• 제목/요약/키워드: Experiences of Illness

검색결과 124건 처리시간 0.028초

치매주간호자의 치매관리전략 영향요인과 부양부담 관계 연구 (A Study on Factors Influencing Dementia Management Strategies and Their relationships with Primary Caregivers' Burden)

  • 이현순;오진주
    • 지역사회간호학회지
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    • 제13권4호
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    • pp.629-638
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    • 2002
  • The impact of chronic diseases on patients and their families depends on how well the family members cope with it. Therefore, research on strategies for facilitating the coping of the families in a desirable manner is very important. Dementia management strategies refer to specific means families of dementia patients use to cope with dementing illness of their family members. This study was designed to examine type of dementia management strategies utilized by families and to identify factors influencing them. The subjects in this study were 103 conveniently selected demented patients and their primary caregivers who were registered to a public health center located in Chungcheong Province. The subjects were visited by 20 home visiting nurses, and the data were collected using a structured questionnaire. The data were collected form May 2, 2001 to June 2, 2001. The findings of this study were as follows. 1. The most frequently used types of dementia management strategies were active management (M=3.36, S.D=.96), and encouragement (M=2.94, S.D=.99). Criticism was least used type of dementia management strategy (M=2.71, S.D=.99). 2. The factors influencing each management strategy were as follows; 1) The criticism management strategy was most frequently used by the primary caregivers who graduated elementary school (F=3.21, p<.05). 2) The encouragement strategy was most frequently used by the primary caregivers in a case when the patients were in the mild stage of dementia (F=2.76, p<.05), when the patients never had any treatment experiences (F=2.01, p<.05), when the family could afford the provision of treatment for the patients (F=-2.44, p<.050), and when the primary caregiver had a job (t=2.90, p<.01). 3) The active management strategy was most widely used by the primary caregivers who could afford the provision of treatment for the patients (F=-2.31, p<.05) and were in their 70s (F=3.04, p<.05). This type of management strategy was significantly more used by those who discussed the difficulties of caring with their family members (F=3.46, p<.05). 3. The use of criticism management strategies was significantly correlated with the total level of burden of the primary caregivers. But the types of encouragement and active management strategies had negative correlations with the caregivers' burden although they were not significant. Since the findings of this study showed that the criticism management strategy had a significant positive relationship with caregivers' burden, those who are more likely to use the negative management strategy should be identified in future studies. The primary caregivers who are more likely to use negative strategy should be more closely monitored and be focused as the group who should be intervened in future studies.

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천담유창여장석순적 「대기」론 (A Study in the Daqi- Theories by Yu Chang and Zhang Xi Chun)

  • 금지수;금경수;정숙이
    • 동의생리병리학회지
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    • 제18권5호
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    • pp.1232-1236
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    • 2004
  • In the Far-Eastern traditional medicine, Oi[Energy] implies a wide range of meaning and is emphasized. There is nothing that is not related to this Qi, as seen in physiology, pathology, the relationship between human body and nature, the movements of intestines and gyeongnak[energy networks], the process of outbreak and change of illness, remedial laws, the features and effects of drugs, and so on. Accordingly, Nei Jing also says, 'every sickness arises from OL' The Qi has multi-meanings, and each of lots Of past physicians researched and analyzed it in different perspective, thus making the Qi-theories much richer. Still. there were not so many physicians who discussed the theme of Daqi. The denomination of Daqi is seen in Nei Jing and Jin Gui Yao Lue, and the physicians like Yu Chang in Ming dynasty and Zhang Xi Chun in Cheng dynasty, etc. applied and utilized Daqi by exploring its functional actions for human life and associating it with clinical practices. Yu Chang said that Daqi is Xiong Zong Yangqi[Positive Energy in Breast] governing every Qi, and that if this Qi is full, it spreads through body and protects the body from sickness, and vice versa. Summarizing his researches on the Daqi in Jin Gui Yao Lue and on the opinions of Yu Chang as well as his experiences, Chang Xi Chun maintained that the Qi accumulated in breast must be named Daqi, which constitutes the contents of Zongqi[Chief Energy] mentioned in Nei Jing. Once the Qi is vacant, breathing is not smooth, whole body is enervated, spirit becomes dim, thinking ability falls drastically. Furthermore, if the Qi is extremely vacant or more worsens, breathing stops. And he prescribed the medicines including Sheng Xian Tang as remedies against the symptom of Daqi XiaXian[Fall in Great Energy]. The recognitions of Daqi by Yu Chang and Zhang Xi Chun are consistent with each other. At any rate, their theories and prescriptions may be high in practical value in contemporary clinics.

