She/they
Post where somebody severely affected by ME/CFS shares relatable messages about the thoughts running through their head due to having to spend so much time alone with their thoughts
https://meglobalchronicle.wordpress.com/2022/09/25/thought-scramble/
@mecfs #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #MyalgicE #PwME #ME #MyE #MEeps #CFSME #CFIDS #SEID #NeuroME #SevereME #SevereMECFS
#SevereCFS #VerySevereME
You know, I want to be wrong about #COVID. I want to learn that my degree of caution is unnecessary. I would love to stop alienating the people I love because their "careful" and my "careful" aren't the same.
It's just that the stakes are so high. The misinformation is so high. The good information that we do have indicates that to be truly confident, you need layers of protection (eg vax + mask + ventilation + distance + testing). My comfort zone is for a lot of those layers, more than most people feel is necessary.
I'd love to be proven wrong.
Image to help explain postexertional malaise (PEM), to use for the upcoming holiday period or indeed any time.
From:
#FacetsOfME-Centering ME During the Holidays
https://meaction.net/2022/12/08/facetsofme-centering-me-during-the-holidays/
#MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MEcfs #CFS #PwME @mecfs
@halcionandon In case you’re not already aware of them, it may be worth contacting this ME charity.
@halcionandon Here and sending đź’ś.
I don’t know many people on here to ask for help but have contacted ME Action via Twitter.