The discovery of chronic renal failure in a child, and the meaning of this experience from the perspective of the child's family caregivers have previously not been described in the literature on aboriginal health. During the summer of 1995, a phenomenological approach was used to explore this phenomena with 10 urban aboriginal family caregivers. These caregivers were providing care for their children who were receiving health care services at the outpatient children's clinic or the transplant unit at one urban tertiary care hospital. The findings of this research have helped create the beginning of a nursing data base of knowledge about aboriginal family caregivers of children who have chronic renal failure. In this paper, three of the main themes: surviving; relocation; enhancing power; and five sub-themes: providing nutrition; getting involved; educating the caregivers; educating the community; and returning to traditional ways are described. Implications of the findings for health care providers of children who have renal failure and their family caregivers are discussed. Issues that need to be addressed to help meet the needs of aboriginal family caregivers are identified. These issues include communication strategies, culturally appropriate teaching methods, access to resources, and community development initiatives.