1. Korea Centers for Disease Control and Prevention & Korean Federation for HIV/AIDS Prevention. National survey on HIV/AIDS knowledge, attitudes, beliefs, and behaviors in the general population, 2015. Seoul: Hanyang University Industry-University Cooperation Foundation;2015. 12. Report No: None.
3. Williams RJ, Stafford WB. Silent casualties: Partners, families, and spouses of persons with AIDS. J Couns Dev. 1991; 69(5):423–427. DOI:
10.1002/j.1556-6676.1991.tb01538.x.
4. Joo HJ. The experiences of the families of persons with AIDS. J Korean Acad Psychiatr Ment Health Nurs. 2009; 18(1):41–50.
5. Bogart LM, Cowgill BO, Kennedy D, Ryan G, Murphy DA, Elijah J, et al. HIV-related stigma among people with HIV and their families: A qualitative analysis. AIDS Behav. 2008; 12(2):244–254. DOI:
10.1007/s10461-007-9231-x.
6. Korea Center for Disease Control and Prevention. Annual report on the notified HIV/AIDS in Korea, 2016. Cheongju: Korea Center for Disease Control and Prevention;2017. 08. Report No.: 117085.
7. Rispel LC, Cloete A, Metcalf CA. ‘We keep her status to ourselves’: Experiences of stigma and discrimination among HIV-discordant couples in South Africa, Tanzania and Ukraine. SAHARA J. 2015; 12(1):10–17. DOI:
10.1080/17290376.2015.1014403.
8. Asiedu GB, Myers-Bowman KS. Gender differences in the experiences of HIV/AIDS-related stigma: A qualitative study in Ghana. Health Care Women Int. 2014; 35(7-9):703–727. DOI:
10.1080/07399332.2014.895367.
9. Kipp W, Tindyebwa D, Rubaale T, Karamagi E, Bajenja E. Family caregivers in rural Uganda: The hidden reality. Health Care Women Int. 2007; 28(10):856–871. DOI:
10.1080/07399330701615275.
10. Krishna VAS, Bhatti RS, Chandra PS, Juvva S. Unheard voices: Experiences of families living with HIV/AIDS in India. Contemp Fam Ther. 2005; 27(4):483–506. DOI:
10.1007/s10591-005-8235-9.
11. Nilmanat K, Street A. Search for a cure: Narratives of Thai family caregivers living with a person with AIDS. Soc Sci Med. 2004; 59(5):1003–1010. DOI:
10.1016/j.socscimed.2003.12.003.
12. D'cruz P. Moments of truth: The experiences of wives in HIV/AIDS affected nuclear households in Mumbai. J Comp Fam Stud. 2003; 34(2):255–281.
13. Yang Y, Lewis FM, Wojnar D. Life changes in women infected with HIV by their husbands: An interpretive phenomenological study. J Assoc Nurses AIDS Care. 2015; 26(5):580–594. DOI:
10.1016/j.jana.2015.05.008.
14. van Manen M. Researching lived experience: Human science for an action sensitive pedagogy. Albany (NY): State University of New York Press;1990. p. 1–173.
15. Lincoln YS, Guba EG. Naturalistic inquiry. Newbury park (CA): Sage;1985. p. 289–331.
16. Paik J. The changing nature in the Korean patriarchal family: Continuity and change. Hyonsang-gwa-Insik. 2009; 33(1-2):204–224.
17. Shin S. A study on health related quality of life in people living with HIV/AIDS in Korea. Health Soc Welf Rev. 2011; 31(4):424–453.
18. Lee IJ, Rhee YS. The moderating effects of social support on the relationship between stigma and quality of life in people living with HIV/AIDS. Korean J Soc Welf Stud. 2013; 44(3):347–369.
19. Korean Statistical Information Service. Survey on the price/household income and expenditure [Internet]. Daejeon: Statistics Korea;c2011. cited 2017 Nov 15. Available from:
http://bit.ly/2AItZE2.
20. Korea Center for Disease Control and Prevention. 2017 HIV/AIDS manage guideline. Cheongju: Korea Center for Disease Control and Prevention;2016. p. 61–64.
21. Kipp W, Matukala Nkosi T, Laing L, Jhangri GS. Care burden and self-reported health status of informal women caregivers of HIV/AIDS patients in Kinshasa, Democratic Republic of Congo. AIDS Care. 2006; 18(7):694–697. DOI:
10.1080/13548500500294401.
22. Wight RG, Beals KP, Miller-Martinez D, Murphy DA, Aneshensel CS. HIV-related traumatic stress symptoms in AIDS caregiving family dyads. AIDS Care. 2007; 19(7):901–909. DOI:
10.1080/09540120601163292.
23. Kim J, Shin G, Park YM, Lim EJ, Nam HA. Experience of people living with HIV working as caregivers for AIDS patients. J Korean Acad Psychiatr Ment Health Nurs. 2011; 20(4):334–344. DOI:
10.12934/jkpmhn.2011.20.4.334.
24. Gordon-Garofalo VL, Rubin A. Evaluation of a psychoeducational group for seronegative partners and spouses of persons with HIV/AIDS. Res Soc Work Pract. 2004; 14(1):14–26. DOI:
10.1177/1049731503257864.
25. Stewart MJ, Hart G, Mann K, Jackson S, Langille L, Reidy M. Telephone support group intervention for persons with hemophilia and HIV/AIDS and family caregivers. Int J Nurs Stud. 2001; 38(2):209–225. DOI:
10.1016/S0020-7489(00)00035-3.
26. Singh D, Chaudoir SR, Escobar MC, Kalichman S. Stigma, burden, social support, and willingness to care among caregivers of PLWHA in home-based care in South Africa. AIDS Care. 2011; 23(7):839–845. DOI:
10.1080/09540121.2010.542122.
27. Vithayachockitikhun N. Family caregiving of persons living with HIV/AIDS in Thailand: Caregiver burden, an outcome measure. Int J Nurs Pract. 2006; 12(3):123–128. DOI:
10.1111/j.1440-172X.2006.00560.x.
28. Ministry of Government Legislation. Act on decisions on life-sustaining treatment for patients in hospice and palliative care or at the end of life [Internet]. Sejong: The National Law Information Center;c2016. cited 2016 Dec 28. Available from:
http://bit.ly/21Q0cV5.
29. Kim DG. Pain and tragedy in Nietzsche's philosophy: From the viewpoint of cultural philosophy. Philos Investig. 2009; 26:139–116.