Sickle Cell Syndrome-Sickle Cell Medical Centers
Health and Human Services
Statewide
Child and Maternal Health
To provide clinical, specialized care, consultation, referrals, genetic counseling, and education to reduce death and sickness of persons affected by Sickle Cell Disease and to enter client data in the NC WCSWeb database.
Provides direct or indirect services (e.g., health care, childcare, inspections, case management, classes/sessions, counseling, referrals, consultations)
Children (0-5), Youth (6-15), Transitional Youth (16+), Families
6,066
$2,547,891
$0
$420
No
Descriptive, Output, Outcome
Yes
* All information is self-reported by the agency or institution and has not been independently reviewed and validated.