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Merged threads "The charity, reMEmber, for people with ME (Chronic Fatigue Syndrome), has been awarded the grant by the Sussex Community...
minutes from CMRC meeting April 2019 https://www.actionforme.org.uk/uploads/images/2019/04/CMRC_minutes_10.4.19.pdf
Stoned rabbits are the anti-marijuana movement's weakest ploy yet...
is there a #tag for Davids crowdfunding? be nice to get one mentioned on MS s twitter.:sneaky:
Cambridgeshire and Peterborough NHS guide to Graded Exercise therapy "To equip people affected by CFS / ME with the skills for self-management...
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...
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.
@rvallee nice comment btw; I think the MP who raised the issue of compensation for harms was Ed Davey (at the Westminster Hall debate).
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Dr Hazel Everitt is also involved in this trial: The Atlantis study: Amitriptyline at Low-dose and Titrated for Irritable Bowel Syndrome as...
Salford Royal (NHS) both assessments with psychologists; where's the biological? recommended websites, top of the list Action for ME and...
Living with an unsociable illness As I’m writing this post, I’m sat in bed, having to take time out to rest, whilst we have a family member...
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...
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...
Kate Kelland @kkelland Award-winning Health and Science Correspondent for Reuters. Also mother of two and aspiring triathlete. Likes: hard...
Bunny therapy......... [MEDIA]
something that many people (outside Australia) have noticed and that maybe advocates in Oz should try and remedy(?) @MyalgicE @Simone
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