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
-
Beliefs about hydroxyurea in youth with sickle cell diseaseBackground: Hydroxyurea reduces complic...
-
Sickle Cell Disease CoalitionThe Sickle Cell Disease Coalition (SCDC)...
-
The Cellie Coping Kit helps sick kids manage the stress of treatmentDesigned by Marsac during her fellowship...
-
Oswaldo L. Castro, MDDr. Oswaldo Castro is Professor Emeritus...
-
Citizens for Quality Sickle Cell CareThe New England Sickle Cell Institute at...
-
Cardiac iron overload in chronically transfused patients with thalassemia, sickle cell anemia, or myelodysplastic sy...The risk and clinical significance of ca...
-
Society of Pediatric Psychology Fall Virtual ConferenceSeptember 29, 2023 | 10 a.m. to 5 p.m. E...
+myBinder