Geriatric Palliative Caregiving aAmong Caregivers in Metro Manila: Experiences and Assessment on of Health Identity and Life Satisfaction

Abbey, J., Palk, E., & Carlson, L., (2008). Clinical practice guidelines and care pathways for people with dementia living in the community. Retrieved from http://eprints.qut.edu. au/17393/1/17393.pdf.

Amano, K., Morita, T., & Tatara, R., (2015). Association between early palliative care referrals, inpatient hospice utilization, and aggressiveness of care at the end of life. Journal of Palliative Medicine, 18, 270–273.

Bolante, M. (2014). Master and servant: Contradictory roles of migrant Filipina domestic worker. Asia-Pacific Social Science Review 14(2), 162–167.

Brinkley, D. (1983). Emotional distress during cancer chemotherapy. British Medical Journal, 286, 663–664.

Brissette, L., Scheier, M., & Carver, C. (2002). The role of optimism in social network development, coping, and psychological adjustment during a life transition. Journal of Personality and Social Psychology, 82, 102–111.

Chandrana, D., Corbina, H., & Shillamb,. C., (2016). An Ecological Understanding of Caregiver Experiences in Palliative Care. Journal of Social Work Iin End-of-Life & Palliative Care, 12(1-2), 162–182.

Corless, I., & Pittman, M. (Eds.). (2006). Dying, death, and bereavement: A challenge for living (2nd ed.). New York, NY: Springer.

Coronel, R., Chua, K., Constantino, M., & Cordova, E. (2009). The Success and Struggles of Filipino Ggeriatric Nurses in Nursing Homes. Educational Gerontology, 35(4), 358-–377.

Coward, D. (1997). Constructing meaning from the experience of cancer. Seminars in Oncology Nursing, 13, 248-–251.

Dane, B., & Moore, R. (2006). Social Workers` Use of Spiritual Practices in Palliative Care. Journal of Social Work in End-of-Life & Palliative Care, 1(4), 63-–82.

Delgado, D. (2015). Discourse, Iidentity, and International Development Cooperation: China, Africa and FOCAC. Asia-Pacific Social Science Review, 15(2), 1-–18.

Durepos, P., Wickson-Griffiths, A., Hazzan, A., Kaasalainen, S., Vastis, V., Battistella, L., & Papaioannou, A. (2017). Assessing Palliative Care Content in Dementia Care Guidelines: A Systematic Review. Journal of Pain and Symptom Management, 54(4),. 804-–813.

Elmore, D. (2013). The Impact of Caregiving on Physical and Mental Health: Implications for Research, Practice, Education, and Policy. In A. Editor, B. Editor, & C. Editor (Eds.), The Challenges of Mental Health Caregiving: Subtitle, (pp. 15-–31). Place of publication: Publisher.

Fox, N., & Ward, K. (2008). What are health identities and how may we study them? Sociology of Health & Illness, 30(7), 1007-–1021.

Hickey, T. (1980). Health and Aging. Belmont, CA: Wadsworth.

Hill, P., & Pargament, K. (2003). Advances in the Conceptualization and Measurement of Religion and Spirituality: Implications for Physical and Mental Health Research.: American Psychologist, 58, 64-–74.

Helminiak, D. (1998). Sexuality and Spirituality: A Humanist Account. Pastoral Psychology, 47(2), 119-–126.

Kahn, W. (1993). Caring for the Caregivers: Patterns of Organizational Caregiving. Administrative Science Quarterly, 38(4), 539-–563.

Perakyla, A. (1991). Hope work in the care of seriously ill patients. Qualitative Health Research, 1(4), 407-–433.

Pines, A., & Maslach, C. (1978). Characteristics of staff burnout in mental health settings. Hospital and Community Psychiatry, 29, 233–237.

Sakakibara, K., Kabayama, M., & Ito, M. (2015). Experiences of “endless” caregiving of impaired elderly at home by family caregivers: a qualitative study. BMC Research Notes, x, 1-–11.

Lamberg, L. (2002). “Palliative Care” means “Active Care.”. Journal of American Medical Association, 288(2), 943-–944.

LeSeure, P., & Chongkham-ang, S. (2015). The Experience of Caregivers Living with Cancer Patients: A Systematic Review and Meta-Synthesis. Journal of Personal Medicine, 2015, 5, 406-–439.

Plante, T., & Sherman, A. (2001). Faith and Health: Psychological Perspectives. New York: The Guilford Press.

Reineck, M., & Furino, A. (2005). Nursing career fulfillment: sStatistics and statements from registered nurses. Nursing Economics, 23(1), 25-–30.

Rogers, N. (1999). Caring for those who care. Adaptation & Aging, 24(1), 1-–12.

Schulz, R., & Beach, S. (1999). Caregiving as a risk factor for mortality: the caregiver health effects study. Journal of American Medical Association, 282(23), 2215-–2219.

Schulz, R., Newsom, J., Mittelmark, M., Burton, L., Hirsch, C., & Jackson, S. (1997). Health effects of caregiving: tThe caregiver health effects study: aAn ancillary study of the Cardiovascular Health Study. Annual Behavioral Medicine, 19(2), 110-–116.

Schulz, R., O’Brien, A., Bookwala, J., & Fleissner, K. (1995). Psychiatric and physical morbidity effects of dementia caregiving: pPrevalence, correlates, and cause. Gerontologist, 35(6), 771-–791.

Shaw, W., Patterson, T., Semple, S., Ho, S., Irwin, M., & Haugler, R. (1997). Longitudinal analysis of multiple indicators of health decline among spousal caregivers. Annals of Behavioral Medicine, 19, 101-–109.

Straight, P., & Harvey, S. (1990). Caregiver burden: A comparison between elderly women as primary and secondary caregivers for their spouses. Journal of Gerontological Social Work, 15(1/2), 89-–101.

Van der Steen, J., Radbruch, L., & Hertogh, C. (2014). White paper defining optimal palliative care in older people with dementia: a Delphi study and recommendations from the European Association for Palliative Care. Palliative Medicine, 28, 197-–209.

Vitaliano, P., Zhang, J., & Scanlan, J. (2003). Is caregiving hazardous to one’s physical health? A meta-analysis. Psychological Bulletin, 129(6), 946-–972.