Regarding varying levels of numbness during intercourse for people with MS; What can be done to increase sensations during sexual activity? Are there programs that focus on the mental experience during sex to circumvent the lack of physical feeling?

Different people have different symptoms and react differently to different medications. I propose a study to see if different physical therapy (PT) regimens may be more effective that others. For instance, land-based PT, vs pool-based, and even Yoga?

What can people with MS following specific diets expect in terms of fatigue improvement, and is this affected by personal characteristics, like age, disability level, or initial fatigue level? Can combining diet with exercise help reduce fatigue further?