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Christine
Graham
When I
was a baby my parents noticed that I was always bruising at even
the slightest touch. The doctors could tell that something was
wrong with my liver, but weren't able to diagnose it until they
performed a liver biopsy. In December 1983 I was diagnosed with
Neonatal Giant Cell Hepatitis at 3 months of age.
Throughout the following year my parents watched over me while my
liver disease got worse. Then in November 1984 my father passed
away in a car accident, leaving my mom alone to take care of a
seriously ill child along with a teenager and toddlers. As time
went on I continued to grow sicker, developing ascites (I was a
3-year-old with a 32 inch waistline) and enduring more than 20
hospitalizations due to uncontrollable nose bleeds. My mom and
oldest sister told me that I used to sit against the corners of
the walls in our house and rub back and forth trying to relieve
the itching sensation I was experiencing due to the liver disease.
We have pictures of those corners all worn down to the metal
bracing thanks to me!
When I was 2-years-old my pediatrician, Dr Victor Alcalde, brought
up the subject of transplantation to my mom. She sought a second
opinion with Chicago's "finest and most knowledgable
pediatric liver physician." This doctor told my mom,
"It's no use. Just take her home, make her comfortable, and
let her die." Well, we all know my mom didn't listen to that! I
was put on the transplant waiting lists at hospitals in Denver,
Miami and Pittsburgh. All of the liver programs said that I was
the "perfect candidate."
In February 1983 we were paged and flown to Pittsburgh.
Unfortunately, by the time I was prepped for surgery we were told
the donor liver was unusable. Then, just six days after my fourth
birthday, on September 27, 1983, we were called a second time and
I received a great liver! Since then everything, with the
exception of one early bout of rejection, has been smooth sailing.
For
the longest time I was embarrassed to talk about my transplant,
but then I grew up and realized how special it is, and how I
should use this gift to help others. One way I would love to help
others is by becoming a physician. I have always wanted to be a
doctor. Most people just laugh and think I would want to stay as
far away from the field of medicine as possible, but it is what
drives me and what intrigues me. This past year I applied and
interviewed at five different medical schools (and I am proud to
say I was accepted to all five schools)!

After my classes ended this semester, I attended the Transplant
Games for the second time. The Games are incredible! It seems no
matter how much you try to prepare yourself for the opening
ceremonies and the donor tribute, you are never quite ready for
them. During these events there was not a dry eye in the entire
sports complex. It is so wonderful at the Transplant Games to be
able to talk with people and have them understand EXACTLY what you
are talking about. The stories are all amazing and all unique, and
the competitions are light-hearted.
In addition to attending the Transplant Games, my year has been
full of many exciting events. My liver became an adult in
September 2001 (turning 18) as I endured my hectic senior year at
the University of Nevada, Reno. In addition to acting as VP of the
school Pre-Med group and as a director of recruitment for the
Student Ambassadors, I worked 20 hours a week, took 17 credits
each semester, applied to medical school, graduated with two
degrees and, oh yeah, I got married!
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