Educate the general population about SCD as a preventative measure.

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Support, empower, and improve the quality of care provided to SCD patients.

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Collaborate with global institutions on SCD research to improve patient outcomes.

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Build an engaged network of partners/ambassadors/volunteers /donors to bring our vision to life

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Our vision is to reduce the burden of Sickle Cell Disease in Nigeria through awareness, care and research.


We raise awareness of SCD in Nigeria through key advocacy initiatives and programs. Our approach combines health education, genotype and genetic counselling. We hope to remove the biases and stigma around SCD through compassion and education. We are blessed with a multidisciplinary team of medical and community-oriented professionals, all working together to empower patients and their families to live better, healthier lives. We work with global institutions to provide cutting-edge research and SCD training to improve patient outcomes. Our efforts are made possible through the generosity of caring individuals, corporations, and foundations both locally and abroad.

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What Makes us different?


A global network of scientists, geneticists, counsellors, healthcare professionals, including a UNESCO awarded scientist and founder

Healthcare Workers

We train nurses and clinic staff to treat SCD patients suffering from leg ulcers

Know Your Genotype
(KYG) Club

Youth empowerment clubs to drive SCD awareness & engagement in local communities

National Youth Service Commission (NYSC) Partnership

Partnering with NYSC graduates to scale SCD awareness across Nigeria

Global Research

We collaborate with international institutions on SCD research and understanding the impact of HIV, Hepatitis and Malaria on patient outcomes

Local Impact

We are deeply rooted in the community – we’ve hosted many grassroots programs across local schools, churches, mosques and universities

News & Updates

Read and enjoy our news updates, and discover what is new!