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Venous Insufficiency and Multiple Sclerosis:Too Soon to Tell

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Old 11-13-2010, 11:14 AM #41
ykonstan ykonstan is offline
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ykonstan ykonstan is offline
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i'm going to have my testing on dec. 15 in Albany and i don't know what kind of procecure they have in mind. I think that placing stents is more appropriate since it keeps veins open but i'm not sure if they do it now.

JM, where did u have your operation? and what name of the doctor? sorry for asking but i'm trying to figure out what is the better way to do this ccsvi procedure and where to go?
I live in central NJ and i'm ready to travel (my husband is my personal help and supporter in everything)
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Old 11-15-2010, 09:24 PM #42
jacksonsmommy jacksonsmommy is offline
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Originally Posted by ykonstan View Post
i'm going to have my testing on dec. 15 in Albany and i don't know what kind of procecure they have in mind. I think that placing stents is more appropriate since it keeps veins open but i'm not sure if they do it now.

JM, where did u have your operation? and what name of the doctor? sorry for asking but i'm trying to figure out what is the better way to do this ccsvi procedure and where to go?
I live in central NJ and i'm ready to travel (my husband is my personal help and supporter in everything)

Mine was done in Bulgaria by Dr. Petrov. All the US places hadn't really opened up when I went overseas. It was all very cloak and dagger in the US six months ago.
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Old 11-25-2010, 01:19 PM #43
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SallyC SallyC is offline
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My Friend's after CCSVI balloon procedure....
It seems to be working, so far......

Quote:
a note to say hi and let you know I am back home. It was a rough trip but successful. had blockage in left jugular veins and azynous about 75 percent,50 pecent on left side, said right side looked good but did get angioplaysted on the left side and azynous veins. today I do not have to use cane to walk as left side is getting stronger about was ready to graduate to a walker then w/c as left leg was getting so bad but now it is getting stronger. Incontenance is so much better, double vision is gone, dizzyness is still there but hope that will get better as times go on. cognitive seems better, attitude is so much better even though I am still a b--ch.lol Fatigue seems to be improving overall am totally amazed and so thankful for the results I have seen and hope to see more improvements as time goes on. I know the neuros will probably say this a placebo effect but it is not as how can inconstinance be a placebo as that is so much more improved,

Trip was rough but got through it. Son was fantastic, treatment was billed to medicare . Don't know how much they will pay but will find out.

Now it is time to heal and let my body get use to blood flowing through the body again. Wish everyone could have this done and see some improvements. Met couple from Canada that was going for treatment and couple from Virginia so many are coming from all over to get this done. Hope it will be for all who has MS. Will not be taking Tysabri again, will keep taking LDN for it now and nothing else.

After I get more rested will let you know of improvements. Did not get video of before and after as I was sick that morning and not up to taping will do a video at Christmas as update as son has video camera that he can tape instead of cell phone. Hope you are doing well.
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Last edited by SallyC; 11-25-2010 at 01:38 PM.
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