Barbara Ferrer
As the City’s Health Commissioner, Barbara Ferrer manages a $172 million budget and oversees 1,200 employees. In addition to operating public health programs, the Commission provides oversight of Boston Emergency Medical Services, several substance abuse treatment facilities, and the second largest homeless services program in New England. A high school principal in the Boston Public Schools from 2004 to 2007, Dr. Ferrer returned to the Commission in 2007 after having previously served as the Deputy Director for six years. During that time she spearheaded a broad-based and comprehensive campaign to reduce racial and ethnic health disparities. Dr. Ferrer has more than 25 years of experience working in healthcare. Prior to joining the Boston Public Health Commission, she spent five years at the Massachusetts Department of Public Health – first as Director of Health Promotion and Chronic Disease Prevention and later as Director of the Division of Maternal and Child Health. In 1988, Dr. Ferrer received a master’s degree in public health from Boston University, and was awarded a Pew Foundation doctoral fellowship to attend Brandeis University. She wrote her doctoral thesis on hospital length-of-stay determinants for AIDS patients and, in 1994, received her doctorate from Brandeis University’s Heller School for Advanced Studies in Social Welfare. Dr. Ferrer also holds a master’s degree in education from the University of Massachusetts, Boston.

For individuals living with complex, often chronic conditions, and their families, palliative care can provide relief from symptoms, improve satisfaction and outcomes, and help address critical mental and spiritual needs during difficult times. Now more than ever, there is growing recognition of the importance of palliative care services for individuals with serious illness, such as advance care planning, pain and symptom management, care coordination, and team-based, multi-disciplinary support. These services can help patients and families cope with the symptoms and stressors of disease, better anticipate and avoid crises, and reduce unnecessary and/or unwanted care. While this model is grounded in evidence that demonstrates improved quality of life, better outcomes, and reduced cost for patients, only a fraction of individuals who could benefit from palliative care receive it. 























































































































































