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Experiencing Chronic Illness
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Items 101–200 of 344
Transient ischaemic attack: a qualitative study of the long term consequences for patients
Croot, E. J., Ryan, T., Read, J., et al. (2014) · BMC Family Practice · doi:10.1186/s12875-014-0174-9 · Cited by 24
“The use of narratives to understand the individual experience of health, healthcare and rehabilitation has a long history [16-19].”
BackgroundSalway, S., Platt, L., Harriss, K., & Chowbey, P. (2007) · Sociology of Health & Illness · doi:10.1111/j.1467-9566.2007.01044.x · Cited by 24
Zhou, T., Yi, C., Zhang, X., & Wang, Y. (2014) · Family Process · doi:10.1111/famp.12099 · Cited by 23
“Secondly, as previous research suggests, chronic illness sometimes relates with experience of shame and social stigma (Bury, 1982; Charmaz, 2000; Crandall & Moriarty, 1995; Joachim & Acorn, 2000).”
Shneider, C. E., Robbertz, A. S., & Cohen, L. L. (2023) · Journal of Clinical Psychology in Medical Settings · doi:10.1007/s10880-023-09973-1 · Cited by 25
“In the context of a chronic illness, Charmaz (2000) theo-rized that it is adaptive for individuals to integrate or incorporate their illness into their sense of self, which requires the individual to merge the concept of the illness and the self.”
Self‐Structure, Identity, and Commitment: Promise Keepers’ Godly Man Project
Armato, M., & Marsiglio, W. (2002) · Symbolic Interaction · doi:10.1525/si.2002.25.1.41 · Cited by 22
Brokerhof, I. M., Ybema, J. F., & Bal, P. M. (2020) · PLoS ONE · doi:10.1371/journal.pone.0228581 · Cited by 22
COMMISSARIAT, P. V., Laffel, L. M., & Gonzalez, J. S. (2019) · Pediatric Diabetes · doi:10.1111/pedi.12932 · Cited by 21
“In “Stigma and Stigma Control,” the person must learn how to manage actual and perceived stigma surrounding their illness.(16) We hypothesize that teens and young adults with T1D who are less successful with these processes of identity change, and instead resist allowing their illness to become part of their sense of…”
BackgroundFrom ‘Gibbering Idiot’ to ‘Iceman’, Kenny's Story: A Critical Analysis of an Occupational Narrative
Finlay, L. (2004) · British Journal of Occupational Therapy · doi:10.1177/030802260406701102 · Cited by 21
Biographical disruption of injured workers in chronic pain
Soklaridis, S., Cartmill, C., & Cassidy, D. (2011) · Disability and Rehabilitation · doi:10.3109/09638288.2011.573056 · Cited by 20
“Other studies have shown that individuals with chronic conditions actively negotiate their roles when interacting with health care professionals and other workplace parties; manage illness and stigma in everyday life; try and regain continuity in their disrupted lives and sometimes become innovators by building new me…”
BackgroundJones, I. R., Ahmed, N., Kelly, M. J., Bothamley, G. H., Rajakulasingam, R. K., Victor, C. R., O’Malley, A., & Griffiths, C. J. (2007) · Social Science & Medicine · doi:10.1016/j.socscimed.2007.09.012 · Cited by 20
“and group identities (Bury, 2001; Charmaz, 2000).”
Caregivers’ Interpretations of Time and Biography
Barken, R. (2014) · Journal of Contemporary Ethnography · doi:10.1177/0891241613514999 · Cited by 23
Illness Narratives of African Americans Living With Coronary Heart Disease
Dubbin, L., McLemore, M. R., & Shim, J. K. (2017) · Qualitative Health Research · doi:10.1177/1049732316645319 · Cited by 13
“Such explorations are important as they provide opportunities for an in-depth understanding of a broad range of micro-, meso-, and macro-contextual factors that influence how people live with chronic disease (Charmaz, 2000; Lawton, 2003).”
BackgroundMediation analysis of relationships between chronic inflammation and quality of life in older adults
Nowakowski, A. C. H., Graves, K. Y., & Sumerau, J. E. (2016) · Health and Quality of Life Outcomes · doi:10.1186/s12955-016-0452-4 · Cited by 20
Illness action rediscovered: a case study of upper limb pain
Calnan, M., Wainwright, D. W., O’Neill, C., Winterbottom, A., & Watkins, C. (2007) · Sociology of Health & Illness · doi:10.1111/j.1467-9566.2007.00543.x · Cited by 20
“This is surprising, given the sizeable theoretical and empirical literature on the illness experience of those with chronic illness (Charmaz 2000).”
