It started at Karson “K.J.” Ross’ 9-month-old
pediatric well-baby visit.
Pretty routine stuff for a family that’s had two older kids
go through those types of regular checkups. Log the baby’s height and weight.
Check ears, eyes and throat. Administer vaccines.
“But they said it felt like his spleen was enlarged,”
recalled Ashley Ross, K.J.’s mom.
The cause, though, was puzzling.
After that appointment in the fall of 2017 came an
ultrasound, followed by test after test at Akron Children’s Hospital.
Sixty-seven in all, by the family’s count. Along the way, doctors ruled out
cancer, but began to suspect a rare hereditary disease, Niemann-Pick.
“We prayed that it wasn’t,” Ashley Ross said.
She and her husband, Matt, who live in southwest Canton,
Googled everything there was to Google about Niemann-Pick.
It wasn’t good. There’s no cure. And one variety can kill a
child by age 4.
The official word came on Aug. 22, 2018.
It was Niemann-Pick type C. It’s a genetic mutation that
causes cholesterol and fats to build up inside a child’s liver, spleen or lungs
— and ultimately affects the brain, too. The disease is sometimes referred to as
“childhood Alzheimer’s.”
Medical research has found only 500 cases diagnosed
worldwide each year.
Symptoms include learning delay, lack of muscle strength,
loss of coordination. The disease causes trouble in a child’s ability to walk
and talk and can include seizures and jerking muscles and a sudden loss of
muscle tone.
To this day, 2-year-old K.J. Ross’ vocabulary is limited to
“dad.”
He’s barely over 2-feet and weighs 21 pounds.
After the diagnosis, Ashley Ross wasn’t about to give up
hope. Using social media, she connected with parents across the country in a
similar situation. One told her to contact Dr. Elizabeth M. Berry-Kravis, a
pediatric neurologist at Rush University Medical Center in Chicago.
“I emailed her and she got right back to me,” Ashley Ross
said.
Berry-Kravis had been administering an experimental drug
VTS-270, from Mallinckrodt Pharmaceuticals, in Niemann-Pick type C patients.
The drug is given through a spinal tap.
Studies have shown the drug can stabilize the disease for
extended periods, according to an article published last year in “Pediatric
Neurology” and co-authored by Berry-Kravis.
In late September, K.J. Ross went to Chicago for his first
treatment. He and his parents make the flight every two weeks, and will
continue to do that for the foreseeable future.
Ultimately, the Ross family would like to see VTS-270 earn
U.S. Food and Drug Administration approval, which could make it available more
locally, or for another treatment to develop.
The non-profit Patient AirLift Services provides the free
flights. And Ashley and Matt Ross recently secured federal Social Security
benefits to support K.J.
His siblings, Matthew Ross Jr., a first-grader at Our Lady
of Peace Catholic School, and Jazminn, a fifth-grader at the same school, often
call their little brother “Beanie.”
It’s a nickname that seemed to fit and they’ve stuck with
it.
Parishioners at Christ the Servant Parish at Our Lady of
Peace Church, which operates the school, have also chipped in with donations to
help the family.
“Everyone always wants to know ‘how is K.J. doing?’” said
Monsignor Lewis F. Gaetano. “We’ve all tried to do what we can ... the mission
is outside of these four walls.”
https://www.the-review.com/news/20190310/canton-2-year-old-battling-rare-childhood-alzheimers-disease
See: https://childnervoussystem.blogspot.com/2018/03/elizabeth-berry-kravis-jamie-chin-anne.html
https://childnervoussystem.blogspot.com/2016/05/newborn-and-rapid-diagnosis-of-niemann.html
https://childnervoussystem.blogspot.com/2018/08/cyclodextrin-for-niemann-pick-type-c.html
https://childnervoussystem.blogspot.com/2016/07/niemann-pick-type-c-therapeutic.html
https://childnervoussystem.blogspot.com/2015/11/modified-amino-acid-acetyl-dl-leucine.html
https://childnervoussystem.blogspot.com/2017/11/diagnosis-of-niemann-pick-disease-type-c.html
https://childnervoussystem.blogspot.com/2016/09/a-homecoming-king-with-niemann-pick.html
https://childnervoussystem.blogspot.com/2019/03/evaluation-of-age-of-death-in-niemann.html
See: https://childnervoussystem.blogspot.com/2018/03/elizabeth-berry-kravis-jamie-chin-anne.html
https://childnervoussystem.blogspot.com/2016/05/newborn-and-rapid-diagnosis-of-niemann.html
https://childnervoussystem.blogspot.com/2018/08/cyclodextrin-for-niemann-pick-type-c.html
https://childnervoussystem.blogspot.com/2016/07/niemann-pick-type-c-therapeutic.html
https://childnervoussystem.blogspot.com/2015/11/modified-amino-acid-acetyl-dl-leucine.html
https://childnervoussystem.blogspot.com/2017/11/diagnosis-of-niemann-pick-disease-type-c.html
https://childnervoussystem.blogspot.com/2016/09/a-homecoming-king-with-niemann-pick.html
https://childnervoussystem.blogspot.com/2019/03/evaluation-of-age-of-death-in-niemann.html
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