Peyronies Society Forums

Please login or register.

Login with username, password and session length
Advanced search  

News:

ALL Members PLEASE Add a Signature line with age, history etc
PROFILE -> FORUM PROFILE -> SIGNATURE
More instructions here -> Signature Line - History - Peyronies Society Forums

Pages: [1]   Go Down

Author Topic: This Forum Should Join the Reddit r/peyroniesdisease  (Read 1726 times)

0 Members and 1 Guest are viewing this topic.

program4004

  • Solid Contributor
  • ***
  • Country: us
  • Offline Offline
  • Gender: Male
  • Posts: 140
This Forum Should Join the Reddit r/peyroniesdisease
« on: January 09, 2019, 05:16:29 AM »

More and more I see this disease ruin ppls lives and make men depressed. I feel like we as a community would make more of an impact on that site. News sites visit there every single day looking for content. Imagine if all the members of this forum upvoted regarding awareness of this. This making r/ all almost every single day. That would be incredible and would definitely increase chances of better research and testing. I know most men here want a solution and want a way to fix Peyronies to get there penis back to original shape. We know what causes it, doctors do to, but, they still haven't gone to the root of the problem, only giving solutions that patch the problem and never reverse it. This as we know needs more awareness. So please I ask of you members here, join the forum, we will reach more people there and attract more urologists and potential doctors to study this disease more intensely. We have to do something on a popular platform. Not denouncing this website as it's very informative, but, we need more mainstream recognition. Tired of hearing ppl experiencing doctors say "there's nothing I can do".
Logged
25,  PrePeyronies possibly, semi erect masturbation injury on Sept 2017.  Erectile Dysfunction for 2017 - Mar. 2019. Semi erect waisting, normal erections. Treatment: Vit E, rice sock heat therapy, abstinence. No official tests yet (doppler, MRI).

skunkworks

  • Global Moderator
  • ****
  • Country: au
  • Offline Offline
  • Gender: Male
  • Posts: 1603
Re: This Forum Should Join the Reddit r/peyroniesdisease
« Reply #1 on: January 09, 2019, 08:10:46 AM »

This is the url https://www.reddit.com/r/peyroniesdisease/

I have joined it, would be a good way to get more exposure for the condition.
Logged
This is an emotionally destructive condition, we all have it, let's be nice to each other.

Review of current treatment options by Levine and Sherer]

program4004

  • Solid Contributor
  • ***
  • Country: us
  • Offline Offline
  • Gender: Male
  • Posts: 140
Re: This Forum Should Join the Reddit r/peyroniesdisease
« Reply #2 on: January 09, 2019, 11:05:22 AM »

Awesome!
Logged
25,  PrePeyronies possibly, semi erect masturbation injury on Sept 2017.  Erectile Dysfunction for 2017 - Mar. 2019. Semi erect waisting, normal erections. Treatment: Vit E, rice sock heat therapy, abstinence. No official tests yet (doppler, MRI).

Whyisthishappening

  • Major Contributor
  • ****
  • Country: 00
  • Offline Offline
  • Gender: Male
  • Posts: 312
Re: This Forum Should Join the Reddit r/peyroniesdisease
« Reply #3 on: February 15, 2020, 05:54:40 PM »

yes thats good
Logged
alc ,vitamin e, propolis,pde5,NAC,nsaids,olive oil massage,nsaids,aspirin,essential oils cockteils,keto,IF,green tea,coffee
Pages: [1]   Go Up
 

Related Topics

  Subject / Started by Replies Last post
0 Replies
3171 Views
Last post January 31, 2017, 08:29:21 PM
by skunkworks
3 Replies
1267 Views
Last post September 01, 2017, 03:28:33 AM
by Jonbinspain
0 Replies
1447 Views
Last post February 07, 2018, 09:07:35 AM
by swiss