Long COVID disability burden in US adults
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