Abstract
This chapter explores end-of-life and existential considerations about illness, injury, or death and provides “helpful hints” and coping tools for the family system. It is divided into several subsections. First, using brain tumors as a prototype, the relatives’ practical and emotional preparation for the loved one’s impending death is delved into. Specific topics include advance directives, hospice care, anticipatory grief, denial, emotional preparedness, and presencing. Positive aspects of caregiving are appraised. Following this, grief reactions and coping techniques after the death of the loved one are examined in family members, including children. The mourning (or emotional reconstitution) and adjustment process after the death of a loved one is then discussed. The concept of “complicated grief” is touched upon. Fundamental existential constructs for caregivers and the family are derived from positive psychology and existential psychology and include: restructuring the assumptive world and lifestyles; integrating ambiguous loss and chronic sorrow; posttraumatic growth; new meaning in life; spirituality; hope; resiliency; learned optimism; as well as personal and family morale. A case study illustrates the therapeutic process and principles. The chapter also incorporates a number of multimedia resources to exemplify the constructs, including websites, songs, books, stories, plays, poetry, broadcasts, and films.
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References
Acorn, S. (1998). The family as caregiver. In S. Acorn & P. Offer (Eds.), Living with brain injury: A guide for families and caregivers (pp. 155–162). Toronto: University of Toronto Press.
Adelbratt, S., & Strang, P. (2000). Death anxiety in brain tumour patients and their spouses. Palliative Medicine, 14(6), 499–507.
Aldrich, J. J., & Peterson, N. M. (2010). Connecting through compassion: Guidance for family and friends of a brain cancer patient. United States of America: Cancer Lifeline Publications.
American Psychological Association. (2012). End-of-life issues and care. http://www.apa.org/topics/death/end-of-life.aspx. Accessed 13 July 2012.
Attig, T. (2002). Questionable assumptions about assumptive worlds. In J. Kauffman (Ed.), Loss of the assumptive world: A theory of traumatic loss (pp. 55–68). New York: Brunner-Routledge.
Ayalong, L. (2004). Cultural variants of caregiving or the culture of caregiving. Journal of Cultural Diversity, 11(4), 131–138.
Bainbridge, D., Krueger, P., Lohfeld, L., & Brazil, K. (2009). Stress processes in caring for an end-of-life family member: Application of a theoretical model. Aging & Mental Health, 13(4), 537–545.
Barry, L. C., & Prigerson, H. G. (2002). Perspectives on preparedness for a death among bereaved persons. Connecticut Medicine, 66(11), 691–696.
Benkel, L., Wijk, H., & Molander, U. (2010). Using coping strategies is not denial: Helping loved ones adjust to living with a patient with a palliative diagnosis. Journal of Palliative Medicine, 13(9), 1119–1123.
Berry, B., Buck, P., Mills, M., & Stipe, M. (1992). Sweetness follows [Recorded by R.E.M.]. On Automatic for the people [CD]. New York: Warner Bros./WEA.
Black, P., & Hogan, S. C. (2006). Living with a brain tumor: Dr. Peter Black’s guide to taking control of your treatment. New York: Henry Holt and Company.
Blomquist, A. C., Hallström, L., Matalon, D., Ohlsson, B., Teper, M. (Producers), & Hallström, L. (Director). (1993). What’s eating Gilbert Grape [Motion picture]. United States: Paramount Pictures.
Boss, P. (2006). Loss, trauma, and resilience: Therapeutic work with ambiguous loss. New York: W. W. Norton.
Boss, P., Roos, S., & Harris, D. L. (2011). Grief in the midst of ambiguity and uncertainty: An exploration of ambiguous loss and chronic sorrow. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 163–175). New York: Routledge.
Bowen, C., Yeates, G., & Plamer, S. (2010). A relational approach to rehabilitation: Thinking about relationships after brain injury. London: Karnac Books.
Boyd, T., Burke, J., Parra, G., Payne, A., Taylor, J. (Producers), & Payne, A. (Director). (2011). The descendants [Motion picture]. United States: Fox Searchlight Pictures.
