Political Quotes

On the recordFebruary 14, 2002
As we commemorate National Duchenne Awareness Week, I express my gratitude to my colleagues and to the Bush administration for their support late last year in passing H.R. 717, the Muscular Dystrophy Community Assistance Research and Education Act. Sadly, at this time, there is no cure for DMD. Little boys with DMD are most often not diagnosed before the age of 2 or 3 years. Most boys with DMD walk by themselves later than average, and then in an unusual manner. They may fall frequently, have difficulty rising from the ground, or experience difficulty going up steps. Calf muscles typically look over-developed or excessively large, while other muscles are poorly developed. Use of a wheelchair may be occasional at age 9, but total dependence is usually established in the teen years. Most boys affected survive into their twenties, with relatively few surviving beyond 30 years of age. I have heard from the parents and family of two little boys in Maine who have DMD. Their names are Matthew and Patrick Denger, and their family members are desperately hoping for a cure so they don't have to watch their sons suffer the long-term impacts of this debilitating disease. While we are far from finding a cure for DMD, I am hopeful that the MD CARE Act, signed into law by President Bush on December 18, 2001, will help Matthew and Patrick and the thousands of other young boys suffering from DMD.
Said by
Susan Collins
Republican · Maine

Editor's note · Context

Discussing the impact of Duchenne Muscular Dystrophy and the importance of the MD CARE Act.

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