Improving Sickle Cell Disease Care: New Medicaid Demonstration Project
This act aims to improve access to high-quality medical care for individuals with sickle cell disease, especially young adults and pregnant women. States will receive financial support to create better medical teams, identify care barriers, and implement best practices. Citizens with sickle cell disease can expect better treatment coordination, access to specialists, and psychological support, which should reduce emergency room visits and treatment costs.
Key points
Enhanced Access to Comprehensive Care: The act establishes a program to provide individuals with sickle cell disease access to multidisciplinary medical teams, including psychologists and social workers.
Financial Support for States: States will receive grants to improve care, including training for healthcare providers and developing provider networks.
Reduced Costs and Improved Health: The goal is to decrease emergency room visits and hospitalizations, leading to lower treatment costs and better patient well-being.
Care Coordination: Patients will have access to care coordinators who will help them navigate the healthcare system and ensure access to necessary services, including transportation.
Expired
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