5 Million Reasons to Live.

We are transitioning from supporting the few to safeguarding the future of the many. Join the movement to reach 5 million Nigerians living with Sickle Cell Disorder by 2030.

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Why We Can't Wait.

Nigeria is the Sickle Cell
Disorder Capital of the World!

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Annual SCD births

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Annual SCD deaths of Children Under 5 years

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Sickle Cell Carriers

Our purpose statement

We are a non-profit leader in the fight against SCD, championing the prevention, care, cure and control of SCD.

Our Mission

Our mission is to ensure sustainability of a world-class Sickle Cell Centre, that will support the Foundation in providing comprehensive solutions to the challenges of sickle cell and related disorders.

Our Vision

Our Vision is to lead global efforts towards reducing the burden of sickle cell disorder and ensuring that affected persons can lead healthy, productive, and meaningful lives.

Our Programmes

Life changing initiatives driving prevention, care, advocacy, and empowerment for sickle cell communities across Nigeria and beyond.

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Our Services

Compassionate, hands on medical care and support for people living with sickle cell. From diagnosis to treatment, we walk every step with you.

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Our Impact

Measurable change improving lives strengthening communities and shaping a healthier future for individuals living with sickle cell across Nigeria and beyond.

See our impact

Real Stories

Sickle Cell is never a burden carried alone.

2026 World Sickle Cell Day Kano Campaign

Nigeria doesn’t wait for SCD crises to pass.

What does it feel like to live in constant pain?

Sickle Cell turns hobbies into dreams

Sickle Cell is never a burden carried alone.

2026 World Sickle Cell Day Kano Campaign

The Champion’s Pulse

Faith, Willpower, and 71 Years of Living With Sickle Cell

Life after Bone Marrow Transplant: Iguehi's Post-Surgery Story

What Happens When a Wrong Genotype Test Destroys a Family?

The Shocking Truth About Sickle Cell and African Beliefs

The Power of Support: Modupe's 67-Year Journey with Sickle Cell

News & events

People We've Helped

Joshua Adenze

Genetic Counseling Program

"I live a much better life because I am more informed now. As a sickle cell warrior, we all need this."

Melody Okpara

Bone Marrow Transplant Patient

"Moving forward, I want to be a doctor, a doctor that stays out of crisis, no pains, but just enjoy myself. I want to say thank you to my mum, dad, siblings, and to SCFN."

Louis Luca

Sickle Cell Patient, Kaduna

"I can't believe I'm still alive. Most of my friends have died. Thank you SCFN for supporting me post my surgeries with funds for my business."

Isa Ibrahim

Adopt to Care Kafanchan

"Three children with sickle cell is difficult manage, but I'm very grateful to SCFN"

Joshua Adenze

Genetic Counseling Program

"I live a much better life because I am more informed now. As a sickle cell warrior, we all need this."

Melody Okpara

Bone Marrow Transplant Patient

"Moving forward, I want to be a doctor, a doctor that stays out of crisis, no pains, but just enjoy myself. I want to say thank you to my mum, dad, siblings, and to SCFN."