Sensitivity subject

Previous topic - Next topic

0 Members and 1 Guest are viewing this topic.

hope794

Hello guys. Since i got Peyronie's, i've had essentially a never-ending inflammation of the dorsal area of my penis. Please note that i havent got an hard, well localized plaque; but rather a "diffuse fibrosis" of that area of the tunica albuginea (not inside the CC, as far as i know).

Now, i've noticed that my sensitivity is "strange" in that area. Sometimes, even the orgasm is quite "unpleasant" because i feel weird sensations there. I have sensitivity, but it has somewhat changed in that area. Sometimes i dont notice it, sometimes i do.

I've opened this post to ask 2 questions:

1) Did anyone here lost ALL the penile pleasure/sensations because of Peyronies, and don't find sex pleasurable anymore?
2) Did anyone experience things like mine?

Thanks!
26 yo from Italy.
Peyronie's since abt 2014
Abt 20-25° bend, w/ a moderate twist to the left
ED for 4 years and getting worse
From pornstar-like to moderately depressed - still fighting for a solution.

trav8701

Ive been experiencing this for a few weeks now. had peyronies for maybe 10+ years now. cant find much success stories here but i'll keep searching

Mikel7

I find that my penile sensitivity is directly correlated with my estrogen/testosterone ratio in my body. I've been on full testosterone replacement for the past 17 years and any imbalance can have a negative affect on me. I think my low T years ago is what lead up to my peyronies.  I am a firm believer that any man who
comes down with peyronies /ED should have their free T levels examined.
Lump 4/2020, age 62 , Dr Levine 6-26-20, Dors Curve 11/2020, Peyronies
Vit E400mg, COQ10, Heat Therapy, Penimaster, Pentox, Cialis, Restorex
SNHL 7/2020 - Stopped all Meds because ototoxicity  Heat/traction/VED are working. CPPS Diagnosis - Stable :)

NeoV

Very common for many of us. Changing my diet restored my penile sensitivity completely.