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Healthcare, Special Issue: ME/CFS ― The Severely and Very Severely Affected
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==Commentaries == *[https://doi.org/10.3390/healthcare9070919 Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: When Suffering Is Multiplied]<ref name="Komaroff2021m">{{Cite journal | last = Komaroff | first = Anthony L. | authorlink = Anthony Komaroff | date = Jul 2021 | title = Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: When Suffering Is Multiplied | url =https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8307552|journal=Healthcare|language=en|volume=9|issue=7 | pages = 919|doi=10.3390/healthcare9070919|pmc=PMC8307552|pmid=34356297|access-date=|quote=|via=}}</ref> (Jul 20, 2021) by Anthony L. Komaroff. ''Healthcare 2021, 9(7), 919.'' <blockquote>'''Abstract -''' Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is an illness defined predominantly by symptoms. Routine laboratory test results often are normal, raising the question of whether there are any underlying objective abnormalities. In the past 20 years, however, new research technologies have uncovered a series of biological abnormalities in people with ME/CFS. Unfortunately, many physicians remain unaware of this, and some tell patients that “there is nothing wrong” with them. This skepticism delegitimizes, and thereby multiplies, the patients’ suffering.</blockquote>
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