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July 26th, 2021 
Awake Goy 
The CDC quietly announced last week that it was withdrawing its request to the FDA for Emergency Use Authorization (EUA) of the 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel — the assay first introduced in February 2020 for the alleged detection of SARS-CoV-2, aka “COVID-19”, according to a new report by VaccineImpact:
Most of the public is probably unaware that similar to the current COVID-19 injections that are not yet approved by the FDA, but only given Emergency Use Authorization, so too the hundreds of diagnostic tests that supposedly detect COVID-19 are also NOT approved by the FDA, but only authorized via an EUA.
What is the reason the CDC is withdrawing its EUA request for the Real-Time RT-PCR Diagnostic Panel?
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. (Source.)Caitlin McFall, writing for Fox News, is the only one in the corporate media I could find that even reported this, and the few reports I found in the Alternative media so far have been mostly inaccurate.
The Centers for Disease Control and Prevention (CDC) urged labs this week to stock clinics with kits that can test for both the coronavirus and the flu as the “influenza season” draws near. The CDC said Wednesday it will withdrawal its request for the “Emergency Use Authorization” of real-time diagnostic testing kits, which were used starting in February 2020 to detect signs of the coronavirus, by the end of the year. “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 agency said. The U.S. has reported more than 34.4 million cases of the coronavirus since the pandemic began in 2020 and more than 610,000 deaths. But while cases of COVID-19 soared nationwide, hospitalizations and deaths caused by influenza dropped. According to data released by the CDC earlier this month, influenza mortality rates were significantly lower throughout 2020 than previous years. There were 646 deaths relating to the flu among adults reported in 2020, whereas in 2019 the CDC estimated that between 24,000 and 62,000 people died from influenza-related illnesses. The CDC urged laboratories to “save both time and resources” by introducing kits that can determine and distinguish a positive test for the coronavirus and flu. (Source.)So there you have it. The CDC just basically admitted that many of the COVID-19 cases this past year could not be distinguished from “flu cases.” No wonder flu cases decreased to zero in so many places.
How is it possible that FDA already has approved diagnostic tests that can detect COVID? — for this to be the case, such tests would have already had to have gone through rigorous testing — and there hasn’t been enough time for that — especially considering that these new tests must have the ability to detect this new, emerging “variants.”
And it is completely misleading to even call the PCR a diagnostic “test” — it is not a test but rather a method to amplify the quantity of fragments of DNA for the purposes of research.
The CDC/FDA cabal chose the PCR as the foundation of the “pandemic” because its results are so easily manipulated to conform to whatever agenda they happen to be pushing at the time.
So basically everyone who would have been diagnosed with the seasonal flu for the last year and a half have been falsely diagnosed as “COVID-19” infections — and no one in the mainstream media challenged this obvious absurdity.
This is how they magically transformed a normal flu season into a “deadly” worldwide “pandemic” that allegedly killed “millions” — leading to the shutting down of the world economies and ushering in deadly, untested genetically modifying delivery systems masquerading as normal “vaccines.”
They have never isolated this so-called “COVID” virus — and without a virus, they cannot have a reliable test to diagnose the presence of a non-existent virus.
New legislation is being introduced to Congress that will give the government the ability to censor and shut down any website or social media source that promotes “disinformation” about their “pandemic.”
Of course, by “disinformation” they mean mentioning an facts that contradict their transparently fraudulent “science” to justify their draconian lockdowns and mandatory “vaccines.”
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