StepOne, that sounds great!  I'm going to discuss it with Dr.Trost for two reasons, my age and Peyronies Disease condition.  I'm getting tired of trying to make it better.

Take it easy!

Could it be because you feel overly worried about traction and if you are doing it right?

I masturbate right after a session sometimes (got back to it after a long time) and i personally have no issues.

What device are you exactly talking about? Can you share that with us?

So I recently came accross an ad of this new device called Neuman™

They claim it fixes ED and peyronies but I'm highly skeptical, has anyone tried it and seen results or does it make sense scientifically that this works?

So I recently came accross an ad of this new device called Neuman™

They claim it fixes ED and peyronies but I'm highly skeptical, has anyone tried it and seen results or does it make sense scientifically that this works?

Hi

Firstly thank you for opening this.


https://www.peyroniesforum.net/index.php/topic,21399.0.html

So I just made a post on the history forum, still trying to figure out how everything works on here.

It is my humble request for anyone reading this to please take out some time to read my history that I have attached a link to above. I know It's long but you would be really helping someone who's in need.


Secondly how do I add files. Like images or pdfs. Cuz I am willing to share pictures I have taken for more than a year now and also share my reports with yall.

Please help me brothers

Age - 24

Age at onset of Peyronies Disease - 22 few days from turning 23 so I usually just consider it being 23

Very First Symptoms - So it all started with me developing a serious UTI. I was doing an internship at the time, was masturbating almost everyday sometimes multiple times, I am still very young and had and still have a girlfriend but different one. So after getting a serious UTI I had a complete loss of erections, which made me very worried but then all the doctors told me to wait it out because of the infection and anti-biotics. After some time however, my UTI went away but I started having severe pain in my lower abdomen, balls and sometimes it would shoot down to my leg and foot. After multiple scans and blood works I discovered that my PSA was extremely tight around 10. But after some time that too went away and I had started regaining my erections albeit with the deadly bend. Initially erections were so hard to get that I never noticed any pain just thought of it as being really hard since I started taking cialis and all sorts of other vitamins and supplements. The pain even when I loom back was never consistent so never knew what to think about it.

My Peyronies Disease progression, Treatments (in order), Doctors, Psychological Stages, observable changes - After noticing the curvature I showed it to my girl at the time and she said it looked the same to her and I mainly thought that's it's all in my head and that's what doctors keep telling me till this day. I did some scans which showed nothing at all but after a lot of research I continued to think that I have the condition as Neo also mentions in one of YouTube videos that any curve that you develop which was not previously there you are most likely a Peyronies Disease case. So on that I continued to take cialis and erections returned. I lost my virginity, though I could only do it laying in one position and I do think I've lost some sensation down there. My curvature seemed to be stable for very long up until now (Nov 2025). I had a scan done during the early stages but being in Pakistan really makes me question the technicians here and even most of the doctor specially when it comes to a young guy with sexual issues. They found nothing at the time after multiple flaccid ultrasounds and even an MRI.

A few months back I decided to get everything tested again since I believe I am loosing size and girth. Also there is a complete loss of morning erections I never wake up with one since the last two months now. Upon that decision I found a very knowledgeable radiologist who does 100s ultrasounds on a daily basis and specialises in the Doppler ultrasound too. He gave me Caverjet not the full dose tho, just 30%. And that gave me an erection score of 2 as it says on the report. The PSV values were incredible and the impression was reported as .9 mm skin thickening at the dorsal aspect posterior to the glans. I discussed with two or three uros and all said it's nothing all I need to do is to work out regularly, fix sleep and all ghat stuff and if the 20-30 degree curvature really bothers me I can get a surgery for it but upon palpating only one said that yes there is thickening but did not officially diagnose me with Peyronie's Disease. I also got an MRI done to rule it out and again nothing showed up however my symptoms continue to worsen. Now there is pain sometimes when erect whereas for over a year I had no pain. I do think that curvature is also increasing slowly. I got another ultrasound done but flaccid this time (cuz a lot of people from Reddit told me you don't need to be erect to detect plaque and fibrosis) and again the impression was "skin thickness at the dorsal aspect posterior the gland measures 4.0 mm, which is increased compacted to the proximal aspect (2.9 mm)
No focal hyperechoic plaques or acoustic shadowing seen
No discrete mass or focal lesion is noted

Will try to attach my reports but trying to figure out how to. Willing to share a year long of picture progressing too for honest opinion.



Where I am today, future plans - Today, I wrote this in order to seek help from people who are much more knowledgeable and experienced than me and all the crap doctor in my country. I don't understand what is wrong and what I need to do. I did order a RestoreX but it will come next month and I'm scared to even start that cuz sometimes after manual stretching I seem to get more buckling. I have so started considering an implant as that surgery seems to be the one with the most amount of positive and happy outcomes. Better than even injections I would say. The main thought process behind that opinion is the fact that waiting and trying other treatments might still result in more size and girth loss and even more curvature. Even if I do manage to reduce my curve gaining size is very difficult even with an implant so why not lock what I have?

Since I'm young, scared and honestly desperate for some real help (cuz the professionals here absolutely useless) I am open to any sort of criticism you may have for me, I just need the truth at this point.

Scooter, I love my implant. I can have sex whenever I want, but we pretty much do it twice a week.
My implant changed my life completely. First, it is bigger, wider, and longer than it's post peyronies size.
When I look at it, I stil think sometimes, this is a great looking cock. LOL.
I have had a few issues with the pump. The pump sticks on this particular model. So it takes a lot more work to deflate sometimes, but it's still worth it.
I went to a Titan specialist in Orlando two months ago and he said yes, there have been problems witht this particular model and year. He suggested I try to hold out, until the pump fails. He said, my penis looked good and why risk another surgery, if it's only a mild inconvenience now. I agreed.
I have since looked at the AMS implants, as they have a new model with an easier pump.
I think if I have to replace the one I have, I will definetly go with the Boston Scientific (with its AMS 700 and TENACIO pump).
But I do love my Titan, I wished I had done it sooner!
I can't believe all the suffering I went through, needlessly.
Stepone

hello I live outside of Philadelphia pa and I need a restorex I will buy your if you still have it just tell me what to do thanks Brian

Stepone,

He was the head of the Male Infertility and Peyronie's at the Mayo Clinic in Minnesota.  Now he has his own clinic in Utah.  I haven't discussed an implant with him yet.  I see from your info that you have an implant.  How has it worked out for you?

Scooter 66