From YMB. Just listened to Sep 2 CC. Around minut

From YMB. Just listened to Sep 2 CC. Around minute 6 Nader says, "we sent an email to FDA and requested status of CYDY potential EUA request filed with them on Sept 12......decision is forthcoming" thats it. He never said we submitted Emergency Use Authorization. As mentioned here by others, this is part of the Pre-EUA submission process. FDA recommends companies have a meeting with them prior to formal EUA submission so they can determine if your drug is a good candidate for EUA. The M/M population is no one's concern right now. That would be the s/c and maybe moderate. But both MHRA and FDA requested p3 s/c interim data and further eind results to make considerations. Do some DD yall. Dont let the shorts #$%$ Fact of the matter is, if the LL wasn't working they wouldn't be in P3 with FDA or MHRA. Yes, maybe NP is to emotionally attached to CYDY, and yes they do have A LOT of pointless CCs, but the fact of the matter is, they are transparent. Why else would they have QAs with unscreened calls. They are not afraid to answer anyones questions. Unless you ask about timelines haha. But jokes aside. Be patient. Dont listen to the noise. If YMB becomes too confusing, go to Facebook or other forums without so many shorters. Do your own DD. And please read up on LL and dont just blindly follow others advice. Including mine. Listen to the CC yourself. But most importantly be patient. This pandemic isnt going away anytime soon and a vaccine will not get approved for another 6 months. The world needs LL and they will get it.