@arewenearlythereyet may have been the innovator but I think TRIPE has taken off as S4ME speak for extra strong BS and I’d say it’s anyone’s call...
I saw on Twitter @Simon M youve been having problems with high traffic to your blog. Nice problem to have :thumbup: I hope it’s not been too hard...
:rofl:
Signed
I don’t think leaflets without 1-1 contact are likely to have much impact more than social media. I barely even look at anything that comes...
This is great thanks @Simon M ive shared it on local ME group. Also although it’s about research and I don’t share about research normally as it’s...
I think she gave some wishy washy fence sitting comment to SMC - maybe on SMILE. Might have remembered wrong. ETA yay my memory is not so bad....
@strategist Under diagnosis is very much a current issue in the U.K. in the context of MUS and downplaying of symptoms people struggle to get...
So just over $10k
I spent the last 10 years of my career working on web content for a public sector organisation where we took information written by technical...
I dont think theres much chance of the main UK charities doing anything
we love you Norway:thumbup:
hi @Hutan i guessed there probably isnt an existing process but it seems a shame if youve got the energy available to build on what youve already...
I think this is a key part of MM speeches and singing is good for visibility but I hope people out there being asked one to one do you know about...
wow thats a big judgment to make on a fellow person with ME
ive not had the swollen glands but I reckon I would if I really pushed myself again over a sustained period
I used to get a lot of sore throats & swollen glands. When I overdo things my voice starts to go croaky. But since I’ve got ill health retirement...
Are NZ patients going to send the people who produce this a formal response with comments? Seems like a good way to demonstrate the value of...
Wot @Esther12 said
This is very useful to have @EspeMor @chicaguapa @Gecko thanks for producing
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