환자 간호에 대한 간호사의 의사결정 내용과 특성 및 의사결정 장애요인에 관한 분석 (An Analysis of Nursing Decision Tasks, Characteristics, and Problems with Decision Making)

  • 최희정
    • 대한간호학회지
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    • 제29권4호
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    • pp.880-891
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    • 1999
  • The purpose of this study was to describe nursing decision tasks, their characteristics, and problems associated with decision making. The subjects were 32 nurses who had at least one-year nursing experience and worked on medical-surgical units or intensive care units(ICU). They were asked to describe their decision making experiences in patient care situations and to identify the characteristics of each decisions. They were also asked to describe perceived problems associated with decision making in nursing. The responses on nursing decision tasks and problems were analyzed with content analysis and the decision characteristics were identified by statistical analysis of variance. It was found that there were 16 nursing decisions which are as follows : decisions related to interpreting and selecting appropriate strategies for pain management(6.6%) ; decisions related to providing emotional support (0.7%) ; decisions related to explaining the patient's condition and rationale for procedures(1.1%) ; decisions related to assisting patients to integrate the implications of illness and recovering into their lifestyles(2.9%) ; decisions related to detecting significant changes In patients and selecting appropriate intervention strategies (17.2%) ; decisions related to anticipating problems and selecting preventive measures(4.2%) ; decisions related to identifying emergency situations(0.4%) ; decisions related to effective management of patient crisis until physician assistance becomes available(2.8%) ; decisions related to starting and maintaining intravenous therapy(2.6%) ; decisions related to administering medications(8.1%) ; decisions related to combating the hazards of immobility(7.3%) : decisions related to treating wound management strategies(5.5%) ; decisions related to relieving patient discomfort(13.9) ; decisions related to selecting appropriate strategy according to the changing situation of the patient(18.2%) ; decisions related to selecting the best strategy for patient management(5.3%) ; and decisions related to coordinating, ordering, and meeting the various needs of the patient (3.1%). The nurses reported the fellowing problems in decision making : difficulties due to lack of knowledge and experience (18.6%) ; uncertainty and complexity of decision tasks(15.2%) ; lack of time to make decisions(2.9%) ; personal values which conflict with other staff(15.7%) ; lack of selection autonomy(30.0%) ; and organizational barriers(7.6%). Continuing education programs and decision support systems for frequent nursing decision tasks can be established on the basis of these results. Then decision ability in nurses will increase through the education programs and decision support systems, and then quality of nursing service will be better.

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정신장애를 가진 노숙 청년의 시설 이용 경험 : 탈시설화의 이면(裏面), 생존을 위한 두 체계의 반복 이용을 중심으로 (Experiences of Institutions Utilization among Homeless Young Men with Mental Health Problems: Inevitable Repeated Usages between Two Facility Systems behind the Deinstitutionalization)

  • 김소영
    • 사회복지연구
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    • 제48권3호
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    • pp.83-116
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    • 2017
  • 정신건강복지법의 개정으로 촉발되고 있는 탈시설화 논의는 정신보건영역의 시설로부터 지역사회로 정신장애인의 삶의 공간을 이동시키는 것에 중점을 두고 있다. 본 연구는 기존의 탈시설화 논의가 이 두 공간에서의 단선적 이동만을 상정한 채, 특히 가족관계가 단절되고 경제적으로 심각한 어려움에 처해 있는 취약한(vulnerable) 정신장애인의 시설 간 순환을 남겨둔 채 진행되는 것에 문제를 제기하고자 하였다. 특히 정신보건시설체계와 노숙인시설체계를 넘나들며 시설에 의존해야 하는 이들의 문제를 조명함으로써 탈시설화의 논의를 보완하고자 하였다. 이 두 시설체계를 반복적으로 이용하는 정신장애를 가진 남성 청년노숙인의 사례를 통해 생존을 위해 정신질환과 노숙이라는 중첩된 위험을 관리하며 끊임없이 장소를 바꾸어가며 시설을 이용하는 패턴을 확인하였다. 또한 이것은 시설 간 의뢰와 자원이 없는 당사자들의 자발성에 기대어 더욱 촉발되고 있음을 확인할 수 있었다. 이러한 상황은 지역사회 내에서 삶을 영위할 수 있을 정도의 자원과 지지체계가 부재한 상황에서 사실상 불가피한 선택으로 여겨졌다. 그럼에도 불구하고 시설을 맴도는 정신장애인의 삶은 여전히 지극히 불안정하고 복지의 관점에서도 바람직하지 않다는 점에서 확장된 탈시설화 논의를 통해 심각히 고려되어야 함을 주장하였다.

