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ME/CFS Resources
useful-resources.md

What is ME/CFS?

Do I have ME/CFS?

What's the latest in the ME/CFS world?

How can I help? How can I advocate?

Why so many names? Why not just CFS?

What are some online communities I can join?

More Communities * Reddit: [The r/cfs Community](https://www.reddit.com/r/cfs/s/FOHNXA7Cu1) Disclaimer: * DO NOT join the r/mecfs or r/cfsme communities on reddit. They are [owned by David Jameson](https://forums.phoenixrising.me/threads/the-moderator-of-reddit-r-cfsme-r-mecfs-pushes-cbt-and-brain-retraining-and-get-and-bans-you-if-you-say-something-about-it.90736/), a notorious psychologiser of the disease. * While generally okay, the r/cfs community has a few users who promote unproven treatments. * Discord: [The MercyME community](https://discord.gg/dQYyXjZ9) * Lemmy: [The lemmy.blahaj.zome community](https://lemmy.blahaj.zone/c/myalgicencephalomyelitis) * Sadly, this community is not very active, but Lemmy is quickly growing, so feel free to be the people who make it active :).

Severe and Very Severe ME/CFS

How to manage ME/CFS?

How do I measure/explain my level of Disability?

  • The FUNCAP Questionnaire is specifically designed to measure disability due to PEM. You can take an online version here.

The Dark History of Psychologisation


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