For the first edition of the World Duchenne Awareness Day in 2014, it was essential to explain to the civil society what is Duchenne muscular dystrophy, what does it mean to live with this disease day by day. Some families and friends filmed the children, the boys and young adults with DMD during one of their typical day. All the stories are part of a small video: following their life it is possible to better understand how this disease can impact the daily life but it is also possible to see how strong are the boys and the families.
