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caregiving

  1. Yann04
    Thread

    Resources for caregiving on the Very Severe end of Very Severe ME

    Hi, I usually can only use my phone for a couple minutes every week or so but sleep deprivation and an unknown allergic reaction gave me lots of...
    Thread by: Yann04, Apr 4, 2024, 4 replies, in forum: General clinical care
  2. Trish
    Thread

    Book - 'Severe ME: More Notes for Carers' by Greg Crowhurst, 2021

    Severe ME: More Notes for Carers by Greg Crowhurst https://www.stonebird.co.uk/
    Thread by: Trish, Feb 2, 2021, 0 replies, in forum: General ME/CFS news
  3. 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
  4. Kalliope
    Thread

    Letter to the editor about ME/CFS in Swedish medical journal

    Note from moderators: First posts merged from thread here. https://www.s4me.info/threads/news-from-scandinavia.647/page-51#post-237731 Good...
    Thread by: Kalliope, Feb 17, 2020, 4 replies, in forum: General ME/CFS news
  5. seeker
    Thread

    First monthly ME PARTNER Caregivers Support Group call this Sunday

    We’re kicking off a new monthly call for ME Partner Caregivers this Sunday, Feb. 10, 1 p.m. PT / 4 p.m. ET. We invite caregivers who are...
    Thread by: seeker, Feb 7, 2019, 3 replies, in forum: Caregiver support
  6. Joh
    Thread

    Caregivers' guide by #MEAction

    New(ish) caregivers' guide by #MEAction #MEAction has crowdsourced the advice in this guide and companion brochure from caregivers who care for...
    Thread by: Joh, Jun 14, 2018, 5 replies, in forum: Caregiver support
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