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Becker Muscular Dystrophy Awareness Week: 6th - 12th October

Home / TREAT-NMD News / Becker Muscular Dystrophy Awareness Week: 6th – 12th October
Becker Muscular Dystrophy Awareness Week

Becker Muscular Dystrophy Awareness Week: 6th – 12th October

 

This week, from 6th to 12th October, we recognise Becker Muscular Dystrophy Awareness Week, a key moment to raise awareness of this rare genetic condition. Becker muscular dystrophy (BMD) is a genetic condition that causes a weakness in the muscles that progresses over time leading to increasing disability and has a significant impact on the lives of those affected. This week offers an opportunity to ensure that individuals living with BMD, along with their families, are not only informed but also supported and connected to a wider community. 

Building Understanding and Community

Receiving a diagnosis of BMD can be life-changing for both patients and their families. During this critical time, access to accurate, up-to-date information is essential. While BMD Awareness Week serves as a valuable platform to share guidance on managing the condition, it’s important that this information remains easily accessible all year round. Providing resources that are tailored to the needs of patients and their loved ones empowers them with the knowledge and tools to face the challenges of BMD with confidence.

Education also plays a key role in advancing the medical community’s understanding of BMD. While this week brings BMD into focus for healthcare professionals, ongoing access to educational materials and training is vital to ensure accurate diagnosis and effective communication with patients and their families. Continuous professional development for clinicians helps to improve the overall standard of care, ultimately advancing medical outcomes for those affected by BMD.

In addition to informing and educating, building the infrastructure to accelerate research and therapy development is crucial for advancing the diagnosis, care, and treatment of BMD. International collaboration between researchers, clinicians, and pharmaceutical companies is essential to ensure clinical trial readiness and improve patient care. By fostering these global connections, we move closer to developing better therapies and achieving improved outcomes for those living with BMD.

Finally, bringing together individuals and families affected by BMD is essential for fostering a sense of community. By sharing experiences and offering support to one another, those living with BMD can find strength in knowing they are not alone on their journey. This sense of connection can be transformative for both patients and their families.

While Becker Muscular Dystrophy Awareness Week is an invaluable initiative, the work must continue beyond these seven days. Ongoing efforts to inform, advance, and connect are crucial in building a future where the diagnosis, care, and treatment of BMD continually improve. Through these collective initiatives, we can create a stronger, more informed, and more compassionate community for all those affected by BMD—supporting them every day of the year.

9 October 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