Jan S. Greenberg, Ph.D. University of Minnesota Professor of Social Work Contact Information Waisman Center UW-Madison 1500 Highland Avenue Madison, WI 53705 608-263-0532 608-265-4862 E-mail: greenberg@waisman.wisc.edu Web: http://www.waisman.wisc.edu/family/

Over the past decade, I have been investigating the challenges faced by families of persons with severe and persistent mental illness. My research has been funded by the National Institute of Mental Health [NIMH] since the early 1990s. With this support, I have conducted three major studies of families coping with mental illness. In a survey of over 1000 Wisconsin families caring for a relative with a severe and persistent mental illness, we documented the importance of professionals involving family members as collaborators in the treatment process. We found that family members had lower levels of distress when professional care providers involved them as partners in their relative's treatment and provided family members with education about mental illness and its treatment, and advice about how to manage their relative's difficult behaviors. The second study, conducted in collaboration with Dr. Marsha Mailick Seltzer (UW-Madison) and Dr. Marty Krauss (Brandeis University), has been to investigate differences in the mental health of aging parents caring for an adult child with mental illness and of those caring for an adult child with developmental disabilities. We found that parents caring for a child with mental illness experienced elevated levels of depression and caregiver burden, and greater pessimism about their child's future care than parents caring for an adult son or daughter with mental retardation. This line of research also has led to new insights into the differential effectiveness of coping and social support across different caregiving contexts. In collaboration with Dr. Marsha Seltzer, I am presently completing a five-year NIMH funded longitudinal study of over 200 aging parents caring for an adult son or daughter with schizophrenia. This study examines the long-term toll that coping with mental illness takes on parental and family well-being. It also explores the involvement of and the effects on the lives of siblings when aging parents are no longer able to remain in a primary caregiving role. This study has been designed to parallel Drs. Seltzer and Krauss' longitudinal study of 461 aging families caring for a son or daughter with Down syndrome (R01 AG08768, Years 1-10), and their funded longitudinal study of 400 families of adults with autism (R01 AG08768, Years 11-15). The availability of these data allows us to conduct the first large scale multiwave longitudinal analysis comparing the experiences of aging families of adults with schizophrenia to those of aging families of adults with Down syndrome and autism. The findings will provide new insights into how the services needs of these families are uniquely shaped by the nature of the adult’s disability. Findings from this study point to the importance of maintaining an optimistic attitude in coping with the challenges of schizophrenia, autism, and Down syndrome. In addition, our findings indicate that mothers caring for a son with a dual diagnosis of mental retardation and schizophrenia are at particularly high risk for experiencing the deleterious effects of caregiving. Also, within the African American community, caregiving takes a greater toll on the physical health than the mental health of maternal caregivers. Finally, we found that siblings of adults with schizophrenia report that they expected to be involved in the future care of their sibling with schizophrenia after their parents’ death. However, there are many factors that will limit their involvement, including geographical distance and competing work and family responsibilities.   Seltzer, M.M., Greenberg, J.S., Floyd, F., Pettee, Y., & Hong, J. (2001). Life course impacts of parenting a child with disability. American Journal of Mental Retardation, 106, 282-303. Greenberg, J.S. (2002). The role of fathers in the lives of their sons and daughters with mental illness. In B. J. Kramer & E.H. Thompson (Eds.), Men as caregivers: Theory, research, and service implications (pp. 269-293). Springer Publications. Kim, H.W., Greenberg, J.S., & Seltzer, M.M. (2003). The role of coping in maintaining the psychological well-being of mothers of adults with mental retardation and mental illness. Journal of Intellectual Disability Research, 47, 313-327. Chen, F.P., & Greenberg, J.S. (2004). Caregiving gains in family care for people with mental illness. Community Mental Health, 40, 423-435. Greenberg, J.S., Seltzer, M.M., Krauss, M.W., Chou, R.J.A., & Hong, J. (2004). The effect of quality of the relationship between mothers and adults with disabilities on maternal well-being: The mediating role of optimism. American Journal of Orthopsychiatry, 74, 14-25. Magana, S., Greenberg, J., & Seltzer, M.M. (2004). The health and well-being of African American mothers caring for an adult with schizophrenia. Psychiatric Services, 55, 711-713. Seltzer, M.M., Greenberg, J.S., Floyd, F., Hong, J. (2004). Accommodative coping and well-being of midlife parents of children with mental health problems or developmental disabilities. American Journal of Orthopsychiatry, 74, 187-195. Seltzer, M. M., Shattuck, P. , Abbeduto, L., & Greenberg, J. (2004). The trajectory of developments in adolescents and adults with autism. Mental Retardation and Developmental Disabilities Research;10(4):234-47. Review.   Click to search National Library of Medicine and PubMed for other publications by Dr. Greenberg

Last updated 9/19/2005 by rowley@waisman.wisc.edu