Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
The Sickle Cell Society was first set up as a registered charity in 1979. It was formed 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 Society is managed by a committee of 10 volunteers elected at the Annual General Meeting, and they meet each month. The Management Committee is accountable to the members and works with a small core of paid staff to further the Society’s aims by providing special services and welfare schemes for sickle cell sufferers.
Sickle Cell Society’s vision is to be the most successful sickle cell organisation nationally with a wide network of well-informed, committed and active supporters working at local, national and international levels.
+myBinderRelated Content
-
Melissa S. CrearyI was working on Gilberto’s narrative ...
-
Red Cell Pain Management Service at St George’s HospitalPeople with sickle cell disease can ofte...
-
Impact of emergency department care on outcomes of acute pain events in children with sickle cell diseaseThe impact of emergency department (ED) ...
-
Annual Sickle Cell Disease and Thalassaemia Conference (ASCAT) 2022The Annual Scientific Conference on Sick...
-
Me Myself and Sickle CellLiving her life with sickle cell anaemia...
-
NYC Health + HospitalsNYC Health + Hospitals are the largest p...
-
Older Blood Used in Transfusions May Be Harmful to Adult Sickle Cell Patients, Review FindsIn an analysis of adults with sickle cel...
