The first national CCSVI treatment study is approved

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

Postby hannakat » Thu Sep 16, 2010 4:26 pm

HP ~ I agree..... KA-BOOM!! POW!

Okay, got that out of my system..... now to my question.

Has anyone heard back about being considered for the trial? Recruiting 600 patients cannot be an easy task but I hoped to hear something by now (fingers drumming against the desk....impatience winning out today).


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Postby 1eye » Thu Sep 16, 2010 4:59 pm

I'm progressive too. I hope he runs a separate trial for that. I'll quote Cordelia's Dad in his hopelessness, to tell you, about the time you should finally stop hoping, or give up, or think you are beyond help, knocked down, left out, hung down, brung down, hung up, disgusted, or flat busted:

"Never, never, never, never, never." -W. Shakespeare

Read the thread on Adventures of Darling Man.
The bottom line on MS is,,. They don't know what causes it. So they can't treat it. And this BUGS THEM.

I am not a doctor. Do not take anything I say as medical advice.
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