JamesB
Member
- Joined
- Aug 18, 2014
- Messages
- 14
- Reason
- Learn about ALS
- Country
- US
- State
- California
- City
- Los Angeles
Wow, Mike. Eloquent. Thanks a lot.
It's just there are personal stories here of having symptoms for a long time, or taking ages to be diagnosed, so the person notices a problem but the doctors can't commit to a diagnosis or whatever, so I was wondering how things present themselves officially. I've had problems moving my leg for months, and it is getting worse but I can still stand on my tip toes, I just can't walk for long, plus there are agonising cramps (which doesn't nec. fit the picture you're talking about).
Is the nerve conduction test as relevant for MND/ALS or is the EMG the biggie?
J
It's just there are personal stories here of having symptoms for a long time, or taking ages to be diagnosed, so the person notices a problem but the doctors can't commit to a diagnosis or whatever, so I was wondering how things present themselves officially. I've had problems moving my leg for months, and it is getting worse but I can still stand on my tip toes, I just can't walk for long, plus there are agonising cramps (which doesn't nec. fit the picture you're talking about).
Is the nerve conduction test as relevant for MND/ALS or is the EMG the biggie?
J