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NEW DATE ANNOUNCMENT: Expert Masterclass on Myotonic Dystrophy Type 1 | 19th November 2026

Home / TREAT-NMD Events and Masterclasses / NEW DATE ANNOUNCMENT: Expert Masterclass on Myotonic Dystrophy Type 1 | 19th November 2026

NEW DATE ANNOUNCMENT: Expert Masterclass on Myotonic Dystrophy Type 1 | 19th November 2026

New Date: 19 November 2026 

Format: Virtual Event

TREAT‑NMD has announced a new date for its Myotonic Dystrophy Type 1 Expert Masterclass, which will now take place virtually on 19 November 2026. The previously scheduled 10 April 2026 session will no longer go ahead.

Aimed at healthcare professionals involved in the diagnosis and care of individuals with DM1, the masterclass will feature international experts covering communication with families, clinical presentations, physiotherapy approaches and other key aspects of DM1 management.

What to expect

  • A high‑quality, interactive learning opportunity for healthcare professionals involved in diagnosing or managing Myotonic Dystrophy Type 1, with updates on current diagnostic pathways and internationally recognised standards of care.
  • A chance to hear directly from patients and patient representatives about the lived experience of Myotonic Dystrophy Type 1.
  • A forum for participants to exchange ideas, challenges and best practices to support optimal DM1 care.

Apply to Attend

Applications are now open (please note, existing registrations will carry over to the new date).

You can apply at:

https://treat-nmd.zoom.us/webinar/register/WN_TcTq63ZNRVaRo50mHbWrlQ

Contact: 

For any enquiries please message us at: education@treat-nmd.com

8 April 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
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  • Conference
    • Registration
    • Sponsorship Opportunities
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