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Support Needed: Translating the LGMD Family Guide

Home / TREAT-NMD News / Support Needed: Translating the LGMD Family Guide

Support Needed: Translating the LGMD Family Guide

TREAT-NMD and Sarepta Therapeutics launched the first plain-language LGMD Family Guide last year to support people living with limb girdle muscular dystrophy (LGMD), their families, and non-specialist clinicians. The guide brings together insights from nine international clinical teams, each pairing a leading medical expert with a patient advocacy representative, and includes clear information about LGMD as a whole plus detailed sections on seven key subtypes (1D/D, 2A/R1, 2B/R2, 2D/R3, 2E/R4, 2I/R9, and 2L/R12).

The long-term aim is to build this into a comprehensive global resource covering all LGMD subtypes. To make sure families everywhere can access it, we are now expanding the project with a major translation effort.

We are therefore are actively looking for individuals, organisations or networks who can help translate the guide. Our first priority languages are:

• German
• French
• Arabic
• Hindi
• Bengali
• Mandarin Chinese
• Russian

If you or your organisation can help, or if you can connect us with someone who might then please contact education@treat-nmd.com. We will provide templates, guidance and everything needed to support the translation process.

30 January 2026

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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
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