Tried finasteride three times.
I mean, REALLY tried. First attempt lasted about four months. Shrunken penis, weak erections, general feeling of lifelessness.
Stopped, waited a year, restarted at .50 every other day. Slightly better erections, lasted eight months. Then the chest pain and gyno swelling started.
Stopped again, waited another year, restarted at .25 every two days. Shrunken penis, next to impossible to get an erection, and sex became increasingly painful. Penis started curving and suspected fibrosis was beginning. Reduced to .25 every three and then four days. Lasted three months. No change in side effects so stopped. It’s been about two months now and I’ve mostly recovered.
I’ve read about people “powering through” sides on this forum. I wish I had the mental fortitude to try again but honestly, looking down at my bent penis throbbing in pain was giving me nightmares.
NW3V now, with diffuse thinning all over the top and probably heading to NW6 or NW7.
Not here to scaremonger or try to warn people away from fin. If you can take it, not experience side effects and maintain your hair…then you’re living in my dream world!!! I’m sick with envy. You’re unbelievably lucky!!!
I can’t describe how insanely frustrated it makes me to read literally anything positive related to this drug. I can’t listen to the Bald Truth Talk show now because it’s nothing but stories about it changing people’s lives and letting them maintain their hair. How ridiculous is it to get hit with both the worst balding genes and a physiology unable to tolerate the one thing that could do anything about it?
So now it seems there’s nothing to do but sit around, go bald and then spend my life savings on as many transplants as my donor hair will allow. I can’t describe how galling and depressing it’s been to drop Norwood after Norwood and not be able to do anything about it without wrecking my body.
I mean, REALLY tried. First attempt lasted about four months. Shrunken penis, weak erections, general feeling of lifelessness.
Stopped, waited a year, restarted at .50 every other day. Slightly better erections, lasted eight months. Then the chest pain and gyno swelling started.
Stopped again, waited another year, restarted at .25 every two days. Shrunken penis, next to impossible to get an erection, and sex became increasingly painful. Penis started curving and suspected fibrosis was beginning. Reduced to .25 every three and then four days. Lasted three months. No change in side effects so stopped. It’s been about two months now and I’ve mostly recovered.
I’ve read about people “powering through” sides on this forum. I wish I had the mental fortitude to try again but honestly, looking down at my bent penis throbbing in pain was giving me nightmares.
NW3V now, with diffuse thinning all over the top and probably heading to NW6 or NW7.
Not here to scaremonger or try to warn people away from fin. If you can take it, not experience side effects and maintain your hair…then you’re living in my dream world!!! I’m sick with envy. You’re unbelievably lucky!!!
I can’t describe how insanely frustrated it makes me to read literally anything positive related to this drug. I can’t listen to the Bald Truth Talk show now because it’s nothing but stories about it changing people’s lives and letting them maintain their hair. How ridiculous is it to get hit with both the worst balding genes and a physiology unable to tolerate the one thing that could do anything about it?
So now it seems there’s nothing to do but sit around, go bald and then spend my life savings on as many transplants as my donor hair will allow. I can’t describe how galling and depressing it’s been to drop Norwood after Norwood and not be able to do anything about it without wrecking my body.
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