• 제목/요약/키워드: Mother's Experiences

검색결과 151건 처리시간 0.018초

기형아 출산 산모의 경험 (Experience of Mothers who Gave Birth to Congenitally Anomalic Babies)

  • 최소영;이미라
    • 여성건강간호학회지
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    • 제3권1호
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    • pp.28-38
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    • 1997
  • Recently, the birth rate of congenitally anomalic babies is increasing in Korea. But there are few studies and articles in nursing field. So nurses are having difficulties in caring those mothers. This study is to reveal experiences of the mothers with congenitally anomalic babies. Subjects were six and data were gathered by interviews. Data were analyzed by Giorgi's method. Mother's responses were organized into five categories-shock, sadness, expectation, attribution and loss of confidence on future pregnancies. Loss of confidence on future pregnancies were categories which were not found in foreign articles. Based on the result of this study, author recommend that another studies which deal only same anomaly will be done, and genetic counseling system will be organized in hospitals.

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중학생이 인지한 가족스트레스 정도와 대응정도 (Family Stress and Coping in Early-adolescence (Middle School Students))

  • 정현숙
    • 한국보건간호학회지
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    • 제7권2호
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    • pp.89-97
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    • 1993
  • The purpose of this study was to analyze early adolescent-family stress and family coping according to differences in general charactiristics. This study is also intended to analyze relationship between early adolescent family stress and coping. The subjects of this study consisted of (292) middle school students of the city of sokcho. The data were collected between Aug. 23, 1993 to Aug. 28, 1993. At tools of measurement, McCubbin & Patterson's 'A-FILE (Adolescent-Family Inventory of Life Events & changes)' and 'A-COPE (Adolescent Coping Orientation for Problem Experiences)' were amended and made use. For the statistical analysis of data, t-test, ANOVA, Pearson Correalation Coefficient were utilized The results were summarized as follows: 1) General characteristics influencing the level of adolescent-family stress were parents status. (p=.000) 2) General characteristics influencing coping were parent's religions. (father: p=. 003) (mother: p=.039) 3) There was a significant difference between the level of adolescent-family stress & coping. (p=.000)

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부모의 원가족 경험이 양육행동에 미치는 영향 : 유아기 자녀를 둔 부모를 대상으로 (Influence of Parents' Family-of-Origin Experiences on Parenting Behaviors : Focusing on Parents with Young Children)

  • 전주혜;박정윤;김양희;장영은;어성연
    • 가정과삶의질연구
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    • 제28권2호
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    • pp.1-15
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    • 2010
  • This purpose of study is the effects of parents' family-of-origin experience on their parenting behaviors of 260 parents with child(ren) aged between 3-7. The results were as follows: First, father's with higher monthly average income showed more frequent responsive parenting behaviors. Mothers with different age, income, employment status, employment of their mother in the family of origin, and current family types showed different levels of limit-setting, intimacy, and responsivenss in their parenting. Second, both parents' experiences from their family of orgin were correlated their parenting behaviors. Third, regression analysis revealed that mothers were found to give their children more reasonable guidance if they experienced more independence from their parents and more acceptance from their mothers, if they raise more than two kids, and if their family of origin was an extended type. Fathers who perceived higher family of health, more acceptance by their mothers showed more limit setting parenting behavior.

산욕기 여성의 경험 - 제주지역을 중심으로 - (The Lived Experience of Postpatal Women in Che-Ju island)

  • 신혜숙;이경희
    • 여성건강간호학회지
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    • 제4권2호
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    • pp.271-285
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    • 1998
  • The purpose of this study is to explore and describe the experiences of postpartal woman, Korean postpatal care that Korean women experience afterbirth, to find the meaning of their lived experiences and to contribute to the base Korean maternal nursing. The method is to phenomenological through participant in depth interview. The subjects of this study were 8 women who are 1 week to less or over 100 days afterbirth. Their age rang from 22 to 33. All available data was collected from 26th of March 1988 to 10 of July 1998. A tape recorder was used with the permission of the subjects to prevent the loss of spoken information. The analysis of the data was made through Colaizzi's. The result of the study was as follow: There were eleven themes and 8 structures, Structure 1 : Acceptance to the traditional Sanhujori, Structure 2 : Powerlessness, Structure 3 : Disappointment and Being sorry, Structure 4 : Attachment as mother, Structure 5 : Anxiety on bring up, Structure 6 : Praying the well being of baby. Structure 7 : Negative body image 8 : Information seeking, Structure. In conclusion, nurses have to help Korean women afterbirth who are in difficulties physically, emotionally, socio-psychologically as direct caregivers and educators. As continually finding out the Korean postpartal care. Sanhujori, we can build the our original maternal nursing.