BackgroundRetractedNiall, F., & Finlay, L. (2008) · International Journal of Qualitative Studies on Health and Well-Being · doi:10.1080/17482620802130407 · Cited by 19
“People with disability often strive to maintain ‘‘normal’’ functioning by minimizing and disguising their problems*a point picked up by several commentators (for example, Charmaz, 2000; French, 1993).”
BackgroundPrevalence of Colorectal Cancer Screening Among a Multimorbid Rural Appalachian Population
Fleming, S. T., Schoenberg, N. E., Tarasenko, Y. N., et al. (2011) · Southern Medical Journal · doi:10.1097/smj.0b013e31823a8879 · Cited by 18
Experiences of apathy in people with Parkinson’s disease: a qualitative exploration
Simpson, J., McMillan, H., Leroi, I., & Murray, C. D. (2014) · Disability and Rehabilitation · doi:10.3109/09638288.2014.939771 · Cited by 19
“It also resonates with Kathy Charmaz’s [75] work on the loss of self in people with chronic illness and participants’ explanations of apathy could also be seen as an attempt to sustain the self against the multiple attacks on it provoked both by their illness and society’s stigmatising and often unhelpful approach to…”
BackgroundRydstad, M., Schult, M., & Löfgren, M. (2010) · Disability and Rehabilitation · doi:10.3109/09638281003734425 · Cited by 18
“Stigma is common among people with chronic illness [18], rendering them more vulnerable to negative social identification from their surroundings and themselves.”
BackgroundInfluentialHope is a four‐letter word: riding the emotional rollercoaster of illness management
Nowakowski, A. C. H. (2016) · Sociology of Health & Illness · doi:10.1111/1467-9566.12403 · Cited by 19
“…I explore the things that have followed since those days – the progressive grind of ‘good days and bad days’ involved in achieving illness management (Charmaz 2000), and the cycle of ‘hope and despair’ that characterises the quotidian experience of living with painful chronic conditions (Corbett…”
BackgroundInfluentialChronic Illness, Self-management and the Rhetoric of Empowerment
Bury, M. (2010) · Palgrave Macmillan UK eBooks · doi:10.1057/9780230297432_9 · Cited by 18
The mother–daughter guilt dynamic: effects of type 1 diabetes during life transitions
Rasmussen, B., Dunning, T. L., Cox, H., & O'Connell, B. O. (2008) · Journal of Clinical Nursing · doi:10.1111/j.1365-2702.2008.02342.x · Cited by 17
“Charmaz (2000a) argued that fear, guilt and shame comprise stigma.”
BackgroundBetween unemployment and employment: Experience of unemployed long-term pain sufferers
Glavare, M., Löfgren, M., & Schult, M. (2012) · Work · doi:10.3233/wor-2012-1394 · Cited by 16
“Their different strategies range from avoiding social contact to innovating new ways to do things [36].”
InfluentialLiving with a pituitary tumour: A narrative analysis
Simpson, J., Heath, J., & Wall, G. (2013) · Psychology and Health · doi:10.1080/08870446.2013.840784 · Cited by 16
“The use of a celebrity comparison could therefore be seen as an attempt by participants to reduce or manage their feelings of stigma and redress their feelings of shame and inadequacy (Charmaz, 2000).”
BackgroundExploring the Sexual Development Experiences of Black Bisexual Male Adolescents Over Time
Morgan, A. R., Saunders, B., Dodge, B., Harper, G. W., & Arrington‐Sanders, R. (2018) · Archives of Sexual Behavior · doi:10.1007/s10508-017-1084-4 · Cited by 19
Collin, J. (2004) · Anthropologie et Sociétés · doi:10.7202/007449ar · Cited by 16
“Il faut en outre repenser l’organisation des structures qui encadrent le rapport social et instrumental au quotidien (Charmaz 2000 ; Kirchgassker et Matt 1987).”
BackgroundStoller, E. P., Grzywacz, J. G., Quandt, S. A., Bell, R. A., Chapman, C., Altizer, K. P., & Arcury, T. A. (2011) · Journal of Aging and Health · doi:10.1177/0898264310397045 · Cited by 15
“Over time, people develop and elaborate strategies for managing illness, becoming very knowledgeable about the treatment regimens that work best for them (Charmaz, 2000; Haug, 1986).”
