The UK Foundation for Muscular Dystrophy Nigeria (MDNG) is dedicated to improving the lives of individuals and families affected by muscular dystrophy. We deliver practical support, raise awareness, improve access to care, and work with partners across the UK and Nigeria to build long term, sustainable change.

What We Do
• Practical Support for Individuals and Families
We help provide mobility aids, assistive equipment, and home adaptations that improve independence, safety, and overall quality of life. Where appropriate, we offer financial assistance to help families manage the challenges associated with muscular dystrophy.
• Awareness and Education
We organise workshops, seminars, and community campaigns that increase understanding of muscular dystrophy among healthcare professionals, educators, families, and the wider public. These initiatives promote early diagnosis, reduce stigma, and encourage inclusive attitudes.
• Partnerships and Collaboration
We work with healthcare professionals, educational institutions, and community organisations to strengthen care pathways and expand access to specialist knowledge. Our trusted partnerships, such as with the Muscular Dystrophy Campaign Nigeria, enhance coordinated support across the country.
• Research and Health Advancement
We support initiatives that contribute to improved medical knowledge, research collaboration, and the development of better diagnostic and treatment approaches for neuromuscular conditions.
• Community Engagement and Outreach
We reach underserved and remote communities through outreach programmes that connect families with information, referral pathways, and available support services.

Why Our Work Matters
Muscular dystrophy is a progressive, life limiting condition that affects mobility, breathing, heart function, and overall quality of life. In Nigeria, access to early diagnosis, specialist care, therapy, and assistive equipment remains extremely limited.

Many people face delayed diagnosis, financial hardship, and stigma, which often lead to preventable health complications and reduced opportunities in education, employment, and community life.

We are committed to addressing these gaps by improving access to care, providing essential support, and promoting inclusion and dignity for people living with muscular dystrophy.

Where We Work
We are a UK based international charity working to improve support for individuals affected by muscular dystrophy across Nigeria. Through operations in both the UK and Nigeria, we collaborate with healthcare providers, academic institutions, charities, and supporters to expand access to care, awareness, and resources nationwide.

Who We Support
We support individuals living with muscular dystrophy in Nigeria, as well as their families and caregivers, by improving access to healthcare, essential equipment, and opportunities that enhance independence and wellbeing.
We also provide training and awareness resources for healthcare professionals, educators, and employers to promote early diagnosis, disability inclusion, and better support practices.

Access to Our Support
Our services are available to:
• Individuals diagnosed with muscular dystrophy
• Families and caregivers
• Healthcare professionals and educators seeking training

Priority is given to those facing financial hardship, limited access to specialist services, or significant support needs.

Eligibility for Support
You may be eligible if you meet one or more of the following criteria:
• Confirmed diagnosis of muscular dystrophy or a related neuromuscular condition
• Financial hardship limiting access to essential care or equipment
• Limited access to specialist healthcare, therapy, or rehabilitation
• Significant support needs affecting mobility, daily living, education, or quality of life

Eligibility is confirmed through appropriate documentation, such as medical reports or referrals from trusted organisations. Decisions are made fairly to ensure support reaches those who need it most.

Our Achievements to Date
We have supported a growing number of programmes and initiatives across Nigeria, including:
• Business start up grants for affected individuals (March 2026)
• Move for Rare NG Community Awareness Campaign (28 Feb 2026)
• Community outreach across South East Nigeria (Feb–Oct 2025)
• Wheelchair procurement (1 March 2025)

Forward Look
Our future goals include:
• Expanding awareness and education programmes
• Increasing practical support for families
• Providing more assistive equipment and home adaptations
• Sponsoring the development of a specialist MD care facility
• Supporting financial empowerment initiatives