Google
Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Howard University Hospital Center for Sickle Cell Disease
1840 7th St NWWashington, DC, United States
Email Phone Web
Transitioning from pediatric to adult providers is an essential step in the care of teens and young adults with sickle cell anemia. The Howard University, Center for Sickle Cell Disease, Adult Transition Program works to educate children and young adults about their disease and personal medical history and develop skill sets required to navigate the adult health care setting.
Howard University’s Center for Sickle Cell Disease (SCD) was founded by the late Dr. Roland B. Scott in 1971 to address the needs of patients and families in the Washington Metropolitan area affected by SCD. The Center is committed to a six-fold goal that includes comprehensive medical care, research, testing, education, counseling, and community outreach. Recently, the Center has expanded its clinical research program and developed a collaborative consortium with Children’s National Medical Center (CNMC) and in working together with Howard University Hospital and NIH, we are the Washington area’s leading provider of patient services for SCD.
+myBinderRelated Content
-
Unanticipated consequences identified after implementation of a pediatric emergency department (PED)-based intranasa...Background: The 2014 National Heart Lun...
-
Patrick Woster, PhDPatrick M. Woster is professor of drug d...
-
The Association Between Timely Opioid Administration and Hospitalization in Children With Sickle Cell Disease Presen...Objective: To evaluate the association ...
-
Joshua Field, MD, MSDr. Joshua Field is an Associate Medical...
-
Methodist Comprehensive Sickle Cell CenterMethodist Comprehensive Sickle Cell Cent...
-
East Carolina University Comprehensive Sickle Cell CenterEast Carolina University Comprehensive S...
-
Sickle Cell Disease: Racism in the American Health Care SystemWednesday, June 28 1-4 pm EDT Massachu...
