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———. ‘The Central Importance of Spirituality in Palliative Care’. International Journal of Palliative Nursing 17, no. 7 (July 2011): 353–58. https://doi.org/10.12968/ijpn.2011.17.7.353.
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Aranda, Sanchia. ‘Silent Voices, Hidden Practices: Exploring Undiscovered Aspects of Cancer Nursing’. International Journal of Palliative Nursing 7, no. 4 (April 2001): 178–85. https://doi.org/10.12968/ijpn.2001.7.4.9034.
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Back, Anthony L.1Rushton, Cynda H.2Kaszniak, Alfred W.3Halifax, Joan S.4. ‘“Why Are We Doing This?”: Clinician Helplessness in the Face of Suffering.’ Journal of Palliative Medicine 18, no. 1 (2015): 26–30. https://doi.org/10.1089/jpm.2014.0115.
Barnard, David. Crossing over: Narratives of Palliative Care. Oxford: Oxford University Press, 2000. https://site.ebrary.com/lib/auckland/detail.action?docID=10375342.
Botti, Mari RN, RM, BN, PhD, MRCNA. ‘Barriers in Providing Psychosocial Support for Patients With Cancer’. Cancer Nursing 29, no. 4 (n.d.): 309–16. http://ovidsp.ovid.com.ezproxy.auckland.ac.nz/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=00002820-200607000-00010&LSLINK=80&D=ovft.
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Byock, I. R. ‘When Suffering Persists’. Journal of Palliative Care 10, no. 2 (n.d.): 8–13.
Carter, Elizabeth A., and Monica McGoldrick. The Expanded Family Life Cycle: Individual, Family, and Social Perspectives. 3rd ed. Boston: Allyn and Bacon, 1999.
Casarett, David J.1,2,3 casarett@mail.med.upenn.eduQuill, Timothy E.1,2,3. ‘“I’m Not Ready for Hospice”: Strategies for Timely and Effective Hospice Discussions.’ Annals of Internal Medicine 146, no. 6 (2007). http://ezproxy.auckland.ac.nz/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=24377897&site=ehost-live&scope=site.
Cassell, Eric. ‘The Nature of Suffering and the Goals of Medicine’. In The Social Medicine Reader. Vol. 1, Patients, Doctors and Illness, 2nd ed. Durham, N.C.: Duke University Press, 2005.
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Chochinov, Harvey Max1 harvey.chochinov@cancercare.mb.caCann, Beverley J.2. ‘Interventions to Enhance the Spiritual Aspects of Dying.’ Journal of Palliative Medicine 8 (2005). http://ezproxy.auckland.ac.nz/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=19902698&site=ehost-live&scope=site.
Chrash, Melany, Barbara Mulich, and Carol M. Patton. ‘The APN Role in Holistic Assessment and Integration of Spiritual Assessment for Advance Care Planning’. Journal of the American Academy of Nurse Practitioners 23, no. 10 (October 2011): 530–36. https://doi.org/10.1111/j.1745-7599.2011.00644.x.
Chur-Hansen, A., S. C. Zambrano, and G. B. Crawford. ‘Furry and Feathered Family Members--A Critical Review of Their Role in Palliative Care’. American Journal of Hospice and Palliative Medicine 31, no. 6 (1 September 2014): 672–77. https://doi.org/10.1177/1049909113497084.
‘Compassion Fatigue and Burnout | CJON’, n.d. https://cjon.ons.org/cjon/14/5/compassion-fatigue-and-burnout.
Cooley, Candy, and Sanchia Aranda. ‘Providing Total Patient Care: The Power of Reflection’. International Journal of Palliative Nursing 11, no. 12 (December 2005): 608–608. https://doi.org/10.12968/ijpn.2005.11.12.20225.
Cort, Elizabeth1Monroe, Barbara1Oliviere, David1. ‘Couples in Palliative Care.’ Sexual & Relationship Therapy 19, no. 3 (2004): 337–54. http://ezproxy.auckland.ac.nz/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=14010868&site=ehost-live&scope=site.
