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
-
The clinical presentation, utilization, and outcome of individuals with sickle cell anaemia presenting to urban emer...Background: Sickle cell anaemia (SCA) i...
-
Nancy M. ReneNancy is the grandmother of a child with...
-
Risk Factors Associated With Increased Emergency Department Utilization in Patients With Sickle Cell Disease: A Syst...Sickle cell disease (SCD), a genetic dis...
-
Ruth Nankanja, BAForty- three year old Ruth Nankanja is t...
-
Let Your Light Shine: Sickle SocialPiedmont Health Services and Sickle Cell...
-
Sickle Cell Community Advisory Council of Northern CaliforniaThe Sickle Cell Community Advisory Counc...
-
Minority Health Counts: Building a More Equitable Community SummitBy Supporters of Families with Sickle Ce...
