QUICK SUMMARY
The Council endorsed House Bill H.1347, aimed at enhancing care for individuals with Sickle Cell Disease (SCD). This legislation, introduced by Representative Bud L. Williams, seeks to improve education, establish partnerships, and secure funding for SCD programs. The bill addresses significant health disparities, as over 90% of those affected in the U.S. are Black or Latino.
The Council passed a resolution supporting House Bill H.1347, aimed at improving care for individuals with Sickle Cell Disease (SCD). Introduced by Representative Bud L. Williams on January 14, 2025, the legislation focuses on expanding education and awareness, establishing partnerships with hospitals, and securing funding for SCD programs. According to the CDC, over 90% of SCD patients in the U.S. are Black or Latino, facing a life expectancy about 20 years shorter than that of the general population. By endorsing this bill, the Council highlights the urgent need for enhanced public health education and community support. The resolution signifies a commitment to health equity and improved quality of life for those affected by SCD. Additionally, this initiative could lead to more comprehensive healthcare access and improved patient outcomes in marginalized communities. The Council aims to address significant health disparities through this legislative support. As SCD disproportionately affects specific demographics, the legislation seeks to create a more equitable healthcare landscape.