I think AfME have a duty of care towards patients to warn them that GET is implicated in harm to patients. I really don't think it's ethical for them to fudge this on their website.
Sick people, some very sick indeed, who are newly ill/diagnosed and may not be best placed to research and weigh...
From the link given by @Joh in the previous post via Google Translate:
All I can say is that Fatigato can't keep this position for ever, if the evidence for ME being physiological continues to mount. The evidence is increasingly against them.
Very short, but clear presentation of the new paper's findings. Comment from Carolyn Wilshire, The ME Association and Dr Jon Stone
Sharpe Chalder and Goldsmith are given the last word.
What I expected from the BBC, and better than we've had in the past.
I like "Goalposts 'moved'" as a...
Hello @JenB and welcome :)
That's a lot of followers. I criticised you earlier in this thread for what I believe to be an error of judgement, but I know that I couldn't handle twitter myself. This forum is a good place for discussion, or you might find starting a blog that you tweet links to...
Well at the end of the day it's just a moment on twitter, I suppose, and none of us are perfect. Twitter isn't where the decision making process happens.
Well you could just up the bad ass-ery a tad to compensate, no problem. :laugh::laugh:
Really, I wouldn't crowdfund for something I'd like to have rather than actually need, it wouldn't seem fair.
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