Bradley, S., Sherwood, P. R., Donovan, H. S., Hamilton, R., Rosenzweig, M., Hricik, A., et al. (2007). I could lose everything: Understanding the cost of a brain tumor. Journal of Neuro-Oncology, 85(3), 329–338.
Brody, T. S., De Niro, R., Gering, C., Guare, J., Palef, B., Rosenthal, J., Rudin, S., et al. (Producers), & Zaks, J. (Director). (1996). Marvin’s room [Motion picture]. United States: Miramax Films.
Buchholz, W. M. (1990). A piece of my mind: Hope. JAMA: The Journal of the American Medical Association, 263(17), 2357–2358.
Calhoun, L. G., & Tedeschi, R. G. (2013). Posttraumatic growth in clinical practice. New York: Routledge.
Callanan, M., & Kelley, P. (1997). Final gifts: Understanding the special awareness, needs, and communications of the dying. New York: Bantam Books.
Carestio, M. A. (2010). Black Jack Jetty: A boy’s journey through grief. Washington, D. C.: Magination Press.
Clarke, D. M., & Kissane, D. W. (2002). Demoralization: Its phenomenology and importance. Australian & New Zealand Journal of Psychiatry, 36(6), 733–742.
Collins, L. G., & Swartz, K. (2011). Caregiver care. American Academy of Family Physicians, 83(11), 1309–1317.
Connor, S. R., Lycan, J., & Schumacher, J. D. (2006). Involvement of psychologists in psychosocial aspects of hospice and end-of-life care. In J. L.Werth Jr & D. Blevins (Eds.), Psychosocial issues near the end of life: A resource for professional care providers (pp. 203–217). Washington, D. C.: American Psychological Association.
Deason, P., Gordon, M., Harlacker, J., Herzberg, I., Panek, M., Porter, A. L., Yorn, J. (Producers), & Crowe, C. (Director). (2011). We bought a zoo [Motion picture]. United States: Twentieth Century Fox Film Corporation.
de Pentheny O’Kelly, C., Urch, C., & Brown, E. A. (2011). The impact of culture and religion on truth telling at the end of life. Nephrology, Dialysis, Transplantation, 26(12), 3838–3842.
Empeño, J., Raming, N. T. J., Irwin, S. A., Nelesen, R. A., & Lloyd, L. S. (2011). The hospice caregiver support project: Providing support to reduce caregiver stress. Journal of Palliative Medicine, 14(5), 593–597.
Engel, G. L. (1968). A life setting conducive to illness. Annals of Internal Medicine, 69(2), 293–300.
Evans, R. P. (1999). The dance. New York: Simon & Schuster Books for Young Readers.
Finerman, W., Flynn, J., Hollond, J., Huntsinger, J., Johnson, B., Kosove, A. A., O’Sullivan, M., et al., (Producers), & LaGravenese, R. (Director). (2007). P. S. I love you [Motion picture]. United States: Warner Bros. Pictures.
Finocchiaro, C. Y., Petruzzi, A., Lamperti, E., Botturi, A., Gaviani, P., Silvani, A., et al. (2011). The burden of brain tumor: A single-institution study on psychological patterns in caregivers. Journal of Neuro-Oncology, Oct. 4. [Epub ahead of print]. doi:10.1007/s11060-011-0726-y.
Gilbert, K. R., & Horsley, G. C. (2011). Technology and grief support in the twenty-first century: A multimedia platform. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 365–373). New York: Routledge.
Goldberg, B. (Reporter/Host). (2012, July 17). Separated [Television broadcast]. In Perskie, J. (Producer), Real sports with Bryant Gumbel. New York: Home Box Office.
Goodman, S., Rabow, M., & Folkman, S. (2007). Orientation to caregiving: A handbook for family caregivers of patients with brain tumors. San Francisco: University of California San Francisco.
Grant, T., Gray, N. J., Sullivan, K. (Producers), & Scaini, S. (Director). (1996). Under the piano [Motion picture]. Canada: Sullivan Entertainment.
Gray, M. (2006). For those I loved: 35th anniversary expanded edition. Charlottesville: Hampton Roads Publishing Company.
Hanson, W. (1997). The next place. Golden Valley: Waldman House Press.
Harvard Health Publications. (2011). Positive psychology: Harnessing the power of happiness, mindfulness, and personal strength. Boston: Harvard Health Publications.
