About two years ago (2015), I was diagnosed with MS, and I thought my life would never be the same again, but as it turns out, its better now that it has ever been.
The initial shock is devastating – besides the physical disabilities, the emotional ones are probably even worse. Brain fog, constant fatigue, and in my case, loss of the use of my left hand and all fine motor co-ordination disappeared.
My wife is an ex nursing sister, so from the outset we started looking for options and as there is no known cure. We started looking at what else was available, and this of course lead to alternative methods…
 
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