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"Meg Embracing Miles" 30" x 24" oil on canvas |
I met Meg on Facebook back in 2010. I painted her portrait (pictured below) as one of the very first in my
Many Faces of NF series. Later she asked me if I could help her out by painting the portraits of three children living in an orphanage in
Nicaragua. I agreed to help out. Truthfully, I can't imagine what life in an orphanage is like, but I'm guessing they could use all the help and donations as they possibly can get. So, it was no trouble at all for me to be able to help her out with her request as she provided many photos of the children and let me decide which ones to paint. The portraits were then auctioned off and the money raised went to support the kids.
Meg sent me her story to accompany the first portrait, in her words:
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30" x 24" oil on canvas - underpainting |
"I was diagnosed with NF as an infant. My case was
caused by a spontaneous mutation, neither of my parents have NF and nor
do my younger brothers. For the most part I had a pretty normal
childhood, other than having a large tumor on my lower back that was
extremely painful when bumped, and also one on my foot. When I was 8, I
had major surgery to remove both tumors. My parents had shielded me
from the seriousness of the surgery and the fact there was a chance I
would not walk again after the surgery, but I did know that without the
surgery I would eventually be paralyzed. The following summer, though,
was when things really changed for me. Our local newspaper ran an
article about Neurofibromatosis and used my family as the subject. The
unfortunate title of this article was "Living with Elephant Man's
Disease." For the next several years I was teased and called names like
"Elephant Girl." It was really the first time I had felt "different"
because of my NF. The worst part of growing up with NF before the
Internet Age was not really knowing anyone else who had NF, other than
the people I would see once a year when my parents would host a cookout
and raffle for NF.
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2011 Watercolor and Wax |
In spite of challenges like that growing up, as well as several more
surgeries, I lead a pretty normal and fulfilling life. I graduated High
School with an Advanced Diploma, went to Virginia Tech and graduated
with a BA in Communication Studies and minors in Theatre Arts and
Liberal Arts, have a job and am active in my church where I volunteer
with our Preschool Sunday School, sing on the Music Team and am involved
in our Women's Ministry and Missions Ministry. I have been to Nicaragua
14 times since 2003 to volunteer in an orphanage, and have more trips
planned. I have also met so many amazing friends through Facebook who
have NF, or whose children have NF and am so grateful for the support
and friendship that has grown, even though many of them I have never met
in person. I pray every day that we will have a cure for NF some day.
The sooner the better!"
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