Carole Parnell @MagaMutt
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🩸Breaking news. share on all platforms: FDA document admits “Covid” PCR test was developed without isolated samples for test calibration, effectively admitting it’s testing something else.

A document just released by the U.S. Food and Drug Administration (FDA) openly admits that the infamous PCR test for the Wuhan coronavirus (Covid-19) was developed not with actual samples, but rather with what appears to be genetic material from a common cold virus.

In the FDA document, it is clearly stated that ordinary seasonal flu genetic material was used as the testing marker in the PCR test kits because the authorities knew that many people would test “positive” for it, thus allowing them to use these results to create the “Covid” narrative.

It is somewhat of a lengthy read, but have a look for yourself and see the deception in plain sight. There is no legitimate test out there that accurately identifies the presence of SARS-CoV-2. From the document:
08:56 PM - Oct 11, 2021
Only people mentioned by MagaMutt in this post can reply
Misna Burelli @Magneticum
25 October, 04:32
In response Carole Parnell to her Publication
There are no reference genetic materials for any virus anywhere, not for covid, not for colds, and not for flu. They are always just testing against "agreed-upon" collected genetic material from some human nose or so. The genetic materials are most likely just a bunch of exosomes produced by the human body in response to a certain stimulus (infection, cancer, emf etc). There is quite a lot of research about exosomes and strangely, under a microscope, they "look similar to viruses"... The German supreme court has ruled that there is no evidence for any "measles virus". It is the same story for any other virus.

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Carol Roberts @InHisHolyName
11 October, 09:20
In response Carole Parnell to her Publication
See two slides from the inventor of the PCR test.

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Carole Parnell donated @MagaMutt
11 October, 09:03
In response Carole Parnell to her Publication
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“Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA (N gene; GenBank accession: MN908947.2) of known titer (RNA copies/µL) spiked into a diluent consisting of a suspension of human A549 cells

The document is the admission by the FDA that test results are “pooled” together to produce numbers that are inaccurate. The FDA is quite literally manufacturing data to support a false narrative

We are now at a crossroads worldwide. The time is upon us to decide if we are going to allow this type of medical fascism to persist, and impact upon the futures of our children. Or if we are finally going to say no to tyrannical government policy

You can DOWNLOAD THE DOCUMENT HERE: https://www.fda.gov/media/...

www.fda.gov (http://www.fda.gov/)

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