DMDF Kenya Logo DMDF Kenya

About DMDF Kenya

Dedicated to improving the lives of children with Duchenne Muscular Dystrophy in Kenya.

Who We Are

The Duchenne Muscular Dystrophy Foundation Kenya (DMDFK) is a community-based organization dedicated to supporting boys living with Duchenne Muscular Dystrophy and their families across Kenya. We provide medical guidance, emotional support, assistive devices, and advocacy to ensure every child with DMD can live with dignity and hope.

Our team works closely with healthcare providers, therapists, and community leaders to create a comprehensive support system for affected families.

Vision

A Kenya where every child living with Duchenne Muscular Dystrophy receives the care, support, and opportunities they deserve.

Mission

To improve the quality of life for children and families affected by Duchenne Muscular Dystrophy through support, awareness, and advocacy.

Core Values

  • Compassion
  • Inclusion
  • Integrity
  • Hope
  • Collaboration

Our Programs

Awareness & Education

We conduct campaigns in schools, communities, and hospitals to reduce stigma and promote early diagnosis.

Family Support

We offer counseling, grief support, and mentorship to help families cope emotionally and practically.

Assistive Devices

We provide wheelchairs and mobility aids to help boys live with independence and dignity.

Advocacy

We engage government and partners to push for inclusion and supportive policies.

Community Building

We connect families through visits, workshops, and mentorship programs to share hope and experiences.

Physiotherapy

Specialized physiotherapy programs to maintain mobility and quality of life.

Meet Our Team

The dedicated individuals working behind the scenes to support families affected by Duchenne Muscular Dystrophy across Kenya.

Schollar

Schollar

Founder & Executive Director

Grace founded DMDFK after her son was diagnosed with DMD, and has championed awareness and family support across Kenya.

D

Dr. Samuel Otieno

Medical Advisor

A pediatric neurologist dedicated to improving care and early diagnosis of Duchenne Muscular Dystrophy.

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Faith Wambui

Programs Coordinator

Faith coordinates support programs, physiotherapy initiatives, and community outreach for affected families.

B

Brian Mwangi

Advocacy & Partnerships Lead

Brian engages government and partners to push for inclusive policies and sustainable support systems.

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Esther Chebet

Family Support Counselor

Esther provides counseling and grief support to families navigating life with Duchenne.

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Kevin Ochieng

Fundraising & Communications

Kevin leads fundraising campaigns and digital communications that amplify the foundation's mission.

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Martha Achieng

Treasurer

Martha oversees the foundation's finances, ensuring transparency and responsible stewardship of donations.

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Peter Kiprono

Secretary

Peter keeps the foundation organized — managing records, meetings, and coordination with our partners.

Join Us in Making a Difference

Whether through donations, volunteering, or spreading awareness, your support changes lives.

Support Our Mission