Children's Cancer Community
Courageous Kid - Alison Levie
Child: Alison Levie
Parents: Cheryl and Jim
From: Sebastopol, CA, USA
Diagnosed with: Ganglioneuroblastoma
Our Story
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I am Ali Levie. When I was eight years I was on vacation with my family
in Utah. I had a flu virus with fever and vomiting and was pretty ill
so my parents took me to emergency at the pediatric university hospital
in Salt Lake City. My mom is an emergency room RN and usually would
have refused a chest xray for me because of the radiation (and I never
had pneumonia or asthma). This one time, for some reason, my mom said
they could go ahead and take an xray of my chest. The emergency room
doctors told me I was going to be fine, that my I did not have
pneumonia, and gave me some fluids and sent me back to my hotel. Later
that night we got a call from the x-ray department that the radiologist
saw a "shadow on my x-ray" and asked us to return the next morning for
more films. When we came back the next day (a Sunday) the radiologist
was waiting for us and immediately took us in for more exams. They
found a baseball size tumor in my chest! This had to be the scariest
day of my life! We were now on a long journey, and I was diagnosed with
what I call the "best of the worst" ganglioneuroblastoma. I actually
had my fourth grade teacher put this word on one of our weekly extra
credit spelling lists! It is one word I wish I never knew. No one needs
the details of the next year and a half......all you need to know is
that the ONLY warning sign I had was I dropped out of gymnastics about
eighteen months prior to my diagnosis because a skill called back
walk-overs caused my excruciating pain in my mid back. I was in a
pre-competitive accelerated gymnastics group and all the skills had to
be completed to keep moving up the levels. Nothing hurt when I did
anything else, in fact I was like a skinny little gumby, and I had no
other limitations or symptoms. My road to recovery has been dotted with
many emotional components including post traumatic stress disorder and
panic attacks. I am now 18, just finished my first year of college, won
the title of Miss American Teen Northern California last year, and am
finally advocating for childhood cancer awareness.
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The SCCF was with me
my entire journey. We were connected after my surgery and we were some
of the first members. Having this type of group to be a part of
benefited my family in many ways. I am forever grateful to such a
caring, grassroots, local organization. Marty Close is dedicated and
does a fantastic job managing and fundraising. I am willing to speak
with anyone about my journey if it helps relieve the pain and fear. I
have a beautiful life ahead and this is ALL that matters!
This is MY story.
Ali
Sonoma Children's Cancer Foundation
P.O. Box 2246
Sonoma, CA 95476-2246
Toll free: 1-866-402-HOPE(4673)
marty@hopeforcancerkids.net
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