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Our mission is dedicated to providing education, screening, counseling and patient support services for Sickle Cell and other abnormal Hemoglobins throughout the State of Georgia. The Foundation has a deep-rooted commitment to making strides in monitoring the occurrence of Sickle Cell, improving the quality of life for those with the disease and cooperating with individuals and institutions conducting research.
The Foundation offers Patient Support Services to include summer camp, tutorial services, and scholarship programs; Outreach Programs with Fulton County Family Project, Georgia Newborn Screening Program and our Anytime-Know Line for clients to access their newborn's test results.
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