Hassan, S. T., Khaw, W. F., Rosna, A. R., & Husna, J. (2011). Traumatic brain injury: Caregivers’ problems and needs. Journal of Nepal Medical Association, 51(181), 53–55.
Hebert, R. S., Prigerson, H. G., Schulz, R., & Arnold, R. M. (2006). Preparing caregivers for the death of a loved one: A theoretical framework and suggestions for future research. Journal of Palliative Medicine, 9(5), 1164–1171.
Hebert, R. S., Copeland, V. C., Schulz, R., & Amato, C. A. (2008a). Preparing family caregivers for the death of a loved one: Implications for hospital social workers. Journal of Social Work in End-of-Life & Palliative Care, 4(4), 269–285.
Hebert, R. S., Schulz, R., Copeland, V., & Arnold, R. M. (2008b). What questions do family caregivers want to discuss with health care providers in order to prepare for the death of a loved one? An ethnographic study of caregivers of patients at end of life. Journal of Palliative Medicine, 11(3), 476–483.
Hebert, R. S., Schulz, R., Copeland, V. C., & Arnold, R. M. (2009). Preparing family caregivers for death and bereavement. Insights from caregivers of terminally ill patients. Journal of Pain and Symptom Management, 37(1), 3–12.
Hemingway, E. (2012). A farewell to arms: The Hemingway library edition. New York: Scribner.
Jacobson, S. (2004). Toward a meaningful life: The wisdom of the Rebbe Menachem Schneerson (new ed.). New York: HarperCollins Publishers.
James, J. W., & Friedman, R. (2009). The grief recovery handbook: The action program for moving beyond death, divorce, and other losses, including health, career, and faith (20th anniversary expanded ed.). New York: HarperCollins Publishers.
Janoff-Bulman, R. (2002). Foreword. In J. Kauffman (Ed.), Loss of the assumptive world: A theory of traumatic loss (pp. xi–xii). New York: Brunner-Routledge.
Jollett, M. (2013). Timeless [Recorded by The Airborne Toxic Event]. On The secret [CD]. Santa Monica: Island Records.
Joseph, S. (2011). What doesn’t kill us: The new psychology of posttraumatic growth. New York: Basic Books.
Judd, T., & DeBoard, R. (2009). Community-based neuropsychological rehabilitation in the cosmopolitan setting. Neuropsychological Rehabilitation, 19(6), 841–866.
Kaplow, J., & Pincus, D. (2007). Samantha Jane’s missing smile: A story about coping with the loss of a parent. Washington, D. C.: Magination Press.
Karst, P. (2000). The invisible string. Camarillo: DeVorss & Company.
Khalili, Y. (2007). Ongoing transitions: The impact of a malignant brain tumour on patient and family. Axone (Dartmouth, N. S.), 28(3), 5–13.
Kipner, S., Frampton, A., O’Donoghue, D. J., & Sheehan, M. A. (2012). If you could see me now [Recorded by The Script]. On #3 [CD]. US: Epic.
Kissane, D. W., & Hooghe, A. (2011). Family therapy for the bereaved. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 287–302). New York: Routledge.
Kitamura, C., Ng, D., Chung, A., Bezjak, A., Garraway, C., Mclean, M., Nyhof-Young, J., & Wong, R. (2011). Development and evaluation of a combined story and fact-based educational booklet for patients with multiple brain metastases and their caregivers. Palliative Medicine, 25(6), 642–649.
Klass, D., & Chow, A. Y. M. (2011). Culture and ethnicity in experiencing, policing, and handling grief. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 341–353). New York: Routledge.
Klonoff, P. S. (2010). Psychotherapy after brain injury: Principles and techniques. New York: Guilford Press.
Klonoff, P. S. (2011). A therapist experiential model of treatment for brain injury. Bulletin of the Menninger Clinic, 75(1), 21–45.
Klonoff, P. S., & Myles, S. M. (2010). Sense of self and identity. In P. S. Klonoff (Ed.), Psychotherapy after brain injury: Principles and techniques (pp. 75–99). New York: Guilford Press.
