Long COVID disability burden in US adults

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Authors: Karen A. Bonuck, Qi Gao, Seth Congdon, R. Kim
Cited by: 1
References: 44

Abstract

Five years since the scientific and patient communities first identified the syndrome now known as Long COVID, affected individuals lack treatments, and the US lacks population-based data on its disability burden and correlation with National Institutes of Health (NIH) funding. Moreover, akin to other debilitating conditions it often co-occurs with, e.g., Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and dysautonomia, Long COVID disproportionately impacts females whose concerns are often marginalized. We quantify Long COVID years lived with disability (YLDs= prevalence x disability weight) in US adults and its actual/YLD-commensurate average annual NIH FY2022-2024 funding versus 68 comparator conditions, by sex predominance. We derive Long COVID prevalence from Census Bureau surveys (9/2022-8/2023) and apply disability weights from the Global Burden of Disease Study. Long COVID YLDs approximate those of Alzheimer’s and Asthma. Long COVID received 14% of its disability commensurate funding: $106 million vs. $739.8 million. ME/CFS is the most under-funded condition, receiving

Fields of Study & Subjects

Long-Term Effects of COVID-19 Fibromyalgia and Chronic Fatigue Syndrome Research Amyotrophic Lateral Sclerosis Research

Publication details

Journal / source
Communications Medicine
Publisher
Springer Science and Business Media LLC
Volume
6
Issue
1
Publication date
31 March 2026
Language
EN