Daaleman, T. P., B. M. Usher, S. W. Williams, J. Rawlings, and L. C. Hanson. ‘An Exploratory Study of Spiritual Care at the End of Life’. The Annals of Family Medicine 6, no. 5 (1 September 2008): 406–11. https://doi.org/10.1370/afm.883.
Dein, S., and J. Stygall. ‘Does Being Religious Help or Hinder Coping with Chronic Illness? A Critical Literature Review’. Palliative Medicine 11, no. 4 (1 July 1997): 291–98. https://doi.org/10.1177/026921639701100405.
Duggleby, W., L. Holtslander, J. Kylma, V. Duncan, C. Hammond, and A. Williams. ‘Metasynthesis of the Hope Experience of Family Caregivers of Persons With Chronic Illness’. Qualitative Health Research 20, no. 2 (1 February 2010): 148–58. https://doi.org/10.1177/1049732309358329.
Egan, Richard, Rod MacLeod, Chrystal Jaye, Rob McGee, Joanne Baxter, and Peter Herbison. ‘What Is Spirituality? Evidence from a New Zealand Hospice Study’. Mortality 16, no. 4 (November 2011): 307–24. https://doi.org/10.1080/13576275.2011.613267.
Fallowfield, LJ1Jenkins, VA2Beveridge, HA3. ‘Truth May Hurt but Deceit Hurts More: Communication in Palliative Care.’ Palliative Medicine 16, no. 4 (2002): 297–303. http://ezproxy.auckland.ac.nz/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=6978408&site=ehost-live&scope=site.
Faulkner, Ann, and Peter Maguire. Talking to Cancer Patients and Their Relatives. Vol. Oxford medical publications. Oxford: Oxford University Press, 1994.
Figley, Charles R., Peter Huggard, Charlotte E. Rees, and EBSCOhost. First Do No Self Harm: Understanding and Promoting Physician Stress Resilience. Electronic resource. Oxford: Oxford University Press, 2013. http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=1201320.
Gallagher, Romayne, and Marian Krawczyk. ‘Family Members’ Perceptions of End-of-Life Care across Diverse Locations of Care’. BMC Palliative Care 12, no. 1 (2013). https://doi.org/10.1186/1472-684X-12-25.
Gaudio, F. D., T. I. Zaider, M. Brier, and D. W. Kissane. ‘Challenges in Providing Family-Centered Support to Families in Palliative Care’. Palliative Medicine 26, no. 8 (1 December 2012): 1025–33. https://doi.org/10.1177/0269216311426919.
Grant, L., S. A. Murray, and A. Sheikh. ‘Spiritual Dimensions of Dying in Pluralist Societies’. BMJ 341, no. sep16 2 (16 September 2010): c4859–c4859. https://doi.org/10.1136/bmj.c4859.
Hall, Sue, Polly Edmonds, Richard Harding, Harvey Chochinov, and Irene J Higginson. ‘Assessing the Feasibility, Acceptability and Potential Effectiveness of Dignity Therapy for People with Advanced Cancer Referred to a Hospital-Based Palliative Care Team: Study Protocol’. BMC Palliative Care 8, no. 1 (2009). https://doi.org/10.1186/1472-684X-8-5.
Hanks, Geoffrey W. C. Oxford Textbook of Palliative Medicine. 4th ed. Oxford: Oxford University Press, 2009.
Harding, Richard1List, Sally2Epiphaniou, Eleni1Jones, Hannah1. ‘How Can Informal Caregivers in Cancer and Palliative Care Be Supported? An Updated Systematic Literature Review of Interventions and Their Effectiveness.’ Palliative Medicine 26, no. 1 (2012): 7–22. http://ezproxy.auckland.ac.nz/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=69872797&site=ehost-live&scope=site.
Harrington, Ann. ‘A Beginning Understanding of Caregivers’ Spiritual Needs When Relinquishing a Loved One to a Palliative Care Setting’. Journal of Religion, Spirituality & Aging 24, no. 1–2 (January 2012): 131–45. https://doi.org/10.1080/15528030.2012.633055.
