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Case Reports
. 2021 Feb 16;9(2):215.
doi: 10.3390/healthcare9020215.

Three Cases of Severe ME/CFS in Adults

Affiliations
Case Reports

Three Cases of Severe ME/CFS in Adults

Leah R Williams et al. Healthcare (Basel). .

Abstract

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex, only partially understood multi-system disease whose onset and severity vary widely. Symptoms include overwhelming fatigue, post-exertional malaise, sleep disruptions, gastrointestinal issues, headaches, orthostatic intolerance, cognitive impairment, etc. ME/CFS is a physiological disease with an onset often triggered by a viral or bacterial infection, and sometimes by toxins. Some patients have a mild case and are able to function nearly on a par with healthy individuals, while others are moderately ill and still others are severely, or even, very severely ill. The cohort of moderately to very severely ill is often housebound or bedbound, has lost employment or career, and has engaged in a long, and often futile, search for treatment and relief. Here, we present three case studies, one each of a moderately ill, a severely ill, and a very severely ill person, to demonstrate the complexity of the disease, the suffering of these patients, and what health care providers can do to help.

Keywords: chronic fatigue syndrome (CFS); myalgic encephalomyelitis (ME); post-exertional malaise (PEM); severe ME/CFS; very severe ME/CFS.

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Conflict of interest statement

The authors declare no conflict of interest.

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References

    1. Institute of Medicine . Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Redefining an Illness. The National Academies Press; Washington, DC, USA: 2015. - DOI - PubMed
    1. Bateman L., Bonilla H., Dempsey T., Felsenstein D., Komaroff A.L., Klimas N.G., Natelson B.H., Podell R., Ruhoy I., Vera-Nunez M., et al. US ME/CFS Clinician Coalition: Diagnosing and Treating ME/CFS. [(accessed on 30 November 2020)]; Available online: https://drive.google.com/file/d/1SG7hlJTCSDrDHqvioPMq-cX-rgRKXjfk/view.
    1. WHO . International Classification of Functioning, Disability and Health (ICF) WHO; Geneva, Switzerland: 2018.
    1. McManimen S.L., McClellan D., Stootho J., Jason L.A. Effects of unsupportive social interactions, stigma, and symptoms on patients with myalgic encephalomyelitis and chronic fatigue syndrome. Community Psychol. 2018;46:959–971. doi: 10.1002/jcop.21984. - DOI - PMC - PubMed
    1. Valdez A.R., Hancock E.E., Adebayo S., Kiernicki D.J., Proskauer D., Attewell J.R., Bateman L., DeMaria A., Lapp C.W., Rowe P.C., et al. Estimating Prevalence, Demographics, and Costs of ME/CFS Using Large Scale Medical Claims Data and Machine Learning. Front. Pediatr. 2019;6 doi: 10.3389/fped.2018.00412. - DOI - PMC - PubMed

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