Are plaques painful?

Previous topic - Next topic

0 Members and 1 Guest are viewing this topic.

uhm

Hey everyone,

Was just wondering if someone could tell me if their plaques are painful?
When erect and I push my plaques inward I get sharp pain.

Thanks  
25 yrs Old
Began 2021 with pain & deformity, Unknown cause
The bend has reduced significantly on its own, I'm left with 2 large lumps on each side at the base

nemo

Yeah, don't do that.  The short answer is that Peyronie's inflammation/plaques/nodules can indeed be painful, sort of the same way a cut on your finger vaguely throbs with inflammation.

However, they can also be completely without pain. Each guy's case can be different. The first time I had Peyronies Disease, I only experienced pain when fully erect, and the scarring was being pulled upon. In my current case (many years later), I have a near constant dull ache in the flaccid state, but weirdly, when I get erect, the pain is only there if I push or press on the nodule area, as you're experiencing.

So, a guy can have no pain, ever, or he can have flaccid pain, or erect pain, or both. And all shades in between.

It's just a really weird, bewildering disease, I'm afraid.

Regards,
Nemo
51 yrs. old, multiple auto-immune conditions. First episode of Peyronies Disease in 2002. Recurred a couple times since. Over the years I have tried Topical Verapamil, Iontophoresis, all the supps and Cialis + Pentoxifylline. Still functional, always worried.

Kobegianna

I just had a new recent injury, I have a hard nodule/plaque I can palpate when flaccid. It only hurts when I push on it. But no pain when flaccid or erect. I don't know if that's a good thing or bad thing  
34 yrs Old, Healthy very active
Possibly injured penis or took too much Cialis
Symptoms starting January-February 2021
First dent seen April 4, 2021, painful erections

nemo

Be grateful there's no flaccid (or erect) pain. It's really unnerving and prevents you from ever forgetting this nightmare, even for a while.

Nemo
51 yrs. old, multiple auto-immune conditions. First episode of Peyronies Disease in 2002. Recurred a couple times since. Over the years I have tried Topical Verapamil, Iontophoresis, all the supps and Cialis + Pentoxifylline. Still functional, always worried.