The MS Society, they have done absolutely nothing for people like me. I was diagnosed on a possitive MRI. I have had all symptoms apart from fatigue oh! and TN. I have spent mainly the last three years researching areas which have been relevant to me, I started with subluxations and progressed from there, what exactly have they been researching obviously not into alternatives as I have.
I shall say nothing more, but make up your own minds as to where it has all gone wrong.
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