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That’s really interesting Trish. I always said the comms around the Tyson project felt like there was stuff in the background we weren’t being told - and not in a paranoid way, it just didn’t quite gel together properly so there had to be some facts or background missing. It never seemed like an...

Out of interest, does anyone know of any ME clinics doing 1-1 work with patients? Having gone around the referral route recently, the two at opposite ends of the country were both offering online group sessions. I think there was an initial assessment and diagnosis appointment but after that...

Perhaps we craft an AGM question to ask the MEA about this use of research funds?

It sounds like what it is - a tool to measure NHS clinic delivery/satisfaction. Which is fine, but don’t tell me you’re doing it for my benefit, when you absolutely are not. The short term clinic intervention also strengthens concerns about the “it’s not GET!” But why not try…doing more...

Anybody want to ask my question? Given that this app moves the admin burden to ME/CFS patients, and given it doesn’t do anything as well as other apps patients can already access*, scrapes free info from the web (like MEA website) and has a function to email professionals which can already be...

I might drop them a line letting them know my thoughts, am sure they will be thrilled. As I said, I do think it was naivety and the mea culpa seems to reflect that.

Same

So the app launch for Clinical Services is tomorrow. And the launch to the ME Community is on Weds.

Ok well I have ME/CFS so this is meaningless, good work Trudie!

Lots of people should know lots of things but they, in practice, do not.

It’s the app trap. It’s added value, isn’t it? Building and supporting the community. Ethically approved research happening now, near you, you can click and sign up. Part of their offering alongside podcasts/blog posts etc.

Basically the same disclaimer. I know I Stan Visible but I really think they’re a bit….pollyanna. They are IT people with LC. They added a research feed feature, it pulls data from a dot gov website, that’s nice, what could possibly go wrong? I think this might be the first difficult...

The correlation (being overweight) is not necessarily causation for sleep apnoea or fibromyalgia. I still don’t meet the majority of the criteria (being male, neck size etc) however having FM, ME/CFS and OSA all untreated (save for GET CBT) can lead to weight gain. No, you are not allowed to...

I once drank a whole bottle of rosė schloer and felt a bit dizzy and guilty as I poured the last glass, I’d been really enjoying it and feeling relaxed. I then remembered that it isn’t wine, it’s just grown-up fizzy juice made to taste a bit like wine. My point being - if your brain recognises...

I was initially diagnosed with Fibromyalgia. Some decade later I started to decline with my undiagnosed Mild ME. I put on weight and a year later, became overweight, started megasnoring, reporting to the GP that it was loud enough to hear outside the building and I was observed stopping...

I could actually believe they didn’t realise the danger.

Ah it’s not a mirror-image of this site, with a forum where they can all hang out and discuss the many different scientific studies they’re going to do which will prove us wrong!

I thought we had a special guest who might have given us some answers. I just wanted to ask why he posted on Sarah Boothby’s Bluesky then failed to engage with her. It kind of seems like an awful appropriation of her daughters death to chase clout and promote his views, because he didn’t reply...

Leeds has not been accepting inpatients from outside of its area for some years now.

My reactions to a new soap, or micropore tape are much worse than any reactions to meds. Cant say Ive ever noticed any difference in reaction to meds since ME, I’ve not heard of it being a thing.