Harwood, Daniel. ‘Grief in Old Age’. Reviews in Clinical Gerontology 15, no. 3–4 (August 2005). https://doi.org/10.1017/S0959259806001912.
Hawken, Susan. ‘REBELS: An Approach to Communication Challenges in the Consultation’. The New Zealand Family Physician., 2008. https://web.archive.org/web/20130207141019/http://rnzcgp.org.nz/assets/documents/Publications/Archive-NZFP/Aug-2008-NZFP-Vol-35-No-4/HawkenAug08.pdf.
Hoffman, Robert D. ‘Buddha in Room Eight’. Patient Education and Counseling 88, no. 1 (July 2012): 2–3. https://doi.org/10.1016/j.pec.2011.12.013.
Hordern, Amanda Jane, and Annette F. Street. ‘Constructions of Sexuality and Intimacy after Cancer: Patient and Health Professional Perspectives’. Social Science & Medicine 64, no. 8 (April 2007): 1704–18. https://doi.org/10.1016/j.socscimed.2006.12.012.
Hudson, Peter., Hayman-White, Karla., Aranda,Sanchia., Kristjanson, Linda. ‘Predicting Family Caregiver Psychosocial Functioning in Palliative Care’. Journal of Palliative Care, no. 3 (n.d.): 133–40. http://search.proquest.com.ezproxy.auckland.ac.nz/docview/214199194.
Imam, Towhid. ‘The Conversation.’ Journal of Palliative Medicine 18, no. 2 (2015): 195–96. https://doi.org/10.1089/jpm.2014.0214.
J. Jacobs and J. Ostroff. ‘Family Therapy: A Systems Approach to Cancer Care’. In Psycho-Oncology. New York: Oxford University Press, 1998.
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Kirk, Peter clinical professor (family medicine and palliative care)1. ‘What Do Patients Receiving Palliative Care for Cancer and Their Families Want to Be Told? A Canadian and Australian Qualitative Study’. BMJ 328, no. 7452 (5AD): 1343–49. http://www.jstor.org.ezproxy.auckland.ac.nz/stable/41707902.
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Klass, Dennis, Phyllis R. Silverman, and Steven L. Nickman. Continuing Bonds: New Understandings of Grief. Vol. Series in death education, aging, and health care. Washington, DC: Taylor & Francis, 1996. https://ebookcentral.proquest.com/lib/auckland/reader.action?docID=1688972&ppg=26.
Krikorian, AliciaLimonero, Joaquin T. ‘An Integrated View of Suffering in Palliative Care’. Journal of Palliative Care, no. 1 (n.d.): 41–49. http://search.proquest.com.ezproxy.auckland.ac.nz/docview/1000455752?accountid=8424.
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Lemieux, Laurie1 llemieux@ucalgary.caKaiser, Stefanie2Pereira, Jose3Meadows, Lynn M.4. ‘Sexuality in Palliative Care: Patient Perspectives.’ Palliative Medicine 18, no. 7 (2004): 630–37. https://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=14797498&site=ehost-live&scope=site.
M. Buchholz, William. ‘Doctor Chaplain, Can You Help Me?’ Journal of Palliative Care & Medicine 04, no. 05 (2014). https://doi.org/10.4172/2165-7386.1000187.
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———. ‘Managing the Difficult Consultation’. Clinical Medicine 3, no. 6 (1 November 2003): 532–37. https://doi.org/10.7861/clinmedicine.3-6-532.
McCarthy, Danielle M., Katherine R. Waite, Laura M. Curtis, Kirsten G. Engel, David W. Baker, and Michael S. Wolf. ‘What Did the Doctor Say? Health Literacy and Recall of Medical Instructions’. Medical Care 50, no. 4 (April 2012): 277–82. https://doi.org/10.1097/MLR.0b013e318241e8e1.
