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?

I've been on this site for a short period and have posted a few times, but haven't introduced myself.  I've had Peyronies Disease for 6 years.  I've been using the Restorex for almost 6 years, had Pentoxifylline for a couple of months early on.  The first symptom was slight pain when flaccid, progressing to an HG deformity, then curvature.  I finally decided to try Xiaflex (6 injections) at Dr Trost's clinic, administered by his PA.  I haven't had intercourse for 3 years ( I'm married), and now have ED.  I've decided to have an implant and have my consult with Dr Clavell today.  Pretty nervous now!

I've used it before for about a year but stopped. I started back in October upon noticing a flare up. I was starting very aggressively, doing essentially the max 7 lbs of traction with the blacks rods essentially totally buried. The last week or so I have backed off and let more of the black rods show. I'm also only doing straight stretching since I have an indent on the opposite side of my curve.

It's weird because I'm noticing less spontaneous erections and morning erections (rarely ever), but I'm ready essentially every single time for my wife. I'm thinking there are some psychogenic factors at play too, just weird that my effect is opposite for erections for me lol.

I was smoking in my bathroom and one of my roaches fell on my penis when the roach hit my penis (flaccid) my penis shrank after that I got scared and masterbated and it's like my entire penis twisted when I got hard I couldn't feel much and penis looked damaged

Ever since then there is a dent when I get erections where the roach hit me and I have been waking up with my penis curved
I went to the hospital twice and they told me to put cream on it the urologist gave me cream also and sent me for a abdominal ultrasound he told me the nerves are farther back than where I hit
Since the urologist visit all my morning erections have been crooked and shorter and some of them have been painful
I also get a sensation of burning on my shaft wasn't there before I saw the uro

Thanks for replying and it just so happens today I have my first consult with Dr Clavell.  I haven't seen one review that was bad.  I told my wife I hope I'm not the first!  I'm pretty nervous now.  I'm thinking I'll also need the scratch technique.  I can't recall, what procedure was done to require the long incision on you? I'm traveling from Colorado and plan to logistically do what you did if all goes well.  I read where the penis will be inflated and the recommended position is up.  How is traveling done regarding having to urinate in a public restroom(wear depends)?  Do you have a hotel recommendation?  I think they'll give me a list.  I'll start to look, but thought I'd ask.  Sorry to pry or bother with questions, but now I'm anxious sense I'm moving forward.