I don’t see oncologists as bystanders. They are directly affected as this MUS and gatekeeping approach is affecting their ability to do their job effectively.
Yeah so the spa music and eye mask don’t make you relax a bit it
absolutely definitely the stickers that are a completely genius new invention. Tale worthy of Hans Christian Andersen
hear hear. I’ve now had a chance to look at the pictures. The woman in the picture that appears to have offended some is a similar build to me. I think the images are intended to be easy to understand for the intended audience. The UK population includes people of all shapes and sizes so...
Chris’ room looks like it is one of those old buildings with pretty high ceilings made me think maybe an acoustic issue?
I had to turn the sound up a bit too and then could hear ok
good conversation - 2 top blokes :thumbup:
These psychosomatic people choose to read normal human reactions to difficult situations as “catastrophisation”. I choose to read it as common sense learning from experience.
Agreed still symptomatic, for me on a good day I am at the upper end of mild, good for me is being able to take part in a social activity out of the house such as watching my team play football or lunch with friends.
eta probably should have said I once every couple of weeks for a big activity...
this
also, if like me you’re not severe, taking the opportunity of talking about how you’re affected to explain that there are people who have severe/very severe ME
Also because the headline was about severity perhaps just using that word made a difference especially to anyone unaware that ME can actually be severe.
When you don’t live with stuff it goes off your radar. Also it’s like learning at school an element of repetition is necessary for information to sink in.
Thus proving there’s no difference between these corporate purveyors of CBT online as a panacea and ‘big Pharma’
CBT deflection tactics used just as antidepressant deflection tactics. Any old product as long as the patient can be fobbed off with it
The fact that for 10/15 years the NHS CFS clinics actively discouraged people with ME from engaging with patient organisations must have contributed to this situation.
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