For those of you that are so young
My MS did not affect my daily life and my work life until I was 47. I'm 51 now. I've been on the same DMT since diagnosed . I am also on disability as well. I just want to express my genuine heartbreak for those of you in your twenties and '30s with small children. my son was already I guess about 18 or 19. I can't imagine this life while trying to manage a family and children. I'm just wishing you all the best. It's harded dealing with people That don't know or don't care or don't care to know.

I appreciate hearing this so much. I was just diagnosed in November of 2025- 3 months postpartum. I also have a two year old. I can’t even begin to explain how hard it has been but finding this page feels nice because other people can at least understand and relate to what I’m going through