• 한국지역지리학회지
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• 제22권3호
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• pp.529-552
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• 2016

본 연구는 물을 매개로 하는 물리적 치유의 경관이 갖는 신체적, 문화적, 공간적, 경제적 의의가 어떤 형태로 여성을 중심으로 하는 공간에서 나타나는지 살펴보고, 이를 여성을 위한 쉼터로서의 기능, 여성을 위한 배려의 기능, 여성을 형상화한 기능으로 나눠 검토하는 것에 목표를 두고 있다. 여성을 위한 쉼터로서의 기능에는 신체적 의의가 가장 두드러지게 나타나며, 온천수와 온천욕, 분위기, 부대시설, 안전한 밤문화 등으로 구체화된다. 이러한 매개를 통해 여성은 자유로움, 온천수가 온전한 상태로 회귀시켜주는 힘, 끊임없이 제공받는 치유의 장치, 안전하게 보호해주는 것, 마음을 열고 자연스럽게 타인과의 교류 등을 느끼게 된다. 다음으로 여성을 위한 배려의 기능에서는 물을 매개로 하는 치유의 경관이 갖는 문화적 의의가 두드러지게 되는데, 이는 온천에서 발견할 수 있는 문화이기도 하지만, 배려에 바탕을 둔 일본의 문화가 자연스럽게 혼합되어 나타나는 현상이라 할 수 있다. 예를 들어, 송영버스, 오카미상 혹은 나카이상의 서비스, 장식품, 장난스러운 설치물, 개인공간의 확보 등을 통해서 다양한 즐거움을 느낄 수 있고, 누군가 지지해주고 혹은 지켜주고 있다는 느낌을 받게 되며, 신체적인 아름다움뿐만 아니라 정신적인 아름다움까지도 추구하게 된다. 마지막으로 여성을 형상화한 기능은 문화적, 공간적, 경제적 의의 등 폭넓게 나타나는데, 광고매체, 온천과 관련된 표식, 신사, 오브제, 상품화된 매개체 등을 통해 다양하게 드러난다. 이러한 기능은 건강함, 쉼, 편안함, 친숙함 혹은 익숙함, 사랑이 이루어지거나 혹은 행복한 결혼 생활로 이어진다는 이미지 등으로 승화된다. 이상을 통해 온천을 중심으로 나타나는 여성을 위한 치유의 요소는 자유로움, 안전함, 신체를 뛰어넘는 효과, 즐거움, 치유의 지속성, 아름다움, 희망 등으로 수렴되며, 이러한 요소들이 유기적으로 결합될 때 여성의 온전하지 않음은 온전함으로 회복되는 치유의 효과가 드러나는 것이라 할 수 있다.

• 한국산학기술학회논문지
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• 제22권5호
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• pp.354-360
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• 2021

사람들은 개인의 삶의 만족을 위하여 일과 삶의 균형을 맞추며 건강하고 행복하게 살아가는 것을 희망하고 있다. 따라서 걱정 없이 행복하고 건강하게 나이가 들어가는 것을 의미하는 웰에이징(well-aging)에 대한 관심이 높아지고 있다. 본 연구는 웰에이징 관련 신문기사를 분석하여 웰에이징과 연관된 요인들을 파악하고자 하였다. 파이썬(Python) 기반의 웹 크롤링(web crawling)을 활용하여 2020년 11월까지 포탈 사이트 다음(daum)의 뉴스 서비스에 게재된 1,199편의 기사를 수집하였으며, 이중 연구 주제에 일치하는 기사 374편을 연구대상으로 선정하였다. 텍스트마이닝의 빈도분석 결과, '노인', '건강', '피부', '웰에이징', '제품', '사람', '노화', '여성', '국내', '은퇴' 등의 순서로 상위 10개의 키워드가 중요하게 파악되었다. 또한 출현 빈도가 높은 45개의 중요 키워드를 기반으로 사회 네트워크 분석을 수행한 결과 '피부-주름', '피부-노화', '노인-건강'이 강한 연결 관계를 나타났다. CONCOR 분석을 수행한 결과 45개의 중요 키워드들은 '삶과 행복', '질병과 죽음', '영양과 운동', '힐링', '헬스산업', '노화와 안티에이징', '건강', '노인서비스'의 8개 군집으로 구성되어, 신문기사들을 기반으로 나타나는 웰에이징과 관련된 요인들을 유추할 수 있었다.

• 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.