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misiu143

11/01/22 7:14 AM

#215249 RE: trding #215245

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 ..

3X Charm

11/01/22 11:51 PM

#215270 RE: trding #215245

“And I believe… he might be technically accurate “ and the tooth fairy and Easter Bunny. Give me a set of stats and I will craft a post hoc credible case for a narrative.

That is not how trials work…so Nader was not in any way accurate in how the data was portrayed, which is why the company was twice reprimanded by the FDA and had to scrub the website and issue a warning label as well.