The Mississippi Sickle Cell Foundation (MSCF) is governed by a Board of Directors that is comprised of patients, parents, caregivers, healthcare professionals, and other interested parties who are all compassionate about sickle cell disease and the people living with the disease in the state of Mississippi. The Board of Directors is governed by a set of bylaws and are all voluntary positions. The MSCF does not compensate members for their time and services to the foundation. Regular board meetings are held monthly, and a special call meeting can be scheduled at any time. Please meet the MSCF Board of Directors.