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
-
GBT launches ACCEL grants program to improve access to care for people with Sickle cell diseaseGlobal Blood Therapeutics, Inc. (GBT) to...
-
World Sickle Cell Day with Special Guest Mr. Tony Adkins, TV Host Sandy Bodeau, Dr. Harrington, and Dr. AlvarezFriday, June 19, 2020 1:00PM to 2:15PM ...
-
Tracee D. PattersonTracee was a Director of operations and ...
-
Carlos GrauperaMr. Graupera is the Immediate Past Presi...
-
Celebratory Scholarship Virtual Gala – Michelle’s House (SCDAA SC)Living with Sickle Cell Disease (SCD) du...
-
Living Well With Sickle Cell: Andre Harris (Video)My name is Andre Harris. We are in Houst...
-
The As One FoundationThe As One Foundation was established in...
