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CONGRESSMAN

COLLIN C. PETERSON
Minnesota - 7th District                         http://www.house.gov/collinpeterson/

FOR IMMEDIATE RELEASE: September 24, 2001
CONTACT: Robin Goracke/202-225-2165

Peterson Bill Overwhelmingly
Passes House Of Representatives

WASHINGTON, DC –U.S. Congressman Collin C. Peterson (D-Minn) joined Representative Wicker (R-MS) in passing H.R. 717, the Muscular Dystrophy Community Assistance, Research and Education Act.  This bill is designed to fight childhood muscular dystrophy by boosting research funding and raising public awareness. 

Peterson urged his colleagues to pass this bill on behalf of an extraordinary 9-year-old boy who has Duchenne Muscular Dystrophy.  Like many children that have Duchenne, his life expectancy is only into the late teens or early 20s.  Children with Duchenne are typically diagnosed between the ages of 3 & 5 years when they start to show signs of slow development of motor skills, and their legs begin to collapse without any warning, even to themselves.  There after, the disease is characterized by progressive weakness, with a gradual deterioration of muscle capacity, first in the legs, then in the arms, back, lungs, and heart.  “Currently, the boy I know uses a motorized scooter to get around but soon he will need a ventilator to breathe,” stated Peterson. 

Duchenne Muscular Dystrophy is the world’s most common and catastrophic form of genetic childhood disease.  Although the Dystrophin gene that causes Duchenne was successfully identified and isolated by medical researchers in 1987, federal research devoted to potential treatment options or a cure since this discovery has been minimal.  Many family physicians and health care professionals lack the knowledge and resources to detect and properly diagnose the disease as early as possible, thus exacerbating the progression of symptoms in cases that go undetected or misdiagnosed.

There is no treatment for Duchenne even though the Dystrophin gene was first identified over 14 years ago.  The life expectancy of a child with Duchenne has not changed since 1859 when it was first identified. 

“It is time for us to focus our efforts and target funds to Muscular Dystrophy research at NIH and CDC,” urged Peterson.  H.R. 717, will fight childhood Muscular Dystrophy by boosting research funding and raising public awareness.  Less than 1/2000 of the NIH budget is focused on research linked to Muscular Dystrophy.

Peterson stated, “I asked my young constituent, if he could trade places with anyone in the world who would he be; I expected him to say a famous athlete or movie star, but he simply answered his older brother, so he can play football with his friends.  You see his biggest wish is to be a regular boy.  Today lets do what we can to help this little boy grow up to play football with his friends.”

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