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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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concerned
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PostPosted: Wed Dec 01, 2010 10:41 am 
Thanks Malden!
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thornyrose76
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PostPosted: Wed Dec 01, 2010 7:30 pm 
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concerned wrote:
I'm sorry thornyrose, I don't know what to say. I was just reading about plavix and I thought those links might be helpful.

From what ladygazelle said, it doesn't seem Siskin is too into CCSVI.


He's doing a trial, I'd say he's definitely "in to it..."
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thornyrose76
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PostPosted: Wed Dec 01, 2010 7:40 pm 
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concerned wrote:
jay123 wrote:
concerned, don't you think you should be researching other treatments for your poor mother rather than spending al your time battling ccsvi? jeez, you'd think you would have something posivitve to do rather than working on negatives.


Please try to stay on topic.


Okay 1/3, 1/3, 1/3 is what Siskin has said, in other words it helps some doesn't help others, period. if you or someone you love has MS and it didn't work, why be using this message board even? Good or bad once I have the procedure, that's it for me. So jay123 has got a good point.
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concerned
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PostPosted: Wed Dec 01, 2010 7:41 pm 
Good for you, and I've never told anybody not to go ahead with anything. I've mostly just said things akin to what Dr. Siskin seems to have said, according to that blog post.
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thornyrose76
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PostPosted: Wed Dec 01, 2010 7:45 pm 
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au revoir!
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concerned
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PostPosted: Thu Dec 02, 2010 12:21 am 
Goodbye!!!

(I'm French if you were trying to be sneaky, pardon my french.)
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thornyrose76
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PostPosted: Thu Dec 02, 2010 1:25 pm 
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and I'm english, what's your point? You seem very negative...
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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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