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I will try anything at this point to make my hands were better. Everything seems to be going fast. My legs feel like they are about to crap. I can't walk straight drives me up the wall.

I do work my hands and feet as much as I can but right now. It is not doing much. The weather. I know may have something to do with a lot of this. It has been raining a lot but still, there has to be something I can do. I would like something to keep my fingers straight, while I sleeping...

the physio therapist is going to train the nurse that comes in, every day things to keep me limber. The physio people come in, may be once a week. I don't know why I asked for more but this is all I get. It is so bad. My son had to feed me tonight at dinner. I cannot lift mine arm at all...

I would just like to know the best way to keep my hands working? The last couple of days I am finding my hands getting very stiff. My right hand is starting to feel cold with this. I am finding it hard to do anything. I can barely eat anymore my wrist well not turn and my food is falling off...

nothing works for me as far as bed goes. I have to use a recliner, because my legs cramp and I can't move.

looks like the same old crap to me. All they're doing is a lot of talking, and that's about it.

yes I am on lithium started a couple of weeks ago. As of yet I find no different. So what it does. I'm not sure

I am on this new test the drug now as of yet. It has done nothing to help me

my doctor says that they are doing no testing. Up here in Canada and seems to think that the treatment if done could take up two years. I have one of the best ALS doctors in the country and as far as going to third world country and paying 30 grand. I don't think so.

don't know how long I can last with this ALS. I can't lift my arms can hardly eat walking is getting so hard for me to do. I can't so many pills for pain and to relax. My muscles, but they don't seem to do any good. I can not sleep in my bed anymore. I have to try to sleep in my power...