| August 15, 2005
BY ROYCE ARMSTRONG
The Mississippi Press
Tragedy, generosity pair up to help
East Central High senior
HURLEY -- Sara Ashcraft may be able
to dance at her prom next spring, something that was once
only a dream.
When other infants are learning to
roll over, sit up, crawl, walk and talk, Sara Ashcraft, now
a senior at East Central High School near Hurley, was learning
the agony of post-surgical pain and the fear of spending nights
in sterile hospital rooms away from her family. When other
little girls started school and began learning to "fit
in," Sara was learning to accept being as "different,"
according to her father, Garry Ashcraft.
Sara Ashcraft, a petite, at-tractive brunette with a quick,
shy smile, was born with multiple severe birth defects, including
a leg that had to be amputated when she was an infant. Born
without hands, she was also born with a mild learning disability.
But Sara Ashcraft wants no pity.
"I am not handicapped,"
Sara says about herself. "I just have a few parts missing."
For Sara, hardship and challenge have been lifelong companions.
Her father is a totally disabled veteran and the family lives
on Social Security, veteran's benefits and her stepmother
Renee's income. Sara, though, appears to thrive on challenge.
She has undergone 56 corrective or reconstructive surgeries
in her young life, an average of three per year.
Through it all, friends, teachers
and family say, she has exhibited tremendous courage and good
humor. These are among the reasons she was selected as the
ideal candidate for the generous donation of a C-Leg.
"Sara is an excellent patient,"
claims certified prosthetist Bobby Leaber, the owner of Adaptive
Prosthetics of Gulfport. "She always comes in with a
smile on her face. Even if she is not comfortable (with a
fitting) it is hard to get it out of her. She never complains.
She is a tough girl."
Computer technology is taking prosthetic
devices to incredible new levels. The C-Leg is just one example.
The knee is crucial to smooth walking and the ability to walk
up and down stairs explained Leaber. In the past, the knee
joint on artificial legs was spring activated. The wearer
was forced to swing his or her body to move the leg. The wearer
must concentrate to make each step and consciously move his
or her body in such a way that the leg moves. Sara must also
listen for cues, generally a clicking sound, that the leg
is in a position that will allow her to stand.
"This leg is much easier on
my back," Sara said. "I do not have to swing it
out to the side. It also doesn't eat up my clothes like the
other one did. This one is safer. I do not fall with it."
Aside from the conscious effort required
for walking, Leaber continued, the wearer often back and hip
problems from the unnatural motions required activating the
leg.
"You can put a child on anything," Leaber said,
"and he or she will get up and walk on it. But, as that
youngster gets older, it gets harder and physical problems
can develop."
Sara has outgrown and had to change prosthetics 15 times since
infancy. Swinging a heavy artificial leg with her back was
beginning to affect her spine.
The C-Leg is an electro-hydraulic
artificial knee joint that is activated by a microprocessor.
It can be programmed to function according to the weight and
gait of the wearer, Leaber said. It reads signals from the
ground, the surrounding area and then "thinks" 50
times per minute, using hydraulics to move the knee. Walking
is much smoother, more natural looking and far easier than
on mechanical prosthetics.
Tragedy and generosity came together to give Sara a mechanical
miracle.
Brad Kimberly, the 27-year-old son of Michael and Dawn Kimberly,
of New York, was fitted with a C-Leg, according to Tony Barr
of the Barr Foundation. Kimberly lost his battle with cancer
early last year. The Kimberly family donated the C-Leg to
the Florida-based foundation. The foundation exists to assist
amputees obtain needed prosthetics.
Leaber contacted the Barr Foundation for assistance in obtaining
a C-Leg or similar device for Sara.
C-Leg manufacturer, Otto Bach Health
Care in Minnesota, was persuaded to fit the C-leg device with
a new pylon (shin) to fit Sara's height and weight, Leaber
reported. Leaber assembled the parts and fitted the device
to Sara. She received her new leg on July 27, days before
school was scheduled to begin.
"Sara is a senior this year,"
her father reported. "Like all girls that age, she is
concerned about her ap-pearance.
"This leg is like the difference
between night and day from her other leg," Ashcraft said.
"Now she can do things that she could not do before,
things like pedaling her three-wheeler and going up and down
stairs with much greater ease."
For Sara, the leg is a great leap forward.
"I can walk like a normal person.
This leg is much safer. It keeps me from falling," Sara
said. "Now, I will be able to take P.E. I want to learn
to play basketball. I am going to learn to dance."
Her teachers have been pleasantly
surprised with Sara's progress with her new leg.
"There is an obvious difference in the way she is able
to function with this leg compared with her other leg,"
said Bertie Johnson, one of her teachers. "She walks
much easier and much more smoothly. As she walks the halls,
it's hard to notice any difference from the other students.
Last year she was having a great deal of trouble with her
other leg. They finally took it off and put her in a wheelchair.
We had teachers and students that were shocked. They apparently
did not realize. She never complains.
"She takes life the way it was given to her and runs
with it," Johnson continued. "She never slows down."
Teacher Renee Carter is equally impressed
with her student.
"You have to admire her courage," Carter said. "I
recently asked my class to write down three things that make
them an interesting person. Sara wrote: I am an interesting
person because I 1) have a computer type leg, 2) because I
only have three fingers, and 3) because I do really good with
both my leg and my hands.'
"A great deal of the credit
for her attitude comes from her parents," Carter added.
"When her father first brought her to school, he told
us to not treat her any differently than the other children.
He told us to challenge her and to not treat her as if she
was handicapped."
"Sara is a very sweet young
lady," Johnson said. "She is studious and tries
very hard. She lives her life normally and does not consider
herself handicapped. She does everything the other youngsters
do."
Life, for Sara, is a struggle for
ac-ceptance and the C-Leg is another step in that direction.
"I want to thank the parents
of that boy for helping me be normal," Sara said.
Reporter Royce Armstrong can be reached by e-mail at rarmstrong@
themississippipress.com or at (601) 947-9933.
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