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MiSCDC Newsletter

The Michigan Sickle Cell Data Collection (MiSCDC) Program gathers health information about people living with sickle cell disease in Michigan to inform policy, health care service improvements and new treatments. The MiSCDC Program is a collaboration led by the Susan B. Meister Child Health Evaluation and Research Center at the University of Michigan and the Michigan Department of Health and Human Services. In partnership with the Centers for Disease Control and Prevention funding a total of 16 states, this national effort aspires to use data to improve quality of life, life expectancy, and the health of sickle cell warriors.

More information at: www.miscdc.org.

MiSCDC Program Form