根据FDA公开的资料，PCR试剂的检测指标采用的是普通flu病毒。这引出了不少问题。
1，得covid的人，鼻内会出现flu病毒蛋白
2，得flu的人，PCR检测会是阳性，自动被归类成covid病人。这解释了为什么去年冬天"没有flu".
3，目前检测covid的最主要手段是PCR。但是，PCR阳性的所谓covid，其中有数目不详的flu.
4，目前所谓的得过covid之后重复感染的病例，有可能是：第一次是flu第二次还是flu; 第一次是以covid第二次还是covid; 第一次是flu第二次是covid; 第一次是covid第二次是flu. 具体是什么情形，按照现在已有的检测手段，科学界和医学界似乎没有办法确认。
5，实际上的covid染病数量肯定比公布的少。因为公布的是以PCR为基准，其中包含了flu病例。至于少多少，这是一个未知数。也许可以用2019年以前历年flu病例数量估算。
6，flu也是会死人的。所以，公布的covid死亡人数，其中包含了flu死亡人数。至于有多少死于真正的covid有多少死于flu，也是一个未知数。也许也可以用2019年以前历年flu死亡数量估算。
7，在covid出现以前，对flu的死亡原因归类比较合理。比如，横穿马路被车撞死的，如果当时患flu, 不会被归类为因flu死亡。这一点和covid很不一样。CDC的covid死亡人数包含了PCR阳性但是死于物理原因的。
8，用于治疗covid的有效药物ivermectin, 也许同时可以用于治疗flu.
Performance characteristics of these extraction platforms with 2019-nCoV (SARS CoV-2) have NOT been demonstrated.
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Equivalence and performance of the following extraction platforms were demonstrated with the CDC Human Influenza Virus Real-Time RT-PCR Diagnostic Panel (K190302) and based on those data are acceptable for use with the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel.
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:
“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.”
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 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: