The NC Sickle Cell Syndrome Program provides clinical care, care coordination and educational services to the pediatric population across the state who are living with sickle cell disease and other related blood disorders. Services included are:
- Education about sickle cell disease and sickle cell trait is provided to individuals and families affected by sickle cell trait and to the general population.
- Ongoing care coordination and counseling services in addition to medical services are provided to patients
Pediatric services to sickle cell clients are offered to reduce death and illness from sickle cell disease by supporting one community-based organization, medical centers and regional sickle cell educator counselors. This service contracts with one community based organization and six medical centers throughout the state.