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Lake Charles resident Ron
Stoddard said he doesn't talk about losing two of his children to cystic
fibrosis.
But, during the recent Great
Strides walk in Lake Charles, a national fund-raiser to help find a cure
for cystic fibrosis, he did.
"I want to talk about
it, but it's so difficult," he said, his voice cracking.
Stoddard's son, Johnny, was
26 and his daughter, Laura Ann, was only 12 when they died of the
disease.
It's a rough, damnable
disease. For years, we had hope," he said.
But that's not the case
anymore.
Researchers have made
significant progress in the past several years in finding a cure for CF,
which is a chronic, progressive and frequently fatal genetic disease of
the body's mucus glands.
CF primarily affects the
respiratory, digestive, and reproductive systems and sweat glands in
children and young adults. It affects about 30,000 Americans.
About 200 people showed up at
the Civic Center for Great Strides. Many of them either suffered
from the disease or knew someone who had it.
Karen Gorum was there with
about 12 members of her Pokeno group. Nicole Gest, a group member,
has a 4-year-old daughter, Elexis, who has CF.
"We're here to help
everyone who has it," Gorum said.
Gest said her daughter's
health has improved.
"She's actually
doing good now," Gest said. "It was tough early
on. We spent weeks and weeks in the hospital for the first two
years. We're still working on it."
Julie Park, team leader of
the group from the Children's Clinic, said clinic employees participate
in walks such as these as often as possible.
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"We see CF patients and
see what they go through, We want to do what we can to help," she
said.
Jodi Zimmerman and Alice
Adams Walked with their two toddlers in strollers. Zimmerman's
13-year-old niece, Courtney George, has CF.
"It's been hard.
She was hospitalized five times this past year," she said.
Courtney's mom, Jill
Stratton, was walking nearby.
"She's doing good now
... as long as winter is over. Winter's hard," she said.
Stratton walks in Great
Strides every year.
Hopefully, this money will
help find a cure," she said.
Adams said she has seen what
Courtney has gone through.
"I've also known others
who have lost children. They need to find a cure for this,"
she said.
Her 9-year-old
Melissa Hansard was also with the group. Her Daughter, Brittni
Hamilton, 9, has CF.
"I love coming out and
doing this kind of thing," she said. "I've always been
too busy to walk, but this year, I said I can't be too busy to do
this."
Hamilton has had a hard year,
health wise.
She missed three-fourths of
the school year because she had to be hospitalized.
She's doing better,
though. She just got off an IV," she said.
Hansard said her daughter's
life is filled with hospital stays, daily treatments, and much
medications.
"She wanted to be here
but it was too soon (since she just got off the IV)," Hansard
said. "Maybe next year."

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Chris Dalme and Michal
Sanchez work at the Louisiana Lions Camp for children with pulmonary
disease in Leesville.
They work with kids suffering
with CF and asthma every day. They're job is not depressing, they
said.
"Kids go out there where
they can get away and be normal. Everyone there has the same
feelings as they do and are like they are. They have fun,"
Sanchez said.
This year,
the two were walking in honor of a 20-year-old friend at the camp who
died of CF just last week. "He
had a lung transplant last year and was doing good. But, he had to
go to the hospital and was put on a ventilator and died," Dalme
said. It was rough on us. It was a shock. He was good
kid." Life
expectancy for the disease has gone from the teens to age 30 currently. Stoddard,
who said this is the first time he's participated in Great Strides, said
a teen-aged relative with CF recently had a lung transplant. "She
was down to 15 percent lung capacity, but now, she's doing great.
She's off and running. Her mom can't keep up with her." Local
businessman and Great Strides chairman, Peter O'Carrol said this year's
walk raised about $11.000 locally for the Cystic Fibrosis Foundation.
For
more information on cystic fibrosis, the Cystic Fibrosis Foundation, or
the programs available to people with the disease, visit the CF
Foundation's Web site at
www.cff.org or call
1-800-FIGHT-CF. |