참고문헌
- Lou Gehing's Disease Association: http://www.kalsa.org. 2015.4.20
- H. S. An, Situation and issues surrounding the will transfer of Korea ALS patients, Core Ethics, 8, pp.13-26. 2013
- J. H Park, & U. H. Sun, Study of interaction changes through family playing therapy among family members with chronically ill patient: focusing on family of Lou Gehrig's disease patient. Korea Christian Counseling Psychotherapy Association. 23(3). pp.117-152. 2012
- H. K. Chong S. M. Heo, A Comparative Study on the ALS Support [31] System between Korean and Japan. Korean Council of Physical, Multiple & Health Disabilities, Vol. 58, No. 2, 4. pp.229-252. 2015
- G. H. Park, Preliminary study on clinical characteristics and caregivers' burden of Korean patients with amyotrophic lateral sclerosis : survey based on database of Korea ALS association: Master's Thesis. Hanyang University, 2005
- Ingrid, B., & Goran, H, Interview with patient, family, and caregiverw in amyotrophic lateral sclerosis: comparing needs. Journal pf Palliative Care, 2001
- H. S. Heo, Related quality of life studies amyotrophic lateral sclerosis. Master's Thesis. Seoulng University, 2013
- J. Y. Oh, Socioeconomic costs of amyotrophic lateral sclerosis according to staging system. Master's Thesis, Hanyang University, 2014
- Department of Health and Human Services. Rare incurable diseases medical support business information. department of Health and Human Services, 2015
- M. Y. Lee, M. H. Yun, Analysis of elements affecting the socio-psychological wellbeing of people with the rare and intractable disorder. Korea Academy of Disability and Welfare. Vol. 12. No, 2010
- G. S. Ko, Stress of patients and family care-giver's burden with rare and incurable diseases in a city. Master's Thesis Chonnam National University, 2006
- Cassileth & Hamilton. The family with Cancer, In B Cassileth, The cancer patient, Philadelphia : Lea & Febiger, 19(4). 236-340. p.179
- J. Son. A Study on the Effects of Home-Staying Patients' Guardians' Experiences of the Social Support System on Their Stress Level- Focused on the Guardians of the Patients relying on the Breathing Machine -Master's Thesis, HanYang University, 2008
- Zarit, S. H., Green, R., Ferraro, E., Townsend, A., & Stephens, M. A. P. Adult day care and the relif of caregiver strain: Results of the adult day care.collaborative study. Symposium presented at the annual meetings of the Gerontological Society of America, Washington, D. C. 1996
- S. H. Beak. (A) study on the burden of family caregivers of amyotrophic lateral sclerosis patients. Master's Thesis, School of Public Health. Yonsei University, 2005
- K. J. Cho, H. J. Jung. Burden and Quality of Life in Caregivers of Patients with Rare and Incurable Disease. Korean Academy Of Coummunity Health Neolsing, 17(3). 2006
- DOL: http;//ableservice.or.kr. 2015.06.20
- Ablenews. (June 5, 2015 article). Those with severe disabilities being selected to work assistants
- U. J. Kang. The Effects on Care-Giving Burden By the visually impaired and the main Care-Givers : The Moderating Effects on Personal Assistance Service. Master's Thesis Kyonggi University, 2009
- J. S Choi, L. S. Lee, J. H. Kim. The Factors Influencing Child-Rearing Burden Recognized By Parents of Children With Developmental Disability Who Use Personal Assistance Service. Journal of community welfare, 32. pp. 31-60. 2010
- J. O. Sin. An Effect of Personal Assistance Services for the Disabled Persons upon the Burdens of Raising a Family -Focusing on Family Resilience Control Effect. Journal of Rehabilitation Research, 18(4). pp. 95-117. 2014 https://doi.org/10.16884/JRR.2014.18.3.95
- M. Konagaya, The Subjective Care Burden of Family Caregivers for Amyotrophic Lateral Sclerosis(ALS) Patients at Home - The Characteristice and Rclatde Factors of Subjective Care Burden. Joumal of Japan Academy of Home Health Care, 5(1), pp.34-41, 2001
- K. T. Isikawa. Role acquisition of family in ALS care - Focusing on active of in nursing practice -. Sosihiorogose, No. 37. 2013
피인용 문헌
- Convergence Study on Burden in Families Caregivers of Patients with Burn vol.7, pp.6, 2016, https://doi.org/10.15207/JKCS.2016.7.6.275