Trusted Resources: People & Places
Healthcare providers, researchers, and advocates
Regina Hartfield
Community Advocate President & CEO
Sickle Cell Disease Association of America
7240 Parkway Drive, Suite 180
Hanover, Maryland, United States
Regina Hartfield is President/CEO of the Sickle Cell Disease Association of America, Inc. (SCDAA).
Prior to joining the Sickle Cell Disease Association of America, Hartfield was a manager for federal, state and commercial contracts for CVP, an information technology consulting firm in Virginia and Maryland. During her time at CVP, she developed strategic outreach initiatives, wrote strategy and implementation plans for the national expansion of a federal health agency’s program and managed a $30-million disaster recovery grant contract for the state of Tennessee, overseeing staff and operations of CVP’s regional office.
Hartfield serves on advisory boards and is a member of the Universal Sailing Club, where she has served on its board in different capacities. Hartfield graduated with honors from Lehman College of the City University of New York with a Bachelor of Arts in community outreach.
Related Content
-
Statement from FDA Commissioner on agency’s efforts to advance development of gene therapiesOnce just a theory, gene therapies are...
-
Southeastern sickle cell conferenceSickle Cell Foundation of Georgia is org...
-
Geographic Differences in Phenotype and Treatment of Children with Sickle Cell Anemia from the Multinational DOVE St...Background: Sickle cell anemia (SCA) is ...
-
Low-molecular-weight heparins for managing vaso-occlusive crises in people with sickle cell diseaseBACKGROUND: Sickle cell disease is one ...
-
Olugbenga Olowokure, MDDr. Olugbenga Olowokure is a hematologis...
-
UConn Health / New England Sickle Cell InstituteThe New England Sickle Cell Institute at...
-
Patient Perspective: The Journey of Pain in Sickle Cell Diseasehttps://www.youtube.com/watch?v=F4raFO0e...