And our drug won't get approved unless doctors and nurses and the media and Govt officials know about it. I say go after every bit of attention.

I have always said go after as much media attention as you can get because NOBODY KNOWS ABOUT LERONLIMAB. Investors raising a stink didn't bring on the FDA letter, doctors talking about, perhaps, but the real thing was when CYDY moved into PI, India and Brazil and out of USA control, then came the letter. Remember Big Pharma/FDA had been trying to block CYDY at every turn using fake law suits, stock shorting, attack articles from AF, etc., etc, etc.... To think that investors complaining caused a hit letter after months and months of hits, come on. Our boards were full of bashers, and what an odd thing to bash a drug that was trying to save people. Who would do that? Investors complaining had very little to do with the forces behind that letter.

I think we will eventually find that someone from Gilead was "helping" advise CYDY on the CD12 trial and was all along slow walking everything, blocking and making trial suggestions to help us fail. That person probably wrote the letter as well.