Hi- Woman hoping for support

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Wired

Did you know that there is very, very little information available on the internet for partner's of men with Peyronie's? Yeah, I didn't either, until I needed to find it.

My boyfriend will probably be getting diagnosed on Wednesday. It's hard to imagine that anything else could be causing his pain with erection. Apparently this started about a month ago, and that's the last time I saw his penis. I don't know what it looks like at the moment, but I believe him when he says that erections hurt. (He doesn't report any curvature or hard spots, but his GP suspected Peyronie's right off the bat, and I'm pretty sure that she had more exposure to his genitals than I have in the past month.)

I have been very supportive. But, I am desperately in need of a place where I can get support, too. I can't unleash all of my feelings on him- I can't imagine how much he is worrying and upset, and I know that my feelings (which are becoming increasingly bleak) will only cause him more upset. I have no one in real life that I can talk to about this.

I've heard that there is a private womens' forum. How would I be able to post there?

james1947

Wired

Send a PM (private message) to Christine, she will guide you to the woman only board.

James
Age 71, Peyronies from Jan 2009 following penis fracture during sex. Severe ED.
Lost 2" length and a lot of girth. Late start, still VED, Cialis & Pentox helped. Prostate surgery 2014.
Got amazing support on the forum

LWillisjr

Wired,
I confirmed that have access to the Women only board "The ladies room". As James mentioned you can also send a message to board member Christine.
Developed peyronies 2007 - 70 degree dorsal curve
Traction/MEDs/Injections/Surgery 2008 16 years Peyronies free now
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