Millions Missing

#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

We've taken the #mecfschallenge and so have some of our friends.
Will YOU do the challenge on May 9?#mecfs #MyalgicEncephalomyelitis #MyalgicE #MillionsMissing pic.twitter.com/qA3WShLoyL

— Emerge Australia (@EmergeAus) May 7, 2020

ME/CFS Awareness Week 2020 – advocating for people with Myalgic Encephalomyelitis.

I am one of the #MillionsMissing.#MECFS #MECFSAwarenessWeek #MECFSAwareness #Emerge #EmergeAustralia #MMSelfie #MECFSAustralia #MEAction @EmergeAus @MMissingAus pic.twitter.com/beK4W3tE0q

— Rebecca Lee Williams (@bec_lee) May 10, 2020

May 12 is International Myalgic Encephalomyelitis (ME) Day (and May is ME Awareness Month)

You can help by retweeting and/or liking this image.

Day #12#MyalgicE #MyalgicEncephalomyelitis #May12 #May12th #MEAwarenessDay #MillionsMissing pic.twitter.com/gFMScrXscK

— Irish ME/CFS Assoc (@IrishMECFSAssoc) May 11, 2020

#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

"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

— A Journey Through the Fog (@JourneyFog) May 12, 2020

📈 Our #millionsmissing 2020 in numbers! With thanks to YOU 🙏💙(1/2)
👩‍💻 70,000+ people saw our content
📹Our 5 top videos reached over 50,000 people!
📹More than 185 #mecfschallenge videos were shared
🤳You helped us create over 100 #MMSelfies

— Emerge Australia (@EmergeAus) May 15, 2020

me, not having the bare minimum energy to participate in #MillionsMissing or #MEAwarenessDay properly because I’m too severe: pic.twitter.com/oj2fNjOsjK

— Katarina✨🍅 (@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.
I think it's important for us all to remember that for many who have #mecfs #MyalgicE… pic.twitter.com/cRBavC3EgM

— 𝔾𝕖𝕞𝕞𝕒 𝔼𝕧𝕖𝕣𝕤𝕠𝕟 – Children's Author (@AuthorGemma) May 11, 2020

#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 Don’t See – https://t.co/wVZjv4r2mT#MillionsMissing “Share you art” 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
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

— Anniken Haga (@AnnikenHaga) May 12, 2020

"I wish people knew that they only see us when we’re ‘well enough’ 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