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This section is a place to share stories about Living with Peyronie's Disease
Below are entries of those who have already shared their stories. We hope that you find their experiences helpful to your own situation.
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March 2008
- six months into peyronie’s - by bb - (Fri, Mar 28 2008)
I first started developing symtoms last fall, bent but not broken. My GP doctor sent me to a urology clinic where a person who is not a doctor has given me 4 weekly sonar treatments.
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- Problems with Caverject - by GeorgeD - (Wed, Mar 26 2008)
In 85 I ruptured three disks in my back. Was told 17% of serious back injuries create sexual problems due to pinched nerve damage. Sure as h***, I’ve had problems for yrs from it.
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- 17 - by mike - (Tue, Mar 25 2008)
i find it annoying to me that all the people i read on the internet complaining about peyronies disease are middle aged men. they dont have it bad at all. i got peyronie’s when i was 14 years old and its so bad that its “impossible” to have sex.
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- Verapamil injections - by Lyle Wammer - (Fri, Mar 14 2008)
I want to strongly advise against verapamil injections. I was told by my health care practitioner that while a cure could not be guaranteed, there was no adverse risks involved. This turned out to be completely false.
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- No Where to Turn - by Wimpy - (Wed, Mar 05 2008)
It is a fate as bad as death. If you are 60 years old, and still have a strong sex drive, there is nothing you can do. Even with Viagra, the erection is not good.
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- thoughts & questions - by Ron - (Wed, Mar 05 2008)
Appreciate all who posted on this site. Appears I am in beginning stage of PD since the last few months (married & 53). Like others, I’m not sure what will happen
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