This Is MS Multiple Sclerosis Knowledge & Support Community

Welcome to This is MS, the leading forum for Multiple Sclerosis research and support. Join our friendly community of patients, caregivers, and researchers celebrating over 20 years of delivering hope through knowledge.
https://www.thisisms.com/forum/

Continue using DMDs after procedure...?

https://www.thisisms.com/forum/viewtopic.php?t=8985

Page 1 of 1

Continue using DMDs after procedure...?

Posted: Sat Nov 28, 2009 9:50 am
by ikulo
Hey all,

those of you who have had the procedure (stent or balloon) or are planning on getting it, are you planning on staying on your current DMDs (copaxone, rebif, avonex, betaseron, etc.)? What are everyone's thoughts on this?

I added a poll, but I'd like to hear why or why not,. I'm just curious about my future options if I decide to get this done - weigh costs/benefits - but wanted everyone's experiences, thoughts, advice.

Posted: Sat Nov 28, 2009 9:57 am
by ErikaSlovakia
I have never been on DMDs and I do not plan to start with them.
I have been on LDN for a year and I continue with LDN aftr the procedure.
Erika

Posted: Sat Nov 28, 2009 1:33 pm
by wobbly
going off tysabri soon / then switching 2 copaxone most likely / he s [dr]\ getting afraid of it/ 32 treatments that is in the range of pml/ the risk seems harder than they thought / MS SUX i wish i could get balloned again :?: :?:
All times are UTC-08:00
Page 1 of 1

Powered by phpBB® Forum Software © phpBB Limited