I believe HADs is one of the questionnaires they used at the CFS clinics I went to.
The only weather I have noticed affects my ME symptoms is very warm weather. When we do get any 30 plus C days I can’t really do anything but lie...
Signed :thumbup:
The only purpose this serves is paying the rent or mortgages of psychosocial researchers thus avoiding the need for catastrophising about their...
Yeah I worked for 12/15 years with ME possibly I could have carried on longer if I’d been diagnosed at the start and hadn’t spent 10 years doing...
:thumbup:You write really well @lunarainbows , succinct and yet comprehensive you should consider contacting AFME/MEA to get this info into...
Only skimmed it but wow those responses by K stink
Got to start somewhere. Hopefully there will have been some people not committed to the old approach speaking up. I would in some sense be more...
If the therapy is blatantly called psychosomatic therapy then presumably this only includes people who accept that diagnosis for whatever reason.
Maybe ask the author to provide their specific reference by CDC to central sensitisation it could be given the article is supposedly only based on...
Saw on AFME social media there have been 99 applications from PWME, 15 carers and 5 professionals
I have put in my application will let you know the outcome
I’m probably going to apply.
Diagnosed 6 years ago in my early 50s due to worsening from mild ME to increasing proportion of time in moderate episodes 10 years or more?...
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