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Bill > S283


NC S283

Expand Sickle Cell Disease Programs & Svcs


summary

Introduced
03/13/2025
In Committee
03/17/2025
Crossed Over
Passed
Dead

Introduced Session

2025-2026 Session

Bill Summary

AN ACT APPROPRIATING FUNDS TO THE DEPARTMENT OF HEALTH AND HUMAN SERVICES, DIVISION OF PUBLIC HEALTH, TO EXPAND PROGRAMS AND SERVICES FOR NORTH CAROLINIANS WITH SICKLE CELL DISEASE. Whereas, recent findings from the North Carolina Sickle Cell Data Collection Program funded by the Centers for Disease Control and Prevention (CDC) estimate that the number of individuals living with sickle cell disease in our State has risen to at least 7,000; and Whereas, this represents a twenty-five percent (25%) increase from the previously estimated 5,578 persons living with sickle cell disease in our State from 2004-2008, based on the North Carolina Registry and Surveillance System for Hemoglobinopathies funded by the CDC; and Whereas, the Department of Health and Human Services, Division of Public Health, requires additional State funds to ensure that essential services are available statewide to support the growing number of North Carolinians affected by sickle cell disease; Now, therefore,

AI Summary

This bill appropriates funds to the North Carolina Department of Health and Human Services' Division of Public Health to expand programs and services for individuals with sickle cell disease. The bill allocates a total of $2,308,273 over two fiscal years (2025-2027), with both recurring and nonrecurring funds. The money will be distributed across four key areas: (1) providing funding to six comprehensive sickle cell medical centers (including Atrium Health, Duke University Medical Center, and others) to support multifaceted needs of sickle cell patients, (2) creating a Transition Coordinator position at each medical center to help patients move from pediatric to adult care, (3) offering directed grants to community-based nonprofit organizations that provide comprehensive sickle cell services in underserved counties, and (4) supporting the North Carolina Sickle Cell Syndrome Program by creating additional staff positions, purchasing office equipment, and developing an evidence-based toolkit to improve emergency department care for sickle cell patients. The bill notes that the number of North Carolinians with sickle cell disease has increased by 25% to at least 7,000 individuals, necessitating expanded support and services. The appropriations will become effective on July 1, 2025.

Committee Categories

Budget and Finance

Sponsors (6)

Last Action

Re-ref Com On Appropriations/Base Budget (on 03/17/2025)

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