We can’t afford to be subtle. There’s just no time. We are fighting for the lives of the 20,000 boys who are born every year with Duchenne Muscular Dystrophy. It can happen in any family. Most of these boys will not live past their teens. Their muscle cells die and won’t regenerate. There is currently no cure. But there is hope. Life saving treatments are on the horizon! <p> CureDuchenne is a not-for-profit organization founded by Corona del Mar (California) parents of a Duchenne boy. We work closely with the leading scientists in the world to determine the most viable research…and moreover…to accelerate the clinical trial process and bring potential life-saving drugs to save this generation of Duchenne boys. Help us give these boys a chance for a lifetime. <p> Visit our website for more information: <a href="http://www.cureduchenne.org" Target=NEW>www.cureduchenne.org</a>.