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liberation treatment - MS

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Posted 12/30/2009 10:24 PM (GMT 0)
Is anyone with MS in Canada able to get tested for restricted veins and has anyone been considered for a study? Iam just so fatigued that I'm willing to try anything since I can barely

walk. Help.

 

     notredame  Dec 30,2009

Posted 12/31/2009 3:41 PM (GMT 0)
As far as I am aware, there is a doctor out in British Columbia who is trying to do the testing (MRV).  Also the University of Buffalo is doing the testing in a study but they won't give you the results, so what good is it?

 

Posted 12/31/2009 5:17 PM (GMT 0)
There is a ton of info on other sites on CCSVI. I am surprised at how little the chatter is on here about it.

Check the http://www.thisisms.com/forums.html they have a lot on CCSVI or hit up facebook.
Posted 1/1/2010 2:49 AM (GMT 0)
Dave,

Yeah that is sorta crazy.  I am so totally excited by the CCSVI development.  I am going to call and make an appointment with Dr. Dake.  I think this is a real breakthrough and will help everyone that has a solid diagnosis of MS.  I am excited to see how many other diseases and disorders this ends up effecting. 

This is a very quiet board compared to MS world, ThisisMS, and MS refugees.  We get more questions as to diagnosistics than anything.

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