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Posted: Tue Oct 17, 2006 6:31 pm
by gabelle
Hello, I'm another newbe to this site. Diagnosed in 2003, (wheelchair dependent). MD's with 2 opinions, one says RRMS now SPMS and the other says PPMS. I have tried all CRAB's, none work. I am now approved for Tysabri and should get 1st infusion soon. This is the best MS site I have found. A lot of good info here and I am looking forward to continued communication and new friendships.

Posted: Wed Oct 18, 2006 2:47 am
by CureOrBust
not only is there a lot of good info, the people are good too. but dont let them know...


I hate it when they keep you guessing.

Posted: Wed Oct 18, 2006 7:17 am
by mick_b
Hi gabelle:


It sounds like you’ve been through ths MS dx mill. I think this has happened to most of us. I went thru it for two years, it’s the nature of the beast.

I think it’s great they approved you for tysabri. I have PPMS and they said no for me. From what I read, It seems pretty effective. Please let us know how it goes.

Don’t hesitate to post often, a lot of watch in case we can relate or help. Sometimes just knowing a lot of us are in the same boat helps a little.

Good luck


Posted: Thu Oct 19, 2006 5:36 pm
by gabelle
Thanks to ALL of you, should get Tysabri this week. Will keep you updated. :D

Posted: Fri Oct 20, 2006 9:27 am
welcome to the group here....hope everything goes well for ya....


Posted: Wed Nov 01, 2006 10:18 am
by Arron
Hi Gabelle,

Sorry I missed your introductory post for so long! Welcome... and best of luck with Tysabri. Please do let us know how you do with it.