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Posted: Mon Jan 17, 2011 12:54 pm
by LR1234
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Posted: Mon Jan 17, 2011 2:28 pm
by L
Well, I assume it is still there. Hopefully I will know after Wednesday morning when I see a vascular doctor.
I had no blood flow in my left jugular vein before the procedure, because of a dysfunctional valve, and I have none after (I presume) thanks to this thrombosis.
The area aches a little, to answer your other question.
I was on clexane and plavix, my neurologist took me off the clexane but continued the plavex.
What would your answers be?
Posted: Mon Jan 17, 2011 2:41 pm
by L
Well, hopefully I'll have news on Wednesday. Good luck with it not recurring. Have you been told that this is a possibility?
Posted: Mon Jan 17, 2011 2:54 pm
by mavis
For those who have had the unfortunate complication of a clot in their jugular
How do you feel MS wise?
--Terrible which just shows CCSVI is real. After my jugular stenosed again due to thrombosis, my legs are much heavier and weaker, I have no energy, and I have increased numbness all over.
How does the clot feel in you neck? (are you aware of it)?
-- Not really. Sometimes I feel a bit of stretching, or pulling in the area, but no pain.
Is your MS worse or better than before the complication and procedure?
-- Worse than before the complication, better than before the procedure.
Are you on blood thinners to stop the clot growing? If so which ones?
-- First Heparin, now Coumadin.