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Thursday, February 23, 2023 5:10:52 PM
I respect that .
But IMO , Dr Recknor as Dr Kelly, didn't have enough of knowledge , and experience for the positions they accepted working for a small biotech company .
Results speak for themselves ...
Of course , FDA working with a BP , and taking legally a lot of money from them is the most important IMO !!!!
I am sure our doctors tried hard ..
No match to FDA and Dr Fauci , imo...
But when Dr Recknor designed a protocol for Brazil , I couldn't believe..
When patient is severe / critical , patient may get up to 4 doses of leronlimab , but only if they still in the hospital..
I saw my son, he was discharged from the hospital after the first injection , on 3-4 L of oxygen , but no way he will survive if he will not have few more injections on the outpatient base.
I wrote all this to Dr Recknor , plus , entire office knew my son progress , wonderful progress , from dying to a live , but with a few shots not two. .
My son treatment showed me how under-treated our CD12 patients were ...Oh , if one is severe / critical it is another miracle to survive after 2 shots , but a beautiful progress with more shots ...
And why to restrict these dying patients ????
All of them..
And at 28 days treatment having 31% mortality benefit ,above all these SOC drugs ,
when the second and last injection was done at 7 days . it was a miracle , and 82% at 14 days when drug was still in the system it is a big miracle ..
Why FDA didn't act on this miracle drug then !!!!!!
Anyway , they could do a fast study in NIH , doing something , anything except saying ,
WE will not look at SOME SUBGROUP , of dying Americans...
and as Dr Lalezari said to NIH doctors ,
"No drug in the world show 82 % signals " when the drug is in the system..
So , I have a big respect to Dr Recknor , but I don't believe he was a proper person on his position in CYDY....
All IMO.
GLTA longs.
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