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
-
Four Solutions for Sickle Cell Disease SupportWhen Precious Lee was a year old, she be...
-
Opioid utilization patterns in United States patients with sickle cell diseaseSickle cell disease (SCD) is the most co...
-
‘I Have Sickle Cell, but Sickle Cell Doesn’t Have Me’: While Raising Awareness, Chicago Man, 25, Dies From...Elijah Powell was determined to live his...
-
Community Health Workers as Support for Sickle Cell CareCommunity health workers are increasingl...
-
SCANJ Holiday Party South with Kenta KlausKenta Klaus (Santa's brother) invites yo...
-
Roland B. Scott Memorial Symposium: I Want Somebody to LoveRoland B. Scott Symposium on Sickle Cell...
-
Gene Therapy & Clinical Trials Webinarhttps://www.youtube.com/watch?v=yYexIUgH...