Women caring for disabled parents and other relatives: implications for social workers in the health services

Revital Gross1, Shuli Brammli-Greenberg, Netta Bentur

  • 1Health Policy Research Unit, JDC-Brookdale Institute, P.O.B. 13087 Jerusalem 91130, Israel. Revital@jdc.org.il

Social Work in Health Care
|November 19, 2003
PubMed

Caring for an ill or disabled relative is a life experience shared by many women. Based on data from a representative sample of women in Israel, this study examined the demographic, employment, and health characteristics of women caregivers, focusing on the extent of care provided and its effect on the caregiver's physical and mental health. Using the conceptual framework of caregiving-related stress, we compared women who care for a parent, and women who care for another relative. The study found more instrumental difficulties, which lead to greater burden, among women who care for a disabled relative who is not a parent. Furthermore, larger proportions of women caring for a disabled relative who is not a parent report depressive mood symptoms, poor health status, and the need for psychological counseling. The findings suggest that formal service providers, chiefly social workers, may better support women caregivers once they are aware of the needs arising from disparate contexts of care.

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