients, she wouldn’t have been cited.”
Doctors who save lives using drugs proven safe over decades of use are stripped of their licenses and ordered to undergo psychiatric evaluation, while doctors who kill patients by either refusing to treat them or by using unproven experimental drugs are “sane” and get to keep theirs. That’s where we’re at. It’s beyond tragic.
In the end, though, Meryl — like the rest of us — will be vindicated, of that I have no doubt. I have had the opportunity to get to know her over the years and have done many interviews with her. I remain confident that although this is clearly a challenge, she will come out better on the other side.
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JD Rucker – EIC @jdrucker
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This article has been archived by Conspiracy Resource for your research. The original version from Based Underground can be found here.
