Curing DMD: Travelling together to find a meaningful destination
disease, DMD, Duchenne muscular dystrophy, Duchenne Parent Project Spain, Joaquim Brites, Marisol Montolio
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DMD Main
Increase collaboration to widen access to DMD drugs, trials and care
access to clinical trials, access to drugs, DMD, Duchenne muscular dystrophy
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DMD campaigners: Advocating for change
disease, DMD, DMD campaigners, DMD campaigning, Duchenne, Klair Bayley, Parent Project Muscular Dystrophy, Pat Furlong, Ricky Andreis, Santhera, Save Our Sons, Swedish Muscular Dystrophy Research Foundation
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Parenting as a DMD patient
DMD, Duchenne muscular dystrophy, Mitch Coles, Muscular Dystrophy UK, Trailblazers
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He ain’t heavy – learning about a sibling’s DMD diagnosis
DMD, DMD diagnosis, Duchenne muscular dystrophy, patient centricity, rare disease
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Living with DMD: Ensuring equal access to quality of life
DMD, Duchenne muscular dystrophy, patient perspective, patient voice, patients
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Making sure everyone with DMD gets access to treatments and the ‘essential’ interventions that can make life worth living is key.
Lights, camera, action – DMD and chasing your dreams
DMD, Duchenne muscular dystrophy, patient perspective, patient voice
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Living with DMD: Inspiring each other’s futures
DMD, Duchenne, Duchenne muscular dystrophy, patient group, patient organisation
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Can people with Duchenne be in charge of their own lives?
DMD, Duchenne, Duchenne muscular dystrophy, patient centricity, patient perspective
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Progress in health and social care in European countries is helping many boys with Duchenne muscular dystrophy (DMD) to extend their lives beyond what was once dreamed possible, and to take control of their lives as they grow up and become men.
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