Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Sickle Cell Disease Coalition
2021 L Street NW, Suite 900Washington, DC, United States
Email Phone Web
The Sickle Cell Disease Coalition (SCDC) was formed to amplify the voice of the sickle cell disease (SCD) stakeholder community to improve outcomes for individuals with SCD. Its membership includes public health, research, and provider organizations, patient groups, faith-based organizations, federal agencies, industry representatives, and foundations.
The future of care for SCD patients will be dependent on advanced and highly targeted approaches to research, discovery, and implementation of proven and new interventions. To ensure that patients with SCD receive state-of-the-art care, there is a need for the SCD stakeholder community to use multi-disciplinary and coordinated efforts to produce the greatest impact. A multi-agency approach would deliver advances faster, more economically, and more efficiently to patients suffering from this debilitating disease in the United States and around the world. That’s what for the SCDC is committed.
+myBinderRelated Content
-
Rare Diseases and Orphan Products Breakthrough SummitEach year, the NORD Summit, one of the l...
-
Crisis OverCrisis Over is a sickle cell disease blo...
-
Sick CellsSick Cells' mission is to elevate the vo...
-
Laura Dortch-Edler, EdDDr. Laura D. Edler is an Assistant Profe...
-
Sickle Cell Disease Association-St. PetersburgAs a non-profit 501(c)3 organization, Si...
-
Emmaus Life Sciences Launches Its Commercial Co-Payment Assistance Program for Endari™Emmaus Life Sciences, Inc., a leader in ...
-
Tina Kay HughesRetired at the age of 34 because of Sick...
