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Advancing diagnosis, care and treatment for people with neuromuscular diseases around the world

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Becker Muscular Dystrophy Awareness Week 2026

Home / Awareness Days / Becker Muscular Dystrophy Awareness Week 2026

Becker Muscular Dystrophy Awareness Week 2026

From 4–10 October 2026, the global community will come together to mark Becker Awareness Week, helping to raise awareness and understanding of Becker muscular dystrophy (BMD).

Becker muscular dystrophy is a rare genetic neuromuscular condition that causes progressive muscle weakness and can affect people in different ways. Raising awareness is important in helping people living with Becker, their families and carers access information, support and appropriate care.

At TREAT-NMD, Becker muscular dystrophy is an important area of our work. We are committed to helping Inform, Connect and Advance progress across the neuromuscular community.

Earlier this year, we brought together people living with Becker, families, carers and healthcare professionals at our Becker Education & Engagement Day in Manchester. The two-day event created an opportunity for the community to learn from experts, ask questions, share experiences and connect with others who understand the realities of living with Becker.

Bringing people together is an important part of advancing care and research. By listening to the experiences of the Becker community, sharing knowledge and connecting people across the field, we can help support continued progress towards better care and treatments.

This Becker Awareness Week, we are proud to stand alongside the Becker community and everyone working to improve understanding, care and treatment for people living with Becker muscular dystrophy.

Explore our BMD resources

21 September 2026

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      • MDX Mouse (DMD)
      • GRMD Dog (DMD)
      • CMD Mouse (CMD)
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      • CMD animal models
      • MDC1A Preclinical Research
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        • Muscle Biopsy
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  • Home
  • Who We Are
    • About Us
    • Partnerships and Collaborations
    • 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
      • LGMD 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
  • Opportunities
  • Conference
    • Registration
    • Sponsorship Opportunities
    • Conference Programme
    • Programme Committee
    • Abstracts
    • Venue
  • News & Events
    • News
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