‘We Don't Have to Prove to People How We're Feeling’: Understanding the Role of Peer Support Groups in Countering Epistemic Injustices in Long COVID at a US Centre
Nandini Sarma, Sam Gage, Catherine L. Hough, Aluko A. Hope
Background
Long COVID, an infection-associated chronic condition...
Abstract:
Endometriosis, a chronic inflammatory condition affecting 10% of biological women, is widely understudied and particularly overlooked in later life. Discussions surrounding endometriosis predominantly centre on medical gender bias during reproductive years, with limited attention to...
I feel like the discourse, the research, and pretty much everything and anything around Long COVID and ME focuses on the “symptoms” and not the functional disability.
I am not disabled by symptoms alone; I am disabled by a profound functional limitation driven by post-exertional malaise (PEM)...
Abstract:
A group of debilitating health conditions disproportionately impacting women, increasingly known as ‘energy limiting conditions’, is associated with a long history of medical and societal disability denial. This article offers reflections on socio-cultural, bio-political and...
Epistemic injustice, healthcare disparities and the missing pipeline: reflections on the exclusion of disabled scholars from health research.
Abstract:
“People with disabilities are subject to multiple forms of health-related and wider social disparities; carefully focused research is required...
The Untapped Power of “We Don't Know”: Epistemological Humility in the Era of COVID-19
Jolaade Kalinowski; Elizabeth A. Hintz; Chigozirim Izeogu
The SARS-CoV-2 (COVID-19) pandemic introduced many challenges and nuances that have transformed medical practice and research. The uncertainty caused...
https://peh-med.biomedcentral.com/articles/10.1186/s13010-021-00110-0
Abstract
Epistemic injustice sits at the intersection of ethics, epistemology, and social justice. Generally, this philosophical term describes when a person is wrongfully discredited as a knower; and within the clinical...
Abstract
In healthcare settings, patient participation is increasingly adopted as a possible remedy to ill people suffering from ‘epistemic injustices’ – that is to their unfair harming as knowers. In exploring and interpreting patient participation discourses within the 2013–2018 Dutch Myalgic...
Spanish title: Síndrome de fatiga crónica: experiencias de las personas afectadas, práctica clínica y justicia epistémica
Looks like it might be a letter to the editor of a Spanish publication. No abstract available.
Paywall, https://www.sciencedirect.com/science/article/abs/pii/S1130862121000371
Looks like it might be interesting and sympathetic
http://ejpch.org/ejpch/article/view/1861
Edited to add:
Prepublication version:
https://garrathwilliams.weebly.com/uploads/1/2/0/7/120771106/wiliams_explaining_epistemic_injustice_in_medicine.pdf
EXPLAINING EPISTEMIC INJUSTICE IN MEDICINE...
I think it is possible it happens with some people with ME/CFS, both men and women
https://www.sciencedirect.com/science/article/pii/S2352552520300839#!
Ethics, Medicine and Public Health
Volume 15, October–December 2020, 100545
Thoughts
Connecting epistemic injustice and justified belief in...
'Wessely has consistently promoted the unsubstantiated suggestion that ME is caused or maintained by patients’ false illness beliefs and abnormal behaviour.
As a result, the integrity of patients’ experience of this devastating illness been destroyed as their testimony is deemed unreliable...
This site uses cookies to help personalise content, tailor your experience and to keep you logged in if you register.
By continuing to use this site, you are consenting to our use of cookies.