
I met a friend with ME for coffee. It was so good.
Way cheaper, and maybe more effective, than therapy.
Fortnightly reflections on myalgic encephalomyelitis (ME) and Long Covid for those who live it and those who want to understand more.
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Way cheaper, and maybe more effective, than therapy.
Cherry picking, misrepresentation, and PACE (again)
Taking the positives from an otherwise flawed piece
Popping my head back in from my travels

Something that cannot be overstated

Bespoke, tailored, expert, specialist - easy to say, harder to define
Psychiatry looms large in NHS care for ME, especially in very severe cases. Why do so many of us resist it?
My last post explained the crash that left me bedbound with ME for 18 months in 2022. Here's what happened in the following days.

An experience I'd rather forget but want to share

Reflections on reading before and after ME