사상의학의 심신치유기법 - 통합심리학의 ILP(Integral life practice)와 대비하여 - (Mental and physical healing techniques of Sa-Sang Constitutional Medicine - In contrast with the Integral life Practice(ILP) of Integral psychology -)

  • 허훈
    • 철학연구
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    • 제131권
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    • pp.353-381
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    • 2014
  • 사상의학은 비단 의학에서뿐만이 아니라, 경영학이나 정치학, 교육학 등 다양한 분야에서 응용되고 있다. 하지만 사상의학이 근본적으로 치심치병(治心治病)을 치료의 근본으로 하는 심신의학임에도 불구하고, 실제 심리나 정신치료에서 활용되는 경우는 극히 드물었다. 실제 임상에서의 치료법은 약물치료나 침구요법(체질침) 정도에 머물고 있다. 하지만 질병 병리 현상에 대해 사상의학이 제시하는 치유법은 개인의 성정(性情)의 다스림은 물론이고, 연령 지역에 따른 환경적 요인, 주(酒) 색(色) 재(財) 권(權)과 같은 사회적 문화적 요인을 포괄한다. 특히, 사상의학의 수양론은 인간의 타고난 성정 가운데 그림자처럼 항상 숨어 있고, 비밀스럽게 간직되어 있는 사심(邪心)과 태행(怠行)을 올바르게 인지하여 박통(博通)과 독행(獨行)으로 나아가는 것이 중요하다고 강조한다. 또한 의학의 통합적 접근을 시도하면서, 지인정기(知人正己)론을 근본으로 의론(醫論)을 전개하기 때문에 대인관계(對人關係)가 중시되는 현대인들에게 많은 시사점을 준다. 마찬가지로, 세계철학과 통합심리학을 주도하는 윌버(Ken Wilber, 1949~)는 실제적이고 체험적인 통합적 접근을 경험 차원에 적용하는 '통합적 삶을 위한 훈련(ILP)'을 제시하고 있다. ILP는 성장가능한(또는 깨어남이 가능한) 영역 전체의 성장을 위한 실제적인 훈련법(수련법)으로 선례가 없는 것이다. ILP에서는 몸 모듈, 마음(Mind) 모듈, 그림자(Shadow) 모듈, 영(Spirit) 모듈이라는 4가지 핵심 모듈과 윤리, 성(性), 일(Work), 정서(Emotion), 관계성(Relationships) 등의 성장을 지향하는 5가지 보조 모듈을 제시한다. 이에 ILP가 제시하는 핵심 보조 모듈과 다양한 심신치유기법들에 사상의학의 심신 치유법을 대입시켜 본다면 양자(兩者) 간에 보다 발전된 심신치유 접근법을 모색할 수 있을 것이다.

정신장애인에 대한 사회편견 연구 (Social Stigma on People with Mental Disorder)

