stigma

  1. Andy

    Social Stigma, Mental Health, Stress, and Health-Related Quality of Life in People with Long COVID 2023 Scholz et al

    Abstract A considerable amount of people who have been infected with SARS-CoV-2 experience ongoing symptoms, a condition termed long COVID. This study examined nuanced experiences of social stigma in people with long COVID and their associations with perceived stress, depressive symptoms...
  2. Sean

    People with invisible disabilities like me are routinely disbelieved — and it can have long-lasting effects (mentions ME)

  3. Andy

    The prevalence of stigma in a UK community survey of people with lived experience of long COVID 2022 Pantelic et al

    Abstract Background Stigma can be experienced as perceived or actual disqualification from social and institutional acceptance on the basis of one or more physical, health-related, behavioural, or other attributes deemed to be undesirable. Long COVID is a predominantly multisystem condition...
  4. cassava7

    Doctors’ attitudes toward specific medical conditions, Scoles, 2022 (includes ME/CFS)

    Bolding mine: This study uses machine learning and natural language processing tools to examine the language used by healthcare professionals on a global online forum. It contributes to an underdeveloped area of knowledge, that of physician attitudes toward their patients. Using comments left...
  5. Andy

    Long Covid stigma: estimating burden and validating scale in a UK-based sample, 2022, Pantelic et al

    Edit: Now published, see post #4 in this thread. Abstract Background: Stigma can be experienced as perceived or actual disqualification from social and institutional acceptance on the basis of one or more physical, behavioural or other attributes deemed to be undesirable. Long Covid is a...
  6. O

    Navigating the social identity of long covid, 2021, Van de Vyver et al

    Opinion piece in the BMJ Conclusion Going forward, we recommend: Acknowledging that patients with long term conditions may experience challenging forms of “identity loss” which may lead them to feel more vulnerable. Addressing stigma in healthcare as well as in communities and workplaces...
  7. Haveyoutriedyoga

    Physician Use of Stigmatizing Language in Patient Medical Records, Park et al, 2021

    Physician Use of Stigmatizing Language in Patient Medical Records Jenny Park; Somnath Saha; Brant Chee, Janiece Taylor; Mary Catherine Beach JAMA Netw Open. 2021 https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2781937 Key Points Question What types of stigmatizing language are...
  8. Andy

    Causal attributions and perceived stigma for myalgic encephalomyelitis/chronic fatigue syndrome, 2021, Froehlich, Jason et al

    Abstract Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a chronic disease with the hallmark symptom of post-exertional malaise. Evidence for physiological causes is converging, however, currently no diagnostic test or biomarker is available. People with ME/CFS experience...
  9. Sly Saint

    Guest Blog MEA: The Shame

    https://meassociation.org.uk/2021/06/guest-blog-the-shame/
  10. Dolphin

    The need for a standardized conceptual term to describe invalidation of patient symptoms, 2021, Bontempo

    I can't access the full text but 6 of the references are to chronic fatigue syndrome papers. https://journals.sagepub.com/doi/abs/10.1177/13591053211024718 The need for a standardized conceptual term to describe invalidation of patient symptoms Allyson C Bontempo First Published June 11, 2021...
  11. Andy

    Elements of Suffering in [ME/CFS]: The Experience of Loss, Grief, Stigma, and Trauma in the Severely and Very Severely Affected, 2021, Fennell et al

    Full title: Elements of Suffering in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: The Experience of Loss, Grief, Stigma, and Trauma in the Severely and Very Severely Affected Abstract People who are severely and very severely affected by Myalgic Encephalomyelitis/Chronic Fatigue Syndrome...
  12. J

    Let’s end the stigma of psychosomatic illness The Times (London) 22/04/2021

    Column (paywalled) by James Marriott in The Times. https://www.thetimes.co.uk/article/lets-end-the-stigma-of-psychosomatic-illness-whfdlwhph Anyone know whether that 'a third of outpatients...' is right? Or where it's from? @dave30th perhaps? I think the article shows what we're up against...
  13. Andy

    Presentation: 'Shame, stigma and the shadows of contested, ‘unexplained’ illness', Katherine Cheston, Thurs 22nd April, 14.30-16.00 UK

    Tweets from Katherine Cheston "I'm presenting a paper entitled 'Shame, stigma and the shadows of contested, ‘unexplained’ illness' this Thursday at the @NNMHRmed Congress (Panel 10, 'Shame and Silences', 14.30-16.00). Registration is free & all are welcome! nnmhr2021.org" "I'll discuss these...
  14. Sly Saint

    Stigma of IBS - dissertation study 2021

    eta: not a recommendation just for info.
  15. John Mac

    Article: Shame, Stigma and “Unexplained” Symptoms

    My bolding https://thepolyphony.org/2020/09/29/shame-stigma-and-unexplained-symptoms/
  16. Kalliope

    Podcast: "The Stigma of Chronic Fatigue" - The Patient is In

    The Patient is In - A Podcast by StuffThatWorks Stories showcasing what's possible when people are empowered to advocate for their own health, or the health of their loved ones. Hosted by Dina Kraft & produced by Skyler Inman September 7 2020 - Episode 11 For 15 years Joe Landson lived with a...
  17. Dolphin

    Healthcare Educational Practices on Stigmatism of Chronic Illness: A Qualitative Narrative Study, 2020, Tolouian

    I imagine this happens with ME/CFS also https://gavinpublishers.com/articles/review-article/Journal-of-Nursing-and-Womens-Health/healthcare-educational-practices-on-stigmatism-of-chronic-illness-a-qualitative-narrative-study
  18. A

    Europe: European Federation of Neurological Associations (EFNA)

    The European ME Alliance has been a member organisation of the European Federation of Neurological Associations since 2015 (https://www.efna.net/emea/) This survey by EFNA includes M.E. https://www.surveymonkey.com/r/EFNA-YS It's open until 21st May and findings will be published on World...
  19. Sly Saint

    “The real me shining through M.E.”: Visualizing masculinity and identity threat in men with ME/CFS using photovoice and IPA.- Wilde et al 2020

    “The real me shining through M.E.”: Visualizing masculinity and identity threat in men with myalgic encephalomyelitis/chronic fatigue syndrome using photovoice and IPA. In: Psychology of Men & Masculinities https://psycnet.apa.org/record/2019-32617-001
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