I faced a glass half full/half empty situation today
when my consultant laid out the possible interventions to tackle my
Parkinson’s. It went something like this: “Current levels of medication aren’t
working so we’ll increase the dose; if that doesn’t work we’ll try a duodopa
pump which administers levadopa directly into the intestine; if that doesn’t
work we’ll stick electrodes in your brain…” With my glass half empty mentality
I could feel myself ticking off and using up the options as fallible steps
towards being totally unprotected from the onslaught of Parkinson’s. But, a
glass half empty is first a glass half full so the options are worth their
weight in gold as something I can try, which is better than laying down and
letting the Parkinson’s tide wash over me...
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