The hardest thing we have ever done - Palliative Care Australia
The hardest thing we have ever done - Palliative Care Australia
The hardest thing we have ever done - Palliative Care Australia
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
Schulz, R. & Beach, S. (1999). <strong>Care</strong>giving as a risk factor for mortality – the caregiver health<br />
effects study. Journal of the American Medical Association, 282 (23) pp 2215-2219.<br />
Silveira, J., & Winstead-Fry, P. (1997). <strong>The</strong> Needs of Patients With Cancer and <strong>The</strong>ir<br />
<strong>Care</strong>givers in Rural Areas. Oncology Nursing Forum, 24(1), 71-76.<br />
Stallard, P., Mastroyannopolou, K., Lewis, M., & Lenton, S. (1997). <strong>The</strong> siblings of children<br />
with life threatening conditions. Child Psychol Psychiatry Rev, 226-33.<br />
Steele, R., & Fitch, M. (1996a). Coping Strategies of Family <strong>Care</strong>givers of Home Hospice<br />
Patients With Cancer. Oncology Nursing Forum, 23(6), 955-960.<br />
Steele, R., & Fitch, M. (1996b). Needs of Family <strong>Care</strong>givers of Patients Receiving Home<br />
Hospice <strong>Care</strong> for Cancer. Oncology Nursing Forum, 23(5), 823-828.<br />
Sullivan, K. (2003). National Indigenous <strong>Palliative</strong> <strong>Care</strong> Needs Study. Department of Health<br />
and Ageing, Sydney.<br />
<strong>The</strong> <strong>Australia</strong>n Psychological Society (2003). Submission to <strong>Palliative</strong> care <strong>Australia</strong> in<br />
response to the National Inquiry into the Social Impact of Caring for the Terminally-Ill. APS.<br />
<strong>The</strong> Standing Senate Committee on Social Affairs, Science and Technology (2002). <strong>The</strong> Health<br />
of Canadians. Available at: www.parl.gc.ca/37/2/parlbus/commbus/senate/com-e/soci-e/repe/repoct02vol6highlights-e.htm.<br />
(accessed Nov 2003).<br />
Toye, C., Kristjanson, L., & Helmes, E. (2003). Factors Influencing the <strong>we</strong>ll-being of family<br />
members of aged care facility residents. Australasian Journal on Ageing, 22(1), 26-30.<br />
Wiley, S (1998). St Vincents Healthcare Campus.<br />
http://www.clininfo.health.nsw.gov.au/hospolic/stvincents/stvin98/index.html.<br />
Wilkes, L., White, K., & O’Riordan, L. (2000). Empo<strong>we</strong>rment through information: supporting<br />
rural families of oncology patients in palliative care. <strong>Australia</strong>n Journal of Rural Health, 8,<br />
41-46.<br />
World Health Organisation. <strong>Palliative</strong> care. Available at:<br />
www.who.int/hiv/topics/palliative/<strong>Palliative</strong><strong>Care</strong>/en/ (accessed Feb 2004).<br />
Vachon, M. (1998). Psychosocial Needs of Patients and Families. Journal of <strong>Palliative</strong> <strong>Care</strong>,<br />
14(3), 49-56.<br />
Yates, P. (1999). Family coping: Issues and challenges for cancer nursing. Cancer Nursing,<br />
22(1), 63-71.<br />
68 THE HARDEST THING WE HAVE EVER DONE: <strong>The</strong> Social Impact of Caring for Terminally Ill People in <strong>Australia</strong>, 2004
Change language