So many thoughts on this, frustratingly brain wont cooperate right now, one thought I can get out though is its a bitter pill to swallow that no one is going to held responsible for my deterioration and zero help/warnings and 19 years wasted on what could at least been monitoring and info...
Haven’t read through it all yet,definitely needs more on severe M.E. but was thrilled to see ‘Pacing should not be seen as a treatment, but more as a way of coping with the impact of ME’
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