1. Sign our petition calling on Cochrane to withdraw their review of Exercise Therapy for CFS here.
    Dismiss Notice
  2. Guest, the 'News in Brief' for the week beginning 11th September 2023 is here.
    Dismiss Notice
  3. Welcome! To read the Core Purpose and Values of our forum, click here.
    Dismiss Notice

petition

Page 1 of 3
  1. Hutan
    Thread

    Petition: S4ME 2023 - Cochrane: Withdraw the harmful 2019 Exercise therapy for CFS review

    The Science for ME forum started a petition on 4 September: Cochrane: Withdraw the harmful 2019 Exercise therapy for CFS review on Change.org The...
    Thread by: Hutan, Sep 4, 2023, 108 replies, in forum: Petitions
  2. Charles B.
    Thread

    Suzy Weiss Manifesto on “Spoonie” Culture

    https://www.commonsense.news/p/hurts-so-good This is merely an intellectually and morally bankrupt regurgitation of long-standing canards against...
    Thread by: Charles B., Sep 8, 2022, 35 replies, in forum: Psychosomatic news - ME/CFS and Long Covid
  3. Peter Trewhitt
    Thread

    Petition: UK Funding for ME & Long Covid research into treatment

    The MEA shared this UK Parliamentary petition on their Facebook page recently, it may have been shared elsewhere, so sorry if this is a duplicate...
    Thread by: Peter Trewhitt, Mar 14, 2023, 6 replies, in forum: Petitions
  4. Sly Saint
    Thread

    United Kingdom: Cases of people with ME/CFS with severe feeding problems, in the media

    This thread is for social media and general media items about people in the United Kingdom with both ME/CFS and severe problems in achieving...
    Thread by: Sly Saint, Feb 23, 2023, 99 replies, in forum: General ME/CFS news
  5. Jaybee00
    Thread

    NIH Recover Initiative—petition against bogus treatments

    There is a petition—looks like all nationalities can sign. Treatments include CBT, exercise. [MEDIA]
    Thread by: Jaybee00, Dec 27, 2022, 8 replies, in forum: Petitions
  6. RedFox
    Thread

    Long Covid drug BC-007 research news

    Change.org petition to fund and expedite BC-007 research BC007 NOW- Chance of a cure for millions of suffering people From the English...
    Thread by: RedFox, Sep 7, 2022, 17 replies, in forum: Long Covid news
  7. SNT Gatchaman
    Thread

    New Zealand: 2022 Petition for the NZ government to recognise ME/CFS as a disability - deadline 29 August 2022 (people living outside NZ can sign)

    Copied post Petition for NZ govt to recognise ME as a disability....
    Thread by: SNT Gatchaman, Aug 9, 2022, 23 replies, in forum: Petitions
  8. Noir
    Thread

    Australia: Petition: Call for Change for ME patients Australia

    "We are looking to submit this Australian version of the Call-For-Change petition to the current Australian Disability Royal Commission and...
    Thread by: Noir, Mar 14, 2022, 3 replies, in forum: Petitions
  9. Noir
    Thread

    2022 Petition: Denmark must follow international evidence-based guidelines for ME (anyone can sign)

    The Danish Health Authorities rejects the new NICE guidelines and keep clinging to CBT and GET. Please sign and share this petition to help put...
    Thread by: Noir, Jan 25, 2022, 32 replies, in forum: Petitions
  10. Lucibee
    Thread

    United Kingdom: Petition: Set up a national harms reporting scheme for non-pharmacological treatments

    OK. I'm off to jump through a few hoops. brb... (in about a week) Seems someone got in there first... :wink:...
    Thread by: Lucibee, Nov 19, 2021, 27 replies, in forum: Petitions
  11. Andy
    Thread

    Austria: Petition: ME / CFS: Recognition, Medical Care and Protection of the Affected, and Research Funding, closes 22 Nov 2021

    I'm relying on Google translation here, if any errors are spotted please let me know. Quote: Myalgic Encephalomyelitis / Chronic Fatigue...
    Thread by: Andy, Nov 5, 2021, 25 replies, in forum: Petitions
  12. John Mac
    Thread

    United Kingdom: Petition Change.org: for a new mechanism by which M.E/C.F.S patients can report harms.

    https://www.change.org/p/department-of-health-and-social-care-we-demand-the-creation-of-a-new-mechanism-by-which-m-e-c-f-s-patients-can-report-harm...
    Thread by: John Mac, Nov 2, 2021, 35 replies, in forum: Petitions
  13. Suffolkres
    Thread

    United Kingdom: Petition, Create a Task Force to Oversee Drug Procurement for ALL Post Viral Conditions - deadline 20 November 2021

    Moved post The great majority of doctors will not get to hear about this. However, quite a high proportion of GPs are likely to take note since it...
    Thread by: Suffolkres, Oct 19, 2021, 0 replies, in forum: Petitions
  14. Andy
    Thread

    Petition 122600 to the German Bundestag: Healthcare, Scientific Research and Political Support for ME/CFS Sufferers!, 2021

    [Can be signed by anybody] Quote: Our Pleas to the German Bundestag We ask the German Bundestag to commit itself to the provision of healthcare...
    Thread by: Andy, Oct 14, 2021, 86 replies, in forum: Petitions
  15. Andy
    Thread

    Petition: #MEAction: Publish the NICE ME/CFS Guideline Now

    "We call on the National Institute for Health and Care Excellence (NICE) to publish the finalised ME/CFS guideline in its current form. People...
    Thread by: Andy, Aug 19, 2021, 87 replies, in forum: Petitions
  16. Andy
    Thread

    UK Action for ME petition: 'Equity for ME' asking UK governments for equity of recognition and research funding with long Covid. closes 26th Nov 2021

    [MEDIA]
    Thread by: Andy, Aug 4, 2021, 21 replies, in forum: Petitions
  17. Andy
    Thread

    Canada: Petition: ME/CFS research funding, closes Sept 10, 2021

    "We, the undersigned, Citizens of Canada, call upon the Government of Canada to: 1. Set Aside $50 Million Dollars for ME/CFS biomedical research;...
    Thread by: Andy, May 15, 2021, 5 replies, in forum: Petitions
  18. Andy
    Thread

    UK: Petition: Specify ME/CFS on the list of neurological conditions under group 6 for UK Covid19 vaccine

    ME (or CFS as some still call it) is a chronic neurological condition that affects around 250,000 people across the UK, 75% are too unwell to work...
    Thread by: Andy, Feb 13, 2021, 21 replies, in forum: Petitions
  19. ME/CFS Skeptic
    Thread

    Press Release from the European ME coalition (EMEC): 'Scientists call for more European research on ME/CFS'

    Press Release from the European ME coalition (EMEC): 'Scientists call for more European research on ME/CFS' Brussels, 10 June 2020 More than one...
    Thread by: ME/CFS Skeptic, Jun 10, 2020, 2 replies, in forum: Advocacy Projects and Campaigns
  20. ME/CFS Skeptic
    Thread

    European ME Coalition (EMEC)

    The advocacy group of Evelien Van Den Brink and Francis Martin (of which I’m part) now has an official name and website. Check it out here:...
    Thread by: ME/CFS Skeptic, Apr 19, 2020, 11 replies, in forum: Advocacy Projects and Campaigns
Showing results 1 to 20 of 53
Page 1 of 3