Don't get me wrong, Cherie. this subject does interest me. I follow the Tysabri story pretty closely. I have friends on this drug, conversations with my neuro and ms specialist about this drug, and might have to consider taking this drug in the future (like anyone else with MS, I realize it behooves me to keep options open). I'll continue to take an interest in Tysabri threads.

I know you're a numbers and stats girl, I can appreciate that - we're similar in that respect, anyway. Whether you continue this discussion here is totally up to you of course; I have no say about that and it's a-okay with me.

I just wanted you to know that some of us are not waiting to hear the verdict you and whomever else comes to, because we've already made our well and fully informed decisions in partnership with our respective neurologists; which ultimately, is as it should be.

For all the rest, I hope they stay tuned if that's their desire (and that they follow up with their neurologists after the fact).