Welcome to the Center for Sickle Cell Disease

The Howard University Center for Sickle Cell Disease was founded by the late Dr. Roland B. Scott in 1971 to address the needs of patients and families in the Washington Metropolitan area, who are affected by sickle cell disease. The Center is committed to a six-fold goal that includes comprehensive medical care, research, testing, education, counseling and community outreach. Currently, the Center has expanded its clinical research program and developed a collaborative consortium with Children’s National Medical Center (CNMC). Working together, Howard University Hospital, CNMC, NIH and the Howard University Center for Sickle Cell Disease are the Washington area’s leading provider of patient services for sickle cell disease.

The Third Roland B. Scott Memorial Symposium

Upcoming Center-Affiliated Events (Archive)

Upcoming Local Events (Archive)

Ongoing Open Events

  • Sickle Cell Screening, Wednesdays, 9:00AM - 12:00PM, HU Hospital Main Lobby. No appointment necessary, call (202) 865-4443 for more information.
  • Center for Sickle Cell Disease Staff Meeting, Mondays, 10:00AM - 11:00AM, 211/Mudd Building.
  • Research Scientists Lab Meeting, Fridays, 10:00AM - 11:00AM, GCRC Conference Room.

Sickle Cell and Anemia News (Archive)

  • NAAC Releases New Slide Set For Iron Deficiency Anemia. The National Anemia Action Council (NAAC) announced today the addition of a new educational presentation about iron deficiency anemia available on their website, www.anemia.org. Created by NAAC's anemia experts, the Iron Deficiency Anemia slide set is the latest in a series of free, downloadable presentations designed to educate healthcare professionals about anemia management practices. National Anemia Action Council (article posted March 5, 2009)

Last updated: June 22, 2009

For questions, comments or concerns regarding this website please contact Ross Heffer