Coping with working out

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westerntown

Before I got penile deformity- before the pandemic when gysm were opened- I was in the gym 4 hours a day 6 days of the week. It was a natrual dopamine boost and loved it there.

Well ever since the pandemic and the gyms closing, I havent been able to get back on the wagon. When the gyms first opened, I went everyday straight for a cool 90 days. However, everytime I would go to the restroom I would notice a profound worsening in the pronouncement of my flaccid hourglass. It was disgusting! SO i stopped working out.

I want to get back into working out as Ive gained quite a bit of weight eating my hear out, however I just feel like I am making my Peyronies Disease situation worse when i do. This is quite the conundrum for a 20 year old boy like. My roomate works out quite a bunch and he takes collagen peptides. We were talking abut experimenting with HGH even..

I am scared to eat more collagen or take hgh because I feel like its going to further my fibrosis but honestly as it stands already, my hourglass and ED are already severe enough to the point where I am honestly ready to not care and just go for it.

The reason I think I would need collagen is because I was on pentox for quite a while and I feel like it made my body weaker. I found my knees and shoulders and back were much weaker when on pentox and cialis and those were one of the reasons i quit working out. Well, I recently quit cialis and pentox as i felt it wasnt helping my penis but rather just exhausting the vessels and tissue in with a constant low flow priapism.

in short, I want to work out but that requires potentially worsening my Peyronies Disease, which is suboptimal.

I want peoples opinions on what they think my best course of action would be
20, late 2020 masturbation injury leads to semi erect hourglass, then try manual stretching leads to pudendal neuralgia like symptoms, corpus spongiosum and glans do not fill, severe ed- floppy unstable erections that feel like water balloon .

Mikel7

I'm 60 and have been exercising about 5 to 6 days a week. I only spend around 30 to 45 min max in the gym at a time. I walk about 2 miles on the treadmill 4 times a week and use light weights the rest of the time.  I think you over training and should not even think about using and HGH or any other assistant peptides.  Get a clean diet and supplement with filtered whey if not allergic. Drink lots of water, eliminate soda etc...
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 :)

Hawk

I too think you are overtraining with inadequate recovery.  That being said, there is zero evidence and little logic that working out would make Peyronies Disease worse.  It naturally increases testosterone which if anything is beneficial.

It could be:
1. You are temporarily pulling blood into the muscles, resulting in more of a flaccid state, making the hourglass more noticeable.
2. You are obsessing (over working out AND your penis) and have lost all objectivity when examining your penis.
3. That it is in fact progressing but that normal workouts are totally unrelated to that progression.
Prostatectomy 2004, radiation 2009, currently 70 yrs old
After pills, injections, VED - Dr Eid, Titan 22cm implant 8/7/18
Hawk - Updated 10/27/18 - Peyronies Society Forums

westerntown

It's not the just the aesthetic though, I also feel my penis contract violently up into my pubic bone and it begins to rub on my pants and I feel all sorts of uncomfortable. Unfortunately, even Trost can't help me, says I have "hard flaccid" whatever that means and he just told me to take antidepressants  
20, late 2020 masturbation injury leads to semi erect hourglass, then try manual stretching leads to pudendal neuralgia like symptoms, corpus spongiosum and glans do not fill, severe ed- floppy unstable erections that feel like water balloon .

AverageBloke

I had the same problem as you, my flaccid penis would become really tight and shrivelled. I had to stop working out because it was so uncomfortable.

The only thing that really helped was hours of light traction daily. Have you had a doppler ultrasound yet to confirm any scar tissue/plaque?
Peyronie's Disease
Titan Touch 22cm - Dr Clavell 06/04/22

westerntown

Yeah I had a Doppler and an mri. Plaque wasn't found. One doctor said I have corporal fibrosis but 4 other doctors said I don't and that u can see whatever u want when u look at the ultrasound (including Trost). Mri also came clean.

Avgbloke, I am wondering did the implant get rid of ur contracting states? I know one person who had "hf" was able to cure it with the implant. Is the same for you?
20, late 2020 masturbation injury leads to semi erect hourglass, then try manual stretching leads to pudendal neuralgia like symptoms, corpus spongiosum and glans do not fill, severe ed- floppy unstable erections that feel like water balloon .