Sickle cell disease is an inherited disorder that causes red blood cells to lose their ability to carry oxygen. While the normal red blood cell is shaped like a smooth and flexible disc, the sickle red blood cell becomes sickle-shaped after oxygen is released from its hemoglobin. A sickle-shaped red blood cell is hard and sticky and forms blockages in small blood vessels. These blockages lead to repeated acute and chronic tissue damage, chronic anemia, and severe painful episodes.
Adult outpatient care for patients with sickle cell disease is held every Monday, Tuesday, Thursday, and Friday at the Mastin Patient Care Center. This clinic is staffed by a team comprised of physicians, nurse practitioners, a registered nurse, and a social worker. In-hospital treatment of adult sickle cell patients is provided at University Hospital.
Outpatient care for children and adolescents with sickle cell disease is held every Tuesday at the Strada Patient Care Center. In-hospital services for patients are provided at Children's & Women's Hospital. We also offer a program for the transition from pediatric to adult care. This transitional time can be very difficult for adolescents.
The mission of the Johnson Haynes, Jr., M.D., Comprehensive Sickle Cell Center, based out of the Whiddon College of Medicine at the University of South Alabama, is to improve the lives of persons affected by this disease through clinical care, basic and clinical research, and through patient and professional education. Semi-annual newsletters provide updates on the center and its programs.