Testimonial

Learning that your son has Duchenne muscular dystrophy (DMD) is watching your child lose his muscular ability month after month. This is Jean-Philippe Morand’s reality: his son Victor is [...]

Do you know the Perfect Lift? Perfect Lift was inspired by Tanner, who has Duchenne Muscular Dystrophy. Tanner cannot stand or use his legs or arms; he is entirely dependent on his family. Her [...]

Notes from the “Living with DMD” web-doc Tecima Productions team. Carl’s resilience. Our small production team travelled across Canada, meeting with families whose children have Duchenne [...]

Duchenne muscular dystrophy seen through the eyes of the families There are over 7,000 rare diseases in Canada. Duchenne muscular dystrophy (DMD) is one of them. DMD afflicts children, especially [...]

Notes from the “Living with DMD” web-doc Tecima Productions team. Our small production team travelled across Canada, meeting with families whose children have Duchenne muscular [...]

The brother movie is the story of the Karouani family in France and their daily life with Kaïs, their son, who has Duchenne muscular dystrophy (DMD). Duchenne is a degenerative muscle disease. In [...]

Victor was diagnosed with Duchenne DMD is an incurable and 100% fatal disease. Duchenne muscular dystrophy is a rare genetic disorder that affects mainly boys. The progression of DMD is [...]

Living with Duchenne muscular dystrophy is difficult. I understand it because I live this reality every day. Duchenne muscular dystrophy forces you to live the moment and enjoy it even more. [...]

A text written by Guylaine Rivard This is a text that has been originally published in the group Les mamans Duchenne. On June 18th in 2009, it’s been almost ten years ago today that the DMD [...]

Only one woman in 50 million is affected by Duchenne muscular dystrophy (DMD). Considered as a male disease, DMD usually affects boys (1 in 3500). Some people don’t know that they exist. [...]