CDC Pulls PCR Tests Because they Can’t Differentiate Between COVID and Flu; Mainstream News Silent

[link to californiaglobe.com (secure)]

The Center for Disease Control is finally pulling the flawed PCR tests because they can’t differentiate between COVID and the Flu. But it appears California news outlets are too busy fear mongering the Delta Variant to notice or care.

source also: [link to www.cdc.gov (secure)]

"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. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives."

The Globe also reported on three doctors in Contra Costa County who were concerned with the excessive COVID PCR testing leading to high numbers of false positive results. Dr. Michael deBoisblanc, Dr. Pete Mazolewski and Dr. Brian Hopkins explain:

“PCR testing has proven to be seriously flawed when used to track disease prevalence, and the number of false positive tests has contributed to fear, panic and unnecessary quarantine of many. The peer review of the original Corman-Drosten PCR paper points out the serious flaws and conflicts of interest in the original article describing the PCR test (Peter Borger Et al., 11/27/2020). This paper is the basis for the PCR test used in the United States. On January 21, 2021 the World Health Organization published direction on the interpretation of a positive PCR test. They now caution about calling a test “positive” without symptoms, a confirmatory test, and physician oversight. They also cite the serious problems with high cycle thresholds leading to a high number of false positives. In short, they agree with what we argued last month.”

“With this information, your COVID positive case numbers are highly suspect and using this data to determine which tier the population falls into has been, and continues to be, completely unreliable and arbitrary. Our recommendation is to move forward quickly with rapid antigen testing. These tests are less expensive, and more appropriately sensitive to detect people with active, contagious disease.”