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I have a journal in here if you want to take a look!
Depends on you. I don't wear pants to bed. I have a sleep apnea test on Monday where they want me to sleep in the clinic and wear my pajamas. I'm scrounging for something to wear. 

The first indicator of Peyronies Disease for me was waking up at 3am every night with a hard erection and lots of pain at the left base, where the plaque started. Made me wonder if even hard erections could cause damage and Peyronies Disease. 

What pants are good to sleep in, in order not to hinder the erection?
This is what I'm currently using. The penis goes out through that "hole".

Last night the hole wasn't aligned with the penis and woke up with a bit of pain.

I used to sleep with the pants pulled down to the thighs, but that's not too good for my low back pain.
I wouldn't risk sleeping with regular pants fully on, no matter how loose they are around there.

Thank you for any suggestions.
Cheers :)
Introduce Yourself / Peyronie worsened due to minor...
Last post by alex88 - Today at 11:40:17 AM

I am 37, living in Europe and this is my history:

teenage years - fibrotic tissue, mild hourglass deformity, neuropathic pain on the penis; all due to masturbation.

8 years ago - mild curvature, at the base, upwards and to the right; probably because I used to sleep on my stomach.

3 years ago - slept in tight pants one night, which hindered the nocturnal erection; woke up in a lot of pain; had painful erections and dorsal tension for months afterwards.
-no change in curvature.

2 years ago - a consult for inguinal hernia has caused me a lot of pain and inflammation in the inguinal and subinguinal area.
-after a few days I have noticed 2 indentations on the penis, a few cm away from the glans, lateral, one on the left and one on the right.
-afterwards the penis curved upwards and to the right, 20-30 degrees, at the point of those indentations.

I did traction by hand last spring for 2 months, 15 minutes/day. Applied force was maximum 0.5kg. Pain and curvature improved a bit.

I've recently started traction again, this time after using a heating pad at 40-45 degrees C for 30 minutes. Traction time is 30 minutes/day, spread out throughout the day. Same force is applied.

Currently the curvature is 20-30 degrees upwards and to the right. (a curve at the base and one a few cm away from the glans).
When 100% erect it's painful, especially when moving it upwards/downwards.

I consider a vacuum pump which I have bought, but haven't yet used (Soma Correct).

If it doesn't improve then I'll buy a penis extender.
My concern is that the neuropathic pain will flare up with it.
Another concern is the fixation mechanism at the glans. I am not sure which is the least traumatic.

Thank you for reading and best of health to everyone.
Introduce Yourself / Desperate and depressed
Last post by DaneS89 - Today at 08:28:45 AM
Hello everyone. Hope you're all doing okay. Here to introduce myself and share my story. I was diagnosed with Peyronies in October of last year (I actually diagnosed myself with it after having Dr Googled the telltale symptoms and then had it confirmed by 2 urologists). I'm just going to jump straight to it - The condition has devestated me. I feel ruined and deeply depressed by it most of the time. It colours my world in a dark and ugly way. I miss my old (sex) life and what I used to enjoy. I miss not having to worry about and manage this dreaded disease. It has consumed me. As much as I try, and persevere, I honestly don't feel up to the challenge it has forced upon me. I wasn't good (mentally) even before peyronies. My reserves of mental strength and energy were low already and then this happened and now they're deep, deep in deficit. It just feels like a nightmare I haven't woken up from. I know this might sound a bit extreme, but that is just my reality at the moment and how I feel about this. The psychological impact has been huge. I hope that maybe some of you here are kind enough to share some advice and wisdom that could help steer me through this (the emotional and philosophical aspects). I do have a good therapist, and they try to support best they can, (and it does sort of help) but its not coming from a place of lived experience. Its such an isolating condition for its sufferers I feel in that hardly anyone in our lives would be able to relate.

To the more practical (or should that be physical?) details of my peyronies. My curve is mid shift with a line/indentation right the way across the top and pinches in slightly either side of that line (so mild hourglassing) It bends up at about 25 degrees. It like my penis is segmented. The half of it closer to the glans sort of bulges out on the sides too, so I'm not sure if I have lost girth in the lower half or if the bulged sides in the other half are due to underlying plaques weirdly somehow adding to  girth. Theres this thing about aspect and angles too - when I stand up, fully erect its as if most of my peyronies imperfections seem to dissapear, if only for a brief moment and while in that position. But when I'm in a semi-erect state or 'on the way up' its a different story and the deformities are apparent.

Its all just so confusing and complicated and this condition frustates me because I'm someone who likes to understand things. And it keeps changing, which adds to the frustration and torment. It might be wishful thinking but I could/can swear the Pentox was/is making a difference to soften the curve. Not just the feel or it but the look of it. But then in that same time since I've been taking it there a new plaques that have formed. And the biggest issue is that my functionality is greatly reduced. My size is almost the same and the visible changes alone I could almost handle - I am fortunate in that (as the urologist said during exam) I have length and girth to lose, and the deformaties are by objective measure quite mild - but if I can't feel pleasure from using it then...thats cold comfort.

