Quote from: kjmarjo677 on December 05, 2025, 03:31:25 PMI am scheduled to see Dr. Darshan Patel in San Diego, who was referred by my local Urologist. I have both Peyronies Disease and ED and likely looking into a penile implant with him based on the recommendations.


It seems like his practice is mostly ED and Peyronies Disease and does a ton of surgeries for both.

I got an appt with Dr. Yafi in Feb. I have never even tried PDE5 inhibitors yet and have had peyronies for 15-16 yrs. Hopefully those measures work, if not I will go try to go implant route with Dr. Yafi.

May I ask, did you try putting your penis into the clamp, unattached from the main device first?

I also do not have much flaccid length but clamping separately and then slowly stretching it re-attach to the main device worked for me.

Hope that makes sense.

Hey everyone,
I'm selling a Restorex device that's practically new, which I bought two weeks ago and I only tried it once. Unfortunately, my flaccid length doesn't seem to be sufficient for proper usage. I'm from Germany and would ideally like to sell it to someone within Germany or Europe.

Sorry, the RestoreX has been sold.  Thanks

Yeah. I mean I don't know if i have those conditions. My family doesn't really have anything like that apart from my cousin having plantar.

I have been feeling some stinging and all in my soles, trying not to pay too much attention to it for now. It's understandable how you feel low because of developing these horrible horrible diseases specially since you're just in your 30's. Maybe it makes you feel better that there's a 24 yo suffering from smth very very similar to you. There's no cure for such disease and that's the worst part really. I hope you find good doctors and I hope everything in your life becomes stable one day and for all of us here on the forum.

I can not really tell you what to do but I can definitely tell you that you gotta learn to adapt to your new body until surgical intervention is absolutely necessary, that's just my humble opinion.

Thank you for sharing, and wishing you all the health!

Peyronies Disease is in chronic phase at the moment, Ledderhose just started on my right foot. It is like a Peyronie's Plaque on tho sole of the foot. I can feel it at thickened fascia and I feel a sting on every step. Similar like a small pebble in the shoe.

My right hand is also a bit less elastic, so I fear Dupuytren's will also start like it did for my father.

I thought I manage again after Peyronie's stabilized, to now learn I have most likely a systemic issues where doctors are even less aware... This put me on a strong mental downward spiral. Quite sad as I think I am quite young for such a disease :/

I tried a fleshlight a while back when I wasn't having regular sex, and it actually helped keep things feeling healthy and blood flowing. Didn't overthink it, just used it regularly. Also, sometimes watching stuff on sex việt nam made it more fun and kept me motivated to stay consistent. For me, it felt better than doing nothing, and it definitely helped with circulation and just feeling normal down there.

I obviously wouldn't masturbate immediately after or before traction but I've noticed that even with a gap of several hours, it can cause irritation.

The doesn't seem to be any firm guidelines on this anywhere or from doctors.

As far as I remember from all that I have read, beta blockers have no effect on the penis in terms of peyronies. A quick search online also came up with the same response.

Could it be that you started taking it at the same time and you mistakenly think they are connected?

Hello!

I had never heard of it before so I had to google it. Apparently not very common and similar to dupuytren's disease. Go figure. Sorry to hear that you are feeling down. What are your symptoms so far, exactly?