There are two members of Project Perfect World’s team who we
don’t see very often, but we know are
indispensible. Brian is a certified orthotist and Jamie is a orthotist/prostetist. They also happen to be brothers.
indispensible. Brian is a certified orthotist and Jamie is a orthotist/prostetist. They also happen to be brothers.
Together Brian and Jamie see 120 patients in clinic of which
they treat 90. They asses and treat the physical and functional limitations of children resulting from illnesses and disabilities. In other words, they create and modify braces to address very specific mobility, function, and correction needs.
A usual day for Brain and Jamie starts at the hospital
around 8 am and ends when they take the last bus back to the hotel at 11 pm or
midnight. The hospital provides them with a shop where the can work and see
patients. Their shop was once a shed behind the hospital, but they have really
moved up in the world. They now have an air-conditioned room INSIDE. They are
kind of spoiled.
Jamie and Brian have worked with a young lady they affectionately
call “Stubby” for a couple of years. When Stubby was 1 year old, she had
surgery and suffered an allergic reaction to the anesthesia. She developed a
systemic infection, and her body responded by shutting down circulation to her
extremities. Eventually her limbs began to die. Both her legs and most her fingers
had to be amputated.
Stubby’s parents brought her to Brian and Jamie’s clinic to
see if there was anything that could be done to her with mobility.
After some trial and error, Brian and Jamie found a solution
they thought would work. From a cast of her legs, they built her a prosthesis
made of lightweight foam and copoly plastic. The battle was not won just yet.
Stubby’s skin is very sensitive. Her legs are a mass of scar
tissue; she could barely tolerate being touched, let alone the contact of a
prosthesis. Brian and Jamie delivered the prosthesis to Stubby’s parents and
instructed them to help her build up a tolerance for it. She should wear it for
as long as she could – increasing the time as much as possible.
When Brian and Jamie saw Stubby in clinic this year, she was
wearing the prosthesis. Ok. She was not only wearing the prosthesis, she was
also walking and running!
With the help of Brian, Jamie, and her parents, Stubby is
now a mobile, happy, beautiful little girl.
As part of Project Perfect World’s education efforts in
Ecuador, two of our physicians spoke to a crowded auditorium of local doctors.
We learned more about scoliosis and spinal cord injuries. Their talks were
translated by the ever present, kind, and tenacious Cesar.
Quote of the day: When beginning his talk on scoliosis, Dr.
Riely asked the crowd to: “Raise your hand if scoliosis is your favorite
thing!” No one did. Tough crowd.
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