"Hi all been a long time since posting on here. Been having a really hard time coming to terms with the way my MS has changed and gotten worse. Most days I'm stuck in bed my hospital bed or my power chair. But that's nothing compared to the physical problems I go through on a daily basis. If I try to walk with my walker I end up falling out especially in the afternoon or evening. I don't know if it's from the spasms or the loss of feeling in my left side. But I still try I just wish that it would get better. I don't know one day maybe."