Peyronies Society Forums

Read This First => Introduce Yourself => Topic started by: she on October 13, 2012, 08:53:17 PM

Title: She - Introduction
Post by: she on October 13, 2012, 08:53:17 PM
HI there, and thank the lord for this forum. My partner possibly has Peyronies Disease and we are going fine with it BUT I MISS INTAMACY!! and of course, what do you say and how to say it.  It doesn't really bother me to not have full on sex, but the other bits that have always been a part of that have gone with it. I have tried to discuss but it is like ok then nothing goes forward.  So, thank you , just knowing that others feel the same, and that there are options. I can keep going for awhile, and it is all new (about a year now) so we are still stumbling along and feeling our way around this.
Title: Re: Re: Breaking new ground!
Post by: Norm on October 13, 2012, 09:58:22 PM
She


I am really sorry for your difficulties. Is there any chance you can get your partner to read and participate on this forum? I know it would help him. Us guys put a lot of stock in our being able to perform sexually. When that ability gets derailed, so does our confidence as a man. There is help here. If he won't come here and try, then maybe you can at least be his liaison to this resource. Has he been to a doctor about it? That is the first step. It needs to be confirmed by a professional to rule out other possibilities that might be readily treatable. Do what you can to encourage him to try. Stay in touch here. If he won't read, then you must. And remember, we tough guys get kinda fragile when our manhood is impugned. I wish you the best.
Title: Re: She - Introduction
Post by: james1947 on October 14, 2012, 05:38:48 PM
She

I am proposing you to read the treatment boards to understand better the treatments for this disease.
I would like also to say that have a "Woman Only" board that is visible and accessible to woman only.
The moderator of the "Woman Only" forum is Christine, you may send her a PM.
She is also the moderator of:
Women Speak Out about Peyronies Disease - PUBLIC Forum - PDS - Peyronies Society Forums (https://www.peyroniesforum.net/index.php/board,40.0.html)
It may be usefull for you also to read the above board

James