I spoke with a dr in the field. This field is in its infancy. They are now only documenting the PFS, no one as far as he knows has any treatment or even solid understanding of the problem.
Unfortunately, an italian study that looks at the genetic differences between patients with PFS vs those that tolerated propecia did NOT find a clue…
What is left? For us to experiment. See legendary’s case, see the progesterone folks (most promising imho) and DONATE to the pfs foundation…
The way i look at it, is we need to work hard, it s not impossible we can do it, but it will not be cracked by others… They r too busy trying to publish…