Paying for CCSVI

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

Paying for CCSVI

Postby Jasmine » Sun Nov 29, 2009 12:29 pm

H, I'm new on here but was wondering if it is possible to go to Europe and be investigated and treated for the ccsvi? If so where do you go and who to see. Is it Poland?

Thankyou 8O
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Postby Mutley » Sun Nov 29, 2009 12:47 pm

Hi Jasmine,

Yes, you can do that. There are a few topics on here with all the info you need but there is lots of reading needed :D Dr Simka in Poland is your European option.

Good luck!
Last edited by Mutley on Mon Nov 30, 2009 2:00 am, edited 1 time in total.
Mutley goes to Poland 1st symptom was Optic Neuritis in 1998, DX RRMS Jan 2001, DX SPMS 2007. Last EDSS by doctor 7.5
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Postby Jasmine » Sun Nov 29, 2009 12:53 pm

Thankyou. I have read quite alot about it and am aware of all the risks. Interestingly, my dad had stent put in his veins years ago 9different weins though as this was for angina) but it does make me think if I have soe hereditory vein insufficiency thing going in. I so want to have the tests for this at least asap. Do you know where Dr Simka is based? :x
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Postby Mutley » Sun Nov 29, 2009 12:56 pm

I think he operates in several hospitals in and around Katowice (Poland)

Good luck!
Mutley goes to Poland 1st symptom was Optic Neuritis in 1998, DX RRMS Jan 2001, DX SPMS 2007. Last EDSS by doctor 7.5
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Postby Pepe » Mon Nov 30, 2009 1:00 am

Welcome Jasmine,

You will find interesting information at topic Going to Poland!!! Page 2
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