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CFS History and Nomenclature Flashcards

6 cards from real CFS practice questions. Tap to flip, then mark Knew It or Still Learning — missed cards come back until you master them.

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  1. What significant step did the NIH take in 2016 regarding ME/CFS research?

    Answer: Launched a major intramural research program to study ME/CFS biology

    In 2016, the NIH launched a large intramural research program to study the underlying biology of ME/CFS, representing a significant increase in federal commitment to the disease.

  2. What is the significance of the 'Nightingale Research Foundation' in CFS history?

    Answer: It is a Canadian organization that has advocated for ME recognition and research since the 1980s

    The Nightingale Research Foundation, founded by Dr. Byron Hyde in Canada, has been an important advocacy and research organization for ME recognition since the 1980s.

  3. Why do some patient advocates prefer the term 'ME' over 'CFS'?

    Answer: 'Chronic fatigue syndrome' is seen as trivializing the illness by focusing on one symptom

    Many advocates prefer 'ME' because 'chronic fatigue syndrome' is seen as trivializing a serious, disabling illness by reducing it to its least specific symptom — fatigue.

  4. Which country conducted the controversial PACE trial on CFS treatments?

    Answer: United Kingdom

    The PACE trial was a large UK study that examined graded exercise therapy and cognitive behavioral therapy for CFS, generating significant controversy about its methodology and conclusions.

  5. What does the historical term 'neurasthenia' refer to in the context of ME/CFS history?

    Answer: A 19th-century diagnosis of nervous exhaustion, sometimes considered a historical predecessor to CFS

    Neurasthenia, a 19th-century diagnosis describing nervous exhaustion with fatigue and multiple symptoms, is considered by some historians to be a historical predecessor to modern ME/CFS.

  6. In which decade did CFS patient advocacy groups first become significantly organized in the United States?

    Answer: 1980s

    CFS patient advocacy groups became significantly organized in the 1980s, galvanized by the Incline Village outbreak and the dismissive response from some medical authorities.