The Children's Sickle Cell Foundation, Inc., provides quality programs and services for children and adults living with sickle cell disease and their families helping them face the educational, social, and economic challenges caused by this chronic disease through integrated community-based and health care systems. The commitment to advocacy, awareness, and support for research are natural extensions of this mission. The CSCF envisions a world where every person living with sickle cell disease is living well, has access to quality care, new therapies, and ultimately, a universally available, accessible, and affordable cure for this rare and neglected genetic disease. Your support is needed and appreciated.