liberation treatment - MS

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Tired LP
New Member

Date Joined Dec 2009
Total Posts : 4
   Posted 12/30/2009 5:24 PM (GMT -6)   
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

New Member

Date Joined Dec 2009
Total Posts : 1
   Posted 12/31/2009 10:41 AM (GMT -6)   
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?

Regular Member

Date Joined Nov 2008
Total Posts : 87
   Posted 12/31/2009 12:17 PM (GMT -6)   
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 they have a lot on CCSVI or hit up facebook.
Learning and living everyday to the fullest. My MS blog

Forum Moderator

Date Joined Jan 2007
Total Posts : 3568
   Posted 12/31/2009 9:49 PM (GMT -6)   
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.
Gretchen  ~  diagnosed with MS July 2006
I have no lesions on my soul and so I will live with no limits.

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