Tips and advice for any sexual side effects of treatment
I also experienced Peyronie's disease post-operatively in 2008. The effects cleared up over the subsequent few years.
How this treatment impacted my life the most
Compomised urinary continence: This is normally under control but is adversely affected by minor infections and when tired from physical exertion. Inability to naturally get or maintain an erection. This has limited my ability engage in sexual activity with my (female) partner.
Why did I give this answer?
I'd want to explore other treatment option (e.g. immunotherapy) before committing to surgery or radiotherapy.
