Hi, and Welcome (I don't think I've seen you around here, yet...).
I just had my 2nd Tysabri infusion last Wednesday. So far, so good. I do notice I'm more tired than usual for the first 24 hrs after the infusion, but then I feel normal (for whatever "normal" is for me these days). I'm hoping for the best...
Good Luck to you!
Cheers,
Guitar_grrrl
Hi there,
We have a couple tysabri users and one about to begin on this list. Hope this helps. Isn't the beating from MS enough? Don't beat yourself up anymore :)
As Quix points out you can exchange private mail with forum members. Just use the hover feature over the members name, and when it says send a message, click there.
http://www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746
Welcome, and tell us how you feel comfortable to share.
-Shell
You also need to know that we have a private (non-public) message system here on MH. Just go to your In-Box - upper right hand of the page. You can exchange emails, phone numbers or just talk and it will all be visible ONLY to the person with whom you are talking.
Q