Plavix and aspirin vs coumadin post procedure ??

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

Postby zinamaria » Sat Jul 23, 2011 8:30 pm

Thanks Cece, yes that was with Dr. Cumming. He said I could change, but I did not see any reason to go with something else at this point. One more week of the plavix for me....

Am doing well, still have a lot of energy but not much change in balance. The heat is tough when it's really hot, but when it's just 'hot' maybe around 85 or so, I feel I can function better than before. My biggest hope is for no relapse and that my body will adjust to better blood flow which will eventually make a difference.

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