Okay... MRV here we come!

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

Okay... MRV here we come!

Postby Jamie » Tue Jun 09, 2009 10:45 am

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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Postby peekaboo » Tue Jun 09, 2009 11:37 am

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Postby mrhodes40 » Tue Jun 09, 2009 2:59 pm

Way to go it is just more information.........
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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Postby Sharon » Tue Jun 09, 2009 3:40 pm

You and Mel are in the driver's seat. You get the tests completed, then you decide about the intervention.

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