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I can't explain the number of doubts
that I have gotten over the years when I tell people that I have a plastic
skull.
Let me guess. If you didn't already
know, you're already second guessing that statement? Understood. That is
why I think it's finally time to make like a press release trying to
convince everyone it's true. I haven't been able to find the paperwork
anywhere, but I will continue to look till I can get all the facts. I'd
like to know all of them as well. It is also near impossible to find
anything on the internet about it. If I remember correctly, I was the
first to have this type of surgery done. Without knowing the exact
diagnosis (till I find the paper work) I wont be able to find anything
online about it. But from my recollection and the stories told to me, it
goes like this:
When I was born my skull was smaller
then normal. This was going to prevent my brain from growing normally. The
result that this was going to have was I was supposed to grow up as a
vegetable. I am not sure that paraplegic is the word, because that deals
more with the spinal cord, but it is basically the same as what could have
happened.
To solve this, they cut out a section
in the upper back part of my skull, and replaced it with some type of
plastic piece. This would (and did) allow the brain to expand normally.
One metaphor I have always used is like baking bread. When you bake bread,
it expands considerably. Picture baking a loaf of bread inside a box that
is just large enough to hold the bread at an uncooked state. Once in the
oven, the bread will try to expand, but there is no room. Thus,
deformities will occur and the bread will not cook properly. This is
basically what was going to happen to me. Once my brain would start
growing, it would start rubbing into the rigid skull, damaging sensors and
doing permanent damage to my body.
I was only 10 months old at the time
of surgery, so I don't remember any pain or anything along those lines. I
remember my father telling me stories of looking into the room and seeing
my scalp folded over my forehead, and how hard that was to watch from his
point of view.
I have found out many small details
over time about my recovery and how lucky I have been. When I was about
12, I was told how lucky I am to be able to grow hair down the middle of
my head. I can't imagine how bad it would look with this 3 inch gap down
the middle like a racing stripe. On my 18th birthday, I was told I am
lucky to be alive. I found this as a major shock. Apparently since I was
the first to have the operation, they didn't know exactly how long I will
live afterwards. The doctor said I will be lucky to make it to 18, and
enjoy an early adulthood.
Well, here I am. 21. I beat the
system.
I have had several times throughout
my life where I would get constant migraines, and the doctors were never
able to explain why. I had what seemed to be a million MRI's and Cat Scans
done on me, but nothing really ever showed up. I always thought it was
linked to my plasto, but there's no hard evidence.
A few big headaches were worth living
this long.
    
Note: I have found the paper work. To
read the real story, click here
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