Scott M.
New member
- Joined
- Feb 2, 2008
- Messages
- 0
- Reason
- Learn about ALS
- Country
- US
- State
- Pa.
- City
- Saxton
Hello, My name's Scott. I just found this support website, and am anxious to talk with any one that can shed some light on my problem. a couple neuro's said ALS a couple said no way. One said a slow moving form. The next said "Is that doc crazy" I've had my nerve damage and am losing all muscle in my arms and shoulders for the past 5 years, maybe longer. I go to a neuro in Pittsburgh, Pa. on the 18th of February for a test that is supposed to tell me if I have ALS or not. But I've also been told there is no test. I've been doing chelation therapy and have a high amount of metals, and I've read about Lyme's disease and a lot of Als patients are testing positive for Lyme's. I've had the least accurate Lyme's test done already and came back negative. The doc who did that wasn't interested in anything I had to say and I feel he basically gave it to me to shut me up. Anyway any help will be appreciated. Even just someone to converse with that is going through the same things I am. thanks for reading. Scott