ideas

I'm wondering what PALS and their caretakers do when the later stages of ALS hit? What do you/they do to stay mentally alert and active. I imagine it must get boring watching TV all day. Any ideas are very helpful. My PALS has trouble talking, is on a cpap (sp?) machine most of the day, is...

Hi, My name is Max and I have been very concerned recently about ALS. I’ve been reading these forums a lot, which has furthered my understanding of the disease, as well as greatly increased my sympathy for those who have it and my empathy for those who think they have it. If possible, I would be...