We were set up in 1979 by a group of patients, parents and health professionals who were all concerned about the lack of understanding and the inadequacy of treatment for people living with sickle cell disorders. The Sickle Cell Society supports and represents people affected by sickle cell disease to improve their overall quality of life. Become a member to help us to raise awareness about the disease; help us to raise vital funds for research, education and welfare services.
Sickle Cell Society
Last updated 01/03/23