considering implant
Posted: Wed Mar 12, 2014 7:38 pm
Hi all-
53 years old. ‘Diagnosed with Peyronies about 3 years ago. Curved downward. At first, there were no other difficulties… a little loss of rigidity, but still could function normally. In the last 6 months, other ED signs have appeared: not always able to get an erection, or not always able to sustain one. I’ve been using the daily Cialis which worked at first, but now is hit & miss with its effectiveness. The other non-daily meds seemed to just not work for me.
Most recently, I’ve also had problems with Premature Ejaculation. Put those issues all together and I’m a mess. It’s frustrating enough for my wife that I’m not sure she even wants to try having sex again until we figure something out.
My family doctor sent me to a urology center where I found a guy that specializes in treatment of PD, ED and Urological prosthesis. I’ve met with him twice. He’s basically given me two options- injections or implant. The injections he said may work fine, but could also make things worse because of the PD- the increased rigidity combined with the curve could make intercourse really difficult. I’m also not crazy about injecting myself, and the lack of spontaneity is a concern.
So… I’m leaning toward an implant. The success rate & knowing that this appears to be the one option that will address all my issues (or at least make the 3rd issue a non-issue) make this pretty attractive. I have decent insurance, so it won’t kill me financially.
I guess I’m looking for a few thoughts (I know that I have to make up my own mind though!). Am I rushing into this? Should I really give the injections some serious thought?
Also- if you’ve had the implant done- how long did you need to stay home from work? (I work at a desk in a private office). What did you tell family, friends, co-workers? I’ve considered confiding in my best friend, but there’s no turning back from opening that door… I’m not sure what to tell my boss when requesting time off for work.
It’s been good to find this forum & realize I’m not alone. Any tips, advice, cautions, encouragement welcome.
Thanks.
53 years old. ‘Diagnosed with Peyronies about 3 years ago. Curved downward. At first, there were no other difficulties… a little loss of rigidity, but still could function normally. In the last 6 months, other ED signs have appeared: not always able to get an erection, or not always able to sustain one. I’ve been using the daily Cialis which worked at first, but now is hit & miss with its effectiveness. The other non-daily meds seemed to just not work for me.
Most recently, I’ve also had problems with Premature Ejaculation. Put those issues all together and I’m a mess. It’s frustrating enough for my wife that I’m not sure she even wants to try having sex again until we figure something out.
My family doctor sent me to a urology center where I found a guy that specializes in treatment of PD, ED and Urological prosthesis. I’ve met with him twice. He’s basically given me two options- injections or implant. The injections he said may work fine, but could also make things worse because of the PD- the increased rigidity combined with the curve could make intercourse really difficult. I’m also not crazy about injecting myself, and the lack of spontaneity is a concern.
So… I’m leaning toward an implant. The success rate & knowing that this appears to be the one option that will address all my issues (or at least make the 3rd issue a non-issue) make this pretty attractive. I have decent insurance, so it won’t kill me financially.
I guess I’m looking for a few thoughts (I know that I have to make up my own mind though!). Am I rushing into this? Should I really give the injections some serious thought?
Also- if you’ve had the implant done- how long did you need to stay home from work? (I work at a desk in a private office). What did you tell family, friends, co-workers? I’ve considered confiding in my best friend, but there’s no turning back from opening that door… I’m not sure what to tell my boss when requesting time off for work.
It’s been good to find this forum & realize I’m not alone. Any tips, advice, cautions, encouragement welcome.
Thanks.