Corpora Cavernosa Fibrosis

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Hard Sponge

I don't have Peyronies but suffer from ED and fibrosis in the CC due to the cavernosal nerves being damaged. I'm currently a math student but thinking about switching to bioengineering to do research in this area. At my current age of 20 I might still be able to make an impact and get to harvest some of the results myself...
If it doesn't work out I might go for an implant.

james1947

Hard Sponge
If you are here already, Welcome to the forum!
Can you explain what is fibrosis in CC? You was diagnosed by an uro?
Regarding switching to bioengineering, well, will be happy to have a friend that will make researches regarding Peyronie's. Don't have too many and some are working for the drug companies and they research is first to make money.
Implant is a last resort and yes, with 90% satisfaction if is done by an expert. You may read the forum to see if don't have nothing else to do.
James
Age 71, Peyronies from Jan 2009 following penis fracture during sex. Severe ED.
Lost 2" length and a lot of girth. Late start, still VED, Cialis & Pentox helped. Prostate surgery 2014.
Got amazing support on the forum

LWillisjr

Quote from: Hard Sponge on March 23, 2012, 06:50:19 AM
I don't have Peyronies but suffer from ED and fibrosis in the CC due to the cavernosal nerves being damaged. I'm currently a math student but thinking about switching to bioengineering to do research in this area. At my current age of 20 I might still be able to make an impact and get to harvest some of the results myself...
If it doesn't work out I might go for an implant.

Do you know they cause of the nerve damage?
Developed peyronies 2007 - 70 degree dorsal curve
Traction/MEDs/Injections/Surgery 2008 16 years Peyronies free now
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