So…. Let’s recap for all the people who still
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1. The FDA writes a hit piece, but refuses to tell us who the author was, even when we go through the proper channels.
2. The FDA attempts to remove our video from YouTube, by using lobbyist from Google to do their dirty work. When we go thru the proper channels to take a look at the emails, they claim they have no record of any emails on the subject.
3. In 2018, Amarex is purchased by a large company and all of a sudden their data collecting becomes sloppy and they make elementary errors and when they are told exactly what needs to be corrected, they decide not to comply.
4. This one is my opinion…. Why the hell does the FDA make us wait 6 months to start our next LH trial when US citizens are living with horrible physical conditions which leronlimab has been shown to improve.
5. Here’s another one…. FDA tells CYDY to stop compassionate use in the US so we can focus on finishing our trials, even though highly recognized doctors are writing papers on the amazing results they are observing when their patients are given leronlimab.
6. Just remembered, the FDA tells us to use 2 doses on our patients instead of 4 like we asked for but let’s make the primary endpoint day 28.
7. FDA tells us that the DSMC checked in on our data and everything looks great… don’t change a thing.
These are 7 instances I can recall while I’m sitting here and I’m starting to get fired up that no one is being held accountable for dicking us around for years while citizens have died and the only therapy they approve is remdesivir, which I guarantee killed more people than it saved. Something is terribly wrong here and I have a feeling the our heavy hitting law firm wants answers to these questions. I hope they get them, and I hope heads roll when people find out how corrupt the FDA has been throughout this pandemic!!!!!!