The Palgrave Handbook of Disabled Children’s Childhood Studies 1st Edition – Ebook Instant Download/Delivery ISBN(s): 9781137544452,9781137544469,1137544457,1137544465
Product details:
- ISBN-10 : 1137544465
- ISBN-13 : 9781137544469
- Author: Katherine Runswick-Cole,Tillie Curran , Kirsty Liddiard
Disabled children’s lives have often been discussed through medical concepts of disability rather than concepts of childhood. Western understandings of childhood have defined disabled children against child development ‘norms’ and have provided the rationale for segregated or ‘special’ welfare and education provision. In contrast, disabled children’s childhood studies begins with the view that studies of children’s impairment are not studies of their childhoods. Disabled children’s childhood studies demands ethical research practices that position disabled children and young people at the centre of the inquiry outside of the shadow of perceived ‘norms’.
Table contents:
1. Part I
Part Frontmatter
The Texting Project
The Tree of Participation: Our Thoughts About Growing a Culture of Participation Between Young People, Parents and Health Team Staff
“What Can I Say?”
The Heaviest Burdens and Life’s Most Intense Fulfilment: A Retrospective and Re-understanding of My Experiences with Childhood Liver Disease and Transplantation
My Sister, My World: From Second Mum to Nurse
Being a Disabled Woman and Mum: My Journey from Childhood
Going ‘Off Grid’: A Mother’s Account of Refusing Disability
2. Part II
Part Frontmatter
The Social Relational Model of Deaf Childhood in Action
‘The Embodiment of Disabled Children and Young People’s Voices About Participating in Recreational Activities’: Shared Perspectives
Making Space for the Embodied Participation of Young Disabled Children in a Children’s Centre in England
Interrogating the ‘Normal’ in the ‘Inclusive’ Early Childhood Classroom: Silence, Taboo and the ‘Elephant in the Room’
The Kids Are Alright: They Have Been Included for Years
Expressive Eyebrows and Beautiful Bubbles: Playfulness and Children with Profound Impairments
My Friends and Me: Friendship and Identity Following Acquired Brain Injury in Young People
Thinking and Doing Consent and Advocacy in Disabled Children’s Childhood Studies Research
3. Part III
Part Frontmatter
The ‘Disability Commons’: Re-thinking Mothering Through Disability
Intersectionality Theory in Research with the Fathers of Children with the Label of Autism
The Construction of Life Trajectories: Reflections, Research and Resolutions for Young People with Behavioural Disabilities
Personalisation Policy and Parents: The Formalisation of Family Care for Adult Children with Learning Disabilities in England
4. Part IV
Part Frontmatter
Anonymity, Confidentiality and Informed Consent: Exploring Ethical Quandaries and Dilemmas in Research with and About Disabled Children’s Childhoods
Supporting Families in Raising Disabled Children to Enhance African Child Development
Normalcy, Intersectionality and Ableism: Teaching About and Around ‘Inclusion’ to Future Educators
“Just Sumaira: Not Her, Them or It”
5. Part V
Part Frontmatter
What’s Wrong with ‘Special’? Thinking Differently in New Zealand Teacher Education About Disabled Children and Their Lives
A Diversity of Childhoods: Considering the Looked After Childhood
A Relational Understanding of Language Impairment: Children’s Experiences in the Context of Their Social Worlds
Resilience in the Lives of Disabled Children: A Many Splendoured Thing
Growing Up Disabled: Impairment, Familial Relationships and Identity
Autistic Development, Trauma and Personhood: Beyond the Frame of the Neoliberal Individual
6. Part VI
Part Frontmatter
Making Policy for Whom? The Significance of the ‘Psychoanalytic Medical Humanities’ for Policy and Practice That Affects the Lives of Disabled Children
Disabled Children’s Childhood Studies and Leadership as Experts by Experience’ Leadership: Learning Activism in Health and Social Care Education
Being a Speech and Language Therapist Speech and Language Therapy : Between Support and Oppression
“You Say… I Hear…”: Epistemic Gaps in Practitioner-Parent/Carer Talk
Disabled Children in Out-of-Home Care: Issues and Challenges for Practice
Easy Targets: Seen and Not Heard—The Silencing and Invisibility of Disabled Children and Parents in Post-Reform Aotearoa New Zealand
Family Voices in Teacher Education
Rights Not Needs: Changing the Legal Model for Special Educational Needs (SEN)
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