I suppose I've known about my mystery disability since I went from forearm crutches to a walkerr and I've definitely known that I'm legally blind since birth, but when I was a child nothing got in my way. I knew that I was legally blind but not as much was based on sight. As for the dysarthria and the tiredness I am pretty certain that those symptoms are fairly new.
Everyone whom I tell about my mystery disability tells me that a diagnosis is just a name, that in the long run it doesn't matter; they don't get it. Instead of a diagnosis I have a list of symptoms and diagnoses that seems to keep growing. Doctors will not treat these symptoms with out this name, without a diagnosis and I wouldn't really care if I wasn't exhausted and weak all the time, if it didn't take multiple times for someone to hear and understand me, if it didn't take the breath out of me when I talk.
Most of the time a diagnosis means a reason and doctors won't treat without a reason. According to almost every test there is no reason for me to have a disability.
I am more aware than I was when I was a child because back then I didn't feel it like I do now. I am a mystery that defies all odds and… I am aware.
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