Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
The Sickle Cell Disease Partnership is a multi-sector collaboration of healthcare stakeholders committed to advancing actionable federal healthcare policies that will improve the lives of patients living with Sickle Cell Disease.
The Partnership’s main objective is to work collaboratively across the Sickle Cell Disease community to translate the recommendations of the National Academies’ foundational report into legislative and administrative actions in Congress and the Executive Branch. Their vision is a day when every individual with Sickle Cell Disease in the United States lives to his or her fullest potential because the individual has timely, sustained access to high-quality, equitable, coordinated care and treatment.
Related Content
-
Update of hematopoietic cell transplantation for sickle cell diseasePURPOSE OF REVIEW: Hematopoietic cell t...
-
Preventing Strokes in Children with Sickle Cell Diseasehttps://www.youtube.com/watch?v=k6h7cb7S...
-
Cognitive function, coping, and depressive symptoms in children and adolescents with sickle cell diseaseOBJECTIVE: The objective of this study ...
-
Cure Sickle Cell Now Move-On Virtual EventWe have re-imagined our annual Stomp Out...
-
14 Tips for Traveling with a Chronic Illness or Disabilityhttps://www.youtube.com/watch?v=fDOHOw3d...
-
2021 WEPSCF Rockin’ the Red – 16th Annual EventJoin us for a Zoom gathering as we celeb...
-
Julie Kanter, MDDr. Julie Kanter is the Associate Profes...
+myBinder