Thanks for the response! My lovely wife found this website. We've been going somewhat crazy with every twitch and weakness. Its great to see so many diverse problems and realizing we aren't alone and that I can get better.MMN is such a rare disease, we've only had each other to talk to. None of the neurologists in our town (Toledo, OH) talked about MMN. We ended up at U of Michigan with Dr.Jim Teener (thank God). He was able to come to this diagnosis with exactly the same test results.

I'm new to any type of diseases (I've been blessed most of my life) and am having a hard time finding my limits. It seems like by the time I start to feel any fatigue, I'm already too far gone and am ehausted for the net few days.
I just started my IVIG treatments at the end of December, so I can't really say if it is doing anything for me yet.

Anyways, thanks again for the kind words.

Scott