References

Ashcroft, R., & Van Katwyk, T. (2016). An examination of the biomedical paradigm: A view of social work. Social Work in Public Health, 31(3), 140-152.

Baumgarten, M., Battista, R. N., Infante-Rivard, C., Hanley, J. A., Becker, R., & Gauthier, S. (1992). The psychological and physical health of family members caring for an elderly person with dementia. Journal of clinical epidemiology, 45(1), 61-70.

Behuniak, S. M. (2011). The living dead? The construction of people with Alzheimer's disease as zombies. Ageing and Society, 31(1), 70-92. https://doi.org/10.1017/S0144686X10000693

Berger, P. L., & Luckman, T. (1976). The social construction of Reality. Penguin Books. 

Čapek, J. (2019). Personal identity and the otherness of one’s own body. Continental Philosophy Review, 52(3), 265–277.

Cohen, C., & Eisdorfer, D. (2001). The loss of self: A family resource for the care of alzheimer's disease and related disorders. W. W. Norton & Company.

Dekker, L. N. (2018). Moral frames for lives worth living: Managing the end of life with dementia. Death studies, 42(5), 322–328. https://doi.org/10.1080/07481187.2017.1396644

Ellis, C., Adams, T. E., & Bochner, A. P. (2011). Autoethnography: An Overview. Forum Qualitative Sozialforschung/Forum: Qualitative Social Research, 12(1), https://doi.org/10.17169/fqs-12.1.1589

Han, S., Chi, N.-C., Han, C., Oliver, D. P., Washington, K., & Demiris, G. (2019). Adapting the resilience framework for family caregivers of hospice patients with dementia. American Journal of Alzheimer's Disease & Other Dementias, 34(6), 399–411. https://doi.org/10.1177/1533317519862095 

Hernández‐Padilla, J. M., Ruiz‐Fernández, M. D., Granero‐Molina, J., Ortíz‐Amo, R., López Rodríguez, M. M., & Fernández‐Sola, C. (2020). Perceived health, caregiver overload and perceived social support in family caregivers of patients with alzheimer’s: Gender differences. Health & Social Care in the Community, 29(4), 1001–1009. https://doi.org/10.1111/hsc.13134 

Hughes, J. C., Louw, S. J., Sabat, S. R., &; Aqualina, C. (2006). The return of the living dead: agency lost and found. In Dementia: Mind, meaning, and the person, 143–161. Oxford University Press. 

Kitwood, T. (1997). The experience of dementia. Aging & Mental Health, 1(1), 13–22. https://doiorg.remote.slc.edu/10.1080/13607869757344

Kumar, G., & Delmundo, A. (2020, June 23). Losing yourself: Alzheimer's and Identity. Grey Matters. Retrieved April 23, 2023, from https://greymattersjournal.org/losing-yourself--alzheimers-and-identity/

Levine, C.  (2014). “Family-Caregiving”. In B. Jennings. (Ed.), Bioethics (pp. 1178-1185). Farmington Hills, MI: Gale. 

Mattingly, C., & Grøn, L. (2022). Imagistic care: Growing old in a precarious world. Fordham University Press. 

Montgomery, R. J. V., & Kosloski, K. K. (2009). Caregiving as a process of changing identity: implications for caregiver support. Generations, 33(1), 47–52.

National Institute on Aging. (2017, May 16). What happens to the brain in alzheimer's disease? National Institute on Aging. Retrieved April 7, 2023, from https://www.nia.nih.gov/health/what-happens-brain-alzheimers-disease 

National Institute on Aging. (2022, October 18). What are the signs of alzheimer's disease? National Institute on Aging. Retrieved April 7, 2023, from https://www.nia.nih.gov/health/what-are-signs-alzheimers-disease 

The Neighbors of Dunn County. (2021, July 20). Best Movies & TV shows for dementia patients: The neighbors. The Neighbors of Dunn County. Retrieved April 17, 2023, from https://neighborsdc.org/news/best-movies-tv-shows-dementia-patients/ 

NYU Libraries. (2023, April 10). Research guides: Primary sources: Objects and artifacts. Objects and Artifacts - Primary Sources - Research Guides at New York University. Retrieved April 14, 2023, from https://guides.nyu.edu/primary/primary-sources/objects-and-artifacts

Reed, P., Carson, J., & Gibb, Z. (2017). Transcending the tragedy discourse of dementia: An ethical imperative for promoting selfhood, meaningful relationships, and well-being. AMA Journal of Ethics, 19(7), 693–703. https://doi.org/10.1001/journalofethics.2017.19.7.msoc1-1707 

Sabat, S. R. (2003). Malignant Positioning and the Predicament of People with Alzheimer's Disease. In R. Harré & F. Moghaddam (Eds.), The self and others: Positioning individuals and groups in personal, political, and cultural contexts (pp. 85–98). Praeger Publishers/Greenwood Publishing Group

Schmid, J. (2022, December 16). Entertainment for alzheimer's - A great way to relax. Best Alzheimer's Products. Retrieved April 18, 2023, from https://best-alzheimers-products.com/activities-for-alzheimers/entertainment-for-alzheimers 

Schweda, M., & Jongsma, K. (2022). Death in advance? A critique of the "zombification" of people with dementia. History and philosophy of the life sciences, 44(3), 37. https://doi.org/10.1007/s40656-022-00512-z

Seaman, A. T. (2018). The consequence of “doing nothing”: Family caregiving for Alzheimer's disease as non-action in the US. Social Science & Medicine, 197,  63- 70. https://doi.org/10.1016/j.socscimed.2017.12.001

Taylor, J. S. (2008). On recognition, caring, and dementia. Medical Anthropology Quarterly, 22(4), 313–335.

The Village. (2022, October 11). TV shows and movies for people with dementia: VGF. The Village at Gleannloch Farms. Retrieved April 17, 2023, from https://villageatgleannloch.com/blog/best-movies-and-tv-for-people-with-dementia/ 

de Vugt, M. E., Nicolson, N. A., Aalten, P., Lousberg, R., Jolle, J., & Verhey, F. R. (2005). Behavioral problems in dementia patients and salivary cortisol patterns in caregivers. The Journal of neuropsychiatry and clinical neurosciences, 17(2), 201–207. https://doi.org/10.1176/jnp.17.2.201

Wendell, S. (1989). Toward a feminist theory of disability. Hypatia, 4(2), 104–24.

Yang, H. D., Kim, D. H., Lee, S. B., & Young, L. D. (2016). History of Alzheimer's Disease. Dementia and Neurocognitive Disorders, 15(4), 115-121. https://doi.org/10.12779/dnd.2016.15.4.115