Talking to the neurologist in Denver, Colorado, back in 2004 he told me in no uncertain terms that I couldn’t just deal with the disease as I wanted to because it was incurable and if I didn’t take the medication which I refused then I would be in a wheelchair within six months.
Talking to my doctor in 2006 he confirmed what the neurologist had told me then basically laid into me because he was far more knowledgeable and experienced and he knew better than I.
Talking to a different neurologist at a very prestigious hospital also in Denver, he was shocked that I was not on the prescribed drugs. While shaking his head from side to side and sucking air through his teeth he then told me that the so called natural ways of curing the incurable were just pipe dreams.
2012, still no drugs.
2013 and back in the UK, at the hospital in Nottingham, the neurologist, an Asian doctor simply said that the MS was at stage 4 and because of this that there was no medication she could prescribe that would help.
2016 and I am feeling more optimistic, stronger and more balanced than at any time in the past several years. Mel, my Sunday carer said that looking at me she couldn’t tell I was sick, bearing in mind she see’s numerous people every week with MS or similar diseases. I know that my determination to continue using the nutritional supplements, drinks and foods I take is making a world of difference.
So far five different neurologists and about six doctors have told me this is incurable and as such returning to good health is impossible. I say sorry but you are all wrong, the way I see this, the fact that I believe 100% that anything can happen to me personally if I have complete confidence and absolute faith which I do.
Note to MS: Sod off, you can’t live here anymore.
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