Chronic Pelvic Pain Syndrome

I suffered from severe pelvic pain before my hysterectomy in March. I can kind of understand. If you want to chat feel free to send me a message anytime.

~Angel

I just came across this, and I'm new to this site. But I completely understand. I have endometriosis, PCOS and pelvic nerve damage. I can relate. If you ever want to talk, I would love to. I'm so sorry you have to deal with this :(

I have been a CPP sufferer for 26 years and I have just finally come to the treatment that may be the one to bring relief. So far I have gone from an average 7 pain a day to about a 3. I'm beginning to wean off meds and am excited to be able to have intimacy with my husband without pain for the first time in our 23 year marriage. There is hope. At times I believed there was none, and my life would be pain and meds and doctors who can't help. My heart breaks for those of you who know that suffering. If I can offer any encouragement or hope or suggestions to try, that is why I'm here. I think I've tried it all. I've diagnosed myself multiple times because doctors just don't know. Thank God for the internet. I want to offer hope.

this thread is old but I want to give HOPE to all those suffering from chronic pelvic pain, which is something I also suffer from & struggle with daily.

You CAN survive. You CAN thrive. You CAN get through today even with the pain. You CAN live through the pain.