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I think you are intentionally pretending you don't get it. The results didn't show a 95% difference; that's the 'fake' part. They decided what percentage they needed and back calculated to know how many positives they needed. Supposedly, they did it repeatedly for 28 thousand people using an inaccurate test with results which are almost random - an impossibility unless they faked the data.
“I think you are intentionally pretending you don’t get it. The results didn’t show a 95% difference; that’s the ‘fake’ part. They decided what percentage they needed and back calculated to know how many positives they needed. Supposedly, they did it repeatedly for 28 thousand people using an inaccurate test with results which are almost random - an impossibility unless they faked the data.”
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The meaning of your above words are almost incomprehensible to me.
Do you understand that the LAB virus testing was done when a trial participant reported feeling SYMPTOMATIC? Feeling symptoms did not mean they had COVID-19. They could have had a cold or other infection. The lab testing was to determine whether they had the COVID-19 virus or not.
Do you understand that ALL the trial participants DID NOT KNOW WHETHER THEY HAD RECEIVED A PLACEBO OR AN ACTUAL VACCINE? Neither did ALL the people giving the shots know who got what shot. That’s what “double blind” means.
Do you understand that the clinical trial workers (to whom the trial participants reported that they felt symptoms) DID NOT KNOW WHETHER AN INDIVIDUAL TRIAL PARTICIPANT REPORTING SYMPTOMS WAS IN THE PLACEBO GROUP OR IN THE ACTUAL VACCINE GROUP. These workers were also “BLIND”. Every time a trial participant reported symptoms, a nasal swab sample was taken to be sent to the lab.
The LAB processing the nasal swabs DID NOT KNOW WHICH GROUP (PLACEBO OR VACCINE). The LAB and its workers were also “BLIND”.
The whole purpose of this BLINDING was to eliminate the possibility of INTENTIONAL OR UNINTENTIONAL BIAS OR CHEATING.