For over a decade, SCHAF has implemented integrated programs designed to address Sickle Cell Disease from prevention to long-term care.
Our programs are designed with patients and families at the center, ensuring comprehensive support at every stage.
We conduct comprehensive awareness campaigns across schools, communities, religious centers, and workplaces to educate people about Sickle Cell Disease, its genetic nature, and the importance of early detection.
We provide holistic support to patients and their families, addressing medical, emotional, and financial challenges that come with managing Sickle Cell Disease daily.
Our screening programs offer accessible and affordable testing to identify carriers and affected individuals early, enabling timely intervention and informed family planning decisions.
We build strong networks within communities to foster understanding, reduce stigma, and create sustainable support systems for affected families.
We partner with academic institutions and research centers to advance understanding of SCD and develop better treatment approaches.
Whether you want to volunteer, donate, or partner with us, there are many ways to support our 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.
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