By Muhammad Amaan
The Federal Government has announced plans to integrate haemophilia and other inherited bleeding disorders into maternal and child health services at primary and secondary healthcare levels nationwide.
Nigeria’s Coordinating Minister of Health and Social Welfare, Professor Muhammad Ali Pate, disclosed this in Abuja during a press briefing to mark World Haemophilia Day 2026.
Represented by Dr Kamil Shoretire, he said the initiative aims to improve early identification and enrolment into comprehensive care.
Prof. Pate expressed concern that although an estimated 21,101 Nigerians live with haemophilia, only about three percent have been diagnosed.
“Poor knowledge of haemophilia among healthcare providers remains a serious public health concern, and this could increase morbidity and mortality if not urgently addressed,” he warned.
The government also launched a National Bleeding Disorders Registry to strengthen data collection and announced the “Road to Clot Initiative” in collaboration with the World Federation of Haemophilia and the Haemophilia Foundation of Nigeria.
The programme will identify undiagnosed patients, link them to treatment centres, and ensure long‑term care.
“This year’s theme, “Diagnosis: The First Step to Care,” aligns with national priorities. Accurate diagnosis is critical to effective treatment,” Pate said, urging stakeholders to intensify awareness campaigns.
Haemophilia Foundation of Nigeria Executive Director, Megan Buckie Adediran, commended healthcare workers and partners, describing the day as a reflection of the struggles and resilience of patients.
Vice President (Medical) of the foundation, Prof. Theresa Nwagha, said the initiative marked a significant step toward health equity, with community‑based screening and improved diagnostics.
As part of the programme, five ambulances were unveiled to support outreach in hard‑to‑reach areas. Officials say the initiative will reduce the socio‑economic burden of bleeding disorders and strengthen Nigeria’s health system.
