Little Hercules Foundation’s mission is to improve the lives of those diagnosed with – and families facing – Duchenne Muscular Dystrophy. Whether we are advocating, spreading awareness, or funding research, we are always working for our greater Duchenne community. We have a responsibility to help push the science forward and enable this generation and future generations to have an opportunity for a better quality of life; a full life. The pictures on our website are real. They are pictures of Ohio-based families that we have encountered on our journey; who fight along-side of us and who stare Duchenne in the face along with us every day. These boys are each unique in their mutations, but all of them just want the chance to grow up. That is why we do what we do. Why we advocate and fundraise and provide assistance to families across the country. And that is why we NEED your help to END DUCHENNE.