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Re: trding post# 215245

Tuesday, 11/01/2022 7:14:08 AM

Tuesday, November 01, 2022 7:14:08 AM

Post# of 232956
Trding , Leronlimab is a great medicine and without one serious side effect …
I witness my family member with acute covid , after HCQ , after ivermectin and prednisone at home , and all the vitamins and minerals , oxygen came down to 72-75 %
In the hospital on IV dexamethasone , and after Tocilizumab treatment there was no improvement , rather getting worse , on high flow oxygen ( step before the ventilator )

And then boom , 2 hrs after first Leronlimab injection I got a text , I am starting to feel better , my oxygen is improving , 4-5 hrs later high flow oxygen was changed to regular ..

I understand why some don’t believe my story , most probably if I will not witness this myself I will also not believe ..

And when someone saying , oh this is anecdotal , I am getting upset , like our patients in video Samantha is saying , I was dying and I know Leronlimab saved my life ..but her doctor said , yes look like Leronlimab MAY have something to do with her recovery .
May ????
But patients know the best in this situation what saved their lives ..

Doing studies is not as accurate as these anecdotal cases often , for egz how one may predict patients reaction , will he need 2 or 4 or maybe 6 doses of drug ..my family member needed more then 2 doses ..he was better , but he will not survive with 2 ..

This can be only evaluated while patients are treated , and not on the paper , and especially what FDA did to our CD12 .

All doctors evaluated that severe / critical patients will need 4 doses ,
Dr Patterson has results from our Montefiore patients showing very high Rantes in a very sick persisting above 2 weeks , and Rantes , he observed going down as patients is improving , he felt that 2 injections for these patients at 0 and 7 days is not enough ,

But what FDA did , they approved toxic Remdesivir , but changed Cydy protocol from 4 injections to 2 only , refusing to change .
And as dr Lalezari said , if Cydy will insist little more , FDA was ready to give them clinical hold .
FDA is bullying small biotechs long enough , and everyone knows what they doing , and why ..

Why would they do that to a very safe drug , and dying patients ?
drug used already in HIV every week for 7 years without one serious problem ??

Why to restrict patients on the ventilators and ECMO to 2 injections only , if not to sabotage our study .

Yes , all this should be investigated very carefully , but who will do it ???
As the FDA executive said in the Veritas video ..
vaccines must be mandated ..

And people still dying daily , and still not one good drug is approve for immune stage of the disease ..
And still Remdesivir is given to everyone admitted to the hospital , regardless of the stage of covid , and now they trying for long Covid , I am sure dr Fauci will conduct the study , results will be “ trending “ and drug approve ..

All imo

GLTA longs ..
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