  • 양옥경
    • 한국사회복지학
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    • 제35권
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    • pp.231-261
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    • 1998
  • 본 연구는 일반인들의 정신장애인에 대한 편견적 태도 및 생각이 어느정도인가를 살펴보고자 하는데 목적을 둔 것으로 크게 3개 차원에서의 비교연구에 초점을 두었다. 하나는 인구사회학적 및 지역별 차이에 따른 일반인의 정신장애인에 대한 편견비교이며, 다른 하나는 지체장애인아 대한 편견과의 비교이며, 마지막 하나는 정신장애인, 그 가족, 그리고 전문가들의 편견과의 비교분석이다. 연구대상은 18세 이상의 성인으로, 일반인 300명, 정신장애인, 그 가족, 전문가 각 100명씩 총 600명이다. 표본은 우선 지역을 선점한 후 지역내 조사답변자를 선점하였다. 지역으로는 서울, 경산, 홍성이 선정되었고, 일반인은 무작위표집하였으며, 나머지는 각 지역의 병 의원을 통해 표집하였다. 자료수집에는 정신장애인 편견척도, 장애인 편견척도를 포함한 설문지를 활용하였다. 분석결과, 우리나라 일반인의 정신장애인에 대한 편견은 그다지 심하지 않은 것으로 나타났다. 한 인간으로서 이들을 수용하는 정도는 높았으나, 이들에게 '사회적응하여 사는 사람'으로 '사회인'으로서의 역할을 부여하는데 있어서는 아직까지 낮은 수용도를 보이고 있었다. 특히 병원에 입원한 정신장애인에 대한 부정적 인식이 컷으며, 사회봉사의 경험이 편견의 정도를 낮추는데 지대한 공헌을 하였다. 장애인에 대한 편견과의 비교에서는 격리치료에서는 정신장애인에게, 불임수술에서는 장애인에게 높은 편견적 태도를 보였다. 대도시에서의 편견은 낮은 반면, 중소도시와 군/읍단위에서의 편견은 항목별로 뚜렷한 차이를 보였다. 나이, 교육적도, 월수입에 따른 차이도 크게 보였다. 정신장애인들의 자기편견의 경우도 항목별 차이를 보이는 가운데 타인과의 관계속에서 이해되는 부분에 대한 편견이 높았다. 가족과 전문가에게서도 대체로 낮은 편견을 보이는 가운데 항목별 차이를 나타냈다. 이같은 결과는 특정편견에 긍정적, 부정적 영향을 미치는 요소들에 대해 전분가의 개입이 필요함을 드러내 준 것이다. 정신보건정책의 수립에 있어서도 입원치료중심의 정책이 아니라 지역사회에서 사회전체가 정신장애인들의 인권을 인정해주는 사회통합의 정책을 마련하여야 함도 시사해주고 있다고 하겠다.

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학교폭력 피해 청소년의 정신의학적 후유증에 관한 사례 연구 (A CASE-ANALYSIS OF THE PSYCHIATRIC SEQUELAE IN ADOLESCENTS VICTIMIZED BY SCHOOL VIOLENCE)

  • 육기환;이호분;노경선;송동호
    • Journal of the Korean Academy of Child and Adolescent Psychiatry
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    • 제8권2호
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    • pp.232-241
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    • 1997
  • 학교폭력의 피해를 입은 경우, 물리적인 측면보다는 정신적인 문제가 더 클 수 있다. 폭력을 당한 이후에 공포심, 우울감, 분노감, 자존심의 저하, 자살, 그리고 만성적으로는 인격장애등이 나타날 수 있다. 학교폭력과 연관하여 사회심리적인 위험요인을 조사하고, 동시에 폭력에 노출된 후에 나타나는 정신의학적 후유증을 알아보는 일은 학교폭력 예방과 해결에 주요한 임상자료를 제공하기 때문에 학교폭력의 실태조사만큼이나 중요하다. 1995년 9월부터 1997년 5월 사이에 학교폭력의 피해를 입고 정신과에 내원한 청소년 환자 13명을 대상으로하여 임상자료와 사회심리적 배경을 조사하였다. 임상자료는 폭력의 정도와 동기, 기간과 방법, 폭력후의 정신과적 증세, 심리검사 소견 및 치료경과 등을 포함하였고, 사회인구학적 자료는 대상들의 성장과정과 가족적 특성, 그리고 학교생활과 교우관계였다. 13명의 전체대상 중 8명은 만성적인 정신장애를 겪은 반면, 5명은 $1{\sim}3$개월동안 불안, 우울, 및 자살기도등의 일시적인 정신과적 증상을 겪은 후에 학교와 가정생활에 복귀할 수 있었다. 만성 정신장애를 보인 8사례 중, 4명은 폭력을 경험한 후에 $3{\sim}6$개월 이상 외상후 스트레스장애 및 우울장애를 나타냈으며, 다른 4명은 폭력으로 인한 정신적 충격을 일정기간 겪은 후 피해에 대한 강한 보상심리 또는 가해자에 대한 동일시 등에 의하여 공격적인 행동장애 내지 폭력가해 사례가 되었다. 만성적 정신장애를 보인 사례들은 일시적인 급성스트레스장애를 나타낸 사례에 비하여 신체적 학대와 정서적 학대, 신체적인 약점이나 질환, 자아기능의 결손, 가족적 지지체계의 결핍 등을 특징적으로 보였다. 결론적으로 학교폭력 피해사례들의 임상적 자료들을 분석한 결과, 심각하고 만성적인 정신장애가 나타난 한편, 임상적으로 유의한 위험요인들이 존재하고 있었으며 이들 중 일부가 가해 사례로 전환되었음을 알 수 있었다.

