Sexual changes affect 40 to 80 percent of women and 50 to 90 percent of men with MS. These questions almost never come up unless you raise them, and most neurologists are prepared to help or refer.
Your Questions
Could MS be causing the changes I am noticing in my sex life?
Could any of my current medications be contributing?
Are there medications, topical products, or devices that can help?
Should I see a urologist, gynecologist, or pelvic floor therapist?
Can you refer me to someone who specializes in sexual health and MS?
Could genital numbness or sensation changes improve with treatment?