Hello Cindy,
Does this mean we can't be angry with the Shared Solutions folks? I was really getting my gander up to give them a hard time for you.

I'm terribly sorry to hear about your new "label", but to be honest, my Neurologist in Fla. never liked to label anyone. He felt that my MS wasn't your MS, and it was a disease that couldn't be "labeled", so I honestly don't know what type of MS I have, although when I read the literature, I suppose I would be "labeled" RRMS. I've come to realise that MS isn't all about labels but rather it's about the differences in each of us and how we react to different therapies.

I was in the original Antegren studies, and did wonderfully well. Now that we've decided to persue other avenues of becoming parents, I'm pretty sure I'm going to go back on Tysabri again too. It seemed to work well for me, and I didn't have any side-effects whilst taking it at all. Enjoy your visit with your friend tomorrow, and don't feel sad that she has to see you "this way". She's coming to visit "Cindy the friend", not "Cindy the one who has MS".

Have a lovely time tomorrow, and take all those trips you've been dreaming of taking. Live one day at a time. That seems to be working for me these days.

All the best,
Chris