Background“A Shrinking Kind of Life”: Gay Men’s Experience of Aging With HIV
Masten, J. (2015) · Journal of Gerontological Social Work · doi:10.1080/01634372.2015.1005786 · Cited by 14
“…the development of axial codes, middle-range theories that influence both the development of theory and the analysis of codes; memo making, writing analytic notes to explicate and fill out categories; theoretical sampling, and delay of the literature review (Charmaz, 1999; Glaser & Strauss, 1965).”
BackgroundDating, Marriage, and Parenthood for HIV-Positive Heterosexual Puerto Rican Men
Sastre, F., Sheehan, D. M., & Gonzalez, A. (2014) · American Journal of Men s Health · doi:10.1177/1557988314532940 · Cited by 14
“A chronic illness disrupts an individual’s everyday life (Charmaz, 2000; Conrad, 1987; see also Bury, 1982).”
BackgroundVenuleo, C., & Marinaci, T. (2017) · Journal of Gambling Issues · doi:10.4309/jgi.2017.36.7 · Cited by 16
“Because gambling is conceived as a chronic illness, gamblers will need the instrumental and affective help of the other members and relatives forever because their chronic illness, unlike an acute illness, lasts (Charmaz, 2000).”
Background‘Chronic’ identities in mental illness
von Peter, S. (2013) · Anthropology and Medicine · doi:10.1080/13648470.2013.772493 · Cited by 13
Markovic, G., Bartfai, A., Ekholm, J., Nilsson, C., Schult, M., & Löfgren, M. (2018) · Neuropsychological Rehabilitation · doi:10.1080/09602011.2018.1482770 · Cited by 14
Perceived HIV Risk Among Black MSM Who Maintain HIV-Negativity in New York City
Dācus, J.-D., & Sandfort, T. G. M. (2020) · AIDS and Behavior · doi:10.1007/s10461-020-02852-y · Cited by 12
“In the interviews we aimed to explore their maintained HIV-negativity in temporal, cultural, and structural contexts by following the constructivist grounded method [29].”
MethodKalhovde, A. M., Elstad, I., & Talseth, A. (2014) · International Journal of Qualitative Studies on Health and Well-Being · doi:10.3402/qhw.v9.23069 · Cited by 12
The Chronic Sick Role: Its Time Has Come
Schipke, T. (2019) · OMEGA - Journal of Death and Dying · doi:10.1177/0030222819852848 · Cited by 12
“A recurrent and predominant theme of her work is that chronic illness, like the end-of-life dying process, can render self and social identity highly problematic (Charmaz, 1993, 1994, 1995, 2000, 2002a, 2002b, 2006).”
BackgroundNowakowski, A. C. H. (2016) · The Qualitative Report · doi:10.46743/2160-3715/2016.2296 · Cited by 12
Roderick, M. (2003) · Leicester Research Archive (University of Leicester) · Cited by 12
The paradox of haemodialysis: the lived experience of the clocked treatment of chronic illness
Cluley, V., Burton, J. O., Hull, K. L., & Eborall, H. (2024) · Health Sociology Review · doi:10.1080/14461242.2024.2319189 · Cited by 12
“…regarding it as: long lasting (WHO, 2022); lasting for a year or longer (NICE, 2015); ongoing and requiring management and treatment over a long period (NHS, 2023); long term and a potentially permanent event in a person’s life (Bury, 1991); or involving plateaus and progression (Charmaz, 2000).”
BackgroundCOME ALONG WITH ME: LINKING LGBTQ YOUTH TO SUPPORTIVE RESOURCES
Wolowic, J., Sullivan, R., Valdez, C. A. B., et al. (2018) · International Journal of Child Youth and Family Studies · doi:10.18357/ijcyfs93201818274 · Cited by 11
“The subset of quotes initially identified as “bridges” were then analyzed further following the second stage of the constant comparison analytic process by the coauthors of the paper (Charmaz, 2000; Glaser, Straus, & Strutzel, 1968).”
