Before I
start this blog I wanted to write a little about my history so that when you
read my future posts, it will all make sense. My name is
Jordan Smith. Early in 2003, I started having minor seizures. They were so
minor that I had no idea what they were, nor did anyone else, simply because
there was very little outward signs. In late October 2003 I was eating
breakfast and when I grabbed the orange juice to fill my cup, I had a seizure
but this time it was more serious. It wasn’t a grand-mal seizure but it caused
me to simply pause and I couldn’t do anything, and my mind was blank. Because
of this, I poured the orange juice all over my French toast! My parents noticed
this and we went to the doctors. They scheduled me to have an MRI on November
2, 2003.
On November
2, 2003, when I was 13, I was diagnosed with brain cancer. If you’re curious on
the type, it was a pilocytic astrocytoma. The tumor was so large that they
operated on the very next day of finding it. It was 8x6x6cm on the left side of
my brain. The first operation was 14 hours long. Besides the fact that I had a
massive tumor, my body was in great health, thankfully.
The main
side-effects were blindness in the right half of each eye, aphasia (the loss of
speech and comprehending language), short term memory loss, cognitive thinking challenges,
and I fell back to a 3rd grade reading level.
Roughly 6
months after the 1st brain surgery we found a cyst growing and
taking the space of the original tumor. We continued to watch the cyst for
another year and a half in hopes of it going down, but it didn’t. I had the
strong impression that we needed to operate again to remove it all. The doctors
agreed and on December 13, 2005 we operated again. They were able to remove it
all and I’ve been cancer free ever since, but there was similar side-effects
like the first surgery. Within an hour after my second brain surgery, I had a
stroke which let me paralyzed on the right side of my body. Thankfully, I was
able to regain almost all major movement within a year.
A lot has happened
since these 2 surgeries. My epilepsy is still lingering and that is what I am
trying to control now. I'd like to share my experiences that are going on now and ones from the past.
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