Hi Everyone,

I have Morbus Ledderhose (started 36yo) and Peyronie's Disease (started 31yo), Knuckle Pads (started at 17yo). My hands are itchy a bit, but not yet clear sign of nodules or contraction. My father had DD, ML and PD.

Now especially my Peyronie's Disease reactivated with a 2nd nodule after being stable for 5 years. I did not have a clear trauma so I suspect I need to be prepared for lifelong progression.

Therefore, I wanted to ask if there are patients in a similar category that have the disease for multiple years or decades and can give me some life advice especially in regards to Peyronie's Disease.

On Peyronie's Disease patient groups there are strangely not many patients with DD or ML and typically consists of patients with a clear trauma or penile fracture.

As this is a quite personal topic I would be super happy to exchange via direct messages or a video call, etc.

Thank you and kind regards
Tobi