MethodRationing health care to disabled people
Albrecht, G. L. (2001) · Sociology of Health & Illness · doi:10.1111/1467-9566.00270 · Cited by 11
The Handbook of Wellness Medicine
Snellings, J. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108650182 · Cited by 11
Hellem, E., & Bruusgaard, K. A. (2018) · Physiotherapy Theory and Practice · doi:10.1080/09593985.2018.1550829 · Cited by 10
Stigma Stories: Rhetoric, Lived Experience, and Chronic Illness
Kessler, M. M. (2022) · Ohio State University Press eBooks · doi:10.26818/9780814214916 · Cited by 13
An Ethical Framework for Outcome Assessment in Psychiatric DBS
Woopen, C., Timmermann, L., & Kuhn, J. (2012) · AJOB Neuroscience · doi:10.1080/21507740.2011.635631 · Cited by 9
Remnant, J. (2019) · Social Science & Medicine · doi:10.1016/j.socscimed.2019.112447 · Cited by 9
A Dutch Study of Remarkable Recoveries After Prayer: How to Deal with Uncertainties of Explanation
Bendien, E., Kruijthoff, D. J., van der Kooi, C., Glas, G., & Abma, T. (2023) · Journal of Religion and Health · doi:10.1007/s10943-023-01750-6 · Cited by 11
“In that respect their experience is not different from that of any other patient with a diagnosis of a chronic illness (Charmaz, 2000).”
BackgroundHunhammar, C., Nilsson-Wikmar, L. B., & Löfgren, M. (2009) · Journal of Rehabilitation Medicine · doi:10.2340/16501977-0421 · Cited by 9
Asthma self-management: What do we really mean?
Aron, R., r, S. S., n, M. A., t, K. S., Fidalgo Robson, N., n, D. G., & S., J. (2003) · Australian Journal of Primary Health · doi:10.1071/py03018 · Cited by 9
Nettleton, S. (2009) · doi:10.1002/9781444314786.ch3 · Cited by 9
The dement in the community: Social work practice with people with dementia revisited
Manthorpe, J. (2014) · Dementia · doi:10.1177/1471301214554810 · Cited by 8
“These stigmatising conditions, with syphilis particularly stigmatising because of its connotations of sexual immorality (Chamaz, 2000), may help in current understandings of the stigma underlying some people’s reactions to a diagnosis of dementia and more general fears of the syndrome (see Alzheimer Disease Internatio…”
BackgroundManaging the need to tell: Triggers and strategic disclosure of thalassemia major in Singapore
Kumar, N., Turbitt, E., Biesecker, B. B., Miller, I. M., Cham, B., Smith, K. C., & Rimal, R. N. (2019) · American Journal of Medical Genetics Part A · doi:10.1002/ajmg.a.61107 · Cited by 8
Kenneth Gergen’s concept of multi-being: an application to the nurse–patient relationship
Hechinger, M., Mayer, H., & Fringer, A. (2019) · Medicine Health Care and Philosophy · doi:10.1007/s11019-019-09897-4 · Cited by 8
“More than acute illnesses, it is chronic illness that relate to experiences of social, interactional, and existential problems such as identity questions and the reconstruction of one’s self (Charmaz 2000).”
BackgroundKathy Charmaz: Theory, Method, and Scholarly Identity
Low, J., & Hyslop‐Margison, C. (2021) · Symbolic Interaction · doi:10.1002/symb.551 · Cited by 13
Rosenfeld, D. (2006) · Social Theory & Health · doi:10.1057/palgrave.sth.8700064 · Cited by 8
Kim, H., Lee, C., Kim, K. T., et al. (2022) · Annals of Leisure Research · doi:10.1080/11745398.2022.2132521 · Cited by 7
“Given the exploratory nature of the study, a qualitative methodology based on constructivist grounded theory was employed, which Charmaz (2000) has described as a way of ‘ discovering reality [that] arises from the interactive process and its temporal, cultural, and structural contexts ’ (524).”
MethodYoung, J. D., Demırdöğen, B., & Lewis, S. E. (2023) · International Journal of Science and Mathematics Education · doi:10.1007/s10763-023-10433-3 · Cited by 7
“Methodologically, this sampling resembles theoretical sampling (Charmaz, 2000), when the researcher chooses forms of data collection to be useful in generation of a theory.”
Out of the shadow: Partners managing illness together
Nowakowski, A. C. H., & Sumerau, J. E. (2017) · Sociology Compass · doi:10.1111/soc4.12466 · Cited by 7
“Violating established norms of the sick role (Varul, 2010) can lead others to withhold social support (Bury, 2000) and engage in microaggressions (Charmaz, 2000).”
