Contact CureDuchenne for event and ticket information.
Friday, May 23, 2008 at 7:00 PM (ET)
Help Save Our Son's Life
Evan Procko of O’Brien is 4 years old. He has Duchenne Muscular Dystrophy. It is 100% fatal. If you saw him, you would hardly know anything is wrong. Yet, he will be in a wheelchair by12 and will die at around 16-19. Help us reach our goals. Fund research to save Evan and the 20,000 boys born each year with Duchenne.
Come Join Us For a Spectacular Night of Entertainment
Hosted by Miss Florida
Tickets may be Purchased at the door or in advance at Branford Fitness and Friends Fine Things.
All Proceeds Will Benefit Cure Duchenne and Evan’s Fund.
www.SaveOurSon.org
CureDuchenne is fighting for the lives of the 1 in every 3500 boys who are stricken with Duchenne Muscular Dystrophy. Most of these boys will not live past their teens. Their muscle cells will die and won't regenerate. It can happen in any family. But finally, thanks to recent scientific breakthroughs, THERE IS HOPE!
CureDuchenne is a not-for-profit organization founded by Corona del Mar (California) parents of a Duchenne boy. Unlike other organizations that simply fund research, CureDuchenne demands more. They are fighting to bring the most promising research out of the labs and into clinical trials that can save THIS generation of Duchenne boys. YOU can help us bring lifesaving treatments to market and give them a chance for a life.
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