McNamara, Beverley, and Lorna Rosenwax. ‘Which Carers of Family Members at the End of Life Need More Support from Health Services and Why?’ Social Science & Medicine 70, no. 7 (April 2010): 1035–41. https://doi.org/10.1016/j.socscimed.2009.11.029.
Miller, Linda. ‘Effective Communication with Older People’. Nursing Standard, no. 9 (n.d.): 45–50. http://search.proquest.com.ezproxy.auckland.ac.nz/docview/219811909?accountid=8424.
Mount, Balfour1 balfour.mount@mcgill.ca. ‘Healing and Palliative Care: Charting Our Way Forward.’ Palliative Medicine 17, no. 8 (2003): 657–58. http://ezproxy.auckland.ac.nz/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=11620175&site=ehost-live&scope=site.
Najjar, N., L. W. Davis, K. Beck-Coon, and C. Carney Doebbeling. ‘Compassion Fatigue: A Review of the Research to Date and Relevance to Cancer-Care Providers’. Journal of Health Psychology 14, no. 2 (1 March 2009): 267–77. https://doi.org/10.1177/1359105308100211.
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Parkes, Colin Murray. ‘Coping with Loss: Consequences and Implications for Care’. International Journal of Palliative Nursing 5, no. 5 (September 1999): 250–54. https://doi.org/10.12968/ijpn.1999.5.5.8966.
Parkes, Colin Murray, Pittu Laungani, and Bill Young. ‘Help for the Dying and the Bereaved’. In Death and Bereavement across Cultures. London: Routledge, 1997. https://site.ebrary.com/lib/auckland/reader.action?docID=10062974&ppg=215.
Pasman, H R W, M L Rurup, D L Willems, and B D Onwuteaka-Philipsen. ‘Concept of Unbearable Suffering in Context of Ungranted Requests for Euthanasia: Qualitative Interviews with Patients and Physicians’. BMJ 339, no. nov16 1 (16 November 2009): b4362–b4362. https://doi.org/10.1136/bmj.b4362.
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Puchalski, Christina. ‘Spiritual Issues in Palliative Care’. In Handbook of Psychiatry in Palliative Medicine, 2nd ed. Oxford: Oxford University Press, 2009.
Rice, Ann Marie. ‘Sexuality in Cancer and Palliative Care 2: Exploring the Issues’. International Journal of Palliative Nursing 6, no. 9 (October 2000): 448–53. https://doi.org/10.12968/ijpn.2000.6.9.9057.
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Showalter, S. E. ‘Compassion Fatigue: What Is It? Why Does It Matter? Recognizing the Symptoms, Acknowledging the Impact, Developing the Tools to Prevent Compassion Fatigue, and Strengthen the Professional Already Suffering From the Effects’. American Journal of Hospice and Palliative Medicine 27, no. 4 (1 June 2010): 239–42. https://doi.org/10.1177/1049909109354096.
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‘The Nature of Suffering and the Nature of Opportunity at the End-of-Life’. Clinics in Geriatric Medicine, n.d.
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Wynne, Lianne1 (NURSE) Lianne.Wynne@clatterbridgecc.nhs.uk. ‘Spiritual Care at the End of Life.’ Nursing Standard 28, no. 2 (2013): 41–45. http://ezproxy.auckland.ac.nz/login?url=http://search.ebscohost.com/login.aspx?direct=true&db=aph&AN=90326067&site=ehost-live&scope=site.
Yedidia, Michael J, and Betsy MacGregor. ‘Confronting the Prospect of Dying’. Journal of Pain and Symptom Management 22, no. 4 (October 2001): 807–19. https://doi.org/10.1016/S0885-3924(01)00325-6.
Zapka, Jane G. ScD. ‘End-of-Life Communication and Hospital Nurses: An Educational Pilot’. The Journal of Cardiovascular Nursing 21, no. 3 (n.d.): 223–31. http://ovidsp.ovid.com.ezproxy.auckland.ac.nz/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&AN=00005082-200605000-00011&LSLINK=80&D=ovft.
