Long Covid and Health Inequalities
What's Next for Research and Policy Advocacy
Bibliographic Data
INTRODUCTION: Organised by the 'Qualitative Long Covid Network', a workshop for qualitative Long COVID (LC) researchers, LC charity representatives and people with LC took place in June 2023, where research on the intersectional inequalities affecting LC prevalence, recognition and care was shared and discussed. METHODS: Five key themes were drawn up from presentations, discussions and reflections during the workshop, which are presented in this study. RESULTS: The following five themes are discussed: the unfairness of LC, difficulties in accessing care, mistrust of the healthcare system, a lack of understanding of LC and experiences of stigma and discrimination. Factors that widen or narrow inequalities related to LC were identified. CONCLUSION: A call to action is proposed to investigate and address inequalities through a robust LC research agenda that speaks with conviction to policy and decision-makers. We argue that there needs to be a strong investment in research and evidence-based policy and practice to mitigate the worst effects of the condition and address the inequalities in experience, treatment and support, which are experienced more often and more acutely by some of society's most vulnerable and disadvantaged individuals. PATIENT AND PUBLIC (PPI) CONTRIBUTION: Projects included in this article had PPI ongoing activity to inform their research. A member of the CONVALESCENCE PPI group presented at the QLC Network 'Long Covid and Health Inequalities' workshop, as did members of Long COVID Kids, Long COVID Support and Long COVID SOS charities. They were all invited to be co-authors of this article
Conviction · Disadvantaged · Disease · Health care · Inequality · Political science · Psychiatry · Public relations · Qualitative research · Social science · Sociology · Amyotrophic Lateral Sclerosis Research · Intensive Care Unit Cognitive Disorders · Law · Long-Term Effects of COVID-19 · Medicine · Psychology
Mind the gap
Barriers to Long Covid Care in the U.S.
Co-creating a social science research agenda for Long Covid
‘We Don't Have to Prove to People How We're Feeling’
Exploring Long Covid Prevalence and Patient Uncertainty by Sociodemographic Characteristics Using GP Patient Survey Data
Socio‐Demographic Inequalities in Covid‐19 Health Care Access and Experiences in the United Kingdom
Symptoms and risk factors for long Covid in non-hospitalized adults
Negotiation of collective and individual candidacy for long Covid healthcare in the early phases of the Covid-19 pandemic
Barriers to healthcare access and experiences of stigma
‘I don't know what to do or where to go’. Experiences of accessing healthcare support from the perspectives of people living with Long Covid and healthcare professionals
Towards evidence-based and inclusive models of peer support for long covid
You're just a Guinea pig
| Citations per year | 6 |
|---|---|
| Citation span | 2025 - 2026 (2) |
| Highly cited | No |