Few people realize that the Moderna vaccine against COVID-19—which the FDA has finally declared “highly effective,” and which is now being distributed to Americans—has actually been available for nearly a year.
But the government wouldn’t let you take it.
The vaccine, a triumph of medical science known as mRNA-1273, was designed in a single weekend, just two days after Chinese researchers published the virus’s genetic code on January 11, 2020.
For the entire duration of the pandemic, while hundreds of thousands died and the world economy was decimated by lockdowns, this highly effective vaccine has been available.
But you, and all the people who died, were prohibited by the government from taking it.
There are some who claim that the FDA “saves lives” by putting the brakes on medical innovation with their requirements for years-long, and often decades-long, billion-dollar medical trial procedures.
Why are hundreds of thousands of “natural” deaths from a rampaging disease considered acceptable to the FDA—while the remote possibility of one or two deaths among well-informed vaccine-testing volunteers are not?
Missing here is the obvious counterpoint—How many lives did the FDA sacrifice to disease in the meantime?
In the case of COVID-19 we know the answer: more than 300,000 deaths so far in the United States and counting.
So why was this vaccine delayed for a full year? Because the FDA prohibited rapid “challenge trials”—where volunteers take the vaccine and then expose themselves to the virus in a lab, rather than waiting agonizing months to see how many catch the virus “in the wild.”
Challenge trials would have proven the vaccine’s effectiveness in a matter of weeks. But the FDA considered the risk to trial volunteers too high.
But why? Why are hundreds of thousands of “natural” deaths from a rampaging disease considered acceptable to the FDA—while the remote possibility of one or two deaths, in the absolute worst case scenario, among well-informed vaccine-testing volunteers are not?
There is no rational answer. The tragic truth is that we are ruled by a cowardly medical bureaucracy, one that would rather allow hundreds of thousands of people to die than face any potential criticism for allowing an accelerated vaccine trial.
By contrast, in a free society, immediately after the vaccine was created, volunteers would have been allowed to participate in challenge trials. The trials would have been conducted either by the vaccine company itself, or more likely by third-party medical-trial specialists, to remove any concerns about bias in the results.
The first small group of volunteers would be vaccinated, and then exposed to the virus. If the vaccine appeared to be safe and effective, then a larger group would be vaccinated.
As each challenge group proved successful…
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