Senate Resolution No. by Senator Barrow urges the Louisiana Department of Health to conduct a thorough review of existing legislation related to sickle cell disease in the state. This review aims to assess whether current laws align with the evolving needs of service delivery and care systems for individuals living with sickle cell disease. The resolution highlights the recognition of sickle cell disease by national health organizations and the need for improved healthcare access, quality, and support services, given the historical barriers faced by patients in Louisiana.

The resolution calls for collaboration between the Louisiana Department of Health, the Louisiana Sickle Cell Commission, and various stakeholders, including individuals with sickle cell disease and relevant professionals. Following the review, the Department of Health is tasked with making recommendations to the governor and legislature to enhance healthcare access and quality, ensuring alignment with national best practices. A written report summarizing the findings and recommendations is to be submitted to key state officials and committees, emphasizing the importance of addressing the unmet clinical needs and stigma faced by those living with sickle cell disease.