Kind of new here, maybe I just need a little encouragement. Went to my Neuro last week, by the way I was DX with PPMS in Oct. 2009, he said basically most of my symptoms I talked to him about, I have to live with. Well that was not encouraging, but oh well. I am currently using a walker and I just foresee in the future ending up in a wheelchair, which is kind of hard to accept. But again I have no choice, I guess I just needed to talk about that, I'm kind of having a bad day. I try and explain to my son who lives about 12 hours away, what my day consists of, all the struggles and symptoms I have and I always get emotional when I talk to him and I hate myself for that. When I do talk to him I feel like the conversation always leads to me and how I am struggling with this disease, I hate talking about my MS all the time, but he always asks me how I am doing. Any suggestions???
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