Any other dudes with eds have the skin on their penis rip from friction? I know women get tears down there all the time but Ive never heard men with eds talking about it.
I also get friction burns on my penis extremely easily.
Anyone else or am I really all alone?
New research
I get really bad kidney stones. They aren't eds related, however Everytime they go inside me to deal with the stones, something gets really screwed up with my nerves down there.
After my most recent kidney stone procedure, my orgasms now start in my lower back after penile stimulation. They are much more intense in my lower back now then anywhere else on my body.
My urologists eyes got really wide and just said "umm that sounds like an odd eds nerve thing. I don't know what to say about that" they then sent me out for a CT that came back completely clear.
I'm mostly just venting, but if anyone else has a really weird experience like this id love to hear it.
I have heard much about pelvic pt for women and issues with constantly needing to pee. Does this work for men as well? Officially diagnosed with HSD, male 53, I have to pee every hour and my doctors want me to literally double my water intake. Thinking about asking for a pelvic pt specialist, but does that work for men or just women?