Companions through cancer
Bibliographic Data
| ID | 5083986 |
|---|---|
| Authors | Carol Thomas (0000-0003-4188-9224, Lancaster University), Sara M Morris, Sara Morris (0000-0002-7701-334X, Lancaster University), Juliet C Harman, Juliet Harman (Lancaster University) |
| Year | 2002 |
| Volume | 54 |
| Issue | 4 |
| Pages | 529-544 |
| Publication date | 2002-02-01 |
| 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/s0277-9536(01)00048-x |
| PMID | 11848273 |
| OpenAlex | W1578604245 |
| Language | EN |
| Citations received | 63 |
| References cited | 37 |
Data collection · Feeling · Psychiatry · Psychosocial · Qualitative research · Sample (material · Sociology · Work (physics · Family Support in Illness · Health, psychology, and well-being · Medicine · Mental Health and Patient Involvement · Nursing · Psychology · Social Psychology
When uncertainty becomes guilt
Psycho-Oncology
Perceived Mood, Health, and Burden in Female Mexican American Family Cancer Caregivers
Exploratory and Confirmatory Factor Analysis of the Burden Scale for Family Caregivers-Short Form
Visible body, invisible care
Cancer Communication and Partner Burden
Casas para os que morrem
Cuidador do idoso com câncer avançado
Follow‐up care in cancer
Participatory research with carers
Experiences of family caregivers caring for cancer patients at home
Contributions of a Retreat Weekend to the Healing and Coping of Cancer Patients’ Relatives
Spouses' grief before the patient's death
Is giving receiving? The influence of autonomy on the association between prosocial behavior and well-being
Assignée au déplacement.Vivre un diagnostic de cancer du pancréas en temps de pandémie
Ambiguous diagnosis, futile treatments and temporary recovery
We Have to Be Strong Ourselves”
Caregivers of Individuals with Cancer in the Covid-19 Pandemic
Families and the transition to specialist palliative care
Changes in Emotion Work at Interdisciplinary Conferences Following Clinical Supervision in a Palliative Outpatient Ward
Caregivers' Communication with Patients about Illness and Death
The emotional landscape of accessing and navigating formal supports for older adults in one Western Canadian city
Openness and Avoidance in Couples Communicating About Cancer
Hidden caring, hidden carers? Exploring the experience of carers for people with long‐term conditions
Home-based palliative care in Sydney, Australia
Informal carers of cancer patients
Lifetime Active Care
Patient companions in the Turkish healthcare system
Bereavement outcomes of carers of patients with high grade glioma
Fear of Death, Mortality Communication, and Psychological Distress Among Secular and Religiously Observant Family Caregivers of Terminal Cancer Patients
Reconsidering the term ‘carer’
Baby-boomers and the ‘denaturalisation’ of care-giving in Quebec
Renegotiating Sexuality and Intimacy in the Context of Cancer
My biggest worry now is how my husband is going to cope
Social Opportunity in the Face of Cancer
We need a little strength as well
Masculinity, moralities and being cared for
The caregiving bind
Rhythmanalysis of care
A qualitative analysis of changes in relationship dynamics and roles between people with cancer and their primary informal carer
The Gendered Construction and Experience of Difficulties and Rewards in Cancer Care
Living Well? Strategies Used by Women Living With Metastatic Breast Cancer
The Encounter Between Informal and Professional Care at the End of Life
Comorbid Suffering
Differential patient-caregiver opinions of treatment and care for advanced lung cancer patients
Getting through' not 'going under
A meta-analytic investigation of the relationship between the psychological distress of cancer patients and their carers
Emotion Work during Colorectal Cancer Treatments
The rise of cancer in urban India
Accounts of disruptions to sexuality following cancer
From Home to 'Home
Moral ambivalence and informal care for the dying
The moral cosmology of cancer
Cancer narratives and methodological uncertainties
When they don't die
Always look on the bright side of life
Mealtime emotion work
The end of life and the family
Experiencing chronic widespread pain in a family context
Performingcare
Health information work and the enactment of care in couples and families affected by Multiple Sclerosis
Confidentiality or continuity? Family caregivers' experiences with care for HIV/Aids patients in home-based care in Lesotho
The cancer may come back
Family obligations and social change
Handbook of qualitative research
Living with chronic illness
The European Organization for Research and Treatment of Cancer QLQ-C30
The Hospital Anxiety and Depression Scale
A Labour of Love
Emotions in Social Life
Who Cares Wins? Women, Caring and Disability
The sociology of chronic illness
Informal care and terminal illness
Some Comments on the Sociology of the Emotions
A problem solving intervention for caregivers of cancer patients
Creating a Space for Absent Voices
De-Constructing Concepts of Care
The Concept of Caring in Feminist Research
Men
Medical sociology, chronic illness and the body
Care = organisation + physical labour + emotional labour
The gaze and visibility of the carer
Genetic, Cultural or Socio-economic Vulnerability? Explaining Ethnic Inequalities in Health
Emotion Work, Feeling Rules, and Social Structure
| Unique citing works | 63 |
|---|---|
| Citations per year | 2,52 |
| Citation span | 2001 - 2026 (26) |
| Citation velocity | current |
| Highly cited | No |
| Citation types | Neutral: 62 |