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Dr. Clarice D. Reid

Year of Birth / Death


Medical School

University of Cincinnati College of Medicine



Career Path

Pediatric medicine
Public health: Government
Dr. Clarice D. Reid


I can't put my finger on a single influence. My father often expressed his desire to become a doctor but starting a family soon after finishing college, he had to seek gainful employment. All of my childhood I competed with my brothers in both physical and mental games, and both [of them] pursued science. One brother was a physician and the other a metallurgical chemist. In looking back, it might have been that I did not want to be a teacher. Pediatrics was a perfect specialty for me as I was very attracted to children and saw this as an opportunity to positively influence their development. At the time of choosing a specialty, I was also a mother.


Dr. Clarice Reid began her education in the segregated schools of Birmingham, Alabama, and went on to become director of the Division of Blood Diseases and Resources, National Heart, Lung and Blood Institute, National Institutes of Health. She was responsible for planning, directing and evaluating research in blood diseases in six national program areas: thrombosis and hemostasis, cellular hematology, sickle cell disease, transfusion medicine, acquired immune deficiency syndrome (AIDS), and bone marrow transplantation.

Born in Birmingham, Alabama, Clarice Reid graduated from the only segregated high school that blacks were then allowed to attend. "There were no circumstances that we considered barriers to education other than travelling across town and bypassing other more convenient high schools which we could not attend."

Growing up in Birmingham, she faced many challenges to success, including an education system that was segregated and lacking in resources. Not that education was a guarantee of success she recalls, "as most educated 'Negroes' could only be employed as postal workers or Pullman porters on the train." But supportive parents and nurturing teachers in the three-room elementary school she attended had high expectations for her and her classmates. "It was understood that we could and would obtain a college education and beyond," she says, "this was a period in African American history in the South where students were highly motivated to excel and our families viewed education as the 'ultimate equalizer.' "

She received her bachelor of science in biology with honors in 1952 from Talladega College in Alabama, a historically black school founded in 1865 by two former slaves to promote education of slaves' descendants. She attended Meharry Medical College, in Nashville, Tennessee, first at the School of Medical Technology and later at the School of Medicine. In 1959, she became the third African American to graduate with an M.D. from Ohio's University of Cincinnati College of Medicine.

Dr. Reid completed postgraduate assignments with a rotating internship and pediatric residency at Jewish Hospital with pediatric training at the Children's Hospitals Medical Center, both in Cincinnati. From 1962 to 1968, she was the only African-American pediatrician in private practice in Cincinnati. In 1969, she became director of Pediatric Education at Jewish Hospital, and in 1970 was named chairman of the hospital's Pediatrics Department. In 1970, she took a leave of absence when her family relocated to Washington, D.C. following her husband's appointment as Deputy General Counsel in the Office of Economic Opportunity.

The move launched her career in federal service, first as a medical consultant at the National Center for Family Planning, Health Services and Mental Health Administration, and then when she joined the National Heart, Lung and Blood Institute in the National Sickle Cell Disease Program in 1973. Under her leadership, the institute made many important advances in sickle cell disease research and hematology, including preventing infections in infants and young children with sickle cell disease with prophylactic penicillin, describing the clinical course of sickle cell disease, using hydroxyurea to reduce painful episodes in adult sickle cell disease patients, exploring the potential for transplantation with umbilical cord blood, and improving the nation's blood supply. From 1979 to 1994, she was also clinical assistant professor of Pediatrics at the Howard University College of Medicine in Washington, D.C.

In 1998, after twenty-six years in federal service, she retired from the Division of Blood Diseases and Resources. In retirement, Dr. Reid enjoys competitive bridge, is vice-president of the American Bridge Association (ABA) and chairs the ABA Foundation.

Among her many professional honors are the Superior Service Award, given in 1989, the highest honor given by the U.S. Public Health Service, and the Presidential Meritorious Executive Rank Award, 1991. She is especially proud to have been included in the Book of Black Heroes, Volume II: Great Women in the Struggle, which salutes eighty-four accomplished black women in the arts, sciences, education, athletics, government and social services. Her second most treasured honor was to be designated a "Distinguished Woman" by the Black Women in Scholarship for Action.

Question and Answer

How do I make a difference?

My greatest accomplishment professionally was the opportunity to oversee the national sickle cell disease program of research and service for a period of over twenty years. This totally tramsformed the management and care of patients and impacted directly on the quality of lives of patients with sickle cell disease.

How has my career evolved over time?

My final career focus in the government, ending at the National Institutes of Health, was just an example of sheer luck, i.e. "preparation meeting opportunity." We came to the D.C. area for two years and during that period, I had planned to continue working in the health care delivery area. Fortunately, with four children and the need to be involved in their daily lives, my plans would have required my working at a distance out of the Bethesda area, which was unacceptable. Friends directed me to the federal agencies in this locality and this allowed me to use my clinical experience at a policy-making level and to work in the program area of sickle cell disease. This was a pathway that I had not planned but one that changed the course of my career.