Reducing the burden of sickle cell disease in Nigeria

Awareness. Care. Advocacy.

Sickle Cell Hope Alive Foundation (SCHAF) advances awareness, patient care, advocacy, and research for Sickle Cell Disease, so families can act early and people living with SCD receive support with dignity.

A child with a doctor wearing masks at a SCHAF outreach
Since 2012Improving lives every day

Why Sickle Cell Matters

Sickle cell disease is one of the most common genetic disorders on earth — and it hits hardest where resources are thinnest.

Global
7.7M
People living with SCD worldwide
Up from 5.46M in 2000 — a 41.4% increase in two decades.
Journal of Hematology, 2024
Africa
650+
Children die per day from SCD in SSA
WHO says 70% could be prevented with low-cost diagnostics.
American Society of Hematology
Nigeria
4–6M
Nigerians living with SCD
Many frustrated, confused, and dying from stigma.
Prof. Adeyinka Falusi / SCHAF

Who We Are (The Statement)

Read More

Since 2012, the Sickle Cell Hope Alive Foundation has worked through four connected pillars — Awareness, Care, Advocacy, and Research. Together they move people from knowledge to early action, from diagnosis to dignified support, and from individual stories to lasting change for everyone affected by sickle cell disease.

Awareness
Care
Advocacy
Research
Click to enlarge

Awareness

Educating communities, schools, and institutions about SCD, genetic inheritance, and prevention.

Care

Providing emotional, medical, and financial support to individuals and families living with SCD.

Advocacy

Collaborating with global institutions on SCD research and pushing for policy change.

Research

Advancing SCD knowledge through research partnerships, data, and evidence-led policy work.

Each program maps directly to one of our four pillars — nothing exists without reason.

School Genotype Education
Awareness

School Genotype Education

Teaching young people what genotype means before marriage decisions are made.

Youth Empowerment Clubs
Awareness

Youth Empowerment Clubs

Student-led clubs driving SCD awareness and engagement among young Nigerians.

Free Screening Drives
Care

Free Screening Drives

Mobile screening in communities, faith centers, and NYSC camps — removing cost as a barrier.

Healthcare Worker Training
Care

Healthcare Worker Training

Training nurses and clinic staff to properly treat SCD patients with chronic leg ulcers.

Research & Policy
Advocacy

Research & Policy

Multi-national research totalling $500K+ — studying SCD with HIV, hepatitis, and malaria.

Patient Support & Empowerment
Research

Patient Support & Empowerment

Annual gifting days, free medication, counseling, and "Mothers of Warriors" programs.

Our Growth and Impact.

Professor Adeyinka G. Falusi is a distinguished Nigerian haematologist and molecular geneticist whose lifelong dedication to science and humanity has transformed the understanding and management of Sickle Cell Disease (SCD) in Africa and beyond. Educated at the University of Ibadan, she obtained degrees in Chemistry, Haematology, and Human Genetics, specializing in haemoglobinopathies and inherited blood disorders.

Professor Falusi remained deeply concerned about the realities faced daily by People Living with Sickle Cell Disease (PLWSCD), particularly in Nigeria where the burden of the disease remains highest.

Driven by compassion and a desire to translate scientific research into practical community impact, she founded the Sickle Cell Hope Alive Foundation (SCHAF) in 2012. Established on the four pillars of Awareness, Care, Research, and Advocacy, SCHAF was created to reduce the burden of Sickle Cell Disease in Nigeria through education, counselling, healthcare support, advocacy, and research-driven interventions.

Since its inception, SCHAF has impacted thousands of individuals and families through genotype awareness campaigns, newborn screening advocacy, rural outreach programmes, patient counselling, empowerment initiatives, and community education. SCHAF has also experienced remarkable growth through collaborations with healthcare institutions, schools, NGOs, pharmaceutical companies, media organisations, and international partners including GANSID, SCDAA, and SCDC.

Today, Professor Adeyinka G. Falusi's legacy stands as a remarkable blend of scientific excellence, ethical leadership, mentorship, compassion, and transformative public health advocacy dedicated to improving the lives of Persons Living with Sickle Cell Disease across Nigeria and beyond.

Click to enlarge
2012
SCHAF founded in Ibadan
1 team
2014
Formal inauguration
200+ reached
2018
Research partnerships
$500K+ funded
2022
100+ schools milestone
5,000+ screened
2025
National recognition
500+ communities

Stories of People Living with Sickle Cell Disease (PLWSCD).

Behind every number is a person whose life SCHAF has touched.

Leadership Team

Prof. Adeyinka Falusi

Prof. Adeyinka Falusi

Founder, Trustee & Co-Chair

Sickle Cell Hope Alive Foundation

Ibadan, Nigeria

Executive Leadership Board

Prof. Abiodun Falusi

Prof. Abiodun Falusi

Trustee & Chairman

Sickle Cell Hope Alive Foundation

Ibadan, Nigeria

Executive Leadership Board

Prof. Oluwatoyin Nwafor

Prof. Oluwatoyin Nwafor

Trustee / President

Medical Doctor

Executive Leadership Board

Mrs. Helen Oduntan

Mrs. Helen Oduntan

Vice President I

Pharmacy

Executive Leadership Board

Prof. Prisca Adejumo

Prof. Prisca Adejumo

Vice President II

Nursing

Executive Leadership Board

Upcoming Events

See all events

Join us on the ground. Every event is a chance to learn, contribute, or simply show up.

SCD Health Assembly 2026Health Assembly
Wednesday, May 20, 20262:00 PM WAT

SCD Health Assembly 2026

An educational session on medicines and their roles in Sickle Cell Disease management, facilitated by Dr. Olayinka Kotila of the University of Ibadan at the Public Health Lecture Theatre beside Virology, opposite UBA, University College Hospital (UCH), Ibadan.

Registration closedLearn More
Annual Gifting DayOutreach
January 14, 202610:00 AM – 4:00 PM WAT

Annual Gifting Day

Our flagship outreach of the year. SCHAF distributes free medication, medical supplies, and care packages directly to sickle cell warriors and their families — a day built around dignity, practical relief, and community celebration.

Community Genotype Screening DriveScreening
March 22, 20269:00 AM – 3:00 PM WAT

Community Genotype Screening Drive

Mobile screening teams visit communities across Oyo State offering free hemoglobin electrophoresis, on-site counseling, and follow-up guidance so families understand their genotype before major life decisions.

Registration closedLearn More