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#MillionsMissing #MECFS #emergeaustralia pic.twitter.com/cuvwoWOc8a
— Terry Field (@AlongsideME) May 8, 2021
#mecfs means that I am one of the #millionsmissing the freedom to strive & thrive, to be spontaneous and to let go; the vitality of my body at one with the world. #emergeaustralia pic.twitter.com/fPu0GgFI8U
— Garth Coghlan (@WildWoila) May 8, 2021
Millions Missing Gallery 2021
Millions Missing Stories 2021
Millions Missing 2020
We've taken the #mecfschallenge and so have some of our friends.
— Emerge Australia (@EmergeAus) May 7, 2020
Will YOU do the challenge on May 9?#mecfs #MyalgicEncephalomyelitis #MyalgicE #MillionsMissing pic.twitter.com/qA3WShLoyL
ME/CFS Awareness Week 2020 – advocating for people with Myalgic Encephalomyelitis.
— Rebecca Lee Williams (@bec_lee) May 10, 2020
I am one of the #MillionsMissing.#MECFS #MECFSAwarenessWeek #MECFSAwareness #Emerge #EmergeAustralia #MMSelfie #MECFSAustralia #MEAction @EmergeAus @MMissingAus pic.twitter.com/beK4W3tE0q
May 12 is International Myalgic Encephalomyelitis (ME) Day (and May is ME Awareness Month)
— Irish ME/CFS Assoc (@IrishMECFSAssoc) May 11, 2020
You can help by retweeting and/or liking this image.
Day #12#MyalgicE #MyalgicEncephalomyelitis #May12 #May12th #MEAwarenessDay #MillionsMissing pic.twitter.com/gFMScrXscK
#MECFS #MyalgicEncephalomyelitis #PwME#MillionsMissing #MEAwarenessDay pic.twitter.com/IRbjNzDGNX
— Manitoba ME/CFS Support Group (@mbmecfs) May 12, 2020
It's ME/CFS International Awareness Day: I used to worry that talking about #MECFS would hurt me professionally or make people think I was a deluded hypochondriac. Thank you, @gdbayliss, for encouraging me to write about it. https://t.co/6wxnkJlB3w #MillionsMissing #pwME
— Sarah Sweet (@catastrophizer) May 12, 2020
#MEwishes
— A Journey Through the Fog (@JourneyFog) May 12, 2020
"My exterior self does not reflect my interior self. Inside, I'm writhing, crying, dying. Outside, I will smile, laugh even. But that's because I have to keep going with some semblance of normalcy." ~ Raadkr, 49, Dakar, Senegal (she/her)#MEawarenessDay #mecfs pic.twitter.com/MwgoGZRC5o
๐ Our #millionsmissing 2020 in numbers! With thanks to YOU ๐๐(1/2)
— Emerge Australia (@EmergeAus) May 15, 2020
๐ฉโ๐ป 70,000+ people saw our content
๐นOur 5 top videos reached over 50,000 people!
๐นMore than 185 #mecfschallenge videos were shared
๐คณYou helped us create over 100 #MMSelfies
me, not having the bare minimum energy to participate in #MillionsMissing or #MEAwarenessDay properly because Iโm too severe: pic.twitter.com/oj2fNjOsjK
— Katarinaโจ๐ (@KatarinaBrandt) May 12, 2020
I'm doing the #mecfschallenge to raise awareness of ME/CFS and people living with Myalgic Encephalomyelitis and @Emerge Australia. Hard to say, harder to live with. #auspol pic.twitter.com/C0p8jURJas
— Patrick Gorman MP (@PatrickGormanMP) May 9, 2020
It's #millionsmissing #meaction awareness week. I wasn't expecting much change from the PMs announcement last night but the realisation of another month in lockdown has really flattened me.
— ๐พ๐๐๐๐ ๐ผ๐ง๐๐ฃ๐ค๐ ๐ – Children's Author (@AuthorGemma) May 11, 2020
I think it's important for us all to remember that for many who have #mecfs #MyalgicE… pic.twitter.com/cRBavC3EgM
#MEAwarenessWeek #MillionsMissing pic.twitter.com/8qNL8wHjB1
— Debs Dakin (@Dakin2Debs) May 16, 2020
It's #MillionsMissing #MEAwarenessWeek and artists with #MECFS are sharing their artwork today! Here's a lovely interview @MEActNet did with me last year about my #symptomatology #embroidery work https://t.co/2L45SPoBYg
— Lia Pas (@lia_pas) May 11, 2020
The ME You Donโt See – https://t.co/wVZjv4r2mT#MillionsMissing โShare you artโ day @MEActNet @PlzSolveCFS #MEAwarenessWeek #MEAwarenessMonth #12MAY #MAY12 #Illustration #Art #Artwork #Art4ME#pwME #MEcfs @mermhart pic.twitter.com/6Dw66aeUi7
— Illustrator Interrupted (@FranceyME) May 12, 2020
#International #MyalgicEncephalomyelitis #MEAwarenessDay
— Anniken Haga (@AnnikenHaga) May 12, 2020
Just gonna leave these here, as they say a lot about the life I and others like me live.
We are the #MillionsMissing pic.twitter.com/F2QTW6pKMF
"I wish people knew that they only see us when weโre โwell enoughโ to be seen. Preparing for a simple afternoon/evening out will often be months in the planning and involve a lot of extra rest time along with managing symptoms with military precision." Hannah West-Smith #MEwishes pic.twitter.com/YprfChgPqL
— A Journey Through the Fog (@JourneyFog) May 12, 2020
