Originally Posted by
op2pig
Hello,
I'm about to start the CDNUTs protocol for PFS. I took Accutuane in 1998 and then 2001 and it took quite a while to rule other causes out. I spent the last 13 years grappling with a supposedly "incurable" autoimmune condition. It's now resolved so I'm riding this victory lap to address my next health crisis: PFS!
I came across testimonials of recovery and was impressed by results and commitment.
In order to stay motivated for the marathon that lays before me, I wanted to connect and ask a few questions:
-Besides observing your subjective symptoms, did anyone track your progress via any biomarkers (lab results/hormone levels)? Tracking quarterly hormone panels will absolutely keep me motivated.
-I took Accutane in 1998 and 2001, so I am worried it will take me much longer to respond to this protocol. Is there a timeframe by which the damage is done and irreversible?
Cheers from Washington, DC!