Founded in 2012, Sickle Cell Hope Alive Foundation (SCHAF) is a registered non-profit organization in Nigeria dedicated to improving the lives of individuals and families affected by Sickle Cell Disease through awareness, early screening, advocacy, research collaboration, and compassionate care.
For over a decade, SCHAF has worked across communities in Nigeria to expand access to Sickle Cell education, screening, and patient support. Every contribution strengthens our ability to reach underserved populations and improve health outcomes.
Our comprehensive approach addresses every stage of Sickle Cell Disease management, from prevention and early detection to long-term care and advocacy.
Educating communities, schools, and institutions about Sickle Cell Disease, genetic inheritance, and prevention.
Providing emotional, medical, and financial support to individuals and families living with Sickle Cell Disease
Offering accessible screening and counseling services to enable early detection and informed decision-making.
Building sustainable support networks that reduce stigma and strengthen community response.
Our systematic approach ensures we reach those who need help most.
Educational campaigns, workshops, and public engagement initiatives across Nigeria.
Free and subsidized screening services for early detection and prevention.
Medical assistance, counseling, and crisis support for affected individuals.
Partnerships with academic and health institutions to advance SCD research and policy.
babies are born annually with Sickle Cell Disease worldwide, making it one of the most common inherited blood disorders.
of the world’s Sickle Cell Disease cases are estimated to occur in sub-Saharan Africa, where access to early diagnosis and treatment is severely limited.
of children in low-income countries who are born with Sickle Cell Disease die before age 5 due to lack of early screening and proper medical care.
SCHAF pioneered the Know Your Genotype (KYG) Club Project across NYSC zones in Oyo State to drive prevention and behavioral change among youth.
For over 14 years, SCHAF has stood alongside warriors, families, volunteers, and partners whose stories inspire resilience and hope.
There are many ways you can support our mission.
Your contribution directly funds patient care, screenings, and awareness programs.
The Sickle Cell Hope Alive Foundation (SCHAF) is a non-profit organization dedicated to improving the lives of individuals and families affected by Sickle Cell Disease through awareness, advocacy, screening, and sustained support.
© 2025 SCHAF. All rights reserved.
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