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
-
‘Talk to Me. There’s Two of Us’: Fathers and Sickle Cell ScreeningStudying kinship has involved doing fami...
-
Emergency Department Utilization for Patients Living With Sickle Cell Disease: Psychosocial Predictors of Health Car...Study objective: Individuals living wit...
-
Successful Gene Therapy for Sickle Cell DiseasePrior to this report, the only curative ...
-
Sickle Cell Disease: Why Is It Hard to Talk About Our Pain?https://www.youtube.com/watch?v=63pgiclv...
-
California Institute For Regenerative Medicine Awards City Of Hope $5.74 Million For Severe Sickle Cell Disease Clin...The California Institute for Regenerativ...
-
Carlton D. Dampier, MDDr. Carlton Dampier is a pediatric hemat...
-
Winthrop-University HospitalNYU Winthrop's pediatric hematologists p...
