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Posted On: 05/17/2021 11:48:15 PM
Post# of 148899
The FDA maybe have actually been messing with the wrong dog here.
1) Because Leronlimab is such a "disruptive miraculous drug", it has attracted sophisticated investors, some investors that have a lot of money, doctors, business owners, seasoned market players. And these guys, many, have broken their personal rules for investing, by placing higher percentages of their portfolios into CYDY, than they've ever allowed themselves to do. Energy is building as forums (and discussions in homes) bring out facts and memories of attacks and as folks come out of denial as to their losses and months of anxiety and expectations.
2) the blatant corrupt action of the FDA today (bold lies) has not only shifted millions of dollars of wealth, some on paper, some actual cash, but also has created enormous action-provoking anger, folks are furious and determined for revenge and retribution. Some of our more sophisticated, educated, financially established investors besides being furious, have huge egos, many are determined to expose the FDA and are determined more than ever, to turn Cytodyn's one drug into a global disruptive grand success.
3) the blatant corrupt action of the FDA today brought many investors angrily over to the other side of the fence, now convinced beyond doubt, that the FDA has been involved in the plots to prevent Leronlimab's success. We want our investment money BACK.
4) It appears that American corporate and bureaucratic corruption by threats and pressure, have forced the FDA to cross a line into flagrant very risky recklessness such that all of this is very likely to be exposed resulting in possibly one of the biggest scandals in American history, because huge numbers of deaths will be considered as possilby having been avoidable.
5) another reason the FDA will probably not get away with this, is because they took the biggest swing at Leronlimab a little bit too late considering activities with Brazil, India and the Phiippines. These desperate countries need and want leronlimab, and they have no therapuetic for suffering, dying criticals. Even IV administered in-patient HGEN if approved, will help only moderate to severe, no criticals, who are the ones who die.
1) Because Leronlimab is such a "disruptive miraculous drug", it has attracted sophisticated investors, some investors that have a lot of money, doctors, business owners, seasoned market players. And these guys, many, have broken their personal rules for investing, by placing higher percentages of their portfolios into CYDY, than they've ever allowed themselves to do. Energy is building as forums (and discussions in homes) bring out facts and memories of attacks and as folks come out of denial as to their losses and months of anxiety and expectations.
2) the blatant corrupt action of the FDA today (bold lies) has not only shifted millions of dollars of wealth, some on paper, some actual cash, but also has created enormous action-provoking anger, folks are furious and determined for revenge and retribution. Some of our more sophisticated, educated, financially established investors besides being furious, have huge egos, many are determined to expose the FDA and are determined more than ever, to turn Cytodyn's one drug into a global disruptive grand success.
3) the blatant corrupt action of the FDA today brought many investors angrily over to the other side of the fence, now convinced beyond doubt, that the FDA has been involved in the plots to prevent Leronlimab's success. We want our investment money BACK.
4) It appears that American corporate and bureaucratic corruption by threats and pressure, have forced the FDA to cross a line into flagrant very risky recklessness such that all of this is very likely to be exposed resulting in possibly one of the biggest scandals in American history, because huge numbers of deaths will be considered as possilby having been avoidable.
5) another reason the FDA will probably not get away with this, is because they took the biggest swing at Leronlimab a little bit too late considering activities with Brazil, India and the Phiippines. These desperate countries need and want leronlimab, and they have no therapuetic for suffering, dying criticals. Even IV administered in-patient HGEN if approved, will help only moderate to severe, no criticals, who are the ones who die.
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