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CDC's Sickle Cell Data Collection (SCDC) program funds 16 states to gather important health information about people living with sickle cell disease (SCD) to assess long-term trends in diagnosis, treatment, and healthcare access in the United States. SCDC helps inform policy decisions and resource allocation within states to improve and extend the lives of people with SCD.
The SCDC programs will showcase their work and highlight how their data are being translated into action.
This online event will not be recorded. Presentation slides may be requested from individual presenters. Direct any registration questions to McKinley Walsh or Mary Hulihan.