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One day post surgery. Dr D performed two CCSVI surgeries yesterday. The earlier is a friend of a TIMS member. After the consult of collar bone placement once the op began he placed my rt. jug stent in the middle of hte jug and the lt jug new stent was placed below or maybe overlap like Sharons. My r...

got my follow up MRI/MRV's and consult w/Dr D. My stents are looking great but....I am going in surgery for 2 new stents Jugular at ea. collar bone. Dake said I will be able to go home afterward if I felt OK to do so. He was totally enthusiastic and excited about it all. Took a short survey re: fati...

Ditto Sharon's post

What about getting stent mfgr's a heads up? They could be the industry back up and $$$

BUMP

WOW a triple whammy. If I may suggest that you wade thru the antibiotic forum and also the copaxone forum where there are tales of success as well as concerns. Great places to gather info.

Here ya go

http://www.thisisms.com/ftopict-7774.html

Welcome and good luck.

Not ot hijack this thread...

lobra going to california at the same time as the symposium...does that mean you are ging to see Dr D?

Oh yeah...how bout Michele Obama?

I'm going bonkers again...this is so exciting....

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Hi Cure - It sounds like you are breaking the CCSVI barrier. Hoperully the vascular doc can turn the lights on your neuro

Good luck on Tues.

H

hlm & mamcitia -

This is very good advice and very organized.

Rokkit - not at all! go for it plus travel in a different part of the world. The only concern is what would you do if you have stenosis or occlusion? Do I remember correctly that Dr D has reccommended a vascular guy in NY?

P.S Erika great post w/ dr Simka findings thanks for sharing!

oh marie - it is so good to hear from you and all your positive news :!: I am going to share your report w/my family (sisters & parents). Since you and I are the later types of MS. They are very supportive of the CCSVI theory and intervention and impressed with all U TIMS folks our there. I am almos...