antman
New member
- Joined
- Jan 12, 2017
- Messages
- 2
- Reason
- Learn about ALS
- Country
- AUS
- State
- QLD
- City
- Brisbane
Good morning to you all.
I have read the "Read this first post" but have some questions regarding my situation.
As a history, I had pins and needles in my feet and hands and reading the "read this first" post showed that this isn't an indicator of ALS.
I visited a neurologist who suggested I have an nerve conduction test and EMG.
I went and saw him and he said I have symptoms "Consistent with mild distal symmetric motor-sensory neuropathy".
However in the test result (this is what is concerning me) he says:-
"EMG of the right tib nerve reveals several high amplitude polyphastic MUP's, no SPA and dense volitional activation pattern.
The right extensor digit brev speals SPA (sparce), polyphastic MUP's and slightly lightened volitional activation"
Lately I have been getting very mild twitching in the leg, arm and sometimes face. They last less that 1 sec and are sporadic.
I have been extremely stressed and my wife reassures me that the Dr said that I don't have ALS however the report he wrote has me confused.
I apologise for posting this but if anyone can assist I would be grateful.
Many thanks.
Antman
I have read the "Read this first post" but have some questions regarding my situation.
As a history, I had pins and needles in my feet and hands and reading the "read this first" post showed that this isn't an indicator of ALS.
I visited a neurologist who suggested I have an nerve conduction test and EMG.
I went and saw him and he said I have symptoms "Consistent with mild distal symmetric motor-sensory neuropathy".
However in the test result (this is what is concerning me) he says:-
"EMG of the right tib nerve reveals several high amplitude polyphastic MUP's, no SPA and dense volitional activation pattern.
The right extensor digit brev speals SPA (sparce), polyphastic MUP's and slightly lightened volitional activation"
Lately I have been getting very mild twitching in the leg, arm and sometimes face. They last less that 1 sec and are sporadic.
I have been extremely stressed and my wife reassures me that the Dr said that I don't have ALS however the report he wrote has me confused.
I apologise for posting this but if anyone can assist I would be grateful.
Many thanks.
Antman