Continue using DMDs after procedure...?

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.
Post Reply

Will you continue to use DMDs after ballooning/stent?

Yes
2
33%
No
1
17%
Not sure
3
50%
 
Total votes: 6

User avatar
ikulo
Family Elder
Posts: 444
Joined: Tue Aug 04, 2009 2:00 pm
Location: colorado

Continue using DMDs after procedure...?

Post 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.
ErikaSlovakia
Family Elder
Posts: 1125
Joined: Wed Jul 29, 2009 2:00 pm
Location: Slovakia, Europe
Contact:

Post 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
Aug. 7, 09 Doppler Ultras. in Poland, left Jugul. valve problem, RRMS since 1996, now SPMS,
- Nov.3,09: one stent in the left jug. vein in Katowice, Poland, LDN, never on DMDs
- Jan. 19, 11: control venography in Katowice - negative but I feel worse
User avatar
wobbly
Family Member
Posts: 73
Joined: Thu Jan 01, 2009 3:00 pm

Post 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 :?: :?:
Post Reply
  • Similar Topics
    Replies
    Views
    Last post

Return to “Chronic Cerebrospinal Venous Insufficiency (CCSVI)”