Peyronie's and Traction Devices
I am new here and probably will do something wrong or dumb because of that so please bear with me.
The use of long-term chronic traction has started to become more routinely used for those of us with Peyronie’s Disease (PD). In my naiveté, I started to research different penis traction devices on the web.
And then I found this place and am sort of more confused than ever! It seems that the bias here is against traction devices as overpriced and perhaps less effective than jelqing, and ADS using cheaper methods. I am open to learning here, so wanted to pose a few Newbie questions.
1) Might the abnormal wound healing process that seems to typify Peyronie’s Disease, make some of the more dramatic methods mentioned here risky for worsening of the Peyronie’s?
2) How might the tendency to fibrosis that characterizes Peyronie’s affect choices regarding longer slower stretching versus harder, but shorter term stretches?
3) If there is a “better” device out there, is there anyone here who would be willing to talk about that? It seems that there are two main reputable vendors of extenders in Europe (Androp***s, and Jes-Exte***r), and the “Fast***e in the US, with another one that includes the letter x in the name (not sure how to hide that one!)(don’t want to spam for anyone inadvertently). It is really hard to tell if one is better than another, when all the “reviews” are biased spam on sites run by manufacturers!
Any help for this newcomer to this site would be greatly appreciated.