If there had been no unusual ‘covid’ measures taken, no unusual illness would have been noticed; was the “pandemic” needed to roll out “vaccines”?
The protocols for the Phase III trials which formed the basis of the authorisation of these products specified clinically irrelevant endpoints and were (in the main) conducted in healthy, younger subjects who were at negligible risk of serious illness. Consequently, they were incapable of measuring the purported benefits. Moreover, there is rapidly accumulating evidence of […]
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