MND progressively destroys Motor Neurones of
the body, and leads to weakness and wasting of the muscles, which in turn cause
increasing loss of mobility of limbs, and difficulties in swallowing, speech,
and breathing: it’s a fatal disease, which has no cure.
The words being added to this blog are mine, started initially when MND robbed me of speech in early 2006, to help the dedicated team of “Professionals” who have tended to my welfare throughout my illness, and also family and friends. I thought it fitting to record my unknown journey “Living with MND” to give a better insight into my progressive deterioration and thoughts.
I have wanted to use my notes to start a blog for some time, to publish what life is like with MND for me, but never quite got around to it until now. I know that time is running out, hopefully slowly, but things are getting more difficult for me by the day, so as I am no computer whiz, I have asked my niece to do the techie bits for me, but honestly, the words and thoughts are mine.
There will be a few posts which are historical, but hopefully this will give a good background for what is to come for anyone who takes the time to read this blog.
If you do read my musings and feel it is of benefit, please do let others know of its existence to help everyone who maybe impacted by MND, here goes....
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