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Cathy Oliver
My mother told me that I was born a 4 lb. premature blue baby,
which means I had a hole inside my heart. I was also born with
a double curvature of the spine, drooping eyelid, clubfoot, and
a general nervous disorder later diagnosed as cerebral palsy (CP).
My early years were spent in doctor's offices with one health
crisis after another. My heart had to work extra hard to keep
me alive. Because of this, I didn't learn to walk without assistance
until I was three and even then my balance was poor.
I didn't start school until I was seven. My older sister Cheryl
and her friends would take turns carrying me on their backs. In
the winter, they would pull me on a sleigh.
When I was in Grade two, I had my first operation to raise my
left eyelid; a second operation was required.
In Grade three, I was very ill with headaches, dizziness and
vomiting. I was diagnosed with a brain abscess and encephalitis
(swelling of the brain). In surgery, the abscess was drained and
the fluid was removed. The operation made my Cerebral Palsy worse,
and decreased my balance due to the massive weight loss.
I had missed a lot of school; it was decided that I would be
transferred to a special education program at another school.
There was speech therapy and physiotherapy during this time. When
I was 13, my cardiologist Dr. Logan, repaired my heart damage.
Four defects were fixed, and my skin turned from blue to pink.
Soon after the surgery, I was diagnosed with CP.
When I was 15, I started High School in the Work Study Program.
It was structured so you went to school in the morning, and worked
in the afternoon. I applied myself, and after the first year,
I won Student of the Year. When I graduated, I worked at the Holy
Cross Hospital as a service aide, where I serviced and sanitized
carts. One day I fell and injured my groin. My employment ended
after 11 years of service.
During the past 13 years, I graduated from Vocational schools
and Mount Royal College, where I finished with a 3.88 GPA. I could
not find employment, so I decided to volunteer at the Cerebral
Palsy Association in Alberta (CPAA). In the five years that I
have been there, I have learned a great deal.
Just because a person is born with disabilities doesn't mean that
they should be treated any differently. We are all human and should
be treated equally.
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