1) Do you think that there’s a slight chance that I’m having a “late” crash?
One of my side effects (puffy and swollen lips) didn’t appear until around 7 or 8 months after quitting finasteride.
It was around this time that my testicular shrinkage was at its worst.
I’m not a doctor, but although you may not have experienced a crash, i believe it may be possible that your endocrine system has down regulated somewhat since quitting finasteride.
If the result will show low T, LH, TSH, will that be considered as a crash since until lately I functioned pretty much ok?
Generally, a crash is an acute and rapid onset of PFS related symptoms.
From reading your posts, it sounds as if you have not experienced a crash, but rather a gradual decline in your health over the course of the last year.
2) What will best indicate if I’m running into pfs or not?
If you have persistent symptoms that continue for several months then this may be an indicator of PFS but you need to see a good doctor to check for possible health related problems, e.g. diabetes, testicular cancer, prostate cancer, chronic fatigue syndrome, liver dysfunction etc.
Hopefully i haven’t scared you too much but what i’m saying is you need to get checked out thoroughly by an experienced doctor.
Check the doctors section on this site and see a good doctor ASAP who can recommend the appropriate tests.
How will I know for sure that fin is the cause? It’s like I feel it is, but how will I know?
This will be dependent on the outcome of your tests.
3) The fact that I had a relatively good year after quitting - is that a positive or a negative sign?
The fact that you are having problems clearly indicates that something is wrong.
What if instead of getting better with time I’m getting worse?!
Follow the advice of your doctors.
See how it goes.
You can always come back and post here.
4) How exactly pfs treatment differs from not fin-related Hypogonadism treatment?
The treatments are similar, HCG/Clomid or Testosterone replacement therapy have been the usual treatments for PFS so far, but i’m not aware of anyone who has been fully cured.
There is medical research underway as per this thread:
viewtopic.php?f=33&t=6581
An update on this research is expected soon and will hopefully explain the mechanism/s that contribute towards PFS.
When the PFS condition is fully understood, then we should have a better chance of working towards proper PFS treatments.
5) Say I have pfs. How do I address an endocrinologist that has no idea what it is and explains to him/her the situation?
I wouldn’t mention propecia/finasteride to your doctor unless he/she specifically asks you.
If you want to provide your doctors with info on the side effects of finasteride, you could always print off some of the medical studies here:
viewtopic.php?f=33&t=6581
and show them to your doctor.
Does one of the famous American doctors who deal with it has a letter or a memo or something I can show a doctor in order that he/her will understand that fin is probably what causes my problem and that it requires special treatment? Since this syndrome considered as relatively new, I guess doctors in my country (Israel) wouldn’t believe fin can cause this.
I doubt that any America doctor would issue a memo/letter.
Over the course of the next few months, try to eat healthy organic foods.
Eat plenty of fruit and vegtables daily.
Avoid alcohol.
Avoid stimulants (including caffeine), grains (including bread and pasta) and sugar
Avoid excessive masturbation/ejaculation. Maybe once every 3 or 4 days to keep things working.
Try to get plenty of rest, at least 8 hours of solid sleep every night.
Moderate exercise regularly such as cardio, walking and light weight training.
Try to get outside regularly for plenty for fresh air.
Natural sunshine is the best source of vitamin d.
sunshinevitamin.org/