A bit late for my first memoir (available on the Kindle, in paperback or hardback) but I discovered this afternoon that my main (ie Neurological) disability is also called "wet brain" and it affects several parts of my brain: the "Thalamus (medial dorsal nuclei)", the "Hypothalamus (Mammillary Bodies)", the "Cerebellum" and the "Brainstem/Periaqueductal gray matter" and what I was put through at the hands of my fellow temp in my first job after moving in with Steve, could very well have started it or at least played a big part in the damage.
Should I start calling it "wet brain" to non-proffessionals so that that it feels more accessible than WKE or should I still keep spouting the mouthful of my diagnosis and watch as it goes flying over everyone's heads though?
Opinions please!
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