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It's the kind of historic document which could be made to disappear. You might need it with the next "Disease X" outbreak.
This legal opinion dates to the hot controversy in 2021 about putting Covid patients on respirators and giving them Remdesivir (a lethal protocol) or simply treating patients at home with the proven pharmaceuticals hydroxy or ivermectin. The government said the latter was deadly and to be avoided. The Nebraska AG office simply reviewed all the science, all the political hype, and showed how the government was misleading people away from an easy, proven, inexpensive, treatment.
This document has protected those careful doctors and patients who bucked the government mandates and went with real science and showed the rest of the country how to deal with Covid responsibly.
The FDA has rejected its strongest safety warning for Covid mRNA vaccines despite acknowledging that children were killed by the products.
This news surfaced during a televised Bloomberg interview with FDA Commissioner Marty Makary, who said the agency has “no plans” to apply its strongest safety warning to Covid mRNA vaccines.
In that interview, Makary confirmed that the FDA’s own safety and epidemiology centre had formally recommended a boxed warning — a step reserved, under FDA rules, for drugs with “special problems, particularly ones that may lead to death or serious injury.”