Klonoff, P. S., Koberstein, E. J., Talley, M. C., & Dawson, L. K. (2008). A family experiential model of recovery after brain injury. Bulletin of the Menninger Clinic, 72(2), 109–129.
Klonoff, P. S., & Koberstein, E. J. (2010). Family life. In P. S. Klonoff (Ed.), Psychotherapy after brain injury: Principles and techniques (pp. 150–170). New York: Guilford Press.
Kobau, R., Seligman, M. E. P., Peterson, C., Diener, E., Zack, M. M., Chapman, D., & Thompson, W. (2011). Mental health promotion in public health: Perspectives and strategies from positive psychology. American Journal of Public Health, 101(8), e1–e9.
Kreling, B., Selsky, C., Perret-Gentil, M., Huerta, E. E., & Mandelblatt, J. S. (2010). ‘The worst thing about hospice is that they talk about death’: Contrasting hospice decisions and experience among immigrant Central and South American Latinos with US-born White, non-Latino cancer caregivers. Palliative Medicine, 24(4), 427–434.
Kreutzer, J. S., Marwitz, J. H., Godwin, E. E., & Arango-Lasprilla, J. C. (2010). Practical approaches to effective family intervention after brain injury. Journal of Head Trauma Rehabilitation, 25(2), 113–120.
Kushner, H. (1981). When bad things happen to good people. New York: Avon Books.
Kutner, J. S., & Kilbourn, K. M. (2009). Bereavement: Addressing challenges faced by advanced cancer patients, their caregivers, and their physicians. Primary Care, 36(4), 825–844.
Landsman, I. S. (2002). Crises of meaning in trauma and loss. In J. Kauffman (Ed.), Loss of the assumptive world: A theory of traumatic loss (pp. 13–30). New York: Brunner-Routledge.
Laufer, J. E. (2012). Where did papa go? Phoenix: Little Egg Publishing Company.
Lewis, L., & Hoy, W. G. (2011). Bereavement rituals and the creation of legacy. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 315–323). New York: Routledge.
Lezak, M. D. (1986). Psychological implications of traumatic brain damage for the patient’s family. Rehabilitation Psychology, 31(4), 241–250.
Lindsay-Abaire, D. (2006). Rabbit hole. New York: Theatre Communications Group.
Linge, F. R. (1990). Faith, hope, and love: Nontraditional therapy in recovery from serious head injury, a personal account. Canadian Journal of Psychology, 44(2), 116–129.
Lowry, H., McDermott, K. J., Netter, G., Rubin, B. J., Zucker, J. (Producers), & Rubin, B. J. (Director). (1993). My life [Motion picture]. United States: Columbia Pictures.
Lubavitcher, R. (2012). Daily Quote. In Chabad.org TODAY IN JUDAISM: Thursday. http://www.chabad.org/. Accessed 11 Oct 2012.
McColl, M. A., Bickenbach, J., Johnston, J., Nishihama, S., Schumaker, M., Smith, K., Smith, M., et al. (2000). Spirtiual issues associated with traumatic-onset disability. Disability and Rehabilitation, 22(12), 555–564.
McGoldrick, M. (1991). Echoes from the past: Helping families mourn their losses. In F. Walsh & M. McGoldrick (Eds.), Living beyond loss: Death in the family (pp. 50–78). New York: W. W. Norton.
Moore, C. D. (2005). Communication issues and advances care planning. Seminars in Oncology Nursing, 21(1), 11–19.
Moore, T., & Wagner, S. (2009). Caregiver and family issues for brain tumor survivors. In S. Goldman & C. D. Turner (Eds.), Late effects of treatment for brain tumors (pp. 331–339). New York: Springer.
Napoli, M. (2011). React or respond: A guide to apply mindfulness for families and therapists. Families in Society: The Journal of Contemporary Social Services, 92(1), 28–32.
Neimeyer, R. A., Harris, D. L., Winokuer, H. R., & Thornton, G. F. (Eds.). (2011). Grief and bereavement in contemporary society: Bridging research and practice. New York: Routledge.
Neimeyer, R. A., & Sands, D. (2011). Meaning reconstruction in bereavement: From principles to practice. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 9–22). New York: Routledge.
