Hello fellow Peyronie's survivors

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MauvaisCoton

Hi everyone!

I'm so glad I found this forum because on the of the worst things about Peyronie's is its psychological impact. It helps to know I'm not the only one battling with this disease and reading some threads gave me some hope.

I'm 30 and got diagnosed with Peyronie's in 2017. I have a congenital curve and didn't know I had to be careful. I think Peyronie's started when my ex-girlfriend was on top. I don't remember feeling pain. It was some sort of pressure or discomfort. If I could go back in time and warn myself about Peyronie's, I would.
I began having painful erections shortly after. I couldn't have sex because it hurt too much. The urologist I saw back then told me there was nothing I could do besides waiting and seeing. Which is what I did. A few months later, the pain was mostly gone but a curve to the left appeared.
Peyronie's took a huge toll on my mental health. I was constantly afraid it would get worse and referred to my penis as broken. But it still worked and I eventually learned to live with it. The curve was stable. I was OK.

That was until a few days ago. After another possible injury during oral sex, the pain started again and I'm terrified at the idea that Peyronie's is coming back or worsening.
I realized I needed to do something about it and one of the steps I took was joining this forum. I took a look at the survival guide and started a treatment with Pentox along with Cialis (I have some pills because of issues with anxiety-based ED) and manual traction in the shower. I strongly hope that my penis will heal properly this time.

Thank you for reading my story. If you any insight or advice, I'm all ears. :)
30. Congenital curvature upward. Diagnosed with Peyronies Disease in 2017. Curvature near the base of the shaft (approx. 45° to the left). Still painful sometimes. Mild ED since summer 2020. Anxious.
Currently using RestoreX (since 04/21) and L-citrulline.

Bud luck

Just don't give up, we are millions out there with the same problem, at least you are trying to find solutions.
My first symptoms started early in 2019
I tried Traction device, Pentofixiline, Q10, TRT, L-Argenine, cialis
I have narrowing/dent/hinge on the left side of my shaft
My ED is getting worse
Had a PRP shot Aug 2021
I have a girlfriend
Age 46

Hawk

Welcome to the forum MauvaisCoton.  You are among friends who understand your battle.  Many have found solutions to many aspects of this condition.

It is essential that you read this more than once to get a solid grasp of the basics.
https://www.peyroniesforum.net/index.php/topic,3180.0.html
Prostatectomy 2004, radiation 2009, currently 74 yrs old
After pills, injections, VED - Dr Eid, Titan 22cm implant 8/7/18
Hawk - Updated 10/27/18 - Peyronies Society Forums

LuisFernandez

IMO manual traction for such low amount of time will not help much. I recommend VED and traction therapy. In your case either light RestoreX or Penimaster Pro. I'd get both devices if you can afford them.

You don't want to make your injury worse, but you want to heal in an engorged and stretched state. Also daily Cialis and L-citrulline is extremely important as early as possible after the injury.

You can ramp up traction time and intensity as the penis is healing and scar tissue begins to form. But for now IMO you want to heal in an elongated state.
Injury in April 2020. Onset of ED.
Started RestoreX and VED 2 months after injury.
Taking 10mg daily cialis, pentox, coq10, vit-e.
Traction (+1 inch)/VED/PGE-1/DMSO+X