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  1. John Mac
    Thread

    Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS): Major Impact on Lives of Both Patients and Family Members, Brittain et al, 2021

    Abstract Background and objectives: To explore the impacts that Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has on the patient and...
    Thread by: John Mac, Jan 7, 2021, 3 replies, in forum: PsychoSocial ME/CFS Research
  2. 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, 1 replies, in forum: BioMedical ME/CFS Research
  3. Andy
    Thread

    The care of younger children (5–11 years) with CFS/ME. A qualitative study comparing families’, teachers’ and clinicians’ perspectives’, 2020, Crawley

    Title including weird quote, “The child’s got a complete circle around him ”. The care of younger children (5–11 years) with CFS/ME. A qualitative...
    Thread by: Andy, Jun 11, 2020, 6 replies, in forum: PsychoSocial ME/CFS Research
  4. Sly Saint
    Thread

    Still to open University of Cincinatti - Department of Psychiatry and Behavioral Neuroscience

    " Women's Health Clinical Trials We are currently recruiting women and men for all of the following studies in the Greater Cincinnati (Ohio) area:...
    Thread by: Sly Saint, Jan 14, 2020, 3 replies, in forum: Recruitment into current ME/CFS research studies
  5. rvallee
    Thread

    Social Services Can Threaten Families of Children with Chronic Fatigue

    Pretty good article from Vice about the reality of social services in the UK threatening sanctions against the parents of children with ME....
    Thread by: rvallee, May 2, 2019, 10 replies, in forum: General ME/CFS News
  6. MeSci
    Thread

    Acceptance and identity change: An interpretative phenomenological analysis of carers' experiences in ME/CFS (2018) Sarah Catchpole

    Source: Journal of Health Psychology Preprint Date: March 21, 2019 URL: https://journals.sagepub.com/doi/full/10.1177/1359105319834678...
    Thread by: MeSci, Mar 22, 2019, 0 replies, in forum: PsychoSocial ME/CFS Research
  7. Sly Saint
    Thread

    Open Impact of ME/CFS on patients & their family

    a clinical research study by a third-year medical student at Cardiff University Aim of the project: The aim of this project is to gain a better...
    Thread by: Sly Saint, Mar 9, 2019, 0 replies, in forum: Recruitment into current ME/CFS research studies
  8. Andy
    Thread

    Home-based family focused rehabilitation for adolescents with severe Chronic Fatigue Syndrome, 2018, Burgess et al (inc Chalder)

    Abstract Aims: The purpose of this article is to describe and evaluate a home based, family focused rehabilitative approach for severely affected...
    Thread by: Andy, Aug 18, 2018, 53 replies, in forum: PsychoSocial ME/CFS Research
  9. arewenearlythereyet
    Thread

    Resources for Parents with ME - helping children come to terms with chronic illness

    I've recently had to do a few internet searches looking for some helpful information. My son has been having difficulties as he realises that dad...
    Thread by: arewenearlythereyet, Jan 29, 2018, 5 replies, in forum: Relationships
Showing results 1 to 9 of 9