Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
The Sickle Cell Association is a not-for-profit organization that strives to diminish suffering and improve the quality of life for those individuals affected by sickle cell disease. They are committed to raising the public’s awareness and providing education to patients, their families, health professionals, legislators and the general public about sickle cell disease, its management and its challenges.
Sickle Cell Association Mission is to support the sickle cell community while working to eliminate the disease through collaborations on research, education and resources.
+myBinderRelated Content
-
Living With Sickle Cell DiseaseIf you or your child has sickle cell dis...
-
Lewis Hsu, MD, PhDDr. Lewis Hsu is a pediatric hematologis...
-
Prevention of acute sickle cell crisis: review of the NEJM reportA recent article in the New England Jour...
-
FDA Awards $2M to Phase 2 Trial of Vitamin D for Reducing Risk of SCD Respiratory ComplicationsThe U.S. Food and Drug Administration (F...
-
Nirmish Shah, MDAs director of Duke’s sickle cell tran...
-
Playing through sickle cellEighteen minutes in with no break, Billy...
-
KNOWvember Webinar: A grandparent’s voice – Advocacy and support for chronic pain familiesWhile parents are often the prim...
