The Muscular Dystrophy Foundation of South Africa (MDFSA) is a non-profit organisation dedicated to supporting individuals and families affected by muscular dystrophy and related neuromuscular conditions. Since its establishment, MDFSA has worked to improve the quality of life of those impacted through awareness, education, advocacy, and support services.

MDFSA provides information and guidance to affected individuals and their families, promotes public and professional awareness, advocates for the rights and needs of people living with disabilities, and facilitates access to resources such as assistive devices, genetic testing support, and community programmes. The Foundation also works to build understanding and create opportunities for inclusion, empowerment, and improved care for people living with neuromuscular conditions.

How You Can Help

• Become a member
• Make a financial donation
• Leave a bequest in your will
• Volunteer your time