My 2 cents: I've said to people before that it's generally not progressive, once people are diagnosed; can reduce their workload and...
I noticed in the latest newsletter of the Solve ME/CFS Initiative it says: It's nice to see people with the illness researching it.
[MEDIA] [MEDIA]
New book: The author, who I know a little from Ireland, has asked me to highlight the book. She recognises it is very expensive but hoped that...
https://www.nih.gov/research-training/medical-research-initiatives/mecfs/cfs-advocacy-call-april-2019 [MEDIA] [MEDIA]
[ATTACH] [MEDIA]
Research Article A possible link between recurrent upper respiratory tract infections and lower cytokine production in patients with Q fever...
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Over the last few hours, I have posted the following in 60-70 (?) Facebook groups: [MEDIA]
I would have preferred to share a link to where they have posted this but I can't find any such link. Here are their social media accounts:...
https://2tired.weebly.com/home/dismissal-of-young-people-with-me-by-nhs-professionals [MEDIA] [MEDIA]
https://www.bacme.info/sites/bacme.info/files/BACME%20CFS%20ME%20National%20services%20survey%20March19.pdf [MEDIA] [MEDIA]
What I and some others have done before with other appeals is to email messages to local and national groups. Different searches will show up...
The Irish ME/CFS Association just has one social media account currently, a Twitter account. We have retweeted a number of tweets on this. We will...
I haven't read this thread so far. But if people want to reach a lot of people with ME/CFS, there are a lot of Facebook groups that could be...
In case anyone wants to share the appeals for funding: [MEDIA] [MEDIA]
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