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Experiences in the therapeutic itineraries of mothers of children with intellectual disabilities

机译:智障儿童母亲的治疗行程中的经验

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The scope of this study is to describe the experiences of mothers of children with intellectual disabilities who have been treated in a specialized institution in Feira de Santana, State of Bahia, during their therapeutic itineraries. The study adopted a qualitative approach and was conducted by means of semi-structured interviews. The results revealed that the discovery that their child has an intellectual disability is accepted by their mothers with emotions of shock, denial, anger, negotiation, depression and subsequent acceptance. The difficulties in therapeutic itineraries begin after the moment the child is diagnosed as having an intellectual disability, due to the lack of experience of health professionals in communicating the fact, which leads the mothers to search for other health services. Despite access to healthcare being one of the principles of the Unified Health System (SUS), therapeutic itineraries are fraught with difficulties at a geographical, economic and functional level. Intellectual disability is a health issue demanding constant care, and its impacts have repercussions in the family dynamics, identities and roles, requiring comprehensive attention to the children and their caretakers, especially in the type of support such that they may maintain their protective roles.
机译:这项研究的范围是描述智障儿童母亲的治疗路线,这些母亲在巴伊亚州费拉德桑塔纳的专门机构接受治疗的经历。该研究采用定性方法,并通过半结构化访谈进行。结果表明,他们的母亲患有震惊,否定,愤怒,谈判,沮丧和随后的接纳情绪,从而接受了他们的孩子患有智力残疾的发现。由于缺乏医疗保健专业人员交流事实的经验,在诊断出儿童患有智力障碍的那一刻之后,治疗行程就开始出现困难,这导致母亲们寻求其他医疗服务。尽管获得医疗保健是统一卫生系统(SUS)的原则之一,但是治疗性行程在地理,经济和功能层面上仍然充满困难。智障是一个需要长期护理的健康问题,其影响会对家庭动态,身份和角色产生影响,需要全面关注儿童及其照料者,特别是在支持类型上,以使其保持保护作用。

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