I started Caverject Injections in Sept of 2008 and switched to Trimix in March of 2009. Then at the end of June, 2009; I was diagnosed with Peyronies Disease. My urologist did not tell me to stop the Trimix Injections but I'm curious to hear of any other's experiences.
On the PD Forums, alot of guys swear that the injections caused the Peyronies. But there really has not been a determination of what causes it. At this point I'm using a Three Tube VED with a daily protocol for the treatment of PD. It's too early to tell if the scarring is receding or not.
Age 60, PSA 2007 4.1, PSA 2008 10.0
Diagnosed April 2008, Biopsy: 6 of 12 cores positive, Gleason 4 + 5 = 9
CT and Bone Scan negative, Open surgery at Shawnee Mission Medical Center May 21, 2008
Right side nerves spared, Radical prostatectomy and lymph node dissection
Cather removed on June 3rd, totally dry on July 9th, pT2c, lymph nodes negative
PSA Sept 28, 2008 0.00, PSA Jan 22, 2009 0.00, PSA June 29, 2009 0.00
ED Status- Currently using Trimix, Levitra daily for increased blood flow.
Noctural Erections have completely returned on a nightly basis, same hardness as before.