BackgroundReflections on Identity: Narratives of Obstetric Fistula Survivors in North Central Nigeria
Degge, H. M., Laurenson, M., Dumbili, E. W., et al. (2019) · Qualitative Health Research · doi:10.1177/1049732319877855 · Cited by 7
“Stigma is a generally known consequence of chronic illness and threatens individuals’ perception of their illness experiences (Charmaz, 2000).”
BackgroundInfluentialQualitative Explorations into Customer Based Brand Equity (CBBE) for Medical Tourism in India
Roy, D. G., Bhattacharya, S., & Mukherjee, S. (2018) · The Qualitative Report · doi:10.46743/2160-3715/2018.3137 · Cited by 8
“Our content analysis in based on a constructivist approach and includes a two-stage coding process (open and axial), memo writing (Charmaz, 2000), clustering the data from the memos, and integration with theoretical framework.”
BackgroundMethodInfluentialHealth Maintenance Activities and Lay Decision-Making Support
Rose, J. H., Bowman, K. F., Deimling, G. T., & Stoller, E. P. (2004) · Journal of Psychosocial Oncology · doi:10.1300/j077v22n03_02 · Cited by 7
“Previously diagnosed patients can serve as mentors, teaching new patients the meaning of their illness and ways of living with the condition (Anderson-Loftin & Moneyham 2000; Charmaz, 2000).”
BackgroundLambert, B. L., Levy, N. A., & Winer, J. A. (2009) · Routledge eBooks · doi:10.4324/9780203929186-12 · Cited by 7
“…not enough training in psychotherapy or the art of medication management; and not enough focus on the meaning of medications and illness experience (Charmaz, 2000; Chewning & Sleath, 1996; Conrad, 1994; Demyttenaere, 1998; Gabbard & Kay, 2001; Holzinger et al., 2002; Karp, 1996c; Lambert et al.,…”
BackgroundMethodInfluentialLe handicap comme épreuve de soi. Politiques sociales, pratiques institutionnelles et expérience
Ville, I. (2015) · HAL · doi:10.13140/rg.2.1.3026.2482 · Cited by 7
Narrative inquiry in diabetes research: Illuminating the psychosocial aspects of diabetes
Acuff, L., & Paulus, T. M. (2016) · PLAID People Living with And Inspired by Diabetes · doi:10.17125/plaid.2016.60 · Cited by 6
“There is, however, a need to go “further outward into the social” when considering illness experiences [6].”
BackgroundThe Salt without the Girl: Negotiating Embodied Identity as an Agender Person with Cystic Fibrosis
Nowakowski, A. C. H. (2019) · Social Sciences · doi:10.3390/socsci8030078 · Cited by 6
“Even if they share the specific experience of being agender, people’s illness biographies and resulting relationships with their own bodies may differ dramatically (Charmaz 2000).”
BackgroundS’engager dans le monde biomédical
Barbot, J. (2001) · Éditions de l’École des hautes études en sciences sociales eBooks · doi:10.4000/books.editionsehess.10903 · Cited by 6
Cheng, Y. H. (2008) · Qualitative Health Research · doi:10.1177/1049732308318037 · Cited by 6
“For some achievers, such as Yuen, who shifted his direction toward working hard instead of enjoying life, the disabling injury was a transcending loss that transformed vulnerability into a source of strength to move ahead (Charmaz, 2000).”
BackgroundAging Partners Managing Chronic Illness Together: Introducing the Content Collection
Nowakowski, A. C. H., & Sumerau, J. E. (2017) · Gerontology and Geriatric Medicine · doi:10.1177/2333721417737679 · Cited by 6
“Some of this buffering against the adverse consequences of chronic disease occurs because supportive partnerships can facilitate effective illness management—a process of adjusting to and coping with changes in health introduced by persistent conditions (Charmaz, 2000).”
BackgroundSimoni, Z. R., Day, P. G., Schneider, D., Strenth, C. R., & Kale, N. J. (2022) · Sociological Perspectives · doi:10.1177/07311214221097086 · Cited by 5
Tipandjan, A., Schäfer, T., Sundaram, S., & Sedlmeier, P. (2011) · Integrative Psychological and Behavioral Science · doi:10.1007/s12124-011-9189-0 · Cited by 5
“In turn, these ideas may later be verified through traditional quantitative methods (Charmaz et al. 2000).”
