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Family needs help getting son to the treatment he needs for his rare genetic disorder

"At home, he has to be surrounded by plenty of cushions, because he will try to hurt himself no matter what you do," said Mary Comer, 4-year-old Jasper Comer's mom.

UNION, Mo. — A young man with a rare genetic disorder needs your help. He has outgrown his main form of transportation and spends a lot of time in the car going to and from doctors appointments.

Jasper Comer is almost 5 years old. Last year, he was diagnosed with Lesch Nyhan Syndrome, a terminal genetic disease.

"He can't sit, walk or crawl," explained Jasper's mom, Mary Comer. Jasper's syndrome also leads him to self-harm.

"At home, he has to be surrounded by plenty of cushions, because he will try to hurt himself no matter what you do," said Comer.

The family commutes a long 50 miles to and from Cardinal Glennon Hospital, in St. Louis, for Jasper's treatment. At this point, he has outgrown his car seat.

"It's a long time for any child to be in a car seat that don't fit them," Mary said.

So, the Comers are in the market for a new wheelchair-accessible lift van that can go the distance. But, vans run anywhere from $39,000 all the way up to $100,000.

"Right now, only one of us can work because he requires 24/7 care," explained Comer, who is working full-time while her husband takes care of Jasper at home.

Pasta House in Union is taking the lead to raise some of the money. It is hosting an all-day fundraiser on Sept. 26. It will donate 10% of the proceeds to Jasper and his family. The fundraiser runs from 11 a.m. to 9 p.m. at 101 East Independence, in Union.

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