Stent 3 months post procedure

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

Stent 3 months post procedure

Postby Gordon » Wed Nov 10, 2010 12:45 pm

Transient Ongoing pain at stent area ?? May have wrenched during sleep.

Suggestions ??

Very stable by the way
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Postby dunkempt » Wed Nov 10, 2010 1:53 pm

I don't know how bad yours it, but I still notice minor transient pain at my stent site (heck, even a little on the other side where I was just ballooned) 7 months in.

I kind of like it as a reminder of what I did.
dx rrms august 2009 (dx CFS spring 1988) off avonex after 3 months
treated katowice 24-25 march 2010 - best thing that ever happened - check tracking thread
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Postby esta » Wed Nov 10, 2010 5:17 pm

ditto drunkemt, and i'm two months in. some weeks good, some not. the stent is the same...very painful, then fine.i was hoping that at 3 months things would change. we'll see...
no suggestion, sorry... well, patience, its all new, and its all forward, which is better than the other way :)
PPMS. Liberated Katowice, Poland
06/05/10 angioplasty RJV-re-stenodsed
26/08/10 stent RJV
28/12/10 follow-up ultrasound intimal hyperplasia
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Update at 3 months

Postby Gordon » Sun Nov 14, 2010 5:05 pm

I am coming along very very nicely, less andless pain and MS symptoms becoming less andless significant. Brian fog gone over 75 % of the time.

Keeping fully aware to ensure maximum water intake is a must. I also spread my Plavix out over 24 hours by splitting the plavix in two, half in the morning and half in the evening.
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Postby NotFound » Sun Nov 14, 2010 11:09 pm


Happy for you, Gordon :)
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