Services

The UK Foundation for Muscular Dystrophy Nigeria provides practical support, education, and advocacy to improve the lives of individuals and families affected by muscular dystrophy across Nigeria. We work in partnership with healthcare professionals, community organisations, and supporters to expand access to care and promote long-term positive change.

Practical Support

We help individuals and families access essential resources that improve independence, safety, and quality of life. Our support may include:

  • Mobility aids and assistive equipment
  • Home adaptations where appropriate
  • Financial assistance for eligible individuals and families
  • Signposting to additional support services

Healthcare Support and Access

We work to improve access to healthcare by:

  • Supporting early diagnosis and referral pathways
  • Connecting individuals with specialist healthcare professionals
  • Promoting access to physiotherapy, rehabilitation, and multidisciplinary care
  • Supporting initiatives that improve health outcomes for people living with muscular dystrophy

Education and Awareness

We deliver educational programmes that increase understanding of muscular dystrophy and promote inclusion through:

  • Public awareness campaigns
  • Workshops and seminars
  • Professional education for healthcare workers
  • Training for educators, employers, and community organisations
  • Resources for individuals, families, and caregivers

Community Outreach

Our outreach programmes ensure that support reaches underserved communities by:

  • Providing information and guidance
  • Connecting families with available services
  • Raising awareness in local communities
  • Supporting families in areas with limited specialist services

Research and Innovation

We support activities that contribute to better care through:

  • Research collaboration
  • Knowledge sharing
  • Healthcare partnerships
  • Promoting improvements in diagnosis and treatment
  • Supporting evidence-based approaches to muscular dystrophy care

Partnerships and Capacity Building

We believe lasting change happens through collaboration. We work alongside:

  • Healthcare providers
  • Universities and academic institutions
  • Disability organisations
  • Community groups
  • National and international charities

Together, we strengthen services, share expertise, and improve support for people living with muscular dystrophy in Nigeria.

Advocacy and Disability Inclusion

We advocate for greater awareness, accessibility, and inclusion by:

  • Challenging stigma surrounding muscular dystrophy
  • Promoting equal access to education, healthcare, and employment
  • Encouraging disability-inclusive policies and practices
  • Giving a voice to individuals and families affected by muscular dystrophy

Who We Support

The UK Foundation for Muscular Dystrophy Nigeria is committed to supporting individuals living with muscular dystrophy and related neuromuscular conditions in Nigeria. Our work also extends to the families and caregivers who play a vital role in their daily care and wellbeing.

In addition, we provide education, training, and awareness resources for healthcare professionals, educators, employers, and community organisations to promote early diagnosis, disability inclusion, and improved support for people living with muscular dystrophy.

Access to Our Support

Our support is available to:

  • Individuals diagnosed with muscular dystrophy or a related neuromuscular condition.
  • Families and caregivers requiring guidance or assistance.
  • Healthcare professionals, educators, and community organisations seeking training, educational resources, or awareness programmes.

Support is provided through an assessment process and is subject to available funding, resources, and programme capacity. Priority is given to individuals and families experiencing financial hardship, limited access to specialist healthcare services, or significant support needs.

Eligibility for Support

You may be eligible to receive support if you meet one or more of the following criteria:

  • You have a confirmed diagnosis of muscular dystrophy or a related neuromuscular condition.
  • You are experiencing financial hardship that limits access to essential healthcare, therapy, or assistive equipment.
  • You have limited access to specialist healthcare, rehabilitation, or support services.
  • You have significant support needs affecting mobility, daily living, education, employment, or overall quality of life.

Eligibility is assessed using appropriate supporting documentation, such as medical reports, referral letters, or recommendations from recognised healthcare professionals or trusted partner organisations.

Meeting the eligibility criteria does not automatically guarantee support. Applications are considered fairly and transparently, taking into account individual circumstances, available funding, programme priorities, and the resources available at the time of assessment.