This child was born unable to move her limbs or even breathe on her own. Over
the first three years of life, she had some spontaneous nerve recovery but muscle
weakness (atrophy) made her helpless. Improved muscle growth and awareness with
Threshold Electrical Stimulation (TES) led to improved function.
About Michelle
Michelle was born in 1982. On admission to the newborn intensive care unit,
she could not move and was unable to breathe. She had a C1-2 spinal cord injury.
Initially her doctors were hopeful for recovery. She showed slow and steady
gains over the first six to 12 months as the spinal shock from her initial injury
wore off. But after three years and despite physical and occupational therapy
five times a week, she had not acquired any new skills for at least a year.
At three years she remained hospitalized, only able to come off a ventilator
and breathe independently for short periods. Like all infants she was developmentally
immature. Adults can cooperate with therapy but Michelle didn't even know she
had legs. Her disability was caused by damage to the brain stem and spinal cord
with subsequent disuse muscle atrophy. The first video clip shows that she could
move short distances, but was very weak.
Michelle’s Treatment and Recovery Progress
The research team, led by Dr. Pape, knew that high-intensity, short-duration
Neuromuscular Electrical Stimulation (NMES) therapy could treat disuse muscle
atrophy. With ethics committee approval, in 1985, a research study program was
developed for Michelle.
Might her overall function be improved by treating the muscles directly using
a high intensity program like athletes?
Unfortunately, when they tried classic NMES, she did not tolerate the contraction
level stimulation. Among other things, she responded with breath holding.
In an “nothing to lose” experiment, Dr. Pape wondered whether low
intensity stimulation over a longer duration might offer the benefit, without
the discomfort. This was the birth of Threshold Electrical Stimulation (TES).
Electrodes were placed on Michelle at night, during sleep. Within five weeks
she showed significant gains, pushing herself into a sitting position. Over
the next three years, she made steady gains in neurologic function and eventually
was able to walk independently. She was off the ventilator 16 hours a day. The
second video clip shows her at age eight years after five years of Threshold
Electrical Stimulation (TES) and continued therapy.
Treating Michelle's muscles unmasked the neurological recovery that had occurred
over the first three years of life. In the presence of severe disuse muscle
atrophy, the true extent of her neurological recovery could not be adequately
assessed.
Update
Today Michelle lives independently and is employed. She still requires some
help with breathing during sleep. She drives a car, has a boyfriend and is living
her goals, day by day.
For more Information on Threshold Electrical Stimulation (TES) (click here)
Important Notice:
The TASC Network is an information only site. Individual medical advice is
not given. If you have questions that relate to your personal situation or your
child's care, please print the article and take it to your health care professional
with your questions.
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