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Sounds like they have got Charles Dickens on the writing

Sorry mr/ms Kalfas I see your name and my brain tells me Kafka :whistle:

:wtf:

9400 now :thumbup: Everyone who has social media please share the link every couple of weeks to help reach 600 more people.

Speechless

Six weeks on from “in the next few weeks”, six weeks til Christmas, chances of “the next few weeks” turning out to be in 2023 are looking slim to impossible.

ME Association have a dental advisor they may have a leaflet about dental care or you could put a question to them through their website or Facebook

Presumably some glitch with publication...

Interesting in the sense that it’s a website based in India so big reach potentially. Maybe it would be worth someone emailing her to point her towards better sources?

That quote :emoji_fire:

Written on the back of a packet of Gauloises

Another article from ME Association about CBT research by Knoop et al https://meassociation.org.uk/2023/11/the-me-association-raises-concerns-about-new-research-promoting-cbt-as-a-treatment-for-me-cfs/

Millions Missing France have included the petition link in this facebook post about psychologisation https://m.facebook.com/story.php?story_fbid=pfbid0mK5CS9xpBY5bcz7BDNKmz2iuTUcgbjW3XBNgZ6jrmxYkHBsgfrtWmVUA4Aw95otNl&id=100067419996509&mibextid=WC7FNe

Based on 33 people recruited through social media I disagree that indicates their findings indicate anything is widespread among people with ME/CFS diagnosis

By more intensive treatment presumably they mean more CBT brainwashing Eta oh so time contingent physical activity ie GET also included the full Monty

:emoji_dart:

https://www.oatext.com/Estimating-the-disease-burden-of-MECFS-in-the-United-States-and-its-relation-to-research-funding.php#:~:text=Using%20the%20above%20formula%2C%20our,impact%20in%20the%20United%20States. Link to the paper by Mary Dimmock and Leonard Jason

https://meassociation.org.uk/2023/11/the-me-association-writes-to-the-president-of-the-royal-college-of-psychiatrists-regarding-their-website-information-on-me-cfs/ The ME Association writes to the president of the Royal College of Psychiatrists regarding their website information on ME/CFS

Or even making the service community based and see people at home

Steungroep ME en Arbeidsongeschiktheid (Netherlands) have also signed. Thanks again for your help @Solstice