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Is he saying that he knows what the thing in the blood is, now?

I'm not, because I never seem to get viruses.

@lunarainbows you might enjoy this

Yes but I find this extremely helpful https://www.completecareshop.co.uk/household-aids/writing-aids/ring-pen-ultra

https://freerice.com/about Here is a website where you can play a little game, and every time you get an answer right, money gets donated to charity.

Funny, I thought it was supposed to be us overachievers who developed MUS.

Windgassen is a brilliant name but I'd expect someone with that name to be writing about bowel issues. Yes, I am childish.

That's not what a false positive means.

Can anyone translate the abstract from Science into English?

@Jonathan Edwards Thoughts?

http://cepuk.org/2020/02/08/guest-blog-nice-depression-guideline-cautious-optimism/?fbclid=IwAR1c2BN81TyQ79EjH8IYSjTeztHESk1i7rP3-GmiJJDLLH3HDrNlaxR8M2c

The population of China is around 1.4 billion...

Why were you refused membership?!

The only "gains" I can think of are that I'm extremely unlikely to be involved in a road accident (given that I'm rarely able to leave the house), much less likely to be a victim of violent crime (for the same reason), and I am never at risk of getting sunburnt. Wahoo. Yay.

If you have the energy to give them feedback, and you consider it a worthwhile use of your time (and if you don't find it soul-destroying), then please go ahead. You're good at articulating these sorts of issues. I don't personally have the energy for it, and in my experience giving them...

Exactly. And when we try to explain our concerns to MEA, all they do is whine that we're criticising them, and bang on about how busy they are. I even saw CS tell one very severely ill PWME that she should set up her own charity if she didn't like what the MEA were doing! Which is totally...

I'm not even surprised by any of this. I have no faith in the MEA. They, like AFME, are trying to keep both PWME and The Establishment happy. Which uh... isn't really possible.

:emoji_joy::emoji_joy::emoji_joy:

Erm. No. I have never heard a single person with ME/CFS say that it enabled them to spend more time with their family. If you're sick enough to be unable to work, then you're generally also sick enough to be limited in how much time you can spend with your family.

This leaflet says that GET is "not appropriate" and not helpful, but it doesn't say that it's dangerous. It doesn't say either that their CBT is inappropriate and dangerous.