This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.

Skip to content

Introductions

New members should feel free to introduce themselves here
Post a reply

Introductions

Postby gabelle » Tue Oct 17, 2006 7:31 pm

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.
User avatar
gabelle
Getting to Know You...
 
Posts: 22
Joined: Mon Oct 16, 2006 3:00 pm
Location: Georgia
Top

Advertisement

hi gabelle

Postby jimmylegs » Wed Oct 18, 2006 1:52 am

hi gabelle, welcome, sounds like you are well on your way to finding a solution that works for you! i think it's the best ms site too. happy communicating!!!
User avatar
jimmylegs
Volunteer Moderator
 
Posts: 10420
Joined: Sat Mar 11, 2006 4:00 pm
Top

Postby CureOrBust » Wed Oct 18, 2006 3:47 am

not only is there a lot of good info, the people are good too. but dont let them know...

welcome.
User avatar
CureOrBust
Family Elder
 
Posts: 3341
Joined: Wed Jul 27, 2005 3:00 pm
Location: Sydney, Australia
Top

I hate it when they keep you guessing.

Postby mick_b » Wed Oct 18, 2006 8:17 am

Hi gabelle:

Welcome.

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

Mick
User avatar
mick_b
Family Member
 
Posts: 40
Joined: Sat Jul 29, 2006 3:00 pm
Location: Western NY
Top

Postby gabelle » Thu Oct 19, 2006 6:36 pm

Thanks to ALL of you, should get Tysabri this week. Will keep you updated. :D
User avatar
gabelle
Getting to Know You...
 
Posts: 22
Joined: Mon Oct 16, 2006 3:00 pm
Location: Georgia
Top

Postby REDHAIRANDTEMPER » Fri Oct 20, 2006 10:27 am

welcome to the group here....hope everything goes well for ya....

chris
User avatar
REDHAIRANDTEMPER
Family Elder
 
Posts: 285
Joined: Mon Nov 07, 2005 4:00 pm
Location: wisconsin
Top

Postby Arron » Wed Nov 01, 2006 11:18 am

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.
Disclaimer: Any information you find on this site should not be considered medical advice. All decisions should be made with the consent of your doctor, otherwise you are at your own risk.
User avatar
Arron
Volunteer Moderator
 
Posts: 893
Joined: Sun Feb 01, 2004 4:00 pm
Location: California, USA
Top
Post a reply

Return to Introductions

 


  • Related topics
    Replies
    Views
    Last post

Who is online

Users browsing this forum: No registered users

This site does not offer, or claim to offer, medical, legal, or professional advice. All treatment decisions should always be made with the full knowledge of your physicians.


This is MS does not create, endorse, or republish any content. All postings are the responsibility of the poster. All logos and trademarks in this site are property of their respective owners. All users must respect our rules for intellectual property rights.

Contact us | Terms of Service