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Duchenne Muscular Dystrophy


Duchenne Muscular Dystrophy is a severe type of muscular dystrophy predominantly affecting boys. It causes muscle weakness throughout the body and progresses rapidly with age. Duchenne also commonly causes further health complications as a result of its symptoms.


Duchenne Muscular Dystrophy is caused through biological gene mutations and/or deletions in the large dystrophin protein, which is essential for maintaining the muscle fiber's cell membrane integrity. Diagnosis can frequently be made at birth through genetic testing.


Unfortunately, there is currently no cure for Duchenne Muscular Dystrophy. However, there are several treatments available to manage the symptoms and improve quality of life. In addition, there are many charities and organizations dedicated to funding research and providing support to individuals and families affected by the disorder.


You can help by donating to Curtis' parents' charity of choice, Action Duchenne, in his memory. Your donation will help fund research into finding a cure for Duchenne Muscular Dystrophy and provide support to individuals and families affected by the disorder. Every donation, no matter how small, makes a difference. Note that this website nor the individuals behind it are officially associated with Action Duchenne in any way, shape, or form.