New York University Child Study Center. (2006). Caring for kids after trauma, disaster and death: A guide for patents and professionals (2nd ed.). New York: New York Child Study Center.
Nichols, T., & Wiseman, C. M. (2004). Live like you were dying [Recorded by Tim McGraw]. On Live like you were dying [CD]. Nashville: Curb Records.
Nixon, A., & Narayanasamy, A. (2010). The spiritual needs of neuro-oncology patients from patients’ perspective. Journal of Clinical Nursing, 19(15–16), 2259–2270.
Norton, S. A., & Bowers, B. J. (2001). Working toward consensus: Providers’ strategies to shift patients from curative to palliative treatment choices. Research in Nursing & Health, 24(4), 258–269.
Olsson, L., Östlund, G., Grassman, E. J., Friedrichsen, M., & Strang, P. (2010). Maintaining hope when close to death: Insight from cancer patients in palliative home care. International Journal of Palliative Nursing, 16(12), 607–612.
Palmieri, R. L. (2007). Responding to primary brain tumor. Nursing, 37(1), 36–42.
Park, C. L., & Halifax, R. J. (2011). Religion and spirituality in adjusting to bereavement: Grief as burden, grief as gift. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 355–363). New York: Routledge.
Pellegrino, M. W. (1999). I don’t have an uncle Phil anymore. Washington, D. C.: Magination Press.
Perakis, C. R. (2010). Soul sickness: A frequently missed diagnosis. Journal of the American Osteopathic Association, 110(6), 347–349.
Peterson, C. (2009). Positive psychology. Reclaiming children and youth, 18(2), 3–7.
Peterson, C., Park, N., Pole, N., D’Andrea, W., & Seligman, M. E. (2008a). Strengths of character and posttraumatic growth. Journal of Traumatic Stress, 21(2), 214–217.
Peterson, C., Park, N., & Sweeney, P. J. (2008b). Group well-being: Morale from a positive psychology perspective. Applied Psychology: An International Review, 57, 19–36.
Planalp, S., & Trost, M. R. (2008). Communication issues at the end of life: Reports from hospice volunteers. Health Communication, 23(3), 222–233.
Power, P. W., & Dell Orto, A. E. (2004). Families living with chronic illness and disability: Interventions, challenges, and opportunities. New York: Springer.
Richman, J. (1995). From despair to integrity: An Eriksonian approach to psychotherapy for the terminally ill. Psychotherapy: Theory, Research, Practice, Training, 32(2), 317–322.
Roos, S. (2002). Chronic sorrow: A living loss. New York: Brunner-Routledge.
Sand, L., Olsson, M., & Strang, P. (2010). What are motives of family members who take responsibility in palliative cancer care? Mortality, 15(1), 64–80.
Sanderson, C. (2010). Mindfulness for clients, their friends, and family members. http://ebookbrowse.com/mindfulness-for-clients-and-family-members-pdf-d28312970. Accessed 19 Aug 2012.
Schmer, C., Ward-Smith, P., Latham, S., & Salacz, M. (2008). When a family member has a malignant brain tumor: The caregiver perspective. Journal of Neuroscience Nursing, 40(2), 78–84.
Schubart, J. R., Kinzie, M. B., & Farace, E. (2008). Caring for the brain tumor patient: Family caregiver burden and unmet needs. Neuro-Oncology, 10(1), 61–72.
Seligman, M. E. P. (2006). Learned optimism: How to change your mind and your life. New York: Vintage.
Seligman, M. E. P. (2011). Flourish: A visionary new understanding of happiness and well-being. New York: Atria.
Seligman, M. E. P., & Peterson, C. (2003). Positive clinical psychology. In L. G. Aspinwall & U. M. Staudinger, (Eds.), A psychology of human strengths: Fundamental questions and future directions for a positive psychology (pp. 305–317). Washington, D. C.: American Psychological Association.
Shadyac, T., Reid, F., Shimizu, E. H., Belic, R. (Producers), & Belic, R. (Director). (2011). Happy [Motion picture]. United States: Wadi Rum Productions.
Shear, M. K., Boelen, P. A., & Neimeyer, R. A. (2011). Treating complicated grief converging approaches. In R. A. Neimeyer, D. L. Harris, H. R. Winokuer, & G. F. Thornton (Eds.), Grief and bereavement in contemporary society: Bridging research and practice (pp. 139–162). New York: Routledge.
