I thought I look into getting involved with the MS community both virtually and physically after 15 years with MS (dx at age 15 and now 30). I assume this site is a good virtual resource, but It would be great if someone could please tell me how I can get in touch with the MS community in my area. I'm not sure how that would help, but I figure it doesn't hurt. I guess I never wanted to get in touch with the community because of denial, which has taken a good 15 years. Thanks in advance!