It seems odd to me that the response, such as it is, comes from the ME Connect team who run the helpline, rather than from someone senior in management.
Ah, but I forgot, they don't have a chief executive.
Why does it make me think this is being seen as us, the signatories of the letter...
Really good. I can see it's taken a huge amount of work to put together key points in the history. You have managed to make it both succinct and comprehensive, and very clearly presented.
Thank you, @Adam pwme.
LCAP are already on Bluesky:
https://bsky.app/profile/lcap.bsky.social
My point was that leaving Twitter doesn't mean the attacks from such groups will stop. Though on Bluesky you have more power to block. I would think if the start the same attacks on Bluesky a lot of people will block them.
Ugh. I find it astonishing that anyone claiming to be a scientist or clinician can take seriously the anecdote of one person who was just one among many who had a short spell of post Covid symptoms and recovered, yet dismisses the millions with serious unremitting Long Covid as social media...
The reply is clearly written by a staff member not by Neil Riley. It focuses entirely on sympathy for an individual's distress and suggesting use of their helpline, while not apologising at all for Riley's awful article. Not good enough.
I hope the body mapping research Oonagh Cousins is involved in is better than the study posted on the forum recently:
Drawing the lines of fibromyalgia: a mixed-methods approach to mapping body image, body schema, and emotions in patient subtypes, 2024, Swidrak
I get what you are saying, Kitty, and I think that's probably the case for many pwME.
For me I think if I'd had real time wearable data when my ME was mild and I was still working and caring for a family it could have made a big difference.
I was always on the edge of tripping myself into...
I noticed that too. If I get dressed and go for a walk in my garden in the morning then go back to bed for the rest of the day, there's no one to get my and my daughters' meals, or do the other things that need doing in a household of two sick people.
Oh, and by the way, Mr Riley, a large...
The people judging the drawings were psychologists or doctors who are experts in pain and didn't know the participants.
Is this an art competition or a scientific study? Participants are asked to draw freely, yet their drawings are being interpreted as revealing psycholical flaws. Surely...
So Riley gets to make a statement on the MEA website that isn't a real apology, it's a string of excuses and self justifcation.
So he sets up the straw man argument that he wasn't advocating GET, as far as I know no one has accused him of doing so. Then he goes on to compound the problem by...
I've just had a quick look at the MEA trustee, staff and volunteer list. I didn't realise they employ so many people.
I see Russell Fleming has worked his way up from part time volunteer through various roles to now Head of Project Development, a full time very responsible position...
I'd vote for closing it down and transferring the materials written by Charles Shepherd to AfME or archving them in accessible form once Charles retires.
Research funds could be transferred to MERUK and funds given for running costs to AfME.
https://www.s4me.info/threads/open-letters-to-the-uk-me-association-trustees-about-a-research-project-developing-proms-led-by-sarah-tyson.37937/#post-524843
The only response by Neil Riley to our complaint about Tyson's behaviour was that the complaint was 'noted', and that the MEA have full...
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