It's not so easy being a superhero
This 9-year-old girl can touch hot burners and chew glass. She can walk barefoot in snow.
She has a rare neurological disorder that lowers her sensitivity to pain and cold.
Kayla Woodhouse's body lacks the ability to regulate temperature. Cooling functions -- sweating -- don't kick in until her body reaches a lethal high temperature. Her skin is overly dry.
She wears a special vest with NASAsigned cold packs. She can only go outside to play after sundown. The house thermostat must stay below 62 degrees.
Kayla has incurable hereditary sensory autonomic neuropathy.
"Nationwide, there are a handful of cases, at best," said her pediatrician, Dr. Margot Crossley.
The disorder has taken Kayla's parents, Kim and Jeremy, far from their sultry
Kayla wasn't diagnosed until she was 14 months old, after passing out on a rare trip to a playground. Her mom said the reason it took that long was a godsend.
"I had postpartum depression and never went anywhere except to church," she said. "The doctors said if I had gotten her out, she would have died."
To save Kayla, they first moved the family, which includes Josh, 11, to
There, the biggest worry was Kayla running outside in 15-below without shoes, but the state also proved too far from medical centers.
A year ago, the family moved to
The tall, blonde Kayla looks healthy.
She jumps around the living room, clutching an oversized teddy bear. She has lots of energy but limited places to go.
"I might want an indoor playground," she said.
She rides her bike after sunset.
Swimming is her only sport, and it's good for keeping her body temperature in check. But she's limited to private, indoor pools.
She plays with her brother, who knows better than to fight with her.
"If I pinch her, it doesn't hurt," he said. "She pinches back -- hard."
Through the back patio door, she watches her two puppies grow up.
Church is the only time she's around other kids, but she's always under the watchful eye of Mom.
"She'll be playing and doesn't want to stop. She pushes herself too hard," Kim Woodhouse said.
Kayla likes to cook and sew. Even these can be hazardous.
"She'll start to reach into the oven without a mitt," her mom said.
Her first sewing lesson a few years ago was a disaster: Kayla sliced her stomach with scissors
and didn't realize it until blood was spilling everywhere.
"She doesn't feel pain until it's 20 to 30 times the normal intensity," Kim Woodhouse said.
"You realize what an asset it is to feel pain."
Still, it's better than when Kayla was a fearless toddler.
She chomped on Christmas lights. She'd slam into walls.
"She was a daredevil and would dive off of things," her mom said. "We had to duct tape socks to her hands so she wouldn't scratch too hard."
The eczema remains a problem. Kayla digs at the sores in her sleep.
She doesn't dwell on her condition. When her dad talks about the good fishing in
"Now we worry about the heat issue, making sure she stays cool enough," her mom said. "What's normal to us is not normal to other people."
They carry spray fans. They pack a cooler with ice packs for Kayla's special vest and drinks to keep her hydrated.
The air-conditioning stays on year-round.
"Our house is freezing. Our friends leave sweat shirts here," Kim Woodhouse said.
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