Expands sickle cell disease programs and services in North Carolina with funding for toolkits, coordinators, and grants.
The bill allocates funds to the North Carolina Department of Health and Human Services to enhance sickle cell disease programs and services. It includes appropriations for an evidence-based toolkit for emergency department providers, full-time Transition Coordinator positions at sickle cell medical centers, and grants to community-based organizations. The funding aims to improve care for patients with sickle cell disease, particularly in transitioning from pediatric to adult care.
Included in complete analysis
- Overview
- Core Provisions
- Implementation
- Impact
- Legal Framework
- Critical Issues
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