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10 - Community rehabilitation in childhood: concepts to inform practice

Published online by Cambridge University Press:  11 August 2009

Michael P. Barnes
Affiliation:
University of Newcastle upon Tyne
Harriet Radermacher
Affiliation:
University of Newcastle upon Tyne
Peter Rosenbaum
Affiliation:
McMaster University, Hamilton, Ontario
Mary Law
Affiliation:
McMaster University, Hamilton, Ontario
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Summary

Introduction

Jenna is a 6-year-old girl, the second of two children of a mother who is 29 and her 32-year-old husband. Jenna was born unexpectedly at 30 weeks gestation following an uneventful pregnancy, and experienced a variety of perinatal difficulties requiring a stay in the special care baby unit. Following discharge she was seen regularly at a newborn follow-up clinic, where her developmental progress was monitored carefully. At 8 months Jenna's motor development was ‘slow’ and she appeared somewhat ‘stiff’. At 1 year of age, adjusting for her prematurity, she was thought to have ‘cerebral palsy’, the prognosis of which was uncertain. At 2 years her language was ‘delayed’, but at 3 she had caught up with speech. She entered school at the usual age but needed special help with mobility, and some extra attention for her learning. Throughout this period from birth to age 6 Jenna's family saw a succession of professionals, received extensive but at times conflicting information and advice, and sought the latest news about therapies from the internet.

How might one approach the ‘rehabilitation’ needs of Jenna and her family? What are realistic goals, and how should they be achieved? What is Jenna's prognosis, and on what evidence is any judgement based?

To understand the ‘rehabilitation’ of children with disabilities professionals need to be familiar with several conceptual underpinnings that distinguish children's needs from those of adults. The purpose of this chapter is to outline and explain these concepts.

Type
Chapter
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Publisher: Cambridge University Press
Print publication year: 2003

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References

Baine, S., Rosenbaum, P. and King, S. (1995). Chronic childhood illnesses: what aspects of caregiving do parents value?Child: Care, Health and Development 21, 291–304Google ScholarPubMed
Breslau, N. (1982). Continuity re-examined: differential impact on satisfaction with medical care for disabled and normal children. Medical Care XX, 347–60CrossRefGoogle Scholar
Breslau, N. and Mortimer, E. A. (1981). Seeing the same doctor: determinants of satisfaction with specialty care for disabled children. Medical Care XIX, 741–57CrossRefGoogle Scholar
Cadman, D., Rosenbaum, P., Boyle, M. and Offord, D. R. (1991). Children with chronic illness: family and parent demographic characteristics and psychosocial adjustment. Pediatrics 87, 884–9Google ScholarPubMed
CanChild: www.fhs.mcmaster.ca/canchild/
Cunningham, C. C., Morgan, P. A. and McGucken, R. B. (1984). Down's syndrome: is dissatisfaction with disclosure of diagnosis inevitable?Developmental Medicine and Child Neurology 26, 33–9CrossRefGoogle ScholarPubMed
Darrah, J., Law, M. and Pollock, N. (2001). Family-centred functional therapy. A choice for children with motor dysfunction. Infants and Young Children 13, 79–87CrossRefGoogle Scholar
Dunst, C., Trivette, C. and Deal, A. (1988). Enabling and Empowering Families – Principles and Guidelines for Practice. Cambridge, MA: Brookline Books
King, G., King, S. and Rosenbaum, P. (1996). Interpersonal aspects of caregiving and client outcomes: a review of the literature. Ambulatory Child Health 2, 151–60Google Scholar
King, G., Law, M., King, S. and Rosenbaum, P. (1998). Parents' and service providers' perceptions of the family-centredness of children's rehabilitation services in Ontario. Physical and Occupational Therapy in Pediatrics 18, 21–40CrossRefGoogle Scholar
King, G., King, S., Rosenbaum, P. and Goffin, R. (1999). Family-centred caregiving and well-being of parents of children with disabilities: linking process with outcome!Journal of Pediatric Psychology 24, 41–52CrossRefGoogle Scholar
King, S., Rosenbaum, P. and King, G. (1996). Parents' perceptions of care-giving: development and validation of a process measure. Developmental Medicine and Child Neurology 38, 757–72CrossRefGoogle Scholar
Law, M., Cooper, B. A., Strong, S. et al. (1996). The person-environment-occupation model: a transactive approach to occupational therapy. Canadian Journal of Occupational Therapy 63, 9–23CrossRefGoogle Scholar
Law, M., Darrah, J., Rosenbaum, P. et al. (1998). Family-centred functional therapy for children with cerebral palsy: an emerging practice model. Physical and Occupational Therapy in Pediatrics 18, 83–102Google Scholar
Law, M., Haight, M., Milroy, B. et al. (1999). Environmental factors affecting the occupations of children with physical disabilities. Journal of Occupational Science 6, 102–10CrossRefGoogle Scholar
Mutch, L., Alberman, E., Hagberg, B. et al. (1992). Cerebral palsy epidemiology: where are we now and where are we going?Developmental Medicine and Child Neurology 34, 547–55CrossRefGoogle ScholarPubMed
Palisano, R., Rosenbaum, P., Walter, S. et al. (1997). Development and validation of a gross motor function classification system for children with cerebral palsy. Developmental Medicine and Child Neurology 39, 214–23CrossRefGoogle Scholar
Palisano, R., Hanna, S., Rosenbaum, P. et al. (2000). Validation of a model of gross motor function for children with cerebral palsy. Physical Therapy 80, 974–85Google ScholarPubMed
Pless, I. B. and Pinkerton, P. (1975). Chronic Childhood Disorder. Promoting Patterns of Adjustment. London: Kimpton
Robards, M. (1994). Running a Team for Disabled Children and their Families. Mac Keith Press. (Distributed by Cambridge University Press.)
Rosenbaum, P. (1988). Children with chronic handicaps: implications for care-giving. In Tonkin, R. S. and Wright, J. R. (Eds.) Redesigning Relationships in Child Health Care, Vol. 2, The Proceedings of a Symposium held February 20–21, 1987, ed. R. S. Tonkin and J. R. Wright, pp. 134–42. Vancouver: British Columbia Children's Hospital
Rosenbaum, P. L. (1997). ‘Alternative’ treatments for children with disabilities: thoughts from the trenches. Paediatrics and Child Health 2, 122–4Google Scholar
Rosenbaum, P., King, S. M. and Cadman, D. (1992). Measuring processes of caregiving to physically disabled children and families. Part I: identifying relevant components of care. Developmental Medicine and Child Neurology 34, 103–14CrossRefGoogle Scholar
Rosenbaum, P., King, S., Law, M. et al. (1998). Family-centred services: a conceptual framework and research review. Physical and Occupational Therapy in Pediatrics 18, 1–20Google Scholar
Stewart, D. (1998). The Transition to Adulthood for Youth with Physical Disabilities: A Qualitative Exploration. MSc Thesis. Hamilton: McMaster University
Taylor, D. C. (1982). The components of sickness: diseases, illnesses and predicaments. In One Child, ed. J. Apley and C. Ounsted, pp. 1–13. London: Heinemann
Sant, A. F. (1991). Neurodevelopmental treatment and pediatric physical therapy: a commentary. Pediatric Physical Therapy 3, 137–41Google Scholar
World Health Organization (2001). International Classification of Impairment, Activity and Participation – ICIDH-2. Geneva: WHO

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