Sherwood, P. R., Given, B. A., Doorenbos, A. Z., & Given, C. W. (2004a). Forgotten voices: Lessons from bereaved caregivers of persons with a brain tumour. International Journal of Palliative Nursing, 10(2), 67–75.
Sherwood, P., Given, B., Given, C., Schiffman, R., Murman, D., & Lovely, M. (2004b). Caregivers of persons with a brain tumor: A conceptual model. Nursing Inquiry, 11(1), 43–53.
Sherwood, P. R., Given, B. A., Donovan, H., Baum, A., Given, C. W., Bender, C. M., & Schulz, R. (2008). Guiding research in family care: A new approach to oncology caregiving. Psycho-Oncology, 17(10), 986–996.
Smith, H. I. (2002). Finding your way to say goodbye: Comfort for the dying and those who care for them. Notre Dame: Ave Maria Press.
Smith, H. I. (2007). A B C’s of healthy grieving: A companion for everyday coping. Notre Dame: Ave Maria Press.
Smith, H. I. (2011). A decembered grief: Living with loss while others are celebrating. Kansas City: Beacon Hill Press.
Strang, S., & Strang, P. (2001). Spiritual thoughts, coping and ‘sense of coherence’ in brain tumour patients and their spouses. Palliative Medicine, 15(2), 127–134.
Strang, S., Strang, P., & Ternestedt, B. M. (2001). Existential support in brain tumour patients and their spouses. Supportive Care in Cancer: Official Journal of the Multinational Association of Supportive Care in Cancer, 9(8), 625–633.
Stark-Vance, V., & Dubay, M. L. (2011). 100 Questions & answers about brain tumors (2nd ed.). Boston: Jones and Bartlett Publishers.
Stroebe, M., Schut, H., & van den Bout, J. (Eds.). (2012). Complicated grief: Scientific foundations for health care professionals. New York: Routledge.
Tepper, S. (2003). A model for care: A transitions program designed to provide comprehensive care in treating individuals with malignant brain tumors. Smith College Studies in Social Work, 73(3), 337–357.
Triplett, K. N., Tedeschi, R. G., Cann, A., Calhoun, L. G., & Reeve, C. L. (2011). Posttraumatic growth, meaning in life, and life satisfaction in response to trauma. Psychological Trauma: Theory, Research, Practice, and Policy. Advance online publication. doi:10.1037/a0024204.
Vaillant, G. E. (2008). Positive emotions, spirituality and the practice of psychiatry. Medicine, Mental Health, Science, Religion, and Well-being, MSM, 6, 48–62.
Vedder, E. (1998). Wishlist [Recorded by Pearl Jam]. On Yield [CD]. US: Sony Records.
Wasserman, L. S. (2008). Respectful death: A model for end-of-life care. Clinical Journal of Oncology Nursing, 12(4), 621–626.
Weiner, J. S., & Roth, J. (2006). Avoiding iatrogenic harm to patient and family while discussing goals of care near the end of life. Journal of Palliative Medicine, 9(2), 451–463.
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(13), 1105–1115.
Williams, B. Y. (2004). The friend who just stands by. In J. Cotner (Ed.), Looking for God in all the right places: Prayers and poems to comfort, inspire, and connect humanity (p. 125). Chicago: Loyola Press.
Wong, P. T. P., & Tomer, A. (2011). Beyond terror and denial: The positive psychology of death acceptance. Death Studies, 35(2), 99–106.
Worden, J. W. (2009). Grief counselling and grief therapy: A handbook for the mental health practitioner. New York: Springer.
Yalom, I. D. (2009). Staring at the sun: Overcoming the terror of death. San Francisco: Jossey-Bass.
Yolen, J. (1997). Birthday box. In J. Hurwitz (Ed.), Birthday surprises: Ten great stories to unwrap (pp. 27–33). New York: Beech Tree.
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Klonoff, P. (2014). Loved Ones’ End-of-Life and Existential Considerations as a Caregiver. In: Psychotherapy for Families after Brain Injury. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-8083-0_10
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