Seeking input from Peyronies Disease partners

[RdubaU]

Firstly. I hope it's okay to post on this board as a man (I'm not sure of the rules here) but I am seeking feed back from women to help with my own considerations about when to consider treatments like surgery.

My question is, at what point in your partners Peyronies Disease progression did you begin to find sex with them worse?

I hear a lot of specific numbers about centimeters lost, girth lost, and degree of curvature but frankly the only metric that matters to me is whether or not my partner is satisfied.

Would anyone be willing to offer insight on what the size/shape/Bend was was like when it impacted your satisfaction while being intimate with your partner.

I'm hoping to decide ahead of time what level of deformity I should begin taking more drastic measures ie surgery.

[Stabler]

Hello RdubalU

I can tell you that in my own experience, I dated a man that was unable to become erect at all. He had had Peyronie's for years before finding out what it was. We had a very active and fulfilling sex life for bother he and I. We found other ways to satisfy each other orally and with outer hands  and toys. He was up front with me from our first date letting me know about the Peyronie's.

My advice to you would be do the research on the type of treatment you are considering. Don't put yourself in a position literally and figuratively that you are causing yourself physical pain. Communicate with your partner so they know to tell you if sex is causing them pain so that you can adjust your positions.

I can tell you that my partner chose to go with Xiaflex injections and it worked very well for him but it was a long process.

Stabler