In a shocking revelation first reported by Dan Dicks of Press for Truth (Canada), an FDA document admits that the CDC and FDA conspired to fabricate a covid-19 testing protocol using human cells combined with common cold virus fragments because they had no physical samples of the SARS-CoV-2 “covid” virus available.
Without physical reference material to use for calibration and confirmation, the test has zero scientific basis in physical reality. And all the PCR analysis based on this protocol is utterly fraudulent, flagging people as “positive” for covid when they merely possess tiny quantities of RNA fragments from other coronavirus strains circulating in their blood.
The document astonishingly admits:
They had no covid virus from which to develop and calibrate the test, so they mixed up a cocktail of human cells and RNA fragments from a common cold virus, then called it “covid.”
The GenBank sequence referred to in this paragraph is simply a digital library definition that’s labeled “covid” but has no supporting reference materials in physical reality either.
That’s because no doctor or researcher has isolated “covid” from any infected, symptomatic patient. As a result, no laboratory instruments can be calibrated against actual covid, and the tests simply rely on digital libraries pushed out by the CDC and WHO, using “covid” as the label.
Continued at link.