COVID Emergency September 2023? Where is the Emergency POTUS Biden to warrant the FDA's new EUA for XBB.1.5 (Omicron) booster that MISMATCHES the BA.2.86 or EG.5 or FL sub-variants? Dr. Marks?
by Paul Alexander
Biden ended COVID (fraud PCR-driven 'false-positive' non-pandemic) EMERGENCY on May 11th 2023, so why has FDA issued a new mRNA booster 'emergency use authorization'? But there is NO emergency NOW!
What in good heavens is going on in the Biden administration and the FDA? Including the corrupted CDC? What? The FDA has moved on September 11th 2023 to approve an EUA for a new booster when there is absolutely NO need societally. Where is the emergency? Why the EUA? What data is the FDA and Biden administration looking at that we have not seen? Then stupid inept corrupt agencies like Health Canada and PHAC, and SAGE etc. will follow same? Their societies must ask for the data to back up any move to approve these XBB.1.5 boosters, even in the high-risk elderly.
There is no need! The vaccine failed with negative effectiveness and the COVID mRNA vaccines are driving the vaccinated to become infected. Did you read that?
Did the idiots, the morons at FDA and CDC and NIH and PHAC and Health Canada not read the seminal research by Shrestha et al. showing a dose-response, that the more doses you took, more boosting, the dramatic increased risk of infection, re-infection?
The potent impact of natural immunity, prior infection on re-infection risk?
Did the clowns, the specious intellectually sloppy and lazy fools at CDC and FDA care to read the seminal Iceland research by Eythorsson et al. showing increased risk of re-infection with more doses of mRNA vaccine?
‘The probability of reinfection increased with time from the initial infection (odds ratio of 18 months vs 3 months, 1.56; 95% CI, 1.18-2.08) (Figure) and was higher among persons who had received 2 or more doses compared with 1 dose or less of vaccine (odds ratio, 1.42; 95% CI, 1.13-1.78).’
Did these FDA, CDC, NIH, Health Canada, SAGE, PHAC et al. moronic dangerous and reckless idiots, these so called ‘scientists’ and regulators, care to read the potent statement findings by Chemaitelly et al. that natural exposure immunity conferred far greater protection than that from the mRNA vaccine, regardless of variant? Did they?
‘Previous natural infection was associated with lower incidence of SARS-CoV-2 infection, regardless of the variant, than mRNA primary-series vaccination.’
And so between now bringing a MISMATCHED XBB.1.5 booster for the fall that is not needed, when there is no public health emergency, that will drive viral immune escape and more variants, coupled to the death path our vulnerable people are placed on with the hospital ‘COVID protocols’ of FALSE POSITIVE PCR testing, sedation (midazolam, diamorphine), dehydration, malnourichment, DNR orders, no antibiotics when it is needed, Remdesivir (kidney and liver toxic, failed Ebola drug), other toxic drugs, isolation that kills, and then put on a ventilator that kills, then what are we setting our people up for this winter? More ‘KILLING FIELDS’?
Do they at the CDC and FDA even care about the science, and what the societal implications of repeat vaccine boosting are, using a vaccine that would not and cannot and never did ‘sterilize’ the COVID virus (stopped infection, replication, and transmission)? That results in inducement of non-neutralizing vaccinal antibodies? Then there will be obvious viral immune escape and Natural (Darwinian) selective pressure when the vaccine-induced antibodies do not match the circulating dominant variant. We have seen this since the COVID vaccines were rolled out! The mRNA vaccines have driven the emergence of sub-variant after sub-variant and Peter Marks knows this, they all know this, CDC, NIH, FDA etc. and now FDA is approving boosters when the society does not need it. When infections etc. are flat and the circulating variants are non-lethal. No doubt we always strongly protect the high-risk vulnerable in our society.
So is there a dark agenda that was always at play and now they at CDC amnd FDA just don’t care anymore. They are operating unchained, unconstrained, devoid of reason. Dr. Peter Marks must be called to congress and under oath, defend why an EUA for XBB.1.5 booster is needed now (XBB.1.5 is for the Omicron sub-variant spike antigen), given there is NO emergency, no COVID emergency. Given XBB.1.5 is circulating the drain as to dominance and BA.2.86 and EG.5 are the present dominants. Other variants are rising too. Then of course there will be original antigenic sin, immune imprinting/fixation effects, viral immune escape, and antibody-dependent enhancement of infection (ADEI) and of disease (ADED). The FDA in this specious unscientific move runs the risk of driving the emergence of more variants that are not only infectious, but could be more virulent and lethal, threatening humanity. It is as if the Biden administration and FDA wants variant after variant to emerge and thus this will continue for 100 years.