I hope to regain my sensitivity and the 'reactivity' of my penis. Its the most disabling feature of this condition I think, for me anyway. It just feels like a bone down there (when erect). And when I'm flaccid I feel uncomfortable in my underwear, having to adjust myself all the time. The tip of my glans feels uncomfortable and sensitive in a not good way when it rubs or moves against my underwear. I have to pull my foreskin forward all the way so that it doesn't touch. I also get a cold sensation down there at times which I find really troubling...hasn't fallen off yet though. But it just adds to the list of things to worry about and the wicked ways in which this condition manifests. Its not just about sex and how peyronies has changed that, I'm uncomfortable and in pain outside of those times too. Theres just no respite.

Anyway, I will persist with the Pentox and the whole suite of other supplements I'm on and do my best to maintain the diet and lifestyle changes I've made. That is difficult though - there were a few vices I enjoyed pre-peyronies that had to go in order to give the treatments a chance to work. The catch 22 of it all - the select few things I enjoyed before had to be sacrificed for continue them would worsen the condition...but to quit them leaves me feeling deprived and depressed, which also happens to be how peyronies makes me feel.

I do want to get more serious about my health though...go further with it to improve blood flow in particular. I don't feel confident to start with traction again or VED until I have reached a state of 'optimal' or 'peak' blood flow, to accommodate the strain and reduce risk of injury (maybe I'm more worried about than need be?). I have both the PMP and RestoreX devices but false started with both of them because I wasn't ready either physically or mentally, I'm not sure.

Alright, that's enough from me for now. Thanks to anyone who sat through and listened to my ramblings. I'm usually more succint in my writings but right now Peyronies has got me down and I had a lot to get off my chest. I hope to have some nice and meaningful chats with you fellows, and contribute something useful of my own if I can. I look forward to it :)

Cheers guys

Priapism only damages the penis after >5 hours of CONSTANT, FIRM erection.  If you partially lose that erection and then return to a full erection, that 5-hour block is broken.  If your penis worked the next day, it stretches the imagination to think there is any issue.
Whether it is someone who mocked a spouse over breast removal, penis issues, a deformity, disability, or any other issue beyond their control, that person is NOT fit to live with unless they are ready to change and work hard at changing. That starts with:
1. Recognizing that they conducted themselves in an inexcusable manner
2. They feel genuine, personal sorrow for their conduct
3. They apologize
4. They dramatically change

Otherwise, I agree with Bensimon. If I had the world's most perfect penis, I would not stick in an evil person who would demean someone they are supposed to love. Your penis is NOT the problem with this relationship. Your penis only revealed the problem. You say you don't understand why she does not want to be with you anymore. The answer is that we can't understand everyone. I don't understand Hitler, Jeffrey Dahmer, or Charles Manson, or many other less notorious people. The question is WHY DO YOU WANT TO BE WITH HER?

I am not saying that you are a perfect part of this marriage. Your drinking only hurts you, and it would harm a good marriage. However, that can not justify her behavior. Unless you were attacking her in a similar evil manner, there could be NO EXCUSE for her behaviour.

On the topic of implants. If you have insurance that will pay for a revision, I would get a 3-piece implant from an EXPERT SPECIALIST. Most women would never even know you have an implant unless you told them.

You will never lay a plan for moving forward and improving your life until you stop drinking alcohol. It undermines your health, your goal-setting, planning, and prevents you from following through on your plans.
Quote from: nevertheless on Yesterday at 08:08:37 PMNot sure how long you've been doing it, but after a few weeks, it solved itself for me and I can bend with long rods since then. Just took time to stretch and such. But you can order a different top piece for cheaper than full device and swap between straight and bent time. 

Also, disagree greatly with last post. I have seen tremendous growth and curve lessening from RestoreX and Cialis. It has made my symptoms basically go away besides slight curve. But not accompanied by any pain or discomfort, so HUGE win. Won't work for everyone, but not need to make sweeping conclusions and just say go right to surgery imo.
Thanks. That's really encouraging.
Personally, I wouldn't let any doctor that does PRP injections for Peyronie's lay a hand on me. There is no medical evidence or case reports to support the use of PRP for Peyronies Disease and any practitioner offering this is very likely simply trying to make a buck. It was snake oil when it was marketed as the "Priapus Shot" here and elsewhere, and that was years ago - you can find the threads through the search function.

It sounds like you guys are dealing with questionable practitioners. I'd be extremely cautious before either giving them your money or entrusting your health to them.