Duchenne Parent Project Fund

We have no time to lose. Duchenne Parent Project therefore wants more and better research into Duchenne Muscular Dystrophy. To develop medications that can stop or slow the breakdown of muscle. Gathering knowledge about the muscular disease is not happening fast enough. Duchenne Parent Project is an independent foundation founded in 1994 by Elizabeth Vroom, mother of a Duchenne son. They are committed to improving the future prospects of Duchenne patients by playing an important role in developing medications that can treat or cure Duchenne Muscular Dystrophy! For all boys worldwide. This can only be done through faster and better research. Through (international) cooperation at all levels. They also develop projects to improve medical care and independence. Through better and faster knowledge transfer, training and, for example, the development of tools. They are achieving success! The results of a number of research projects are promising.