BackgroundKonradi, A. (2017) · The Journal of Law Medicine & Ethics · doi:10.1177/1073110517750598 · Cited by 5
Lampe, N. M., Desai, N., Norton‐Brown, T., Nowakowski, A. C. H., & Glueckauf, R. L. (2022) · The Qualitative Report · doi:10.46743/2160-3715/2022.4917 · Cited by 5
“These narratives about facilitator experiences, personal needs, and recommendations may serve as valuable resources in educating researchers and clinicians (Charmaz, 2000).”
BackgroundMarkman, E. S., Moore, D. A., & McMahon, C. E. (2018) · Current Oncology Reports · doi:10.1007/s11912-018-0677-y · Cited by 5
Ives, H. (2014) · University of Bedfordshire Repository (University of Bedfordshire) · Cited by 5
Bewältigung chronischer Krankheit
Schaeffer, D., & Haslbeck, J. W. (2023) · Springer eBooks · doi:10.1007/978-3-658-42103-8_16 · Cited by 4
Experiences and management of uncertainty following treatment for prostate cancer
Green, R. (2024) · Health Risk & Society · doi:10.1080/13698575.2024.2345631 · Cited by 4
“Such experiences can be explored through a lens of uncertainty, a core facet of chronic illness experience (Charmaz, 2000; Royer, 2000).”
Brown, R. L. (2010) · Cited by 4
Löfgren, M., Schult, M., Öhman, A., Julin, P., & Ekholm, J. (2015) · Handbooks in health, work, and disability · doi:10.1007/978-1-4899-7627-7_26 · Cited by 4
Back to the Future: Irving K. Zola’s Contributions to the Sociology of Disability
Welch, M. J. (2016) · Emerald Group Publishing Limited eBooks · doi:10.1108/s1479-354720160000009007 · Cited by 4
Living with dementia during the COVID-19 pandemic: insights into identity from the IDEAL cohort
Stapley, S., Pentecost, C., Collins, R., Quinn, C., Dawson, E., Morris, R. G., Sabatini, S., Thom, J. M., & Clare, L. (2023) · Ageing and Society · doi:10.1017/s0144686x22001350 · Cited by 5
“…on identity has commonly considered chronic conditions as triggering a loss of self (Charmaz, 1983) or biographical disruption (Bury, 1982) wherein identity is under threat from the social consequences of the illness, with individuals striving to manage or adapt to this threat (Charmaz, 2000).”
Jefferson, L., Atkin, K. M., Sheridan, R., Oliver, S. E., Macleod, U., Hall, G. D., Forbes, S., Green, T., Allgar, V. L., & Knapp, P. (2019) · British Journal of General Practice · doi:10.3399/bjgp1919x706625 · Cited by 4
Stigmatization, discrimination and illness
Bohle, L. F. (2013) · doi:10.17875/gup2013-289 · Cited by 4
Human infrastructure in health: a commentary on networks of supports
Muenchberger, H., Kendall, E. A., & Han, H. (2010) · Australian Health Review · doi:10.1071/ah09774 · Cited by 4
Gesundheitsinformationen im Internet
Rosenkranz, N., Eckhardt, A., Kühne, M., & Rosenkranz, C. (2013) · WIRTSCHAFTSINFORMATIK · doi:10.1007/s11576-013-0369-z · Cited by 4
Personal illness experience of my adolescent self: a narrative inquiry self-study
Aksenchuk, S. (2022) · doi:10.32920/19749976 · Cited by 4
Illegitimate Pain: Dimensions, Dynamics, and Implications
Kenney, J. S., & Slowey, J. (2010) · Deviant Behavior · doi:10.1080/01639620903231407 · Cited by 3
Sharma, S., & Mishra, A. J. (2021) · Diabetes & Metabolic Syndrome Clinical Research & Reviews · doi:10.1016/j.dsx.2021.06.015 · Cited by 3
Deacon, M., & Rickards, E. (2013) · Contemporary Nurse · doi:10.5172/conu.2013.44.1.76 · Cited by 3
“Therefore Deacon (2008) analysed and faithfully reworked the themes described by Charmaz (2000) and Von Korff et al. (1997) into a series of tasks (see Table 1, below) conceived of as a job description.”
