Established in 2003, we are dedicated to improving the lives of individuals and families affected by muscular dystrophy through support, awareness, advocacy, and research.
Learn More About Our MissionThe Muscular Dystrophy Foundation Nepal (MDF Nepal) is a non-profit, non-governmental organization established in 2003 by a group of dedicated parents, healthcare professionals, and social workers. Our foundation was born out of the pressing need to address the challenges faced by individuals with muscular dystrophy and their families in Nepal.
"Our mission is to empower individuals with muscular dystrophy and other neuromuscular disorders by providing comprehensive support, fostering awareness, advocating for inclusive policies, and advancing research for improved quality of life."
Operating from Kathmandu with outreach across Nepal, MDF Nepal serves as a beacon of hope for hundreds of families affected by muscular dystrophy. We work to bridge the gap in healthcare services, social support, and awareness about these complex disorders.
Founded in 2003 by parents of children with muscular dystrophy and concerned medical professionals, MDF Nepal began as a small support group. Over the years, we have grown into a nationally recognized organization serving patients across all seven provinces of Nepal.
Our journey has been marked by significant milestones including the establishment of the first patient registry for muscular dystrophy in Nepal, organization of regular multidisciplinary health camps, and successful advocacy for better healthcare policies for neuromuscular disorders.
We believe in a holistic approach to supporting individuals with muscular dystrophy. Our work encompasses:
Guiding principles that shape our work and define our aspirations
To empower individuals with muscular dystrophy and neuromuscular disorders through comprehensive support services, awareness programs, advocacy for inclusive policies, and advancement of research for improved diagnosis, treatment, and quality of life.
A Nepal where individuals with muscular dystrophy and other neuromuscular disorders live with dignity, have equal opportunities, access to quality healthcare and rehabilitation services, and are fully integrated into society without discrimination.
Compassion, Integrity, Collaboration, Empowerment, and Innovation guide our every action. We believe in the inherent dignity of every individual and work to create an inclusive society where everyone can thrive regardless of their physical abilities.
Comprehensive programs addressing the diverse needs of the muscular dystrophy community
Regular health camps providing free consultations, diagnostic support, and treatment guidance for MD patients across Nepal.
Community awareness programs, school workshops, and educational materials to increase understanding of muscular dystrophy.
Counseling services, support groups, and financial assistance for medical equipment and treatment costs.
Collecting data on MD prevalence, supporting research initiatives, and advocating for policy changes to improve patient care.
Making a difference in the lives of individuals and families affected by muscular dystrophy
Whether you're a healthcare professional, a volunteer, a donor, or someone who wants to learn more about muscular dystrophy, there are many ways you can contribute to our mission.