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
-
Social Determinants of Health and Emergency Department Use Among Children With Sickle Cell DiseaseSickle cell disease (SCD) is associated ...
-
Eric E. Bouhassira, PhDDr. Eric E. Bouhassira joined the Albert...
-
Hope for SCDHope for SCD strives to bridge the gap b...
-
Sickle Cell Disease Program at Children’s HealthThe Sickle Cell Disease Program at Child...
-
Global Sickle Cell Disease Treatment Market 2019–2023| Evolving Opportunities with ADDMEDICA and Bristol-Myers Squ...The global sickle cell disease treatment...
-
Ify Osunkwo, MD, MPHDr. Ify Osunkwo, a specialist in hematol...
-
Opioid Abuse Backlash Could Hurt Sickle Cell Patients’ Medication Needs, Some FearWith drug overdoses now the leading caus...
