Re: A few major concerns
Does anyone here know, from their journey to diagnosis--if atrophy is possible with MS? I keep thinking that if I had ALS, I'd be worse than I am after a year of atrophy in my hands. Is that a valid assumption?
I know the neurosurgeon was concerned--but do EMG/NCVs...
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Ok. Here is my story. I came here last year scared and concerned about widespread twitching. I went to the neuro in July 2010 and I had 3 visits with him from July to September. He only did an EMG of my arms at this time. I have always had pulse twitching. Meaning heart beat twitching. It...
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Hi and welcome to our forum blee--
I have fibromyalgia and my flare ups feel exactly like-- cramping. We usually use our muscles bilaterally, so often times, it will hit me on both sides. Now don't start worrying about fibro..... I guess I shouldn't have mentioned that...... there are many more...
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Hello everyone,
I have not been diagnosed with als but am very scared that i have it. I have a long story but I will try to shorten it as much as possible. i got the swine flu back in april and have been having weird neurological symptoms ever since. It first started out with my arm feeling...
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we tried to relieve your fears the last time you was posting but nothing convinced you that you really don't sound like you have als.
it sounds like mentally you are still in a bit of a state as you were before.
you said you was not going to come back,what has happened to bring you back to the...
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