The NC SCDC is one of 16 states participating in the Sickle Cell Data Collection program, funded by the Centers for Disease Control and Prevention.
The NC SCDC program collects and links data from several sources to better understand the healthcare needs of people with sickle cell disease in North Carolina.
The findings and conclusions in this presentation are those of the authors and do not necessarily represent the views of the North Carolina Department of Health and Human Services, Division of Public Health.
