Literature DB >> 11560735

Being a parent of an adult son or daughter with severe mental illness receiving professional care: parents' narratives.

A Pejlert1.   

Abstract

The aim of this study was to illuminate the meaning of parental care-giving with reference to having an adult son or daughter with severe mental illness living in a care setting. The parents were asked to narrate their relationship to offspring in the past, in the present, and their thoughts and feelings concerning the future. The study was guided by a phenomenological hermeneutic perspective. The meaning of parental care was illuminated in the themes 'living with sorrow, anguish and constant worry', 'living with guilt and shame', 'relating with carer/care; comfort and hardships' 'coming to terms with difficulties' and 'hoping for a better life for the adult child'. Parental care-giving emerged as a life-long effort. The narratives revealed ongoing grief, sorrow and losses interpreted as chronic sorrow. The narratives disclosed a cultural conflict between the family system and the care system, which was interpreted as a threat to the parental role, but also experiences of receiving comfort and having confidence in the care given. Experiences of stigma were interpreted from the way of labelling illness, narrated experiences of shame and relations with the public and mental health professionals. Parents' persisting in the care-giving role, striving to look after themselves and expressing hopes for the future were interpreted as a process of coming to terms with difficulties. Results suggest that mental health professionals need to be aware of their own attitudes and treatment of families, improve their cooperation with, and support to families, and provide opportunities for family members to meet one another.

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Mesh:

Year:  2001        PMID: 11560735     DOI: 10.1046/j.0966-0410.2001.00301.x

Source DB:  PubMed          Journal:  Health Soc Care Community        ISSN: 0966-0410


  9 in total

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3.  Self-stigma and affiliate stigma in first-episode psychosis patients and their caregivers.

Authors:  Emily S M Chen; Wing Chung Chang; Christy L M Hui; Sherry K W Chan; Edwin Ho Ming Lee; Eric Y H Chen
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4.  Multiple perspectives on mental health outcome: needs for care and service satisfaction assessed by staff, patients and family members.

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Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2011-08-18       Impact factor: 4.328

5.  Experiences of Siblings of Children With Neurodevelopmental Disorders: Comparing Qualitative Analysis and Machine Learning to Study Narratives.

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Journal:  Front Psychiatry       Date:  2022-04-28       Impact factor: 5.435

6.  Attitudes and perceived barriers to working with families of persons with severe mental illness: mental health professionals' perspectives.

Authors:  Hea-Won Kim; Michelle P Salyers
Journal:  Community Ment Health J       Date:  2008-04-25

7.  First-time primary caregivers' experience of caring for young adults with first-episode psychosis.

Authors:  Terence V McCann; Dan I Lubman; Eileen Clark
Journal:  Schizophr Bull       Date:  2009-08-13       Impact factor: 9.306

8.  Positive and negative impacts of schizophrenia on family caregivers: a systematic review and qualitative meta-summary.

Authors:  Nao Shiraishi; Jacqueline Reilly
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2018-10-22       Impact factor: 4.328

9.  Complicated Grief, Depression, Health and Attachment Style in First Degree Relatives of Individuals with a Chronic Psychotic Disorders.

Authors:  Lilach Rachamim; Nitsa Nacasch; Inbal Sinay
Journal:  Community Ment Health J       Date:  2021-06-16
  9 in total

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