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The lived experience of parenting a child with a life-limiting condition: A focus on the mental health realm

Published online by Cambridge University Press:  13 February 2009

Alison Rodriguez*
Affiliation:
Department of Behavioural Sciences, School of Human and Health Sciences, University of Huddersfield, Queensgate, Huddersfield, United Kingdom
Nigel King
Affiliation:
Department of Behavioural Sciences and Applied Psychology Research Group, School of Human and Health Sciences, University of Huddersfield, Queensgate, Huddersfield, United Kingdom
*
Address correspondence and reprint requests to: Alison Rodriguez, Department of Behavioural Sciences, School of Human and Health Sciences, University of Huddersfield, Queensgate, Huddersfield, HD1 3DH, United Kingdom. E-mail: [email protected]

Abstract

Objective:

As medical technology has improved, there has been a marked increase in the numbers of children with life-limiting conditions being managed in the community. Few studies have evaluated the life worlds of the parents of these children. However, there have been studies that have reported feelings of isolation and depression among mothers. This article reports a study that highlights the mental health implications of the lived experience of parenting a child with a life-limiting condition.

Method:

Semistructured interviews were conducted with 10 parents of children with life-limiting conditions and analyzed using a phenomenological method.

Results:

The essential meaning of the phenomenon “the lived experience of parenting a child with a life limiting condition” is understood as a full-time emotional struggle involving six continuous constituents: inner drive, feeling responsible, psychological effects, threatened self image, social withdrawal, and a fear of reaching the bottom line.

Significance of results:

Very little clinical attention is focused upon the wider issues that affect parents dealing with caring for a child with a life-limiting condition.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 2009

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References

REFERENCES

Andrews, F. & Hood, P. (2003). Shared care: Hospital, hospice and home. Peadiatric Nursing, 15, 2022.CrossRefGoogle Scholar
Edmond, A. & Eaton, N. (2004). Supporting children with complex healthcare needs and their families: An overview of the research agenda. Child: Care, Health and Development, 30, 119135.Google Scholar
Frank, N.C., Brown, R.T., Blaint, R.L., & Bunke, V. (2001). Predictors of affective response of mothers and fathers of children with cancer. Psycho-Oncology, 10, 293304.CrossRefGoogle ScholarPubMed
Harding, R. & Higginson, I. (2003). What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness. Palliative Medicine, 17, 6374.CrossRefGoogle ScholarPubMed
Patenaude, A.F. & Last, B. (2001). Cancer and children: Where are we coming from? Where are we going? Psycho-oncology, 10, 281283.CrossRefGoogle ScholarPubMed
Polit, F.D. & Beck, C.T. (2004). Nursing research, principles and methods. Philadelphia: Lippincott Williams & Williams.Google Scholar
Schwandt, T.A. (1994). Constructivist, interpretive approaches to human inquiry. In Handbook of Qualitative Research, Denzin, N.K. & Lincoln, Y.S. (Eds.), pp. 118137. Thousand Oakes, CA: Sage.Google Scholar
Van Manen, M. (1990). Researching Lived Experience: Human Science for an Action Sensitive Pedagogy. Albany, NY: New York Press.Google Scholar
Dahlberg, K., Drew, N., & Mystrom, M. (2001). Reflective Lifeworld Research. Sweden: Studentlitteratur AB.Google Scholar