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.
Related Content
-
Kathryn E Scott, MDDr. Scott is affiliated with General Ped...
-
New Pre-transplant Treatment Regimen Improves Survival of Kids with Sickle Cell Disease, Trial ShowsA new pre-transplant conditioning regime...
-
Sickle Cell Disease Virtual Forum: Historically Black Colleges and Universities 16-Day ChallengeYou’re invited to the Sickle Cell Dise...
-
Children and adolescents with sickle cell disease have worse cold and mechanical hypersensitivity during acute painf...Sickle cell disease (SCD) pain associate...
-
Children’s Hospital Oakland Research InstituteDuring our first 50 years, Children’s ...
-
‘Every time it’s a battle’: In excruciating pain, sickle cell patients are shunted asideAmy Mason had toughed it out for hours o...
-
Lisa M. Shook, MA, MCHES, CCPLisa M. Shook is an Assistant Professor ...
+myBinder