Tuesday, August 28, 2007


Excuses-- something that I think about quite a bit and guard against. Making excuses can be confused with that amotivational stuff that I fight with due to the t.b.i.

Do I make explanations for myself out in public? Usually, I consider things as "need to know info." The casual human being I meet in a store does not have to know that I have mild expressive aphasia. My talking is too soft but understandable even if I miss a word and find a similar one to stick in there instead. The jogger that appears down the street does not need to know that I might see him as having two heads, two necks, four arms, two trunks somehow connected to one waist like a morphed out hydra. [The double vision in one eye thing].

It is important for me to know when I am tired and to pace myself so my energy is more even.
And important for me to know when taking time for healing turns into a convenient sort of laziness and unwillingness to extend myself and get out there and job-hunt [again]. Maybe I can't do what I used to do. Maybe I can do something. Even if it is part-time, "something" is better than sitting home crying about my unlucky break and all of that. Taking risks is risky.
And yes, I have used my own t.b.i. as an excuse not to take risks because I am afraid.

The c-t scans and the m.r.i.s don't always show the extent of the damage. Mine showed the specific damage in the left frontal-temporal lobe but not the stretching of the axons that were part of the more diffuse damage. No way am I allowing radiation to be shot into my head [PET or SPECT scans] even if some insurance company would like to spend that kind of money.

The hyperreflexia and double vision in one eye,
the refusal of my eye muscles to move unless forced,
the inability of my eyes to work together or with my brain,
the borderline hearing loss [which has now cleared up],
the difficulty navigating on uneven ground,
the true photophobia,
the objective vertigo [not dizziness, not a balance problem--
the room slides to the left],
the pervasive lack of ability to multi-task;
all are things I live with daily.

I don't get to add those things up in an attempt to justify quitting. I don't get to whine about things being harder for me than the average person even if sometimes they might be.

I am alive and I shouldn't be. My car was rammed into a house at a high speed. I opened the one door that wasn't stuck and let myself out of that car. The last neurodoc didn't understand why I "walk so well" as he put it. My hyperreflexia is very high on the spastic scale. I'm glad he wasn't checking me out in the emergency room. Else I might not be walking today. I walked because no one told me that I shouldn't be able to.

I was lazy before my t.b.i. That didn't go away. I got another crack at life. Maybe I can do it a bit better this time. I hope so. I've got to try. And that means attempting to blend in whenever possible and being as productive as I can be in whatever form it takes. It means not blaming others for my problems. It means being able to see my self as a sacred human being, not as my symptoms or my labels. It means ignoring those who tell me that I am not able to. I can wallow in my self-pity or I can turn my excuses into determination to get back up again and get going. I have to keep striving. I am part of this society, a citizen of the world, and I intend to make my contributions to the society that I live in.

sapphoq healing tbi

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