Brilliant 👏

(By ImAliceElla)

#ME AwarenessMonth #pwme #ME #MyalgicEncephalomyelitis

Today is #WorldMEDay . My partner Soph continues to get worse and I have written a small piece to try to describe - in a tiny way - what it is like a the moment. She has also allowed me to share one of the most recent photos of her. #pwme #MECFS #severeME #MEAwarenessDay

#MECFSawarenessday #pwME

How #MyalgicEncephalomyelitis shrinks your world...

Illustration by Kornelia Paulsen

#pwME
#MillionsMissing
#WorldMEDay
#MEAwarenessDay

A friend sent this to me and it gave me a little optimism in this phase called #longcovid may it give someone out here a glimmer of hope too. They have to help us. We are too many to ignore and will double and triple sooner than they think. #stayvigilent #mecfs #pwME

thank you. #pwME

#MEAwarenessDay

Acronyms explained

#MEcfs #CFS #PwME

UK #MyalgicEncephalomyelitis research spend with [sic] 1.3 million people affected.

£800,000 per year

61.5p per person per year

Then they punish us for not being well enough to work

#pwme #ME #MyalgicEncephalomyelitis #ME AwarenessDay

For #MEAwarenessDay , I’ve written a poem to try to express how I’ve felt at my worst. It’s sad, it’s dark, it’s certainly not sugar coated. This is the reality of people living with #MyalgicEncephalomyelitis #pwME #MECFS #LongCovid #PEM

#pwME
#MyalgicEncephalomyelitis
#MillionsMissing
#MEAwarenessDay
#WorldMEDay

Crushed and chained by #SevereME for 20 years.

Self portrait by Ruth Braham 🔥

#pwME
#MyalgicEncephalomyelitis
#WorldMEDay
#MEAwarenessDay
#MillionsMissing

Hoe dystopisch is het biomedisch onderzoek van Rosmalen dan? Waar liggen haar belangen dan? Hoe kan je #pwME nog meer schofferen?
Het aan de kant gooien door ZonMw van het aannemen van het amendement Drost door ons parlement geeft Rosmalen kennelijk alle vrijheid.

My daughter is forgotten, it’s time for that to stop - 9+ years now!!
#MEAwarenessWeek
#DontForgetME #PwME #MECFSawarenessday

I'm Nevra. I'm 28 years old, I have ME & I'm permanently trying to escape abuse and World ME Alliance have done a writeup on my story. Please click the link below to learn more about me. The article has a GoFundMe link at the very end. Thank you worldmealliance.org/2024/04/people… #pwme

Diagnostic test with 91% accuracy from Oxford UK can identify hallmarks of M.E./CFS in blood cells eng.ox.ac.uk/news/diagnosti… This M.E. Diagnostic test needs more money to continue. Action for M.E. ME Association Elon Musk #pwME #MyalgicEncephalomyelitis

Powerful account of being a carer for #pwME and devastating toll it can take. Thank you Colin Vallance #IstandwithUkraine#FBPE 🙏💙

#MEAwarenessWeek
#ExposeMENow
#SevereME

Wow...Jess Phillips MP has joined the #ME train 😀👏

#welcome #pwme #MyalgicEncephalomyelitis

Gracias infinitas a quienes habéis participado 💙

🆘️NECESITAMOS
👁VISIBILIDAD
🙏RECONOCIMIENTO
🔬INVESTIGACIÓN
🏥CUIDADOS

Nos va la vida en ello
#12Mayo #DiaMundial #EncefalomielitisMialgica

#WorldMEDay
#MECFS
#GlobalVoiceForME
#MEAwarenessDay
#MEAwarenessMonth
#pwME

If you watch one thing today, make it this powerful video on behalf of the millions of people living with #MECFS and be part of the #GlobalVoiceForME at worldmeday.org.

#WorldMEDay #MEAwarenessDay

#MyalgicE ncephalomyelitis #pwME #MyalgicE