At this point I suspect that I will once again be part of the statistic that I will be somehow disabled from the Multiple Sclerosis. I’ve tried to be as mentally and emotionally prepared for this as much as you can be in advance. The neuro wouldn’t say my MS is more aggressive than most at my last appointment, probably just being reserved, but I’m sure it will be confirmed at the next appointment and when I get a copy of the report later this week. The worst part is that the primary focus seems to be my arms and hands so I suspect that any disability will be in those areas. At least voice recognition software has come a long ways in the last few years!