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

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Jamie
PostPosted: Tue Jun 09, 2009 11:45 am 
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After much discussion over the past couple of weeks we've decided to look into all of this.

I've emailed Dr. Dake, Mel is going to talk to her PCP.

I've asked him if there's anyone locally he'd trust to do the MRV. Then we've got the intervention to worry about if a problem is found.

Right at the very beginning of the process but it feels good to do something.
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peekaboo
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PostPosted: Tue Jun 09, 2009 12:37 pm 
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Congrats
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mrhodes40
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PostPosted: Tue Jun 09, 2009 3:59 pm 
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Way to go it is just more information.........

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I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you...
http://www.thisisms.com/ftopic-7318-0.html This is my regimen thread
http://www.ccsvibook.com Read my book published by McFarland Health topics


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Sharon
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PostPosted: Tue Jun 09, 2009 4:40 pm 
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You and Mel are in the driver's seat. You get the tests completed, then you decide about the intervention.

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

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