Early Diagnosis. Lifelong Impact.

The Mich Sickle Cell Foundation (MSCF) is committed to improving the lives of children living with sickle cell disease through early diagnosis, timely treatment, family support, and community partnerships in western Kenya.

ABOUT MSCF

Our Story

The Mich Sickle Cell Foundation (MSCF) was inspired by the founder’s journey as both a caregiver and a physician assistant caring for individuals and families affected by sickle cell disease. Through years of personal and professional experience, she witnessed the challenges families face and the life-changing impact that early diagnosis and quality care can have on a child’s future.

Named after the founder’s son, Mich-a Luo name meaning gift-the foundation exists to ensure that children born with sickle cell disease have the opportunity to receive early diagnosis, timely treatment, and lifelong support.

WHAT WE DO

Early Screening

MSCF supports newborn and infant screening to identify sickle cell disease before serious complications develop. Early diagnosis allows children to receive lifesaving interventions from the very beginning of life.

Linkage to Care

Diagnosis is only the first step. We work closely with healthcare providers to ensure that every child diagnosed is connected to appropriate medical care, receives regular follow-up, and has access to essential medications.

Community Education

We partner with healthcare workers, Community Health Promoters, schools, and local leaders to increase awareness about sickle cell disease, reduce stigma, and promote early healthcare seeking.

Medication Support

MSCF seeks to improve access to evidence-based treatments including: Penicillin prophylaxis Hydroxyurea Folic acid Malaria prevention where appropriate These interventions significantly improve survival and quality of life.

Families Supported

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Community Events

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Healthcare Partners

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Years of Service

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Your Support Changes Lives

Every donation helps us improve access to screening, strengthen community education and advocacy, connect children to life-saving care, and improve outcomes for children living with sickle cell disease across Western Kenya.

Dr. Johnson has led the Mich Sickle Cell Foundation since 2015. Under her leadership, the foundation has expanded its programs statewide and established key partnerships with major healthcare systems across Michigan.

Rachel oversees all foundation programs, ensuring they meet the evolving needs of the community. She holds a Master's in Public Health and has 12 years of experience in community health program management.

David leads fundraising, donor relations, and strategic partnerships. His background in nonprofit management and corporate philanthropy has helped grow the foundation's impact significantly.