A coalition of health advocates has called for stronger awareness, prevention, and improved care for people living with sickle cell disease in Nigeria.
The appeal was made in Calabar during a Sickle Cell Health Promotion and Sensitization Programme organized by the She for She Initiative in partnership with the Niger Delta Development Commission (NDDC) and the Sickle Cell Awareness Initiative Ireland–Nigeria. The programme, themed “Bridging the Gap in Sickle Cell Disease Management and Care,” focused on educating the public on symptoms, treatment, and management.
Nigeria has the world’s highest burden of sickle cell disease, with an estimated 4–6 million people living with the condition and about 150,000 babies born with it every year.
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NDDC Managing Director, Dr. Samuel Ogbuku, represented by Mrs. Afiong Eshiet, said the Commission is committed to supporting communities across the Niger Delta and ensuring the programme reaches all states in the region.
He described the initiative as a compassionate effort that offers patients access to essential drugs and mental-health support, noting the emotional and financial strain on families caring for sickle cell warriors.
Consultant pediatrician, Dr. Jimoh Abdulrasheed, highlighted how new technologies — including virtual patient models, smartphone diagnostic tools, and AI-powered wearables — are improving early detection and treatment outcomes.
Some sickle cell warriors shared motivational messages, encouraging others to stay strong, maintain regular check-ups, and avoid triggers that could lead to crisis.
The event featured free medical check-ups, counselling, and distribution of essential medications.
