In the beginning, a treatment plan that featured old, no longer patented anti-malarial drugs surfaced and was shouted down in favor of a drug that ended up not working, a protocol that forced victims on ventilators, and the development of a vaccine.
Each of these methods to prevent or treat the disease has seen less than visible success next to the original treatment plan put forth by doctors in the field, and true anti-body cocktails that work if taken early.
This week, Anthony Fauci, a man who has never practiced medicine, but works for the government and happens to be the highest-paid employee, announced that a NEW product looks promising for preventing death in COVID patients if taken early.
The White House chief medical adviser said that using the lab-made antibodies (monoclonal antibodies) to fight the virus before a patient is hospitalized can prevent the chances of severe illness by between 70 and 85 percent.
“That’s when you get the best effect. And again, being an underutilized intervention, we want people out there, including physicians as well as potential patients, to realize the advantage of this very effective way of treating early infection.”
Weren’t the “vaccines” supposed to do that? Prevent getting the disease? Don’t vaccines build up natural antibodies in the body that prevent further illness? Oh, that’s right. Now, the COVID shots just lessen the symptoms in “breakthrough” cases.
If such a therapeutic is available, how is it that we need vaccines in the first place?
And why is the Food and Drug Administration falling all over itself to approve one brand of shot over all the others when such a new, patented treatment is available.
These are questions that need answers before the annual cold and flu season.
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