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암 환아 부모의 경험에 대한 질적 연구 (The Experience of Parents Whose Child is Dying with Cancer)

  • 조영숙;김수지
    • 대한간호학회지
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    • 제22권4호
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    • pp.491-505
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    • 1992
  • The purpose of this research was to understand the structure of the lived experience of parents of a child terminally ill with cancer The research question was “What is the structure of the experience of parents of a child terminally ill with cancer\ulcorner” The sample consisted of 17 parents of children admitted to the cancer units of two university hospitals in Seoul. The unstructured interviews were carried out from October 10, 1991 through January 10, 1992. They were audio-recorded and analysed using Van Kaam's method. Parents ascribed the cause of the cancer to the mother's emotional imbalance during pregnancy, the mother's stress, failure to observe religious rites, food, the parent's sin, misfortune and pollution. The theme clusters were tension, fear and depression experienced during pregnancy, stress that children suffer from abusive parents, failure to observe religious activites, bad luck, and sins committed during a previous life. When the child suffered a recurrence of cancer, the parents experienced negative emotions, nervousness, sorrow. depression and death. The theme clusters were feelings of despair, helplessness, regret, guilt, insecurity, emptyness and apathy. The long struggle with cancer resulted in the loss of economic security, loss of psychological and physical well being, and social withdrawal. The theme clusters were the economic burden of medical cost, giving up treatment, debt, limited medical insurance coverage and blood transfusion. The loss of psychological well being included stress, lack of support systems, inability to carry out responsibilities, lack of trust of the medical ten family breakdown, inappropriate expression of emotion and not disclosing the diagnosis to the child. Physically the parents suffered fatigue, insomnia, loss of appetite, loss of weight, dizzness, headache, psychosomatic symptoms, and increased consumption of liquor and cigarettes. Social withdrawal was manifested by taking time off from work to look after the child, decrease of outside social activities and feelings of isolation. Influences on family life were spousal conflicts, negative response of siblings, separation of the family members and economic hardship. The theme clusters were blaming a spouse for the cause of the illness and disagreements, maladjustment, lonliness, hostility and depression of siblings. The high price of medical care over the long period was a major factor influencing the life of the family. Positive experiences during the child's long illness were the strengthening of support systems and religious beliefs and financial help from social organizations. The support of one's spouse primarily helped to overcome the stress of the long illness. In addition, support was received from parents of other children with cancer and from nurses and religious leaders. The nurse, by providing empathetic support, should be a person with whom parents can express their feelings and share their experiences.

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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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양육 결정 미혼모의 초기 모성 경험에 관한 연구 -해석학적 근거이론 방법- (A Study on the Initial Motherhood Experiences of Non-married Mothers who Decided to Raise Their Babies -Hermeneutic Grounded Theory Methodology-)

  • 임해영;이혁구
    • 사회복지연구
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    • 제45권3호
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    • pp.35-69
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    • 2014
  • 이 연구는 양육 결정 미혼모의 초기 모성 경험을 탐색하고자, 7명의 연구 참여자를 대상으로 Rennie의 해석학적 근거이론 방법을 활용하였다. 분석 결과, 145개 의미단위, 34개 하위 범주를 통해, '출산 선택', '바닥을 치는 기분', '뱃속 생명에 대한 양가감정', '모성 인식', '모성 불안', '사회적 꼬리표라는 굴레', '모성 희망', '새로운 나를 만남', '고단한 삶의 얼굴' 이란 9개의 해석학적 범주를 구성하였다. 연구 참여자들의 모성 경험을 통합하는 핵심범주로는 "약이면서 독이고, 독이면서 약인 모성의 갈등적 두 얼굴로 살아가기"로 상정하였다. 그리고 이들의 모성 경험 과정은 출산 선택, 심리적 좌절, 모성 인식, 모성 혼란, 희망과 좌절의 공존 5단계로 나타났고, 모성 경험 유형은 순응형, 갈등형, 저항형으로 분석되었다. 이러한 연구 결과를 토대로 양육 결정 미혼모의 모성 경험은 어머니라는 새로운 주체를 출현시키는 과정으로 드러났다. 그리고 이들은 사회문화적으로 부여된 모성 이데올로기를 내면화하는 과정 속에서 사회적으로 지향된 모성과 현실적인 모성 역할 사이의 간극으로 인해 혼란을 경험하는 것으로 나타났다. 이를 기반으로 양육결정 미혼모의 초기 모성을 지지해줄 수 있는 개입 방안을 제언하였다.