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HIV/AIDS 감염인의 감염 이후 삶의 긍정적 경험 : "추락하는 것에는 날개가 있다" (Life Experience of People Living with HIV/AIDS: rising up from despair)

  • 김경미;김민정
    • 사회복지연구
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    • 제41권1호
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    • pp.251-279
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    • 2010
  • 2009년 11월 30일 보건복지가족부는 1985년 국내에서 공식적으로 에이즈 '1호' 환자로 확인된 박모씨가 24년이 지난 지금도 매우 건강한 상태라고 발표하였다. 치료를 받은 환자라면 HIV/AIDS 감염인도 대부분은 일반인과 마찬가지로 HIV/AIDS가 아니라 암, 심혈관 질환 등의 질병으로 사망한다는 것이다. 그러나 아직 국내에서 HIV/AIDS는 죽음의 병이라고 알려져 있으며, HIV/AIDS 감염인은 사회에서 '추방된' 느낌을 가지고 살아간다. HIV/AIDS에 대한 치료가 발전했음에도 불구하고 HIV/AIDS 감염인에 대한 국내의 연구는 아직 초보적인 상태이다. 이에 이 연구는 HIV/AIDS 감염임들의 관점에서 이들의 생존경험을 기술하였다. 이를 위해 현상학적인 방법을 이용하여 6명의 HIV/AIDS 감염인을 인터뷰하고 그 결과를 분석하였다. HIV/AIDS 감염인의 감염 이후 삶의 경험은 시간에 따라 상호 연관되어 나타난다. HIV/AIDS에 감염되었다는 사실을 통보받고 감염인들은 "하늘이 무너져 버릴 것 같은" 충격을 경험한다. 또한 HIV에 감염되었다는 사실의 강제적인 노출은 세상으로부터 강요된 단절과 소외를 안겨주고, 직장에서 내몰려 생계의 위협을 받게 하며, 이들은 죽을 날만을 혼자 외롭고 무기력하게 기다린다. 그러나 몇 몇 의료진과의 접촉은 이들에게 HIV/AIDS는 평범한 '관리의 질병' 이라는 인식을 갖게 하며, HIV/AIDS를 "알아가며 이해해 가는" 시간을 갖게 한다. HIV/AIDS 감염을 긍정적으로 수용함으로써, 이들은 현재의 '삶' 에 충실하게 살며, 삶의 새로운 의미를 만들어간다. 주위 사람들에게 HIV/AIDS 감염을 떳떳하게 말하지 못하는 '거짓된 삶' 이 아닌 "진실된 모습으로 거듭나기 위해" 이들은 주위사람들에게 HIV/AIDS 감염사실을 알린다. HIV/AIDS 감염 사실을 알리는 것은 "내가 나를 인정하고", "나 자신을 강하게 만드는 원동력" 이 되어 이전보다 더 성숙해진 자신을 발견할 수 있게 한다. HIV/AIDS와의 이러한 상생의 전제는 바로 병에 대한 인식의 변화이다. '더러운 병, 죽는 병' 이 아니라 '관리가능한 질병' 이라는 인식의 변화는 HIV/AIDS 감염인들이 새롭게 태어날 수 있는 토대가 된다. HIV/AIDS 감염 이후 새로운 삶에는 자기만이 아닌 다른 사람들이 있다. 이는 나에게로만 향하던 관심에서 타인에 대한 관심으로의 변화를 의미하며, HIV/AIDS와의 상생을 촉진했던 것은 가족과 친구들의 변함없는 지지였다.

