Childhood and Disability in the Nordic Countries

Childhood and Disability in the Nordic Countries

Kaup valmöguleikar

This collection provides a comprehensive insight into disabled children and youth in Nordic countries. It seeks to understand the experiences of children from their own perspectives and takes a multidisciplinary approach grounded in the new social studies of childhood and the Nordic relational approach to disability.

Nánar um bókina

Útgefandi
Springer Nature
ISBN
9781137032645
Print ISBN
9781137032638
Format
ePub
Útgáfa
0
Höfundar
Tungumál
English
Útgefið
2015-05-05
Prent takmörkun á líftíma
100
Prent takmörkun
2
Afritunar takmörkun
2

Kaflar

  • Cover Page
  • Title Page
  • Copyright
  • Contents
  • List of Tables
  • List of Figures
  • Foreword
  • Tom Shakespeare
  • Acknowledgements
  • Notes on Contributors
  • Introduction: Disabled Children and Youth in the Nordic Countries
  • Snæfrídur Thóra Egilson, Borgunn Ytterhus, Rannveig Traustadóttir and Berit Berg
  • Why this book?
  • Theoretical foundations
  • Nordic welfare and disability policies
  • Organisation and content of the book
  • Note
  • References
  • Part I: Theories and History
  • 1 Perspectives on Childhood and Disability
  • Borgunn Ytterhus, Snæfrídur Thóra Egilson, Rannveig Traustadóttir and Berit Berg
  • Theoretical and conceptual underpinnings
  • Disabled children’s perspectives and experiences
  • Future directions
  • References
  • 2 Disabled Children and Welfare Policy in the Nordic Countries: Historical Notes
  • Jan Tøssebro
  • Two fundamental changes
  • Three discourses
  • After normalization – trends from the 1970s to the 1990s and beyond
  • References
  • 3 Inclusion, Diagnostics, and Diversity: Ethical Considerations
  • Simo Vehmas
  • Introduction
  • Disability as an ethical and political issue
  • Capabilities and inclusion
  • Diagnostics, medicalization, and moral responsibility
  • Conclusion
  • References
  • Part II: Identity and Images
  • 4 ‘I Am Different, But I’m Like Everyone Else’: The Dynamics of Disability Identity
  • Anders Gustavsson and Catarina Nyberg
  • Disability and identity – from dichotomies to dynamics
  • The family and ‘the first generation of integration’ in Sweden
  • Taking the normalization and integration policy seriously
  • The family as a supportive space for positive self-identifications
  • Multiple identifications
  • Sven’s self-identifications
  • Positive self-identifications
  • Normal, but thinks in a different way
  • Explaining, proving and defending self-identifications
  • Multiplicity, fluidity and continuity
  • The dynamics of disability identity
  • Notes
  • References
  • 5 Childhood Disability, Identity and the Body
  • Eiríkur Smith and Rannveig Traustadóttir
  • Identity and the body
  • The research
  • Childhood disability
  • Entering the teenage years
  • Experiencing differentiation
  • Embodied obstacles and explorations
  • Conclusion
  • References
  • 6 Ethnicity, Disability, and Identity
  • Anna M. Kittelsaa
  • Introduction
  • The study: immigrant families with disabled children in Norway
  • Parents’ narratives about identity
  • Individual identity and disability
  • Identifying children with severe impairments
  • Ethnic identity and disability
  • The importance of belonging to a family
  • Professional narratives
  • Professionals’ narratives about identity and disability
  • Professionals’ narratives about ethnicity
  • Conclusion
  • References
  • 7 Cultural Representation of Disability in Children’s Literature
  • Hanna Björg Sigurjónsdóttir
  • Icelandic folk tales
  • Translated fairy tales and fantasy literature
  • Classic children’s books
  • More realistic books
  • Discussion: images of disability
  • References
  • Children’s books
  • Part III: Interaction and Inclusion
  • 8 Social Inclusion as a Theoretical Concept and a Social Practice
  • Karin Barron
  • Introduction
  • The emergence of ‘social inclusion’ as a significant concept
  • A question of power
  • Claiming social inclusion on one’s own terms
  • All the children contributing
  • Playing alone, but not necessarily lonely
  • The complexity of identity
  • Gendered pathways
  • Interests and gendered agency
  • References
  • 9 Does One Size Fit All? Physical Placement, Organizational Structure, and Parental Satisfaction in Norwegian Day Care Centres
  • Borgunn Ytterhus
  • Introduction
  • Nordic welfare and day care for children
  • Data and analysis
  • Major political changes – few empirical changes
  • What characterizes the day care centres where parents and staff are most satisfied?
  • Discussion
  • Note
  • References
  • 10 Trendsetters and Followers: Disabled Young People’s Computer Use during Leisure Time
  • Helena Hemmingsson
  • The digital generation
  • Information Communication Technology and impairments
  • The digital divide
  • Surveying young people’s media habits
  • Young people’s use of ICT in 2006
  • Different views on the results
  • Trendsetters and followers
  • In search of explanations
  • Concluding remarks
  • Note
  • References
  • 11 A Comparison of Social Life among 11-Year-Old Disabled Children and 11-Year-Olds in General
  • Maria Lomborg Røgeskov, Helle Hansen and Steen Bengtsson
  • Children’s development and social relations
  • Method
  • Disabled children
  • Social life outside school
  • School and social life
  • Bullying
  • Friendship and peer relations
  • Conclusions and perspectives
  • Notes
  • References
  • Part IV: Families and Services
  • 12 Ordinary or Not? Families of Children Growing Up with Disabilities
  • Jan Tøssebro and Christian Wendelborg
  • Ordinary families?
  • Family experiences with the service system
  • Conclusions
  • References
  • 13 Immigrant Families with Disabled Children in Norway
  • Berit Berg
  • Introduction
  • The study: immigrant families with disabled children in Norway
  • Survey methods and ethical considerations
  • Family attitudes towards disability
  • Sameness and differences
  • Stereotypes, misunderstandings, and myths
  • Interactions with the service system
  • A demanding situation
  • Conclusion
  • Note
  • References
  • 14 User Perspectives on Support Services to Disabled Children and Their Families
  • Snæfrídur Thóra Egilson
  • Eliciting family perspectives and priorities
  • Measuring processes of care
  • What parents think and want
  • Children’s and adolescents’ views
  • Discussion and implications
  • References
  • Concluding Remarks
  • Borgunn Ytterhus, Snæfrídur Thóra Egilson, Rannveig Traustadóttir and Berit Berg
  • Increased emphasis on disabled children
  • Importance of families
  • Human rights perspectives
  • Social inclusion and exclusion
  • Future challenges of the Nordic welfare states
  • References
  • Index