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 and treatment for individuals living with sickle cell disease, as well as the inadequacies in current policies that may not align with national standards or adequately address the needs of patients. It emphasizes the importance of improving healthcare access, quality, and supportive services for those affected by the disease, which has been recognized as a significant public health issue by various national health organizations.

The resolution calls for the Louisiana Department of Health to collaborate with the Louisiana Sickle Cell Commission, affected individuals, and relevant stakeholders to ensure a comprehensive evaluation. It mandates that the Department submit a written report of findings and recommendations by February 14, 2025, aimed at strengthening legislation to better serve individuals with sickle cell disease. The resolution underscores the necessity of coordinated care and the elimination of stigma, while also addressing the financial burdens and healthcare access challenges faced by patients.