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Parent Project Muscular Dystrophy Holds 15th Annual Connect Conference in Atlanta
Date:6/22/2009

ore than just entertaining or even an awareness piece about Duchenne, the film has been hailed for the attention it brings to accessibility issues in our country. Additionally, Mr. Weems and Mr. Smalley decided to sell the DVD of the film themselves so that a majority of the proceeds of each copy sold will go towards Duchenne research. Their goal is to sell one million copies in one year.

For more information about PPMD's 2009 Annual Connect Conference in Atlanta, Georgia from June 25 - June 28, 2009 at the Atlanta Marriott Marquis, please visit the PPMD website or call 1.800.714.5437.

About PPMD

Parent Project Muscular Dystrophy (PPMD) is a national not-for-profit organization founded in 1994 by parents of children with Duchenne and Becker muscular dystrophy. The organization's mission is to improve the treatment, quality of life and long-term outlook for all individuals affected by Duchenne muscular dystrophy through research, advocacy, education and compassion. PPMD is headquartered in Middletown, Ohio with offices in Fort Lee, New Jersey. For more information, visit www.parentprojectmd.org.


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