Policy Development / Program Planning Skills
Module 2.4: 5-Minute Summary
Here we summarize the knowledge you've gained over the previous modules with a 5-minute conversation with John Richards, Co-Director of NCEMCH and Suzanne Bronheim, Associate Professor and Senior Policy Analyst within the Georgetown University Center for Child and Human Development. In this conversation, Dr. Bronheim answers questions that you have submitted throughout the module.
Click below to: Learn more about our speaker, Comment on the conversation, and Interact with other MCH professionals who are also taking Public Health Pronto.
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About Our Speaker
Suzanne M. Bronheim, Ph.D., is Associate Professor in the Department of Pediatrics and a Senior Policy Analyst within the Georgetown University Center for Child and Human Development (GUCCHD). As faculty within the National Center for Cultural Competence (NCCC), she has leveraged her 30-year career to advance MCH issues of cultural competence, family-centered care, CYSHCN, and systems development.
Currently, Dr. Bronheim helps to lead the National Partnership to Promote Safe Sleep; she previously served as the Director of the Sudden Unexpected Infant and Child Death and Pregnancy Loss Project within the NCCC for 15 years
As a pediatric psychologist, she was director of the learning disabilities/neuropsychology service at Georgetown for twenty years, was co-director of the Tourette Syndrome Clinic at Georgetown, provided evaluation and consultation for adults with developmental disabilities, and served as the psychologist in the Pediatric Pulmonary Center, the Cystic Fibrosis Center and the renal dialysis and transplant team at Georgetown University Hospital. For over ten years, she coordinated Communities Can!—a national network of communities dedicated to using collaborative, systems integration strategies to support and serve all children and families, including those with or at risk for special health care needs.
Dr. Bronheim served as PI for a MCHB-funded research project to address racial and ethnic disparities in access to information by families of children with special health care needs and is part of research teams conducting validations studies on measures of provider cultural and linguistic competence and family-centered care. She has provided training and technical assistance related to cultural and linguistic competence to state Title V and other public health programs, health and mental health care systems, non-profit organizations, health care providers, and family advocacy and support organizations. She has also developed resources on the role of cultural and linguistic competence in infant mortality disparities, approaches to implementing cultural and linguistic competence in health promotion, and providing culturally and linguistically competent services and supports to families.
COMMENT
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Next steps and thoughts to consider for the field:
- I think it would be interesting to actually have to use the tools provided to put together potential policy. The hands on potential of learning by doing something like that could be really valuable.
- How difficult is it for agencies to avoid lobbying? It seemed like there were lots of disclaimers on the cdc site about this?
- Why do we let services for children/young adults with disabilities drop off after a certain age?
- While the materials are great, the amount of steps seems somewhat daunting. I think as a semester project, with each portion broken out, it could be a great learning tool.