Bella77

Hello, Bella77, from another Michigander. i have ALS and my husband is the cALS. Just recently diagnosed early this year and still mobile. But progressing. :-( Have you been in contact with ALS of Mich? or ALSA? Both organizations have been helpful to me. ALS of Mich has support groups. I strongly suggest you attend some if you are not. It was hard to go to the first one, but now I love them. Often, at our meetings, we will have more cALS there than pALS. So, feel free to go by yourself if you have to. You won't be 'out of place'.

This is very helpful information, and very good diagrams. Thanks