People can still access this online ME/CFS art exhibition at the moment
https://mecfssa.org.au/event/forever-in-lockdown
#MECFS #mecfsawareness #MillionsMissing #chronicillness #spoonie #invisibledisability #invisibleillness @mecfs
People can still access this online ME/CFS art exhibition at the moment
https://mecfssa.org.au/event/forever-in-lockdown
#MECFS #mecfsawareness #MillionsMissing #chronicillness #spoonie #invisibledisability #invisibleillness @mecfs
In Deutschland sind ca. 80.000 Kinder und Jugendliche an ME/CFS erkrankt.
"Anyone can help by learning about ME/CFS, for example here: https://me-pedia.org, or over on Sammy's Instagram: https://instagram.com/m.e_and_more, by supporting research and advocacy organizations like https://instagram.com/openmedf and https://instagram.com/meactnet, and engaging with our content to help get as many survey participants as possible!
#ChronicFatigueSyndrome #MyalgicEncephalomyelitisAwareness #MECFSAwareness #CFSAwareness #MEAwareness #LongCovid #LongCovidAwareness
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I thought I would repost this to highlight again some of the many varied symptoms that can be found in #MyalgicEncephalomyelitis/#ChronicFatigueSyndrome
Particularly relevant when similarities with the #LongCovid presentation in some people are being missed
#MEcfs #CFS #PwME @mecfs @cfs #meeps #cfsme #mecfsawareness
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Today's Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) International Awareness Day.
Please take some time to learn more about this illness, for example on the CDC website https://www.cdc.gov/me-cfs/resources/awarenessday.html or the website of Solve M.E.
https://solvecfs.org/
And please consider contributing to existing research (as a patient, control or researcher) as well as pushing for more research (donate, advocate).