Just over three years ago I heard about CCSVI and its treatment. After a couple weeks of fevered research, I decided that Zamboni's theory made a lot of sense, and that given the rapid deterioration in my MS symptoms, I should take the earliest possible opportunity to be tested and, if appropriate, treated for CCSVI.
I'm SO glad I didn't wait for the testing and treatment to be made available in Canada because, if I had, I'd STILL BE WAITING FOR THE RESEARCH TO BEGIN! Geez, what a travesty!
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Me too !! Bureaucrats certainly take their time. Perhaps its time to prod the process. Wonder how the studies in NF are doing?
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