میں زندگی کو بہت غور سے دیکھ آئی ہوں
سب کچھ ہے اس میں مگر اعتبار نہیں ہے
#MillionsMissing

#pwME #MillionsMissing #MyalgicEncephalomyelis
#MEAwarenessDay

🔹5月12日はME/CFS世界啓発デー🔹

なおるもん！のボイコミ作りました( ´•ᴗ•ก )

若干目がチカチカするので動画苦手な方はパスして明日公開の漫画版を見てね！

#筋痛性脳脊髄炎
#慢性疲労症候群
#コロナ後遺症
#MEAwarenessDay
#MECFSAwarenessDay
#MillionsMissing
#WorldMEDay
#LongCOVID

How #MyalgicEncephalomyelitis shrinks your world...

Illustration by Kornelia Paulsen

#pwME
#MillionsMissing
#WorldMEDay
#MEAwarenessDay

No one should have to go years without a diagnosis to a disease that affects millions. At #MEAction , we are working to change this by educating clinicians & med students about myalgic encephalomyelitis (ME aka ME/CFS) in a campaign called #TeachMETreatME . millionsmissing.org

- #MillionsMissing #TeachMETreatME @meactnet 's campaign to educate hospital systems and medical schools about ME/CFS by encouraging medical schools to Teach ME, and major hospitals to Treat ME. millionsmissing.org
Jo's fate may have been alot different if ME was more widely

We asked our community how long it took to receive their diagnosis of myalgic encephalomyelitis (ME, aka ME/CFS). Most diagnoses took years not months.

#MEAction ’s annual #MillionsMissing campaign has a theme of #TeachMETreatME this year. Learn more at millionsmissing.org.

Thank you to Emily (Kara Jane sister) for sending in this video to be part of #TeachMETreatME #MillionsMissing . Kara Jane touched so many.

Please join in today. Info at millionsmissing.org.

Full video:
youtu.be/h_PlrK0Nprg?si…

#WorldMEDay #pwME

Jennie Jacques #Vikings Actress FULL interview with #merryncrofts Family & Friend Smile For ME WATCH NOW
^*
We will not continue to be silenced
🔕 🤐 💙 ‼️ COMMENTS are ON
*
#MECFS #MillionsMissing
⤵️⤵️⤵️⤵️
*
m.youtube.com/watch?v=NrRpTJ…

𝟱𝟱 𝗹𝗲 𝗻𝗼𝗺𝗯𝗿𝗲 𝗱𝗲 𝘁𝗿𝗼𝗽 ! ❌
Ensemble, mobilisons-nous pour soutenir les personnes atteintes d’ #EncéphalomyéliteMyalgique
World ME Alliance
#MillionsMissing #MillionsMissing France #EM #EM SFC #WorldMeAlliance #WorldMeDay #journeeinternationaleEM #OMS #GlobalVoiceForME

Der internationale #MECFS -Tag ist auch beim 32ten Mal so wichtig. Zwar gibt es jetzt eine Versorgungsrichtlinie des G-BA. Doch für die tatsächliche Versorgung fehlt es an fast allem. Das müssen wir ändern!
Infos👉sbk.org/magazin/cfs-da…

#MillionsMissing #LongCovid

Welke arts wil jij 📘Landziek laten lezen?

Vandaag op #MEAwarenessDay wil ik kennis en begrip over de ziekte ME verder verspreiden.

Laat me weten wie & waarom ⬇️, ik kies een reactie uit en stuur het boek namens jou aan de arts!

#TeachMETreatME #MillionsMissing #MEAction

STEMMEN UIT DE SCHADUW 💬

Vandaag is het #MEAwarenessDay .

Graag vragen we je aandacht voor patiënten met de ziekte ME (Myalgische Encefalomyelitis)

Veel van hen moeten we al jaren missen in onze maatschappij.

🧵👇🏻

#NietHersteld #MECVS
#MillionsMissing

Or have to think about fighting for my life, everyday... Fighting for simple supports, like a MSP category of coverage for #myalgicencephalomyelitis or housekeeping +tests/treatments
#pwd #bcpoli #canpoli #meaction
#Disability #pwME
#MillionsMissing tumblr.com/myalgicencepha…

Mein Beitrag zu #ArtforMECFS , der nur mit professioneller Hilfe zustande gekommen ist. Meine kognitiven Kapazitäten hätten es niemals zugelassen.
Danke nochmal dafür. 🙏

Mein sehnsüchtiger Blick in ein normales Leben. 💙

#MEAwarenessDay #MECFS #millionsmissing

This is from 1997. Nothing has changed. Nothing. #MillionsMissing #ExposeMENow