Anyone with less severe ME will be trying to return to work in their existing job starting on reduced hours and many will not be able to achieve that.
Fatigue will mean something different to each of the 100
I’d expect a substantial minority 30? to have had a gradual onset and would have been Ill for years rather than months before getting a diagnosis.
Exercise is medicine…… Ok then Medication can be deleterious in the wrong circumstances Exercise can be deleterious in the wrong circumstances
maybe try emailing
Obviously they would pick up stuff from social media to use in segments but I always wonder about trying to catch people’s attention using social...
The psychosomatic proponents have effectively sucked up government research funding as well as dominated guidance on MECFS until very recently....
BPS as in the Psychological Society presumably? Oops Sorry just seen the thread title
Who gets the advantage :whistle:
Psychosportbabble
:thumbup::thumbup:
Are the participants informed their “illness perception” is the subject of the research they are taking part in. I wonder if anyone has...
There’s been other papers posted I think “linking” inflammation and “functional” Tripe
Sorry for stating the obvious but might help others that erythrocytes are red blood cells (I had to google it)
Good riddance
Only 38 signatures from 11k now looks likely to go over that hurdle by the end of May
It’s on 80% now £52k.
Nobody has ever suggested LP to me. I think most people are aware that I keep up to date with developments and if something was a good idea I’d be...
https://www.change.org/p/cochrane-withdraw-the-harmful-2019-exercise-therapy-for-cfs-review 73 short of 11k now 10,927
They should just go off into a corner and spend their time analysing the personality profiles of psychosomatic proponents
Separate names with a comma.
