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  1. Sly Saint

    United Kingdom: reMEmber news

    Merged threads "The charity, reMEmber, for people with ME (Chronic Fatigue Syndrome), has been awarded the grant by the Sussex Community Foundation for its Clinical Network and Children’s Service Project."...
  2. Sly Saint

    Thread for all minutes of the UK CFS/ME Research Collaborative [CMRC] Executive Board Meetings

    minutes from CMRC meeting April 2019 https://www.actionforme.org.uk/uploads/images/2019/04/CMRC_minutes_10.4.19.pdf
  3. Sly Saint

    BBC News website: 'Rabbits gave me a reason to live'

    Stoned rabbits are the anti-marijuana movement's weakest ploy yet https://www.theguardian.com/commentisfree/2015/mar/03/marijuana-stoned-rabbits-utah-weakest-ploy-yet-legal-weed
  4. Sly Saint

    David Tuller crowdfund: Trial By Error: Reporting on ME/CFS and Related Controversies

    is there a #tag for Davids crowdfunding? be nice to get one mentioned on MS s twitter.:sneaky:
  5. Sly Saint

    ME/CFS services in the United Kingdom

    Cambridgeshire and Peterborough NHS guide to Graded Exercise therapy "To equip people affected by CFS / ME with the skills for self-management towards a better quality of life’." Jan 2017, reviewed in Jan 2019 http://www.cpft.nhs.uk/PDF/Miscellaneous/Graded Exercise Therapy Booklet May...
  6. Sly Saint

    Michael Sharpe skewered by @JohntheJack on Twitter

    The article he tweeted is by a girl in England who 'recovered' after 3 years using 'graded activity' which, from her description, sounds a lot like pacing having been off school for a year and a half (post glandular fever). maybe someone could ask him what happened to the PACE 10 year...
  7. Sly Saint

    NDIS: NDIA meeting with Emerge and ME Australia

    In the UK in the CMO report 2002 (I think) said that prognosis for recovery after 5 years was not good or words to that effect.
  8. Sly Saint

    A general thread on the PACE trial!

    @rvallee nice comment btw; I think the MP who raised the issue of compensation for harms was Ed Davey (at the Westminster Hall debate).
  9. Sly Saint

    "Answer to IBS is in the mind" - media coverage of new Chalder/Moss-Morris trial

    Dr Hazel Everitt is also involved in this trial: The Atlantis study: Amitriptyline at Low-dose and Titrated for Irritable Bowel Syndrome as Second-line Treatment: A Double-blind Placebo-controlled Trial Duration: Start date 1st September 2018 - End date July 2022...
  10. Sly Saint

    ME/CFS services in the United Kingdom

    Salford Royal (NHS) both assessments with psychologists; where's the biological? recommended websites, top of the list Action for ME and AYME. http://www.srft.nhs.uk/about-us/depts/clinical-health-psychology/patients/about-our-service-cfs-me/
  11. Sly Saint

    Living with an unsociable illness - blog April 2019

    Living with an unsociable illness full blog here http://notjusttired.com/2019/04/18/living-with-an-unsociable-illness/
  12. Sly Saint

    Experiences with Insurance Companies

    I know this is an 'advert' for this lawyer but he gives potentially some useful information for Insurance claims re ME/CFS Andrew Kantor Helps Get Chronic Fatigue Syndrome Sufferers the Benefits They Deserve
  13. Sly Saint

    David Tuller On Exposing the Bad Science Behind the Biopsychosocial Effort to Define ME/CFS (Cort Johnson, HealthRising)

    I appreciate that; the US have only fairly recently started to realise that by using 'chronic fatigue' it in effect puts it and them "in the BPS camp", and although a lot of the researchers in particular don't like ME as a name, by using it (eg ME/CFS) it tends more to identify with the...
  14. Sly Saint

    Special Report - Online activists are silencing us, scientists say Reuters March 2019

    Kate Kelland @kkelland Award-winning Health and Science Correspondent for Reuters. Also mother of two and aspiring triathlete. Likes: hard work; asking questions; learning new things. yeah right.
  15. Sly Saint

    BBC News website: 'Rabbits gave me a reason to live'

    Bunny therapy.........
  16. Sly Saint

    David Tuller On Exposing the Bad Science Behind the Biopsychosocial Effort to Define ME/CFS (Cort Johnson, HealthRising)

    something that many people (outside Australia) have noticed and that maybe advocates in Oz should try and remedy(?) @MyalgicE @Simone
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