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World Duchenne Awareness Day 2024: Raising Our Voices for Duchenne

Home / TREAT-NMD News / World Duchenne Awareness Day 2024: Raising Our Voices for Duchenne
World Duchenne Awareness Day 2024

World Duchenne Awareness Day 2024: Raising Our Voices for Duchenne

 

This Saturday, September 7th, marks World Duchenne Awareness Day (WDAD), an important occasion to raise awareness for Duchenne. Around the globe, communities come together to shine a light on these conditions, highlighting the need for greater support, research, and care.

The theme for WDAD 2024 is ‘Raise your voice for Duchenne’, emphasising the importance of creating a society with equal opportunities for all individuals affected by Duchenne muscular dystrophy (DMD). This year, we call on everyone to help amplify the voices of those living with DMD and their families, advocating for better diagnosis, care, and access to treatments.

At TREAT-NMD, we are deeply committed to advancing the diagnosis, care, and treatment of DMD through our ongoing work and collaborations. We proudly support the efforts of amazing patient organisations like Parent Project MD, World Duchenne, Duchenne UK, Action Duchenne, and Cure Duchenne, who are leading the way in raising awareness and fighting for a brighter future for all those impacted by DMD.

You can find out more about World Duchenne Awareness Day (WDAD) here.

Join us this Saturday in raising your voice for Duchenne and helping to make a difference. Together, we can create a world of equal opportunities for those living with Duchenne muscular dystrophy.

5 September 2024

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  • Home
  • Who We Are
    • About Us
    • Partnerships and Collaborations
    • Governance
    • Our Team
  • Who We Support
    • Patients
    • Clinicians / Researchers
    • Life Sciences Industry
  • What We Do
    • Advisory Committee for Therapeutics
      • Members of the Advisory Committee for Therapeutics
      • Take Part in TACT
      • Past Applicants
    • The Global Registry Network
      • Members of the Registry Network
    • Core Datasets
      • DM dataset
      • DMD dataset
      • FSHD dataset
      • LGMD
      • SMA
    • Education
      • Masterclasses and Events
      • Digital Resources
      • Endorsement of External Programmes
    • Post-Marketing Surveillance
  • Resources and Support
    • Neuromuscular Disease Information
      • Becker muscular dystrophy
      • Charcot-Marie-Tooth
      • Congenital muscular dystrophy
      • Congenital myasthenic syndromes
      • Duchenne muscular dystrophy
      • Facioscapulohumeral muscular dystrophy
      • GNE myopathy
      • Limb girdle muscular dystrophy
      • Myotonic dystrophy
      • Myotubular and centronuclear myopathies
      • Spinal muscular atrophy
    • Research Overview
      • DMD
        • Gene Therapy for DMD
        • Mutation Specific Approaches
        • Cell Therapy
        • Drug Therapy
    • Standards of Care & Family Guides
      • CM Care
      • CMD Care
      • DM Care
      • DMD Care
      • BMD Care
      • FSHD Care
      • SMA Care
    • SOP Library
      • MDX Mouse (DMD)
      • GRMD Dog (DMD)
      • CMD Mouse (CMD)
      • SMA Mouse (SMA)
      • CMD animal models
      • MDC1A Preclinical Research
      • Cell Lines
        • Clinical Outcome Measures
        • Functional Evaluation Tools
        • NMR (MRI/MRS) Imaging
        • Muscle Biopsy
    • Social and Ethical Issues
  • Conference
    • Registration
    • Sponsorship Opportunities
    • Conference Programme
    • Sponsors of the TREAT-NMD 8th International Conference
    • Programme Committee
    • Abstracts
    • Venue
  • News & Events
    • News
    • TREAT-NMD Events
    • All Events
    • Submit an Event
    • Newsletter Sign-up
    • Contact Us