BackgroundMethodKilgore, K., Leinfelder, J., Campbell, J., et al. (2023) · Global Advances in Integrative Medicine and Health · doi:10.1177/27536130231206122 · Cited by 3
Schaeffer, D., & Haslbeck, J. W. (2013) · Springer eBooks · doi:10.1007/978-3-642-28201-0_16 · Cited by 3
SOCIAL REPRESENTATIONS IN DIABETICS: IMPLICATIONS FOR GLYCEMIC CONTROL
Amorim, M. M. A., Ramos, N., & Gazzinelli, M. F. (2018) · Psicologia Saúde & Doenças · doi:10.15309/18psd190211 · Cited by 3
The Handbook of Wellness Medicine
Snellings, J. E. (2021) · Family Medicine · doi:10.22454/fammed.2021.204951 · Cited by 3
Gesundheit und Krankheit als soziales Problem
Gerhardt, U. E. (1999) · VS Verlag für Sozialwissenschaften eBooks · doi:10.1007/978-3-322-99640-4_13 · Cited by 3
Developing trust and balancing control : social interactions in work accommodations
Kwan, H. C. (2014) · cIRcle (University of British Columbia) · doi:10.14288/1.0165642 · Cited by 3
Nettleton, S. (2021) · doi:10.1002/9781119633808.ch6 · Cited by 3
A qualitative analysis of patients' day-to-day living with functional cognitive disorder (FCD).
Mantovani, N., Poole, N., Cope, S., Vanzan, S., Duffus, A., Williams, T., Smith, J. G., Barrett, B., Scicluna, M., Beardmore, S., et al. (2025) · Disability and Rehabilitation · doi:10.1080/09638288.2025.2460725 · Cited by 2
“Experiencing stigma is a common consequence of chronic illness and is perceived as a constant threat by some individuals impacted by it [33] which has been documented with patients with FND [17,18].”
Disaster victim identification: UK practitioners’ experiences and wellbeing
Gorton, N.-L., & Roach, J. O. (2026) · Policing & Society · doi:10.1080/10439463.2026.2634111 · Cited by 2
“Social support is crucial for maintaining wellbeing, with managers playing a key role (Stephens & Long, 1999, 2000).”
O doświadczaniu choroby Parkinsona. Socjologiczne spojrzenie na chorego
Szluz, B. L. (2020) · Annales Universitatis Mariae Curie-Skłodowska sectio J – Paedagogia-Psychologia · doi:10.17951/j.2020.33.1.209-218 · Cited by 2
The Trend and Prospect of Medical Sociology: Its Concepts and the Interface with Medical History
Kim, J., & Lee, H. A. (2020) · Korean Journal of Medical History · doi:10.13081/kjmh.2020.29.843 · Cited by 2
Assessing and Achieving Quality in Qualitative Research: Clues for Researchers in Training
de Alicante, U., & Benjumea, C. D. L. C. (2024) · Investigación y Educación en Enfermería · doi:10.17533/udea.iee.v42n1e02 · Cited by 2
Trazendo corpos – e cuidados de saúde – “de volta”
Pols, J. J. (2024) · Novos Debates · doi:10.48006/2358-0097/v9n1.e9s03 · Cited by 2
Metadata
- Authors
- Charmaz, K.
- Corresponding author
- Charmaz, Kathy
- ORCID
- Charmaz, Kathy
- Venue
- Handbook of Social Studies in Health and Medicine
- Publisher
- SAGE Publications Ltd
- Published
- 2000
- Pages
- 277-292
- OpenAlex
- W2487022057
- Cited by
- 352
- References
- 0
- Citations by year
- 2026: 8 · 2025: 7 · 2024: 9 · 2023: 17 · 2022: 14 · 2021: 7 · 2020: 62 · 2019: 19 · 2018: 10 · 2017: 9 · 2016: 20 · 2015: 11 · 2014: 15 · 2013: 13 · 2012: 14
- FWCI
- 26.85
- Type
- book chapter
- Language
- en
- Open access
- closed
- Locations
- SAGE Publications Ltd eBooks (publishedVersion)
- Topics
- Health Sciences › Medicine › Epidemiology › Chronic Disease Management Strategies
- Social Sciences › Arts and Humanities › History and Philosophy of Science › Medicine, History, and Philosophy
- Social Sciences › Education › Qualitative research in health
- Keywords
- chronic disease, lived experience, patient experience
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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