Flyby
Active member
- Joined
- Jul 2, 2012
- Messages
- 40
- Reason
- PALS
- Diagnosis
- 10/2012
- Country
- CA
- State
- British Columbia
- City
- Nanaimo
Well folks, a year ago they finally gave me a diagnosis of atypical NMD and assured me I didn't have ALS. Two weeks ago, this all changed. The diagnosis is now ALS. It wasn't a h:smile::smile:uge surprise as I am deteriorating quickly. Still there is a big difference between thinking you might have and being told that you do. The only good thing about this is that my neurologist has left town and I willl now be followed by the experts in Vancouver. I will now have that "team" behind me instead of playing guess and only having the forums to get info from. The forums have been a great help and I am truly grateful for the information that all the others have posted on line for newbies like me to read. (Trying to put a smile here but it isn't going in. The important thing though is that no matter what the diagnosis I will live my life to the fullest possible with the help of my dear husband and CAL Don. Even if it will be shorter and more of a challenge, I will live each day to the fullest and anyone can remind me of that when I get feeling the blues. Mdy best to each and every one of us with this challenge ahead!