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#1
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#2
Penile Implants / Overseas surgery
Last post by universalbread - Yesterday at 06:55:09 PM
I'm 33 I've had Peyronies Disease for 2 years and Ed for 5. I'm interested in surgery but it cost too much to do in the us. Does anyone have any experience outside of the US having the implant
#3
Introduce Yourself / Overseas Surgery
Last post by universalbread - Yesterday at 06:38:45 PM
I'm 32 I've had Peyronies Disease for about 2 years and ed for about 5 I'm looking to have the ipp surgery but the price within the US is extremely high. I've read online about clinics in turkey, Mexico and India does anyone have any experience with this
#4
Penile Implants / Re: Deciding to get an implant
Last post by Pdxguy - Yesterday at 12:47:40 PM
3/25 13 days post op
Today my scrotum swelling has increased quite a bit, which I'm fairly sure is from the pump slipping out of my hand and shooting around like a marble. 

3/27 15 days post op
My scrotum has continued to swell on one side. I spoke with my doctor last night and he told me to stop cycling for one week but keep taking hot baths and massaging the pump the best I can. The swelling feels puffy and squishy. I don't think it's an infection, my doc thinks it's inflammation from the pump slipping and causing trauma.
Has anyone else experienced this after having their pump slip a number of times?
#5
Alternative Treatments of Peyronie's Disease / Re: New Member
Last post by Mikel7 - Yesterday at 05:50:19 AM
Welcome Ronaldo77 to the forum. The first thing you need to do is to fill out your signature line -->Signature Line . Then please download and read our survival guide -->Survival Guide . This will give you a better understanding of peyronies and it's different treatments.

Usually new members post their introduction here in our, " Introduce Yourself board". -->Introduce Yourself .
Here you can give as much detail about yourself and your situation. You have a total of 10 postings here that other members chime in to greet and meet you.
Welcome!
:)
Mikel7
#6
I started taking tadalfil/cialis 5mg daily early 2021 during acute phase of Peyronies and it gave me good nocturnal erections . I never tried sex on it , but on masturbating I could tell it was helping a lot with the blood flow and how warm it used to feel so the the blood rushing in. Ate it from 2021- end of 22. Then did not have mutch of it in 2023, skipped a few months . Fast forward to today and I it just doesn't have the same effect it feels to me. It doesn't seem as potent as before . A couple of things could be possible -

1) Is it possible RestoreX desensitized my glans a bit ? On cialis earlier I tried clamping my glans, it would immoderately give me an erection , now my glans seems used to it and doesn't try to induce an erection on clamping.  But this would not impact my nocturnal erections so can't be it .
2) peyronies worsened ?  . I don't see a new relapse , only some nodules that hardened after xialflex injections over the years despite restore x . No curve change. ( really hoping that's not it )
3) Earlier I was on cialis ( brand) and now on generic tadalafil , maybe it does make a  difference ?
4) there is indeed some cialis tolerance that builds for it to not work the same ?

Despite daily 5 mg cialis , I only wake up with a chubby , not a full fledged erection like I used to when I just started cialis.

*This nightmare never ends. Any ideas ?
#7
Penile Implants / Re: T.E.P (tunica expansion me...
Last post by GaussRifle - March 26, 2024, 10:19:15 PM
Any update jj21 ? I avidly follow your journal ?
#8
Alternative Treatments of Peyronie's Disease / New Member
Last post by ronaldo77 - March 26, 2024, 08:01:20 PM
I'm new to this and looking for advice on how to deal with this peyronies disease please advise
#9
Alternative Treatments of Peyronie's Disease / E4 Peptide
Last post by happyman - March 26, 2024, 06:04:11 PM
Hey everyone,

Ive been spending a lot of time researching the e4 peptide, and while i do feel like ive learned a lot, im still confused on some things. i want to be able to have a group of people that can think together and come to conclusion cause right now its difficult just being one person

for anyone interested in talking about the ant fibrotic e4 peptide, heres a server i created:"  link removed "
#10
Well, here is it, March of 2024. Does anyone have any updates on this topic? I'm about to begin traction therapy (RestoreX) for Peyronie's, mainly for shortening, and I'm very interested in heat as an adjunct therapy.