We're tired, not sad
Benefits and burdens of mothering a child with a disability
Bibliographic Data
| ID | 4600992 |
|---|---|
| Authors | Sara Eleanor Green (University of South Florida, corresponding author) |
| Year | 2007 |
| Volume | 64 |
| Issue | 1 |
| Pages | 150-163 |
| Publication date | 2007-01-01 |
| Peer Reviewed | Yes |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | Social Science & Medicine (JOURNAL) |
| Journal identifiers | ISSN: 0277-9536 • E-ISSN: 1873-5347 |
| Publisher | Elsevier BV (PUBLISHER) |
| DOI | 10.1016/j.socscimed.2006.08.025 |
| PMID | 17014946 |
| OpenAlex | W2084874157 |
| Language | EN |
| Citations received | 115 |
| References cited | 41 |
Caregiver burden · Developmental psychology · Distress · Political science · Poverty · Psychiatry · Stigma (botany · Clinical Psychology · Disability Rights and Representation · Family and Disability Support Research · Family Support in Illness · Medicine · Psychology
Una noción triádica
Extreme Caregiving
Disabilities and DevelopmentPreparation of this chapter was partially supported by grant R40 MC08956 from the Maternal and Child Health Bureau (Title V, Social Security Act), Health Resources and Services Administration, U.S. Department of Health and Human Services.
Hard Labor
Grounded theory, mixed methods, and action research
Affiliate Stigma Among Caregivers of People with Intellectual Disability or Mental Illness
The quality of life of parents of children with autism spectrum disorder
Teenage wheelchair users experience multiple geographies of waiting
Satysfakcja i wymagania w roli matki i ojca dziecka z niepełnosprawnością
Experiences of Parents as Caregivers for Children Diagnosed With Mild Intellectual Disability
Reframing Parental Caregiving for Individuals With Developmental Disabilities Through a Life Course Care Stress Model
The mothering/scholaring self
Parents of children with special educational needs’ shared work in fully online learning
‘Everything is there, but they don't bring it to your front door … ’ An analysis of the perception of early childcare by parents of children with disabilities
The Rare Life
Health literacy among children living with a long-term condition
Activism, Growth, and Empowerment of Israeli Parents of Children With Disabilities
“It is important that we also remain a person ourselves”
Identifying the Impacts, Obstacles and Information Barriers for Parents of Children Living With Genetic Neurodevelopmental Disorders
Parents' experiences of living with a child with a long‐term condition
Parents' experiences of parenting a child with profound intellectual and multiple disabilities in France
Components of perceived stigma and perceptions of well-being among university students with and without disability experience
Care-giving experiences of parents of young people with PMLD and complex healthcare needs in the transition to adulthood years
Taking care
Congenital zika syndrome and family impacts
Síndrome congênita do zika e impactos para as famílias
It’s Like I Have an Advantage in All This
Tactics and Strategies of Family Adaptation among Parents Caring for Children and Youth with Developmental Disabilities
Understanding Maternal Role in Caring for Children with Severe Cognitive Impairment in Paediatric Palliative Care
Gender Differences in Caring for Children with Genetic or Rare Diseases
Perceptions of caring for children with disabilities
Needs of families of children with intellectual and developmental disabilities in Addis Ababa
Living with disabled children in Malawi
Anxiety, Stress, and Resilience Strategies in Parents of Children with Typical and Late Psychosocial Development
Health-Related Quality of Life and Related Factors among Primary Caregivers of Children with Disabilities in Shanghai, China
Being a Parent of Children with Disabilities during the Covid-19 Pandemic
Quality of Life, Needs and Fears of Mothers of Children with Disabilities in Saudi Arabia during the Covid-19 Lockdown
Children with Developmental Disabilities in Low- and Middle-Income Countries
Caregiver Burden and Preventive Dental Care Use for US Children with Special Health Care Needs
Mothering children with developmental disabilities
An Ecological Approach to Reducing the Social Isolation of People With an Intellectual Disability
Appréhender l’invisible
Looking at Life through a Different Window
Disadvantage, discrimination, and despair
Contenu et utilité d’un forum de discussion sur Internet destiné aux parents d’enfants autistes
Who Is Willing to Foster Children With Disabilities
The impact of disablism on the psycho-emotional well-being of families with a child with impairment
