Teen speaks about her disease
Monday, June 14, 2004
By D.L. STEPHENSON
dstephenson@repub.com
SPRINGFIELD - When Laura Beth Jacquin first started speaking publicly
about her struggle with muscular dystrophy, she was so shy she could
barely get the words out.
Not these days.
Jacquin, 16, one of the more than 200 people who took
part in yesterday's Stride & Ride third annual walk for the Muscular
Dystrophy Association in Forest Park, not only talks the talk and walks
the walk, but can also raise money - lots of money.
"I'm finally getting to a point where I'm not
nervous speaking anymore," said the Longmeadow High School student,
who raised more than $16,000 this year for the MDA. Three years ago, she
raised $5,000. Last year, wanting to double that amount, she raised
$16,000, and this year a little more than that, said her mother, Patti
N. Jacquin of Longmeadow.
Pledge totals for the walk were not available
yesterday, but organizers said they were hoping to exceed the $22,000
brought in by last year's walk.
Diagnosed at age 11 with Friedreich's Ataxia, a rare
recessive neuromuscular disease that strikes one in 50,000 children
between the ages of 11 and 15, Jacquin decided not to be a victim but an
advocate for a cure.
"I was able to dance and do gymnastics, but some
kids are diagnosed at 4 and never get the chance to have the childhood I
had, so that's why a cure is so important," Jacquin said of her
regular speaking engagements and fund-raising activities.
Margaret A. Wheble, district director for the Western
Massachusetts chapter of the MDA, said funds raised from yesterday's
walk will go to local groups and organizations such as the pediatric and
adult clinic at Baystate Medical Center and the MDA summer camp, Camp
Florian, in Canton.
Wheble said the most common form of the disease in
children is Duchenne Muscular Dystrophy, a progressive neuromuscular
disease that affects mostly boys.
There are more than 43 neuromuscular diseases,
including Lou Gehrig's disease, which the MDA seeks funds to help cure
and treat, she said.
Though there are no cures for these neuromuscular
diseases, families like the Jacquins do what they can to help find one.
After her parents' trip to Paris to meet with doctors
doing research, Jacquin is now taking the drug Idebenone, an antioxidant
used to help prevent cardiomyopathy, a malfunctioning of the heart
muscle that often leads to death.
Munroe, an assistant dog, helps Jacquin with turning
out lights, fetching her shoes and pulling her wheelchair up a ramp.
Trained by the National Education Assistance Dog
Services, Munroe's $6,000 cost was paid for by Pet Co. Inc. of New
England, Patti Jacquin said.