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COVID19 PCR Tests Are Scientifically Meaningless


Aug 13, 2020
COVID19 PCR Tests are Scientifically Meaningless

What is required first for virus isolation/proof? We need to know where the RNA for which the PCR tests are calibrated comes from.

If the authors of these studies concede that their published electron micrographs (EMs) do not show purified particles, then they definitely do not possess purified particles claimed to be viral.

This actually means that one cannot conclude that the RNA gene sequences, which the scientists took from the tissue samples prepared in the mentioned in vitro trials and for which the PCR tests are finally being “calibrated,” belong to a specific virus — in this case SARS-CoV-2.

For instance, the alleged “infected” laboratory mice did not show any relevant clinical symptoms clearly attributable to pneumonia.

Also, no animal died except those they killed to perform the autopsies.

And let’s not forget: These experiments should have been done before developing a test, which is not the case.


Feb 18, 2016
The CDC are withdrawing emergency support for PCR tests, they are not accurate, too many false positives, incredible, won’t be covered by MSM.
This article doesn’t cover it but they are moving to another PCR test that covers the common cold/flu and covid, keep an eye on this, it could be a case of too many becoming aware of the casedemic effect and how it’s fraudulent.
It’s likely the new test will be fraud, why change.

The Centers for Disease Control and Prevention (CDC) will no longer recognize PCR tests as valid methods of diagnosing COVID-19 by the end of this year. The CDC announced in a lab alert on its website that it will be withdrawing its standing request to the Food and Drug Administration (FDA) to grant emergency use authorization for PCR tests to be used to detect SARS-CoV-2. The request, which was issued in February 2020, will be withdrawn on December 31, 2021, a move which signals that the CDC no longer approves of the use of PCR tests as valid diagnostic methods for COVID-19.
In the CDC’s own words: “After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only.”

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