Everyday travel for families with children using wheelchairs
Not a nurse but more than a mother
Becoming the mother of a child with disabilities
A powerful glimpse from across the table
Power together”
Recurrent grief in mothering a child with an intellectual disability to adulthood
Hope and subjective well‐being among parents of children with special needs
Social determinants of state variation in special education participation among preschoolers with developmental delays and disabilities
Understanding the parental experiences of raising deaf children in Ghana
Redefining parenting among parents of children with profound intellectual and multiple disabilities in Poland
Negotiating the normative
Caregiving and quality of life
Parental Experiences of Engaging With the National Disability Insurance Scheme for Their Children
Parent Advocacy” as an Ideological Code
The changing face of the ‘good mother’
Public health policy and social support for immigrant mothers raising disabled children in Canada
This is real now because it’s a piece of paper’
Raising a child with a disability
Caregiving mothers of children with impairments
Negotiating work and care in Chinese families of children with autism
Representations of mothers having children with disability in Hindi cinema
We create our own small world’
Benefit-finding or finding benefits? The positive impact of having a disabled child
Mother of a person
It takes a sister
Social class, disability, and institutional interactions
Fighting the odds
I am because I have to be
Partnership in practice
The effect of caregiving on women in families with Duchenne/Becker muscular dystrophy
Maintaining exceptionality
Prenatal Genetic Screening, Epistemic Justice, and Reproductive Autonomy
Transitioning to University with a Mental Illness
It's not really Michael who wears me out, it's the system’
It's Really a Roller Coaster”
Grandchildren Caring for Grandparents
Narratives of single, black mothers using cultural capital to access autism interventions in schools
Forms of Capital in Navigating Health and Welfare Services for Disabled Children
Being a ‘good’ mother
Everyday activisms
Narratives on the Autism Journey
Improving the Likelihood of Positive Outcomes for Survivors of Sexual Violence, Considering Intersections Between Justice, Gender, and Trauma
Repercussões do nascimento e do cuidado de crianças com deficiência múltipla na família
A personal geography of care and disability
We were on our own
Disability stigma resistance by parents at the intersection of psychosocial and structural levels
"My child is my job now" - Care, work and careers of mothers with disabled children in the Norwegian welfare state
I'm not a saint
A consideration of medicalisation
Children's bullying victimization and maternal suicidal ideation among multicultural families in South Korea
Perceived discrimination among caregivers of children with disabilities in China
Is caring associated with an increased risk of mortality? A longitudinal study
Complexity
Causal attribution, perceived benefits, and morbidity after a heart attack
Parents of Children with Disabilities
Prospective Patterns of Resilience and Maladjustment During Widowhood.
Positive aspects of caregiving
Handbook of Disability Studies
The Politics of Disablement
Positive Aspects of Critical Life Problems
Where Are the Children's Experiences? Analysing Social and Cultural Exclusion in 'Special' and 'Mainstream' Schools
Perceived burden among caregivers of adults with serious mental illness
Age and family burden among parents of offspring with severe mental illness
Ethnicity, social status, and families' experiences of caring for a mentally ill family member
Interpretive Ethnography
A Modified Labeling Theory Approach to Mental Disorders
What do you mean 'what's wrong with her
Emplotting children's lives
Mothering children who have disabilities
The impact of stigma on maternal attitudes toward placement of children with disabilities in residential care facilities
Does It Hurt to Care? Caregiving, Work-Family Conflict, and Midlife Well-Being
Minority Stress and Mental Health in Gay Men
Caregiving as Reciprocal Exchange in Families with Seriously Mentally Ill Members
Ethnic Differences in Caregiving Duties and Burdens Among Parents and Siblings of Persons with Severe Mental Illnesses
The Consequences of Caring
Mothers Who Care
Living Stigma
Attitudes Toward Control in Uncontrollable Situations
Oh, those therapists will become your best friends
| Unique citing works | 115 |
|---|---|
| Citations per year | 6,05 |
| Citation span | 2007 - 2026 (20) |
| Citation velocity | current |
| Highly cited | Yes |
| Citation types | Neutral: 114 |