5 Years with Peyronies suffering

[goawaypeyronies]

Hi everyone,

I have been struggling with peyronies since 5 years, Have been visiting doctors since day 1 yet no hope.

I got peyronies during covid due to excessive masturbation and it's still horrifying me as its increased a lot.

I have got peyronies on the ligaments of my penis - on the left and the right and probably developing on the under side too, and it goes way down till the anus. Where the ligaments attaches to the below muscles.

I have down ESWT got no response, lately did vacuum therapy got fantastic results - revived by erection penis to 6.5 inches and then it activated more fibrosis and now back to 5.5 inches. Traction hasn't been also helping. Also taking multiple supplements didnt work.

The doctor says we won't d surgery as you are really young. 32  years, we'll try all the method for reducing inflammation

Can someone help me? Been psychologically affected a lot with it. I'm sure everyone is. I hope we find the cure that helps and supports everyone.

[Nihal]

I have DMed you

[GaussRifle]

Just saying that our stories are really similar . Got it during Covid and been struggling since 5 years. I think I have a certain degree of erection dysfunction and loss of girth which makes the erection unreliable. I don't really know a permanent cure except getting an implant. I don't know how longer to wait since I haven't been able to have sex since years.