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


Postby dbsandiego » Mon Aug 10, 2009 9:02 pm

This sounds too good to be true! What is Dr. Dake's success rate? How do I contact Dr. Dake?
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Postby peekaboo » Tue Aug 11, 2009 6:37 am

Here ya go

Welcome and good luck.
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Postby mrhodes40 » Tue Aug 11, 2009 9:59 am

we don't know if it is too good to be true--there are no published peer reviewed success rates yet. this is still experimental though there is a fair amount of early work on it and we do expect the results of the Liberation group next winter. The research "sticky" at the top of the forum with the papers associated with this will show you what IS done and out there now to read.

I hate to be a wet blanket but people have to know that... it is only fair.

that having been said, I am doing well and am glad I got treated even with the unknowns because the heat tolerance thing and the reduction in fatigue levels is so wonderful. I hope my MS goes away and never progresses again, but I don't know that will be true and it would be unfair to promise it or suggest this is a sure thing at this point.
I'm not offering medical advice, I am just a patient too! Talk to your doctor about what is best for you... This is my regimen thread Read my book published by McFarland Health topics
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