The Nigerian Senate has taken an important step toward improving care for sickle cell disorder nationwide.
A bill to establish Sickle Cell Disorder Research and Therapy Centres across Nigeria’s six geopolitical zones and the Federal Capital Territory has successfully scaled its second reading in the Senate.
The bill, titled “A Bill for an Act to Establish Sickle Cell Disorder Research and Therapy Centres to Expand Access to Specialised Sickle Cell Disorder Care, Improve Data Collection and Research, Support Education and Assistance for Patients, Families, Providers and Communities Affected by Sickle Cell Disorder, and for Related Matters, 2025 (SB. 893),” was sponsored by Senator Sunday Marshall Katung
Senator Katung, leading the debate on the bill, explained that it aims to expand access to specialised care, improve data collection, and enhance education and support for patients and families affected by sickle cell disorder.
Chief Whip of the Senate, Senator Tahir Monguno from Borno North, urged relevant agencies to increase public sensitisation on genotype compatibility ahead of marriage to prevent transmission of the disorder.
In support, other Senators described the bill as long overdue and critical, highlighting the genetic nature of the disease and the urgent need for public awareness about its causes.
After extensive debates, Deputy Senate President Jibrin Barau put the bill to a voice vote, and it was passed for second reading, bringing Nigeria closer to a stronger framework for sickle cell disorder research and care.
This development marks a significant legislative effort to address sickle cell disorder through specialised centres strategically located across the country.
