ok i’ll bite. you will probably end up calling me delusional or throw home brew somewhere
studies will bring about an official diagnosis which will be useful for legal reasons (lawsuits, insurance, disability etc)
as for cure, lets be realistic here.
even if they could patent the cure into a pill we would have to take everyday cause that’s how pharma works…
no company will make it because there’s no money in it
even if they could patent the cure into a one time injectable shot if that’s all we needed to reset our receptors…
no company will make it because there’s even less money in it
that means we will have to rely on existing medicine to treat out condition. unfortunately, effects of pfs can be progressive (aka rapid premature aging) for the worst affected. there’s no treatment for aging. well there is but we dont really respond to it (TRT+HGH).
existing medicine cannot treat tinnitus, peyronies, visual snow, skin thinning, shrinking dicks, muscular atrophy, etc. these conditions exist outside PFS and have been studied for decades.
so what does this mean? enroll in studies. then taper your expectations. no one here is speculating about anything. medicine is backed by greed and money and we’re billions short