Detecting Cold and Flu
August 4, 2021
A new document released by the U.S. Food and Drug Administration (FDA) admits that the PCR test are detecting the common cold and flu: worldwide PCR testing protocol was fabricated using human cells combined with common cold virus fragments because they had no (and to date there are no) physical samples of the SARS-CoV-2 “covid” virus available.
Sincere thanks to NaturalNews
“I know your works, your toil and your patient endurance, and how you cannot bear evil men but have tested those who call themselves apostles but are not, and found them to be false” (Revelation 2:2)
Articles by NaturalNews
1) In a shocking revelation, 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 FDA document, available from the FDA.gov website, is entitled, “CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel.” The document astonishingly admits: “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 and viral transport medium (VTM) to mimic clinical specimen.”
In other words, 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. The PCR tests are then instructed to look for these genetic sequences obtained from the fabricated digital libraries, meaning the entire scheme is junk science circular logic with no basis in physical reality.
WHY ARE THERE SEEMINGLY NO CERTIFIED REFERENCE MATERIALS FOR COVID AVAILABLE TO LABORATORIES FOR INSTRUMENT CALIBRATION?
I am the founder and owner of an analytical laboratory that routinely conducts quantitative analysis of food contaminants, producing high-precision analysis results for pesticides, herbicides and heavy metals. In every case where we conduct lab analysis, we calibrate the instruments against known physical samples called “external standards” or “certified reference materials.” (CRM)
Any lab can purchase CRMs for mercury, arsenic, glyphosate and even salmonella. … Labs can purchase those reference materials and use them to calibrate their instruments, making sure their analysis is traced back to physical, real-world samples of a purified material. These CRMs, in turn, must be NIST-traceable in order to confirm their origin and authenticity. All CRMs are therefore labeled with lot numbers and expiration dates.
While labs can purchase reference materials for microbes, heavy metals, pesticides, etc. — all physical materials — I have searched far and wide and have not been able to locate any certified reference materials for SARS-CoV-2 or even a weakened, non-viable version of it. As far as I can tell, there appear to be no physical specimens of isolated covid viruses available for instrument calibrations and testing protocol quality control.
To be clear, I’m NOT saying that viruses don’t exist, and it’s quite clear that the Wuhan Institute of Virology colluded with Fauci, Daszak, the NIH, Baric and others to develop a weaponized spike protein. But the spike protein is NOT a virus by itself. It’s simply a toxic nanoparticle that can be synthesized in quantity and then either dumped on cities or added to vaccines and injected into people via immunization protocols. …
In essence, if “covid-19” is a real virus that can be isolated, why are there apparently no physical reference materials to calibrate laboratory instruments for covid detection? And why were no such materials used in the development of the FDA-approved, CDC-endorsed PCR testing protocols?
CDC PULLS ITS OWN FRAUDULENT COVID PCR TESTING PROTOCOL, IMPLYING IT CANNOT DIFFERENTIATE BETWEEN COVID AND INFLUENZA
What adds to the mystery in all this is the fact that the CDC just issued a “laboratory alert,” announcing their intention to withdraw the faulty PCR testing protocol by the end of this year. As part of their announcement, they implied that the current PCR test — the same one the FDA mentioned above, which was developed without any physical covid samples for calibration — cannot tell the difference between influenza and covid.
From the CDC document: “In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test. CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses.”
Why might it be important to differentiate covid from influenza? Because, as it seems, influenza cases nearly disappeared in 2020 as influenza was re-labeled “covid” due to the faulty testing. “Percentage influenza positivity decreased by 64% (p = 0.001) and estimated daily number of influenza cases decreased by 76% (p = 0.002) in epidemiologic weeks 5–9 of 2020 compared with the preceding years,” reported the CDC in 2020.”
In essence, the medical establishment simply took all the people who would normally be diagnosed with colds and the flu, and shifted them into the “covid” category in order to push a covid mass hysteria narrative that would drive people into vaccines. The vaccines, then, were formulated with spike protein toxic nanoparticles to cause the “delta” panic wave, which is largely occurring among vaccinated individuals. …
The CDC has just published a science document that confirms the entire scam. … It’s entitled, “Outbreak of SARS-CoV-2 Infections, Including COVID-19 Vaccine Breakthrough Infections, Associated with Large Public Gatherings – Barnstable County, Massachusetts, July 2021” and it shockingly admits that 74% of infections occurred in fully vaccinated (double dose) people: “During July 2021, 469 cases of COVID-19 associated with multiple summer events and large public gatherings in a town in Barnstable County, Massachusetts, were identified among Massachusetts residents; vaccination coverage among eligible Massachusetts residents was 69%. Approximately three quarters (346; 74%) of cases occurred in fully vaccinated persons (those who had completed a 2-dose course of mRNA vaccine [Pfizer-BioNTech or Moderna] or had received a single dose of Janssen [Johnson & Johnson] vaccine ≥14 days before exposure).”
2) 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 of the Chinese virus, but rather what appears to be genetic material from a common cold virus. Since the (Chinese virus) in any of its “variant” forms has yet to be properly isolated, the FDA instead used regular cold/flu viruses to produce PCR tests – meaning everyone who tests “positive” for Chinese germs is actually just testing positive for the seasonal flu.
This would, of course, explain why the flu nearly disappeared in 2020, as everyone who got sick was assigned a “covid” diagnosis. Many were saying this from the beginning and being called “conspiracy theorists,” but now the FDA is fessing up to the truth that this whole thing was a scam all along.
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 the (Chinese virus), and this is the smoking gun.
Another revelation in 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 as part of the plandemic narrative, and it is all revealed in the document.
What this all proves is that the plandemic narrative, as it was spread over the past year and a half, is contrived and false. What people are truly testing “positive” for remains unknown, or is just the common flu, because the tests are inherently fraudulent. If more people would simply take a closer look at the facts, perhaps we could put a stop to the government’s vaccine genocide agenda, which aims to forcibly vaccinate everyone against their will under the cover of a public health “emergency.” … Especially with regard to children, what the government is pushing using these fraudulent PCR tests as backing is nothing short of genocide.