In line with the three articles about care considerations for DMD recently published in Lancet Neurology 1-3, a new Duchenne Family Guide has been developed and was launched online on World Duchenne Awareness Day, September 7, 2018.
The development of the updated care considerations was funded by the U.S. Center for Disease Control. These updates offer the latest clinical considerations to improve care, services, and quality of life for people living with Duchenne, raise the standards of care for Duchenne and will assist clinicians in making the best possible recommendations for these patients.
Thanks to the collaboration of four not-for-profit organizations — the Muscular Dystrophy Association, Parent Project Muscular Dystrophy, TREAT-NMD and the World Duchenne Organization — a thoroughly updated and re-drafted Duchenne Family Guide was developed.
This guide will give patients, families and caregivers access to the information necessary to enable them to work with their health care and support providers in ensuring optimal care. The Duchenne Family Guide will be translated and published online on the TREAT-NMD website in many languages, with the help of the global Duchenne community.
Help spreading the best possible care information
Cathy Turner, TREAT-NMD
Elizabeth Vroom, World Duchenne Organization
Nancy Intrator, Muscular Dystrophy Association
Will Nolan, Parent Project Muscular Dystrophy (PPMD)
TREAT-NMD: www.treat-nmd.eu
PPMD: www.parentprojectmd.org
MDA: www.mda.org
Educational videos: www.dmd-care.org
Implementing the latest Standards of Care
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