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me/cfs

Page 41 of 49
  1. chrisb
    Thread

    Normal muscle strength and fatiguability in patients with effort syndromes, 1988, Stokes at al

    I realise that this is hardly news but thought it worth a reread as Chalder and Butler in a 1989 MEA newsletter considered it one of the two...
    Thread by: chrisb, Jul 3, 2020, 34 replies, in forum: Historical Documents
  2. Esther12
    Thread

    Chapter on Chronic Fatigue, Sharpe, in Science and Practice of Cognitive Behaviour Therapy

    When my stomach is stronger I must try to reread the chapter by Salkovskis and Bass on Hypochondriasis in the Science and Practice of Cognitive...
    Thread by: Esther12, Jul 3, 2020, 25 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  3. Andy
    Thread

    Altered Structural Brain Networks Related to Adrenergic/Muscarinic Receptor Autoantibodies in CFS, 2020, Fujii, Sato, Yamamura et al

    BACKGROUND AND PURPOSE Recent studies suggest that the autoantibodies against adrenergic/muscarinic receptors might be one of the causes and...
    Thread by: Andy, Jul 2, 2020, 3 replies, in forum: ME/CFS research
  4. Andy
    Thread

    Blog: Frozen in Amber, "Energy systems and pacing in ME/CFS"

    Summary The aerobic energy system is “broken” in ME/CFS and cannot be fixed with exercise (i.e., graded exercise therapy, also known as GET). The...
    Thread by: Andy, Jul 2, 2020, 12 replies, in forum: General ME/CFS news
  5. Ravn
    Thread

    Post-Exertional Malaise - a discussion including defining and measuring PEM

    Moderator note: This post has been copied and following posts moved from this thread: Epidemiological and clinical factors associated with...
    Thread by: Ravn, Jul 2, 2020, 326 replies, in forum: Post-Exertional malaise and fatigue
  6. Dolphin
    Thread

    (Thesis) Autoimmune aspects in ME/CFS: A literature study on indications of autoimmunity in ME/CFS [Swedish), 2020, Strahle

    From: Dr. Marc-Alexander Fluks Source: Digitala Vetenskapliga Arkivet (DiVA) Date: June 23, 2020 URL:...
    Thread by: Dolphin, Jun 30, 2020, 2 replies, in forum: ME/CFS research
  7. John Mac
    Thread

    Two-Day CPET in Females with a Severe Grade of ME/CFS: Comparison with Patients with Mild and Moderate Disease. van Campen et al. 2020

    Full title: Two-Day Cardiopulmonary Exercise Testing in Females with a Severe Grade of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome:...
    Thread by: John Mac, Jun 30, 2020, 28 replies, in forum: ME/CFS research
  8. Dolphin
    Thread

    Hypothalamic-Pituitary-Adrenal (HPA) Axis and Chronic Fatigue Syndrome in Older Adults: The Rehabilitation Perspectives, 2020, Ho-Yin Lai et al

    Open access peer-reviewed chapter...
    Thread by: Dolphin, Jun 29, 2020, 7 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  9. Sly Saint
    Thread

    Open The impact of food on cognition: Potential implications for brain fog in ME;24 June 2020 online

    " The impact of food on cognition: Potential implications for brain fog in ME 24 June 2020 This study is looking to recruit both healthy...
    Thread by: Sly Saint, Jun 28, 2020, 18 replies, in forum: Recruitment into current ME/CFS research studies
  10. Andy
    Thread

    UK: Haywards Heath ME charity announces new patron

    Mid Sussex ME charity reMEmber has announced its newest patron alongside important news about the after-effects of Covid-19 and new funding for a...
    Thread by: Andy, Jun 26, 2020, 0 replies, in forum: General ME/CFS news
  11. lunarainbows
    Thread

    The Times: Infectious diseases expert warns of spike in ME cases

    The NHS is facing a “post-viral tsunami” with thousands of people struggling to recover from Covid-19 and experiencing symptoms of the...
    Thread by: lunarainbows, Jun 25, 2020, 34 replies, in forum: General ME/CFS news
  12. Robert 1973
    Thread

    United Kingdom: ME/CFS in The Times (including Sean O'Neill)

    Times Letters: Research into Chronic Fatigue Syndrome...
    Thread by: Robert 1973, Jun 25, 2020, 72 replies, in forum: General ME/CFS news
  13. Andy
    Thread

    The Times view on taking myalgic encephalomyelitis seriously: Chronic Condition

    It has taken a long time for myalgic encephalomyelitis (ME), or chronic fatigue syndrome as it is also known, to be treated with the seriousness...
    Thread by: Andy, Jun 24, 2020, 24 replies, in forum: General ME/CFS news
  14. Andy
    Thread

    The Times: Chronic fatigue syndrome: ME families accused of child abuse

    Hundreds of families whose children suffer from the debilitating condition ME have faced child protection investigations in the past decade, The...
    Thread by: Andy, Jun 24, 2020, 68 replies, in forum: General ME/CFS news
  15. Dolphin
    Thread

    Juvenile myasthenia gravis unmasked: a case of a teenage female (with CFS diagnosis) who presented in acute respiratory failure, 2020, Leyens

    I've no idea where this should go https://pediatrics.aappublications.org/content/146/1_MeetingAbstract/316 Juvenile myasthenia gravis unmasked:...
    Thread by: Dolphin, Jun 23, 2020, 3 replies, in forum: ME/CFS research
  16. Andy
    Thread

    What ME/CFS caregivers want you to know, 2020, Ausubel

    Eight stories comprise this paper: Stories were written in 2019 from caregivers, parents, and spouses, most of whom live with a pwME (person with...
    Thread by: Andy, Jun 23, 2020, 1 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  17. Andy
    Thread

    Impact of myalgic encephalomyelitis on treatment of comorbidities: A lived experience, 2020, Lopez-Majano

    Myalgic Encephalomyelitis (ME) is a complex, chronic, disabling, multi-system disease with no FDA-approved treatments. ME greatly impacts quality...
    Thread by: Andy, Jun 23, 2020, 4 replies, in forum: ME/CFS research
  18. Andy
    Thread

    Environmental accommodations for university students affected by myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), 2020, Chu et al

    BACKGROUND: Today, 24% of college and university students are affected by a chronic health condition or disability. Existing support programs,...
    Thread by: Andy, Jun 23, 2020, 1 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
  19. Andy
    Thread

    Inclusion of family members without ME/CFS in research studies promotes discovery of biomarkers specific for ME/CFS, 2020, Tokunaga et al

    BACKGROUND: The search for a biomarker specific for ME/CFS (myalgic encephalomyelitis/chronic fatigue syndrome) has been long, arduous and, to...
    Thread by: Andy, Jun 23, 2020, 2 replies, in forum: ME/CFS research
  20. Andy
    Thread

    Documenting disability in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), 2020, Podell et al

    Background: According to the 2015 National Academy of Medicine report, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) “is a serious,...
    Thread by: Andy, Jun 23, 2020, 2 replies, in forum: Psychosomatic research - ME/CFS and Long Covid
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