Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Sickle Cell Partners of the Carolinas
PO Box 480714Charlotte, North Carolina, United States
Email Web
Sickle Cell Partners of the Carolinas was formed in January of 2009. At that time, patients, families and members of the medical community came together informally to meet and discuss ideas involving care and support in the Sickle Cell community. From those conversations, Sickle Cell Partners of the Carolinas came into being and is an organization that consists of patients of all ages; families; caregivers; healthcare providers; social workers and an at large community that cares deeply about those affected by Sickle Cell Disease. The original founders of the organization included patients, families and members of the medical community. The need for a support group was expressed to engage patients and families affected by Sickle Cell Anemia, Sickle Cell Trait, and Thalassemia.
+myBinderRelated Content
-
U.S. Government Awards Missouri Researcher $4.3 Million to Study Sickle Cell in Teens, AdultsThe National Institutes of Health (NIH) ...
-
Translating sickle cell guidelines into practice for primary care providers with Project ECHOBackground: Approximately 100,000 perso...
-
Today’s Faces of Sickle Cell Disease: Pat Corley, RNIn 1979, while she was volunteering at a...
-
Cayenne Wellness CenterCayenne Wellness Center and Children’s...
-
Pacific Sickle Cell Regional CollaborativeThe Pacific Sickle Cell Regional Collabo...
-
2018 World Sickle Cell Day “In Good Spirits & Good Health” EventTuesday June 19th is World Sickle Cell D...
-
Understanding the Impact of Sickle Cell Diseasehttps://www.onescdvoice.com/wp-content/u...
