Note: I was going to post all about what happened in the past two weeks, but I realized that I really hadn't talked much about how all this other stuff is going for me. I'll make my next post about how that all works.
I then got to have some tests on my brain and how signals from my eyes, ears, hands and feet made it to my brain. And again the tech asked what they were testing. Once again my response and then once again a reaction of "Well yeah, things are not what would be seen as 'normal' results." Finally in January, a repeat MRI, this time lots of time on my neck and head, and no reaction at all from these techs, but they were much more careful getting me off their machine that they were when I showed up. And then later that month Dr. Mary Amir (my neurologist) had me in her office to tell me that she knew exactly what the problem was and where it was located. We got to work getting me up to speed on how to deal with MS.
It seems that I have an area in my spinal chord near as it's in my neck, about the diameter of a toothpick and about 1/3 of an inch long that just doesn't work. I'm just missing parts of my spinal chord. Sort of a strange feeling when you think about it. How something that little could mess with your left foot, parts of your left leg, and the signals from your inner-ear.