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IT´S OFFICIAL. Pfizer VAXXTARDS LOSE THEIR ANTIBODIES 3 MONTHS faster than "unvaxxed infected" people!! big Israel STUDY
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[quote:Sandman1!:MV80ODg4ODk0Xzg5Mjk0ODE1XzUyQjUwN0ZC] Bitch about 8 months late! If you got one YOU Consented!!!! LOL The same day they Authorized it!! Bitch tells you this! They can only deceive you under the Emergence Use Authorization (EUA)! You should be very concerned! HEAD OF CDC CHANGES DIRECTION AGAIN. Says early vaccinations can now have serious illness [bitchute]https://www.bitchute.com/video/tISBnX85rFKP/[/bitchute] She be covering her ASS!!! They did this knowingly! They published it 8 months ago on their own sites! [face=Verdana]Suckers read the fine print![/face] The Edited Highlights you should know listed below. Please read the whole linked document/report Link Here Informed consent disclosure to vaccine trial subjects of risk of COVID‐19 vaccines worsening clinical disease https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7645850/ [b]International Journal of Clinical Practice Published online 2020 Dec 4.[/b] [b]Informed consent disclosure[/b] to vaccine trial subjects of risk of COVID19 vaccines worsening clinical disease via Antibody Dependent Enhancement (ADE). COVID19 vaccines were reviewed to determine if risks were properly disclosed. [b]Patient comprehension is a critical part of meeting medical ethics standards of informed consent to disclose the specific risk that COVID19 vaccines could worsen disease upon exposure to challenge or circulating virus[/b]. COVID19 vaccines designed to elicit neutralising antibodies may sensitise vaccine recipients to more severe disease than if they were not vaccinated. Vaccines for SARS, MERS and RSV have never been approved. irrespective of delivery method, may worsen COVID19 disease via antibody dependent enhancement (ADE). This risk is sufficiently obscured in clinical trial protocols and consent forms for ongoing COVID19 vaccine trials that adequate patient comprehension of this risk is unlikely to occur, obviating truly informed consent by subjects in these trials. The specific and significant COVID19 risk of ADE should have been and should be prominently and independently disclosed. After vaccine approval, in order to meet the medical ethics standard of patient comprehension for informed consent. A recent study revealed mediated acute lung injury in vivo in macaques infected with SARS that correlated with a vaccine elicited, neutralising antibody response. Inflammation and tissue damage in the lung in this animal model recapitulated the inflammation and tissue damage in the lungs of SARS infected patients who succumbed to the disease. The time course was also similar, with the worst damage occurring in delayed fashion in synchrony with ramping up of the immune response. Remarkably, neutralising antibodies controlled the virus in the animal, but then would precipitate a severe, tissue damaging, inflammatory response in the lung. This is a similar profile to immune complex mediated disease seen with RSV vaccines in the past, wherein vaccinees succumbed to fatal enhanced RSV disease because of the formation of antibody virus immune complexes that precipitated harmful, inflammatory immune responses. Thus, a finite, non theoretical risk is evident place vaccinees at higher risk for more severe COVID19 disease when they encounter circulating viruses. vaccine candidates, commonly exhibited ADE associated with high inflammatory morbidity. unknown variable is how long this tissue damage lasts, possibly resulting in permanent morbidity (eg, diabetes from pancreatic damage ). ADE evidence in COVID19 vaccine data risk of enhanced disease to vaccine trial participants, and it remains a realistic, non theoretical risk to the subjects. Signed consent forms from the COVID19 vaccine trials All three protocols mention the risk of disease enhancement by the vaccine, but all three list this risk last or next to last in the list of risks, risks for pregnancy and birth control (which are said to be “unknown”), risk of vaccine elicited disease enhancement as “theoretical.” Finally, in citing the risk, Pfizer and Moderna note prior evidence of vaccine elicited disease enhancement AstraZeneca form clearly discloses the specific risk of ADE, COVID19 vaccine could convert a subject from someone who experiences mild disease to someone who experiences severe disease, lasting morbidity or even death .. Medical ethics standards required that, given the extent of evidence in the medical literature reviewed above, the risk of ADE should be clearly and emphatically distinguished in the informed consent. Based on the published literature, it should have been obvious to any skilled medical practitioner in 2019 that there is a significant risk to vaccine research subjects that they may experience severe disease once vaccinated. while they might only have experienced a mild, self limited disease if not vaccinated. The consent should also clearly distinguish the specific risk of worsened COVID19 disease from generic statements about risk of death and generic risk of lack of efficacy of the vaccine. Given the strong evidence that ADE is a non theoretical and compelling risk for COVID19 vaccines and the “laundry list” nature of informed consents, disclosure of the specific risk of worsened COVID19 disease from vaccination. [/quote]
Original Message
antibodies go away much faster with Pfizer double shot than natural recovered people
very crystal clear large study
https://twitter.com/_/status/1430536332338663432
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