References
- Albert, S. M., Im, A., Brenner, L., Smith, M., & Waxman, R. (2002). Effect of a social work liason program on family caregivers to people with brain injury. Journal of Head Trauma Rehabilitation, 17, 175–189.
- British Society of Rehabilitation Medicine, & Royal College of Physicians. (2003). Rehabilitation following acquired brain injury: National clinical guidelinesLondonThe Lavenham Press
- Degeneffe, C. E. (2001). Family caregiving and traumatic brain injury. Health and Social Work, 26, 257–268.
- Department of Human Services. (1995). Public hospital patient charter. Available online at: www.health.vic.gov/patientcharter/resources/materials , accessed 8 May 2009.
- Ergh, T. C., Rapport, L. J., Coleman, R. D., & Hanks, R. A. (2002). Predictors of caregiving and family functioning following traumatic brain injury: Social support moderates caregiver distress. Journal of Head Trauma Rehabilitation, 17, 155–174.
- Fyffe, C., & McCubbery, J. (1996). ‘If only we had somewhere to turn …’ The service needs of people with acquired brain injury in a rural community. Australian Journal of Rural Health, 4, 232–236.
- Knight, R. G., Devereux, R., & Godfrey, H. P. (1998). Caring for a family member with a traumatic brain injury. Brain Injury, 12, 467–481.
- Kreutzer, J. S., Gervasio, A. H., & Camplair, P. S. (1994). Primary caregivers' psychological status and family functioning after traumatic brain injury. Brain Injury, 8, 197–210.
- LeFebvre, H., Pelchat, D., Swaine, B., Gelinas, I., & Levert, M. J. (2005). The experiences of individuals with a traumatic brain injury, families, physicians and health professionals regarding care provided throughout the continuum. Brain Injury, 19, 585–597.
- Machamer, J., Temkin, N., & Dikmen, S. (2002). Significant other burden and factors related to it in traumatic brain injury. Journal of Clinical and Experimental Neuropsychology, 24, 420–433.
- Marsh, N. V., Kersel, D. A., Havill, J. H., & Sleigh, J. W. (1998). Caregiver burden at 6 months following severe traumatic brain injury. Brain Injury, 12, 225–238.
- Miles, M., & Huberman, A. (1994). Qualitative data analysis (2nd ed.)Thousand Oaks, CASage Publication
- Murray, H. M., Maslany, G. W., & Jeffery, B. (2006). Assessment of family needs following acquired brain injury in Saskatchewan. Brain Injury, 20, 575–585.
- Nabors, N., Seacat, J., & Rosenthal, M. (2002). Predictors of caregiver burden following traumatic brain injury. Brain Injury, 16, 1039–1050.
- New Zealand Guidelines Group. (2006). Traumatic brain injury: Diagnosis, acute mangagement and rehabilitationWellingtonNew Zealand Guidelines Group
- O'Callaghan, A. M., McAllister, L., & Wilson, L. (2010). Experiences of care reported by adults with traumatic brain injury. International Journal of Speech-Language Pathology, 12, 107–123.
- Ponsford, J., Olver, J., Ponsford, M., & Nelms, R. (2003). Long-term adjustment of families following traumatic brain injury where comprehensive rehabilitation has been provided. Brain Injury, 17, 453–468.
- Rotondi, A. J., Sinkule, J., Balzer, K., Harris, J., & Moldovan, R. (2007). A qualitative needs assessment of persons who have experienced traumatic brain injury and their primary family caregivers. Journal of Head Trauma Rehabilitation, 22, 14–25.
- Sample, P. L., & Darragh, A. R. (1998). Perceptions of care access: The experience of rural and urban women following brain injury. Brain Injury, 12, 855–874.
- Serio, C., Kreutzer, J., & Gervasio, A. (1995). Prediciting family needs after traumatic brain injury: Implications for intervention. Journal of Head Trauma Rehabilitation, 10, 32–45.
- Sinnakaruppan, I., & Williams, D. M. (2001). Family carers and the adult head-injured: A critical review of carers' needs. Brain Injury, 15, 653–672.
- Smith, J. E., & Smith, D. L. (2000). Family caregivers' perspectives on their journeys through the system. Care Management Journal, 2, 27–33.
- Stebbins, P., & Leung, P. (1998). Changing family needs after brain injury. Journal of Rehabilitation, 64, 15–22.
- Turner, B., Fleming, J., Cornwell, P., Worrall, L., Ownsworth, T., Haines, T., et al. (2007). A qualitative study of the transition from hospital to home for individuals with acquired brain injury and their family caregivers. Brain Injury, 21, 1119–1130.
- Wells, R., Dywan, J., & Dumas, J. (2005). Life satisfaction and distress in family caregivers as related to specific behavioural changes after traumatic brain injury. Brain Injury, 19, 1105–1115.