As it is a Regional paper there’s a strong possibility this will also pop up elsewhere in the country due to common ownership or syndication.
And don’t forget to donate to the gofundme :whistle:
Oops must be an England Rugby fan
how about some tiny mouse shopping bags, or standing on a paper sheet and squeaking stop in mouse. Eta. Just to say this comment ^ is obviously...
As a simple non scientist I think that whatever movement the step counter reacts to for that individual if a given intervention results in them...
On the Guardian article specifically I just went to the home page and I had to do some scrolling it wasn’t highlighted near the top of the health...
They are all adding their names because they are all believers in psychosomatic cause.
Oh specific multidisciplinary care when you really mean CBT/get
Wish he would properly retire.
Haven’t checked but surely as a public body they are subject to FOI
Maybe nowadays, they published some of the worst articles in the past - militant patients
Probably best referred to ME Association to tackle. As they have done with LP website
It’s a real mix. At least those who normally live in the alternative bubble will potentially be exposed to more sensible ideas. What is...
I use cuticle oil to improve the condition of my nails I have ridges that are more noticeable nowadays. Buffing the nails makes them a bit...
If it was patient centric it would say online as default, the approach taken of breaking a one day event into 3 zoom meetings over 2 weeks by the...
Agreed on hybrid meetings. Unless everyone is wearing a headset and the meeting is disciplined with no talking over or side chat it is very...
Also on this point of LC people not getting ME diagnosis it’s highly unlikely to be something LC advocates would be interested in engaging with...
Yep both definitely happen for me. Both physical and cognitive. As well as getting physically drained mostly linked to orthostatic issues...
@JemPD interesting idea of approaching Ed Stafford. Maybe picking up from his approach of engaging with people to get their first hand experience...
On NICE implementation I just reiterate my usual point, there are places, ICBs now, that have literally nothing for people with ME/CFS they would,...
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