House Resolution No. by Representative Miller urges the Louisiana Department of Health to conduct a thorough review of all existing legislation related to sickle cell disease in the state. The resolution highlights the need for this review due to the evolving barriers to care, advancements in treatment, and the importance of aligning state policies with national standards and best practices. It emphasizes the historical context of legislative efforts in Louisiana to improve healthcare access for individuals with sickle cell disease, while also acknowledging the ongoing challenges such as underfunded programs, limited specialized services, and the stigma faced by patients.

The resolution calls for the Department of Health to collaborate with the Louisiana Sickle Cell Commission and other stakeholders, including individuals living with sickle cell disease, to ensure a comprehensive evaluation. It mandates that the Department submit a report of findings and recommendations by February 14, 2025, aimed at strengthening healthcare access, quality, and supportive services for those affected by sickle cell disease. The ultimate goal is to enhance the overall care and quality of life for individuals living with this condition in Louisiana.