EMG is next step for me. Actually meet with neuro today and EMG has been set up for end of this month. My main problems are arm/hand weakness in one side, some muscle atrophy in forearm and shoulder area of that side. A lot of fascics throughout body, especially in affected arm (most of all in shoulder and lats). Increased sensory disturbances, weakness, and fatigue over last two months.
The thing that brought me here was that I actually had cervical spine surgery about three months ago for a ruptured disc, and while all of the pain has been relieved, many of the other neurological and muscle problems that I was having before the surgery have remained. MRIs have ruled out any problems with the surgery, so my neurosurgeon and primary doctor are stumped. I came across a journal article online that talked about a small percentage of people in the early stages of ALS unnecessarily having the surgery I had to "correct" their symptoms. Now, I realize that a small percentage of people with ALS would mean a REALLY small percentage of the general population, but at this point I am concerned and a little scared about the things going on with my body. I have had far more questions than answers, which is probably the norm for quite a few of the people on here. The EMG will hopefully shine some light on things.
You also don't know how grateful I am to the people that have actually been diagnosed that provide some insight. You are all very courageous people. No matter how this turns out for me, I will do my best to raise awareness and support of ALS in the future.