조선시대(朝鮮時代) 전기(前期)의 의료제도(醫療制度)에 대한 연구(硏究) (A study of the Medical System in the Early Chosun-Dynasty)

  • 한대희;강효신
    • 대한한의학원전학회지
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    • 제9권
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    • pp.555-652
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    • 1996
  • Up to the present the scholastic achievements in the history of the medical system have been rather scare despite its importance in the Korean History. Hence, this dissertation attempts to examine the significance of the institute in the Korean History, covering the period from the ancient times through the early Chosun-Dynasty. In the ancient times, the medical practice relied primarily upon human instincts and experiences at the same time, shaman's incantations were widely believed to cure diseases, the workings of evil spirits supposedly. For the period from the Old Chosun through Samhan(巫堂), Chinese refugees brought a long medical knowledge and skills of the continent. New Chinese medicine, traditional practices and incantations were generally used at this time. Medicine and the medical system were arranged by the period of the Three Countries(三國時代). No definite record concerning Koguryo remains now. As for Paekje, however, history shows that they set up the system under the Chinese influence, assigning medical posts such as Euibaksa(medical doctor), Chaeyaksa(pharmacist), and Jukeumsa(medicine man) within Yakbu(department of medicine). Scientifically advanced, they sent experts to Japan, giving a tremendous influence on the development of the science on ancient Japan. After the unification of the three countries, Shilla had their own system after the model of Dang(唐). This system of the Unified Shilla was continued down to Koryo and became the backbone of the future ones. In the ancient time religion and medicine were closely related. The curative function of the shaman was absolute. Buddhism played a notable part in medical practice, too, producing numerous medical monks. The medical system of Koryo followed the model of Dang with some borrowings from Song(宋). Sangyakkuk(尙藥局) was to deal exclusively with the diseases of the monarch whereas Taeeuigam(太醫監) was the central office to handle the national medical administration and the qualification test and education for doctors. In addition, Dongsodaebiwon(東西大悲院), Jewibo(濟危寶), and Hyeminkuk(惠民局) were public hospitals for the people, and a few aristocrats practiced medicine privately. In 987, the 6th year of Songjong(成宗), local medical operations were installed for curing the sick and educating medical students. Later Hyonjong(顯宗), established Yakjom(clinics, 藥店) throughout the country and officials were sent there to see patients. Foreign experts, mainly from Song, were invited frequently to deliver their advanced technology, and contributed to the great progress of the science in Korea. Medical officials were equipped with better land and salary than others, enjoying appropriate social respect. Koryo exchanged doctors, medicine and books mainly with Song, but also had substantial interrelations with Yuan(元), Ming(明), Kitan(契丹), Yojin(女眞), and Japan. Among them, however, Song was most influential to the development of medicine in Koryo. During Koryo Dynasty Buddhism, the national religion at the time, exercised bigger effect on medicine than in any other period. By conducting national ceremonies and public rituals to cure diseases, Taoism also affected the way people regarded illness. Curative shamanism was still in practice as well. These religious practices, however, were now engaged only when medication was already in use or when medicine could not held not help any more. The advanced medical system of Koryo were handed down to Chosun and served the basis for further progress. Hence, then played well the role to connect the ancient medicine and the modern one. The early Chosun followed and systemized the scientific and technical achievement in medicine during the Koryo Dynasty, and furthermore, founded the basis of the future developments. Especially the 70 years approximately from the reign of Sejong(世宗) to that of Songjong(成宗) withnessed a termendous progress in the field with the reestablishment of the medical system. The functions of the three medical institute Naeeuiwon(內醫院), Joneuigam(典醫監), Hyeminkuk(惠民局) were expanded. The second, particualy, not only systemized all the medical practices of the whole nation, but also grew and distributed domestic medicaments which had been continually developed since the late Koryo period. In addition, Hyeminso(惠民局, Hwarinwon(活人院)) and Jesaenwon(濟生院)(later merged to the first) played certain parts in the curing illness. Despite the active medical education in the capital and the country, the results were not substantial, for the aristocracy avoided the profession due to the social prejudice against technicians including medical docotors. During the early Chosun-Dynasty, the science was divided into Chimgueui (acupuncturist), Naryogeui(specialist in scrofula) and Chijongeui (specialist in boil). For the textbooks, those for the qualification exam were used, including several written by the natives. With the introduction on Neoconfucianism(性理學) which reinforced sexual segregation, female doctors appeared for the female patients who refused to be seen by male doctors. This system first appeared in 1406, the sixth year of Taejong(太宗), but finally set up during the reign of Sejong. As slaves to the offices, the lowest class, female doctors drew no respect. However, this is still significant in the aspect of women's participation in society. They were precedents of midwives. Medical officials were selected through the civil exam and a special test. Those who passed exams were given temporary jobs and took permanent posts later. At that time the test score, the work experience and the performance record of the prospective doctor were all taken into consideration, for it was a specialized office. Most doctors were given posts that changed every six months, and therefore had fewer chances for a goverment office than the aristocracy. At the beginning the social status of those in medicine was not that low, but with the prejudice gradully rising among the aristocracy, it became generally agreed to belong to the upper-middle technician class. Dealing with life, however, they received social respect and courtesy from the public. Sometimes they collected wealth with their skills. They kept improving techniques and finally came to take an important share in modernization process during the late Chosun-Dynasty.

