Anything about current clinics/community based services only picks up a minority of the picture. The ICBs who do nothing should be engaged to ask how they consider the needs of people with ME/cFS are currently being addressed.
Yes. I didn’t vote https://www.s4me.info/threads/was-there-a-gap-between-trigger-and-onset-of-your-me-cfs.40505/page-2#post-557531
but I think comments about how difficult/impossible for some are still relevant
True Peter. I had Gastroenteritis and then Chicken pox within a month 15 years before ME/CFS symptoms started. It might have contributed but who knows.
If I got ME/CFS from a virus it was a normal level cold/flu/laryngitis or gastro. I have no idea. From early 40s my health gradually got worse with regular episodes of such illnesses but also ok spells. Then at some point in early 50s I was either poorly enough to be off work or felt like I was...
When I moved 5 years ago I went to a local furniture manufacturer’s factory shop to buy a sofa. I insisted on lying down to make sure it was long enough to stretch out
Madan et al MECFS guidelines for occupational health 2006
https://www.s4me.info/threads/occupational-aspects-of-the-management-of-chronic-fatigue-syndrome-a-national-guideline-2006.2604/
MEA already have an area on their website for clinicians including links to the nice guidelines, how to obtain a purple book and a link to the existing e learning module.
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