On #InternationalMensDay, some articles on men & #MyalgicEncephalomyelitis
Not So Macho: A male perspective on M.E. https://t.co/gUo64nX9a4
Men with #CFS https://t.co/PuOG4ZeN6d
'Men & M.E.' booklet (2007) Intro: https://t.co/pbFTjctOPn
Booklet: https://t.co/rTfknFxHSD
#MEcfs
#MECFS#chronicallyill
3 years in which my feet haven't touched the ground.
Days of pacing. Be brave.
5 seconds on my feet.
Now rest. The body has to rest. But my mind is calm.
I can and will win this battle. Someday.
🧵
Here are the only shoes I’ve bought* in the 28 years I have been virtually housebound with ME/#CFS.
This is covering ages 22-50 which
could be called your prime years. I think they get across how limited
my life has been due to the illness. 🙁
#MEcfs#PwME#MyalgicE
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