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The Sickle Cell Disease Association of America, Michigan Chapter (SCDAAMI) is a non-profit healthcare organization dedicated to improving the lives of individuals affected by sickle cell disease. Founded in 1971, the organization provides a comprehensive range of services including patient advocacy, public education, and social support. A key component of their mission is the administration of the Newborn Screening Follow-up Program for sickle cell disease in the state of Michigan. They offer genetic counseling, support groups, and educational workshops to empower patients and their families. SCDAAMI also works closely with healthcare providers and researchers to promote better clinical outcomes and access to care. Through its various initiatives, the chapter serves as a vital resource for the hematology community in the Great Lakes region.
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