Since it is April Fools day, I thought it fitting
Post# of 153822
(Total Views: 537)
Posted On: 04/01/2021 8:03:16 AM
Since it is April Fools day, I thought it fitting to ask everyone a question. What will be the next fiasco to delay LL from saving lives? Will it be a blantant rejection from the FDA? Will they try to bleed us of cash through additional trials? Will they decide all therapuetics given by shots are now illegal because needles are sharp and can be used to stab people?
How will they manipulate the rules to keep Americans from being helped by LL while bending the rules to give inferior drugs unwarranted approval?
This is actually a fun exercise and is a way to reduce the frustration with the games the FDA is playing with CYDY.
Another point that is interesting to observe is how much BS can the government get away with?
So many people have suffered needlessly from this virus. It is blatantly obvious that saving American lives by any means neccesary is not their concern.
This in turn leads to another fun activity to watch, how much covering up will mainstream media and social media perform in an attempt to keep people from learning about what is happening right under their noses?
With all this being said I am going to give my best guess at the next FDA excuse for keeping lives from being saved...
My kick the can down the road theory is in fact that the FDA outlaws needles which means we will have to make LL in a pill form, which will then require all new trials for LL at FDA mandated dosing requirements and intervals.
12 months later, when we finally jump through all the trial hoops and are still proven to be the most effective and safe therapeutic in existence, and after we have shown stat significance and fashioned our trials to be FDA BS proof, the FDA will then say that LL can not be distributed in pill form because pills present a choking hazard. You see 1 out of every 35,000,000 US residents die from choking on pills each year and it is the FDA's duty to protect the US citizens and keep them alive. Therefore we will not recieve approval.
All of this would be a funny April fools day joke if it was not actually looking more and more likely that the FDA would try to pull this kind of shit if it meant giving more time for BP to develop a competing therapeutic...
How will they manipulate the rules to keep Americans from being helped by LL while bending the rules to give inferior drugs unwarranted approval?
This is actually a fun exercise and is a way to reduce the frustration with the games the FDA is playing with CYDY.
Another point that is interesting to observe is how much BS can the government get away with?
So many people have suffered needlessly from this virus. It is blatantly obvious that saving American lives by any means neccesary is not their concern.
This in turn leads to another fun activity to watch, how much covering up will mainstream media and social media perform in an attempt to keep people from learning about what is happening right under their noses?
With all this being said I am going to give my best guess at the next FDA excuse for keeping lives from being saved...
My kick the can down the road theory is in fact that the FDA outlaws needles which means we will have to make LL in a pill form, which will then require all new trials for LL at FDA mandated dosing requirements and intervals.
12 months later, when we finally jump through all the trial hoops and are still proven to be the most effective and safe therapeutic in existence, and after we have shown stat significance and fashioned our trials to be FDA BS proof, the FDA will then say that LL can not be distributed in pill form because pills present a choking hazard. You see 1 out of every 35,000,000 US residents die from choking on pills each year and it is the FDA's duty to protect the US citizens and keep them alive. Therefore we will not recieve approval.
All of this would be a funny April fools day joke if it was not actually looking more and more likely that the FDA would try to pull this kind of shit if it meant giving more time for BP to develop a competing therapeutic...
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