
Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.

deleted_user
Hi everyone, I was told I had CIS Clinically Isolated Syndome. Which means CIS which I found out from this website through good friends. My neuro never said anything, not a word, just put me on avonex and had me join a MS Alliance Support Group. I came into the hospital with my whole left side numb. Now, the only thing that is sort of numb is my foot when I do move around too much.
I would like to know if anybody has had one attack and also for the people who have had more "how long did it take before you had your second attack"
Please answer me, because I am really scared right now and I am wondering if anyone is going through the same thing.
Thanks alot everyone
You guys are the best!!!!!!!!!!!
HUGS and prayers, Margaret.
I would like to know if anybody has had one attack and also for the people who have had more "how long did it take before you had your second attack"
Please answer me, because I am really scared right now and I am wondering if anyone is going through the same thing.
Thanks alot everyone
You guys are the best!!!!!!!!!!!
HUGS and prayers, Margaret.
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