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뇌성마비아 어머니의 경험 (Lived experience of mothers who have child with cerebral palsy)

  • 이화자;김이순;이지원;권수자;강인순;안혜경
    • Child Health Nursing Research
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    • 제2권1호
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    • pp.93-111
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    • 1996
  • The purpose of the study is to identify the lived experience of mothers who have children with cerebral palsy in order to understand their agony. Moreover, the result of study was to find some nursing intervention for disabled children and their mothers. For this purpose, ten mothers who are willing to cooperate with this research were selected at random from those who have children with the cerebral palsy, currently using the municipal facilities for the handicapped with cerebral malfunction. Data collection was done from October 4, 1994 th December 31, 1994. The data were collected by asking the mothers mentioned above with some unstructured open-ended questions, recorded on the tapes with permission by the interviewee in order to prevent missing of the interviewed contents. These collected data have been substantiated and properly analyzed on the basis of phenomenological approach initiated by Colaizzi's method. The results and validity are proved to be credible by means of the individual checking of the interviewed mothers. The results of this study are as follows : 1. When the mother is first informed of the diagnosis of cerebral palsy on her child, she usually misses the crucial timing needed for proper treatment of the child's disorder because she is notified through the doctor's indifference and his apparently inactive, matter-of-fact attitude. At first she suspects the doctor's diagnosis and tries to attribute it to the unknown cause from a certain genetic problem and then she quickly wants to deny the whole situation that her child is really suffering from the cerebral palsy. The reality is too much for her to accept as it is and she would not believe her child is abnormal. Therefore, she even attempts depend on the power of God for its solution. 2. The mother, who goes thorough this kind of uncommon experiences, is totally devoted to the treatment and care of the child and completely ignores her own life and happiness. At the same time, she feels sorry for her other normal children she believes having not enough care and concern. Also, she feels sorry for the sick child when the child's brothers or sisters show special concern for the patient out of sympathy. It is sorry and not satisfied for her that the child is growing with abnormality and neighbor other around have inappropriate attitudes. Likewise, she is discontent with her husband's lack of concern about the child's treatment. She believes that the health care system in this society isn't fulfilling its due purpose. In the state of her utmost distress and anxiety, she always feels the need of competent consultants, and is angry about that her child is treated as an abnormal being, she is trying to hide the child from other people and to make him or her disappear, if possible. Although she doesn't have harmonious relation with her husband, she id happy when he shows his affection for the child and she feels relieved and thankful when the relatives don't mention about the child's condition Since the child's overall status of health is continuously in unstable conditions, requiring her all-time readiness for an emergency, she feels guilty of her child's illness toward the fEmily members as if it was her own fault to have borne such an abnormal child and she feels responsible for the child morally and financially if necessary Because her life is centered on taking care of the child, she cannot afford to enjoy her own life and happiness. She is a lonely mother, fatigued, with no proper relationship with other people around her. With this sense of guilt and responsibility as a mother of an unusual disease, she has no choice but to grieve her destiny from which she is not allowed to escape. 3. Nevertheless, the mother with the child suffering from the cerebral palsy does not easily give up the hope of getting her child cured and she believes that in the long run, though slower than hoped, her abnormal son or daughter will be eventually cured to become a normal sibling someday. This kind of hope is sustained by the mother's strong faith coming from observing the progress of other similar children getting better. Sometimes she is encouraged to have this faith by other mothers who share the same painful experiences, believing that her child will improve even more rapidly than others with the same palsy. Full of hope, she painstakingly waits for the child's healing. Moreover, she plans to have another child. she thinks that the patient child's brothers and sisters only can truly understand and look after the patients. However, when she notices that the progress of other children under the treatment does not look so hopeful, she is distressed by the thoughts that her child may never get well. Too, she is worried that the patient's brother or sister will be born as the same invalid with the cerebral disease. She is discouraged to have another baby as much as she is encouraged to. She is also troubled by the thought that in case she has another baby, she will have to be forced. to neglect the patient child, especially when she does have an extra hand or some reliable person to help her with taking care of the patient.

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