Hi
I just wanted to thank those who have this terrible disease for their kindness and concern to those who worry about having ALS and to those who do have ALS. Also, I would like to thank those who did respond to my previous posts. For me, it hurts to read of those who are newly diagnosed, yet encouraging to see people care enough to respond.
I am waiting to see another neurologist, who will decide on a muscle biopsy, another EMG, or ?. I think the most difficult thing, for me, is the waiting and not knowing, and as I wait, my twitches wait along with me...twitch, twitch, twitch...all day long.
I just wanted to thank those who have this terrible disease for their kindness and concern to those who worry about having ALS and to those who do have ALS. Also, I would like to thank those who did respond to my previous posts. For me, it hurts to read of those who are newly diagnosed, yet encouraging to see people care enough to respond.
I am waiting to see another neurologist, who will decide on a muscle biopsy, another EMG, or ?. I think the most difficult thing, for me, is the waiting and not knowing, and as I wait, my twitches wait along with me...twitch, twitch, twitch...all day long.
