Friends of Muscular Dystrophy Kenya (FOMDK) supports individuals and families affected by muscular dystrophy through healthcare, emotional support, and awareness. We aim to improve lives, promote inclusion, and advocate for research, all with compassion and integrity.
Muscular dystrophy refers to a group of genetic disorders characterized by progressive muscle weakness and degeneration. Each type of muscular dystrophy affects different muscles and has varying degrees of severity.
About Us
Friends of Muscular Dystrophy Kenya (FOMDK) is a foundation dedicated to supporting individuals and families affected by muscular dystrophy — a group of genetic disorders that cause progressive muscle weakness and degeneration. Common types include Duchenne, Becker, and Limb-Girdle muscular dystrophy. FOMDK works to improve quality of life through support services, awareness, and community empowerment across Kenya.
To empower and support individuals and families affected by muscular dystrophy in Kenya through care, awareness, advocacy, and community engagement for improved quality of life.
Comprehensive Support
Awareness & Advocacy
Community Empowerment
Through your donations, we spread kindness and support to our children and families.
Donate NowAt FOMDK, we are committed to empowering individuals and families living with muscular dystrophy, providing care, hope, and opportunities for a better quality of life.
Ensure access to essential drugs and treatments to manage muscular dystrophy symptoms.
MedicationConnect patients with qualified doctors and healthcare professionals for continuous care.
SupportFacilitate regular physiotherapy sessions to help improve mobility and muscle strength.
PhysiotherapyAssist families with basic needs to ease the financial and emotional burden of care.
Family & CommunityOffer guidance and counselling to patients and caregivers for mental and emotional well-being.
CounsellingEducate the public about muscular dystrophy and inspire acceptance, inclusion, and hope.
AwarenessWhy Us!
At Friends of Muscular Dystrophy Kenya (FOMDK), we go beyond care — we walk the journey with every family affected by muscular dystrophy. Our compassionate approach, professional medical support, and strong community network make us a trusted source of hope and help. We believe in empowering lives, spreading awareness, and creating an inclusive environment where every person feels supported and valued.
Compassionate & Professional Care
Community & Family Support
Awareness & Advocacy
Events
We organize workshops and learning sessions to educate families, schools, and communities about muscular dystrophy and how to support affected individuals.
Through visits and support activities, we engage with families and local communities to provide care, resources, and raise awareness about muscular dystrophy.
We offer health check-ups, therapy sessions, and counseling to individuals and families affected by muscular dystrophy, helping them improve quality of life.
Through your generous donations, Friends of Muscular Dystrophy Kenya (FOMDK) helps improve the quality of life for individuals and families affected by muscular dystrophy. Your support enables us to provide care, raise awareness, and build a stronger, more inclusive community for those living with this condition.
We strive to bring hope, support, and a better quality of life to individuals and families affected by muscular dystrophy.
Bernadette is the Co-founder of FOMDK. As a parent of a child with Duchene muscular dystrophy (DMD), she understands firsthand the challenges families face and is deeply committed to making the journey easier for other parents navigating similar experiences.Her passion for advocacy and support drives her work at FOMDK, where she focuses on improving access to medical care, raising awareness, and creating a strong support network for families affected by DMD. Through her dedication, Bernadette strives to ensure that no parent feels alone in their journey and that every child with DMD receives the care and opportunities they deserve
Joyce is the Co-founder of FOMDK. As a passionate special needs teacher, she brings a unique perspective to the foundation, advocating for inclusivity and tailored support for children with DMD. Her commitment to the cause goes beyond medical assistance—she works closely with families and healthcare professionals to ensure that boys with DMD receive the care and support they deserve. Through FOMDK, Joyce continues to drive awareness, empower caregivers, and create a nurturing environment for affected children.