I am not the kind of woman who complains of everything
Illness stories on self and shame in women with chronic pain
Dados Bibliográficos
| ID | 4796893 |
|---|---|
| Autores | Anne Herrmann‐werner (0000-0003-2413-7047, University of Oslo), Anne Werner (0000-0003-1883-4700), Lise Widding Isaksen (0000-0002-6717-2830, University of Bergen), Kirsti Malterud (0000-0001-9556-616X, University of Bergen) |
| Ano | 2004 |
| Volume | 59 |
| Fascículo | 5 |
| Páginas | 1035-1045 |
| Data de publicação | 2004-09-01 |
| Peer Reviewed | Sim |
| Open Access | Sim |
| Tipo | ARTICLE |
| Periódico | Social Science & Medicine (JOURNAL) |
| Identificadores do periódico | ISSN: 0277-9536 • E-ISSN: 1873-5347 |
| Editora | Elsevier BV (PUBLISHER) |
| DOI | 10.1016/j.socscimed.2003.12.001 |
| PMID | 15186903 |
| OpenAlex | W2092127529 |
| Idioma | EN |
| Citações recebidas | 101 |
| Referências citadas | 37 |
Anger · Chronic pain · Credibility · Disgust · Distrust · Epistemology · Narrative · Plot (graphics · Psychiatry · Psychotherapist · Shame · Skepticism · Sociology · Empathy and Medical Education · Mental Health and Psychiatry · Pain Management and Placebo Effect · Psychology · Social Psychology
“Brave Men” and “Emotional Women”
Pain as social representation
Credibility work and moral evaluation at the ED
The Legitimacy of Pain as an Object of Study
Performative public health in Fannie Hurst’s ‘T.B.’ (1915)
Unheard Voices
Living with Sjögren’s Syndrome
The Paradox of Patient Consent
Smerte, visshet og mistillit
L’endométriose, une fabrique genrée de l’ignorance
A Grounded Theory of Credibility Work and Illness
Invisible pain
Explanation for symptoms and biographical repair in a clinic for persistent physical symptoms
Exercising an individualized process of agency in restoring a self and repairing a daily life disrupted by fibromyalgia
Words connecting communities
“I Don’t Claim to Be the World’s Foremost Expert, But . . . ”
I used to dream of lupus as some sort of creature
The social construction of fibromyalgia as a health problem from the perspective of policies, professionals, and patients
‘Move it or lose it’
The social construction of fibromyalgia as a health problem from the perspective of policies, professionals, and patients
Appropriating and asserting power on inflammatory arthritis teams
Between Public Guidelines for User Involvement and Ideals About Free Research
Medication and the patient–doctor relationship
Painful subjects
Making pain social
Agents in time
Chronic pain across clinical settings
Play the Pain
Paying Attention to Women's Ageing Bodies in Recovery From Substance Use
Patients’ Lived Experience in a Multicomponent Intervention for Fibromyalgia Syndrome in Primary Care
Provider Bias in prescribing opioid analgesics
Satisfaction with life in adults with Marfan syndrome (MFS)
Symptoms without disease
Diagnosis
When pain never goes away
Pain communication
Inequality in the Origins and Experiences of Pain
Implementation of integrated care for type 2 diabetes
Restorying the Defendant's Life
Haunting and the ghostly matters of undefined illness
Before narrative
Light-Writing and Photography’s Bodies of Memory
Depletion through Social Reproduction and Contingent Coping in the Lived Experience of Parents on Universal Credit in England
Balancing attendance and disclosure
How do patients and General Practitioners talk about pain and negotiate empathy in consultations? A direct observational study
Temporal Experience Among Women Gynecological Cancer Survivors
Connecting Place to Disease and Gender
Gender Bias in the Perception of Others’ Fatigue
The Meanings of ‘Pain’ in Historical, Social, and Political Context
Women exaggerate, men downplay
Thinking Like a Climate
Pain, Shame, and Power
Disruption foreclosed
Exploring the emotional experiences of young women with chronic pain
Obstetric gaslighting and the denial of mothers' realities
Do type, timing and duration of life course non-employment differentially predict dementia risk? An application of sequence analysis
Conducting dyadic, relational research about endometriosis
An exploratory study of the experience of fibromyalgia diagnosis in South Africa
Re-working biographies
Gender, Body, and Medicine in Urban Ecuador
Just Advil
Contesting misrecognition online
Nothing and Everything
Gendered Portraits of Depression in Swedish Newspapers
Staying Healthy From Fibromyalgia Is Ongoing Hard Work
Living With a Contested, Stigmatized Illness
Moral Economy and Moral Capital in the Community of Clinical Practice
Mothers' Experiences of Supporting Adolescent Children Through Long-Term Treatment for Substance Use Disorder
Embodied Accounts of HIV and Hope
Women's Lived Experiences of Chronic Pain
Studying Narrative-in-Action in Women With Chronic Rheumatic Conditions
It Was Not Me That Was Sick, It Was the Building
Women in Chronic Pain
I just want permission to be ill
Rhetorical work and medical authority
Painful lives
Men's accounts of depression
Contested illness, contested identity
Long Covid - The illness narratives
Credibility work in disenfranchising patient-clinician conversations for Mono/Multiracial women of color with autoimmune disease in the U.S
Working the boundaries of 'whining' - how patients and care professionals make sense of informal complaining practices
Ethnic boundary-making in health care
Disease frames and their consequences for stigma and medical research funds
Even my sister says I'm acting like a crazy to get a check
Different logics of pain
Establishing the (extra)ordinary in chronic widespread pain
Factors facilitating patient satisfaction among women with medically unexplained long-term fatigue
It's not all nice and fun
Maintaining face in the presentation of depression
Embodying occupational overuse syndrome
The dreaded body
This really explains my case
Establishing Self and Meaning in Low Back Pain Narratives
Erasure of the Credible Subject
On Illegitimacy, Suffering and Recognition
Suffering, recognition and reframing
Works of Illness and the Challenges of Social Risk and the Specter of Pain in the Lived Experience of TMD
Resisting medications
The challenge of fitting in
Of butterflies and wolves
Chronic illness – a disruption in life
The Wounded Storyteller
Medicine, Rationality and Experience
Illness as Narrative
Beyond the “Fetishism of Words”
Prenatal Care Use Among Women of Low Income
Telling Sexual Stories
InterViews
Encountering the Continuing Challenges for Women With Chronic Pain
Pain as Human Experience
Beyond Female Masochism
Strategic uses of narrative in the presentation of self and illness
The concept of therapeutic 'emplotment
The Standpoint of Storyteller
Women's Experiences of Stigma in Relation to Chronic Fatigue Syndrome and Fibromyalgia
Chronic back pain sufferers-striving for the sick role
Back pain and the resolution of diagnostic uncertainty in illness narratives
Complaining about chronic pain
Ideal versus reality
Patients' and professionals' understandings of the causes of chronic pain
It is hard work behaving as a credible patient
From Paralysis to Fatigue
Suffering and the Social Construction of Illness
The illness experience
Chronic illness as biographical disruption
Loss of self
Illness and narrative
Vicissitudes of pain and suffering
| Obras citantes distintas | 101 |
|---|---|
| Citações por ano | 4,59 |
| Intervalo de citações | 2004 - 2026 (23) |
| Velocidade de citação | current |
| Altamente citado | Sim |
| Tipos de citação | Neutras: 101 |