Eke
Foundation

Sickle Cell Awareness

Every life
deserves
to be lived
fully

We educate, support, and advocate for people living with sickle cell disease across Nigeria and beyond.

Healthcare worker with patient

1 in 4

Nigerians carry the
sickle cell trait (AS)

2,000+

People educated

200+

Screenings conducted

580+

Patients supported

12

States reached

What is sickle cell disease?

A disease that shapes every moment of life.

Sickle cell disease (SCD) is an inherited blood disorder where red blood cells become rigid and crescent-shaped — blocking blood flow and causing severe pain, organ damage, and life-threatening complications.

Nigeria has the highest burden of SCD in the world. Approximately 150,000 babies are born with SCD in Nigeria every year — many of whom don't survive to their fifth birthday due to lack of awareness and access to care.

SS

Sickle cell disease

Both parents pass sickle gene

AS

Sickle cell trait

Carrier — usually no symptoms

SC

Sickle-haemoglobin C

Milder form of SCD

AA

Normal

No sickle genes inherited

Read the full guide

Common symptoms

  • Painful crises

    Sudden, severe pain in the chest, joints, or abdomen — often requiring hospitalisation

  • Anaemia & fatigue

    Sickled cells break down faster than normal, causing persistent tiredness and weakness

  • Stroke risk

    Blocked blood vessels in the brain can cause stroke, even in young children

  • Organ damage

    Kidneys, spleen, and eyes are particularly vulnerable to long-term damage

Patient stories

Real lives. Real courage.

Adaeze's story

Lagos, Nigeria

"I refused to let SCD define me.."

Adaeze was diagnosed with sickle cell disease at age 3. Growing up, she faced countless hospital visits, painful crises, and moments of despair. But...

Read Adaeze's story
Emeka's story

Abuja, Nigeria

"Knowledge saved my family from heartbreak."

Emeka and his wife were planning their wedding when they decided to get genotype tested. Discovering they were both AS carriers was a shock, but it al...

Read Emeka's story
Ngozi's story

Port Harcourt, Nigeria

"My daughter will not grow up afraid."

When Ngozi's daughter was diagnosed with SS genotype, she was terrified. "I didn't know what to expect, and I was scared for her future," she recalls....

Read Ngozi's story
All stories

Upcoming events

Join us in the field.

Aug

15

Caregivers Training Program — Online

Online Online

Register

Aug

22

Warriors Walk — Annual Fundraising Walk

Millennium Park, Abuja

Free entry

Sep

10

SCD Research Symposium 2026

Lagos Continental Hotel, Victoria Island, Lagos

Register
All events

Latest from the blog

News & insights.

New Gene Therapy Trial Shows Promise for SCD Patients in Africa
Research

New Gene Therapy Trial Shows Promise for SCD Patients in Africa

A landmark clinical trial across three West African countries is showing early positive results in reducing painful crises for sickle cell disease patients.

June 10, 2026

Why Genotype Testing Before Marriage is Non-Negotiable
Awareness

Why Genotype Testing Before Marriage is Non-Negotiable

Knowing your genotype is the single most important step every Nigerian couple can take before starting a family. Here's why it matters.

May 28, 2026

How to Support a Loved One Living with Sickle Cell Disease
Support

How to Support a Loved One Living with Sickle Cell Disease

Practical advice for families and friends — from crisis management at home to navigating hospital visits with confidence.

May 14, 2026

All posts