청소년기 자녀 어머니의 양육경험에 대한 질적 연구 (A Qualitative Study of the Parenting Experience of Adolescents)

  • 최지원;김수영
    • 한국콘텐츠학회논문지
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    • 제21권5호
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    • pp.837-854
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    • 2021
  • 본 연구는 청소년기 자녀 어머니들을 대상으로 양육 경험을 탐색하기 위해 이루어졌다. 연구 참여자는 서울지역의 중학교 1~3학년 자녀의 주 양육자 7명으로 2019년 9월부터 12월까지 심층 인터뷰를 진행하였다. 각 참여자들의 인터뷰 내용을 녹취한 후 전사한 축어록과 인터뷰 요약 내용인 문서 등을 자료로 수집하였다. 본 연구에서는 참여자들이 서술한 경험과 행위에 대한 인식을 연구자가 의미화 할 수 있는 Smith & Osborn (2003)의 해석현상학적 방법으로 분석하였고, 자료 분석 결과 6개의 대주제와 25개의 소주제가 도출되었다. 청소년기 자녀 어머니들의 양육 경험에서 도출된 결과는 크게 6가지로 자녀와 함께 시간보내기의 함의, 당연하지 않은 당위 행동, 표현의 미학, 에너지의 충전 방법, 자녀에게 남기고 싶은 정신적 유산, 유연성이다. 본 연구의 연구결과는 임상 실천 분야에서 어머니들이 어떻게 청소년기 자녀와 상호작용해야할 지에 대한 보편성과 특수성의 양방향을 제시해줄 수 있다고 본다. 따라서 본 연구 결과는 예방적이고 교육적인 차원에서 청소년기 자녀의 어머니들이 양육자로서 자녀와 어떤 상호작용을 하면 좋을지에 대한 건강한 반응의 제시를 제공할 수 있을 것이다.

고학력 전문직 중년여성의 이혼 후 삶의 경험 (Life's Experiences of Middle-aged Divorced Women with Higher Education and Profession)

  • 박형숙;배영실;이성화;유수정;전소영
    • 여성건강간호학회지
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    • 제22권1호
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    • pp.11-20
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    • 2016
  • Purpose: Today, an increasing number of divorce is shifting family forms and gender role practices. The purpose of this qualitative study was to understand life's experiences of middle-aged divorced women with higher education and profession lives in Korea. Methods: For this study, 6 middle-aged divorced women with similar backgrounds were recruited from December 2013 to June 2014, using in-depth individual interviews. Data analysis was performed using Giorgi's phenomenological methodology. Results: Individual interviews revealed the following 15 meaning of themes and 5 themes. 1) A woman considering herself to be ashamed that she has not lived an ordinary life. 2) The destiny of a woman not having a fortune. 3) An exhilarated mood like a teenage girl's 4) Suppressing an instinctive desire of sex. 5) Being a mother as a woman head of household. Conclusion: This study provides deep understanding of middle-aged divorced women with higher levels of education and professional lives of women who experienced difficult times and overcame their problems. Based on the results of this study, nursing strategies for enhancing quality of life need to be created and implemented for all professional women by Korean community networking gradually.

호스피스 환자의 임종증상

  • 최화숙;김수지
    • 호스피스학술지
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    • 제2권1호
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    • pp.75-86
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    • 2002
  • Prupose: The purpose of this study was to identify signs and symptoms of hospice patients during their dying processes. Method: The subjects of this study were 76 patients who received hospice care services in 2 different hospice care programs in Seoul area. Data was obtained from January, 1999 to June, 2001 by hospice nurse's observation, interviews with patient's primary caregiver and hospice volunteers, patient's self report, nursing records and questionnaires which had been developed by selecting from various references and refining them based on the result of preliminay studies. The collected data were analyzed with the SPSS PC+ program and content analysis. Results: Mean lengths of hospice patient's dying process were 3.6 days. Physical signs and symptoms of hospice patients during their dying processes were 'increased sleep'(89.5%), 'decreased oral intake of food'(88.2%) and 'liquids'(86.8%), 'change of respiration'(82.9%), 'decreased urine output'(80.3%), 'cold extremities'(69.7%), 'death rattle'(67.1%), 'cyanosis'(57.9%), 'restlessness'(55.3%), etc. And psychological, spiritual and social signs and symptoms were 'decreased interpersonal relationships'(61.8%), 'panorama of memories from childhood'(60.5%), 'experiences as like hallucination'(56.5%), 'saying bye with family'(69.7%), 'forgiveness', 'make a will', etc. Experiences as like hallucination were seemed not as dream but reality were shown by 43 dying patients. They had experienced to see and to talk with their deceased mother(18.6%) and/or relatives(30.2%), angels(20.9%), heaven(11.6%), old house in which they had lived, someone from the world beyond with black clothes, etc. Conclusion: The above results indicate that death of hospice patients is ongoing process with dying signs and symptoms during several days contains not only in physical aspects but also among psychological, spiritual and social aspects including family dynamics.

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