I Value What You have to Say'. Seeking the Perspective of Children with a Disability, Not Just their Parents
Datos Bibliográficos
| ID | 12312002 |
|---|---|
| Autores | Belinda Garth (0000-0003-3937-4790, La Trobe University, autor de correspondencia), Rosalie Aroni (0000-0003-2945-0403, La Trobe University) |
| Año | 2003 |
| Volumen | 18 |
| Número | 5 |
| Páginas | 561-576 |
| Fecha de publicación | 2003-08-01 |
| Peer Reviewed | Sí |
| Open Access | No |
| Tipo | ARTICLE |
| Revista | Disability & Society (JOURNAL) |
| Identificadores de la revista | ISSN: 0968-7599 • E-ISSN: 1360-0508 |
| Editorial | Taylor & Francis (PUBLISHER • GB) |
| DOI | 10.1080/0968759032000097825 |
| OpenAlex | W1981578409 |
| Idioma | EN |
| Citas recibidas | 18 |
| Referencias citadas | 41 |
The UN Convention on the Rights of the Child acknowledges the right for children to express opinions about issues affecting them and the right to have these views heard (Davis, 1998). There has been an increase in the number of international studies including children as informants in research, but there is noticeably less published research including children as informants in Australia if they have a disability. Rather, there has been a reliance on parents/carers for insight into their child's experiences. In this article we present the results of a qualitative pilot study where we interviewed parents and their children who have cerebral palsy about their perceptions and experiences of communication in the medical consultation. We found that the views of children and parents were different, further reiterating the need to seek the perceptions of children as well as their parents
Cerebral palsy · Developmental psychology · Perception · Perspective (graphical · Psychiatry · Qualitative research · Social science · Sociology · Value (mathematics · Children's Rights and Participation · Ethics and Legal Issues in Pediatric Healthcare · Family and Disability Support Research · Psychology
‘I Do Often Feel Like We Were Given a Magic Wand’ – Children's and Families’ Experiences of Allied Health Services for Developmental and Disability Needs in Rural and/or Remote South Australia
The impact of Covid-19 on secondary school Students
Portraying people with disability in Indonesian online news reports
Communicating with disabled children when inpatients
Saving Delaney … by white privilege
Disability-based inequity in youth subjective well-being
Speaking Softly and Listening Hard
What is Important to Young Children Who Have Cancer While in Hospital
Being an ordinary kid’ – demands of everyday life when labelled with disability
The potential of the fractions of lifeworld for inclusive qualitative inquiry in the third space
Inclusion of children with disabilities in mainstream child development research
Factors that influence elementary school teachers’ attitudes towards inclusion of visually impaired children in Turkey
Facilitating and hindering factors in the realization of disabled children’s agency in institutional contexts
Representations of disabled children and young people in Irish newspapers
I want support, not comments’
Photo Elicitation Interview (PEI)
Disability and Deleuze
Troubling power dynamics
Doctor–parent–child communication. A (re)view of the literature
Researching Children'S Perspectives
Independent Living and the Medical Model of Disability
The ethics of participatory research with children
The Ethics of Social Research with Children
Understanding the meanings of children
The Ethics of Social Research with Children
Methodological aspects of collecting data from children
Did You See That Guy in the Wheelchair Down the Pub?’ Interactions across Difference in a Public Place
A Qualitative Study of the Perceptions of Individuals with Disabilities Concerning Health and Rehabilitation Professionals
Refocusing on the Parent
The Social Experiences of Children with Disability and the Influence of Environment
Consulting the Children
Disabled People, Health Professionals and the Social Model of Disability
Learning to Partner, Disabling Conflict
Handbook of Qualitative Research
Interactive Frames and Knowledge Schemas in Interaction
Quality in services for disabled children and their families
Learning Difficulties', the Social Model of Disability and Impairment
Communicative styles and adaptations in physician-parent consultations
Models of disablement, universalism and the international classification of impairments, disabilities and handicaps
The doctor-patient relationship and the management of asthma
Looking means listening
First diagnosis of severe mental handicap
Medical professionals and parents
International Journal of Sociology of the Family
| Obras citantes distintas | 18 |
|---|---|
| Citas por año | 0,9 |
| Intervalo de citas | 2006 - 2026 (21) |
| Velocidad de citación | current |
| Altamente citado | No |
| Tipos de cita | Neutras: 17 |