The study investigates the rights of individuals with sickle cell disease (SCD) in Nigeria, focusing on their access to quality healthcare, education, and employment, and the attitudes of both government and families towards these rights. Drawing on a mixed-methods approach, the research aims to provide insights into the experiences and perceptions of people living with SCD, as well as the roles and responses of key stakeholders. Through surveys, interviews, and analysis of policy documents, the study seeks to address gaps in understanding and support for individuals with SCD, shedding light on challenges such as stigma, discrimination, and access to essential services. By examining the intersections of health, social, and human rights issues, the findings aim to inform advocacy efforts, policy development, and healthcare practices to better meet the needs and rights of individuals with SCD in Nigeria.