tabney
Active member
- Joined
- Jan 15, 2007
- Messages
- 53
- Reason
- PALS
- Country
- US
- State
- ky
- City
- Shelbyville
I have been diagnosed with PLS. The good news is I do not have ALS. At least my neurologist is 85 percent sure it is not ALS. An EMG in three months will give a final diagnosed. I have been looking for a support group all over and never noticed it right under my nose.
I don't know what to say right now. I have limitations to deal with daily. So weak in the legs that standing up is difficult. Once I am on my feet, I have to be careful to walk slowly. My legs cramp alot. Baclofen is not helping yet but I have not been taking it for long. My hands are weak and don't want to do what I need. They are stiff and have
some atrophy. I have no clue what to do now. I have a diagnosed but not much information on
what comes next. Any ideas?:?
I don't know what to say right now. I have limitations to deal with daily. So weak in the legs that standing up is difficult. Once I am on my feet, I have to be careful to walk slowly. My legs cramp alot. Baclofen is not helping yet but I have not been taking it for long. My hands are weak and don't want to do what I need. They are stiff and have
some atrophy. I have no clue what to do now. I have a diagnosed but not much information on
what comes next. Any ideas?:?