Over 160 Experts Slam COVID Vaccines as ‘Unnecessary, Ineffective and Unsafe’ in Powerful Letter
by Raymond Wolfe | LifeSiteNews
Dozens of medical experts issued a warning this month about COVID-19 vaccines, slamming the jabs as “unnecessary, ineffective and unsafe” and likely to lead to “foreseeable mass deaths.”
“In short, the available evidence and science indicate that COVID-19 vaccines are unnecessary, ineffective and unsafe,” Doctors for COVID-19 Ethics said in an open letter two weeks ago. “Actors authorizing, coercing or administering experimental COVID-19 vaccination are exposing populations and patients to serious, unnecessary, and unjustified medical risks.”
Doctors for COVID-19 Ethics, a group co-founded by former Pfizer vice president Michael Yeadon, counts more than 160 medical experts from around the world among its signatories. Other founding members include Prof. Sucharit Bhakdi MD, former chair of the Institute of Medical Microbiology and Hygiene at Johannes Gutenberg University of Mainz, Germany and Dr. Wolfgang Wodarg, former head of the health committee of the Parliamentary Assembly of the Council of Europe.
The doctors have penned multiple letters to the European Medicines Agency on COVID-19 vaccine issues and are facing censorship, though their most recent letter can be found archived here. The group also can be found on Twitter. Their testimony reflects growing calls from experts, like Dr. Janci Chunn Lindsay and Dr. Peter McCullough, to halt the jabs.
‘The tip of a huge iceberg’
In their letter earlier this month, Doctors for COVID-19 Ethics emphasized serious health implications of the vaccines for both the healthy and ill, saying that the shots “are not safe, either for recipients or for those who use them or authorize their use.”
They pointed to risks of “lethal and non-lethal disruptions of blood clotting including bleeding disorders, thrombosis in the brain, stroke and heart attack,” “antibody-dependent enhancement of disease,” autoimmune reactions, and potential effects of “vaccine impurities due to rushed manufacturing and unregulated production standards.”
“Contrary to claims that blood disorders post-vaccination are ‘rare’, many common vaccine side effects (headaches, nausea, vomiting and hematoma-like ‘rashes’ over the body) may indicate thrombosis and other severe abnormalities,” the experts said. “Clotting events currently receiving media attention are likely just the ‘tip of a huge iceberg.’”
“Due to immunological priming, risks of clotting, bleeding and other adverse events can be expected to increase with each re-vaccination and each intervening coronavirus exposure,” Doctors for COVID-19 Ethics added. “Over time, whether months or years, this renders both vaccination and coronaviruses dangerous to young and healthy age groups, for whom without vaccination COVID-19 poses no substantive risk,” they argued.
“Just as smoking could be and was predicted to cause lung cancer based on first principles, all gene-based vaccines can be expected to cause blood clotting and bleeding disorders, based on their molecular mechanisms of action,” they said. “Consistent with this, diseases of this kind have been observed across age groups, leading to temporary vaccine suspensions around the world.”
“Since vaccine roll-out, COVID-19 incidence has risen in numerous areas with high vaccination rates. Furthermore, multiple series of COVID-19 fatalities have occurred shortly after the onset vaccinations in senior homes,” the doctors said. “These cases may have been due not only to antibody-dependent enhancement but also to a general immunosuppressive effect of the vaccines, which is suggested by the increased occurrence of Herpes zoster in certain patients.”
“Regardless of the exact mechanism responsible for these reported deaths, we must expect that the vaccines will increase rather than decrease lethality of COVID-19,” they continued.
The group stressed that the jabs remain technically experimental – a fact that legally precludes mandatory vaccination in many cases:
“The vaccines are experimental by definition. They will remain in Phase 3 trials until 2023. Recipients are human subjects entitled to free informed consent under Nuremberg and other protections, including the Parliamentary Assembly of the Council of Europe’s resolution 2361 and the FDA’s terms of emergency use authorization.” Read Full Article >