#meawarenessmonth

[theshoegirldiaries]

For #TeaPartyForME2021 See Tea Party For M.E. for how to participate and donate to M.E. charities to raise funds into the research we so desperately need and do not get.  Post viral illnesses are on topic these days, but they are not new.  I’ve suffered for almost 2 decades after a bout of glandular fever and my life has been devastated by it.  We’re not faking being ill, we’re not exaggerating, most of the time we’re downplaying it and pretending to be well.  See us. Listen to us.  Understand us.  Help us.   

[cherylbenson]

#Repost @meactnet with @get_repost ・・・ #Repost @myillnessmythoughts with @insta.save.repost • • • How amazing would it be if that apology came via education & biomedical M.E research in these communities. Now that would effect change. * It’s time for change 🙌🏻 it’s time for #understanding #awareness the end of #neglect & for governments to allocate adequate funding for this life destroying disease known as ‘the living death’ #facts #meawarenessmonth #meawareness #millionsmissing #missingbutnolongersilent #endcfs #mecfs #meadvocacy #maymomentum #openmed #actionforme #endtheneglect #cfsme #thetruthoflifewithME #canyouseeMEnow

[komaeda-nagayto]

Graphics from @meassociation Chronic Fatigue Syndrome/Myalgic Encephalomyelitis is so much more than “just being tired”. I struggle every day. Over the years of being sick it has just gotten worse over time, from a mild case to a moderate case. These are various symptoms that people with #mecfs have to live with every single day. I can’t even begin to describe what I go through. The muscle aches. The weak limbs. The sleep issues. The fatigue I feel in my bones. It’s #meawarenessweek and #meawarenessmonth. I try to be open about it all year because I feel it’s important to bring it to light. There is not enough going in to studies for it. There is no cure, just management. #cfsme #cfs #chronicfatiguesyndrome #myalgicencephalomyelitis https://www.instagram.com/p/CO6WoeFpC9r/?igshid=dfvyehsn0tcz

[alishawhittam]

Remember people like me when you get to go back to your life, I will never get to go back to mine 😢#ME #SevereME #meawareness #meawarenessweek #meawarenessmonth #helpmeplease #raiseawareness https://www.instagram.com/p/B_1gKmTHMlt/?igshid=1omt7ztoloed4

[myalgicencephalomyelitiscfstom]

[lanakilamiller]

Welcome to my world & im sure many others in our community. Keep fighting. #Repost @myillnessmythoughts with @repostapp ・・・ #mecfs painful truths 🔵 Liking & reposting these posts helps raise awareness for much needed understanding & research so one day we might get to be able to LIVE instead of EXIST. 💙THANK YOU💙 #meadvocacy #MEawarenessmonth #meawareness

[jenicorn88]

Last night I was absolutely bone crushingly exhausted, in pain and wishing I could have a new body. I was listening to an audiobook but couldn't follow the story, the narrators voice was soothing to me. this has been my reality recently. Suffering a 'dippy-dip' (as my mum described it to the doc) #spoonie #meawarenessmonth #selfie

[elizabethbcn]

Dosed up on magic beans this afternoon! Also took my mitochondrial supplements this morning 😧💊👌I'm pretty sure there's no way I'd be up and out of bed without this bomb of a concoction 😉💁🏼 Going out for a lil walk 😛 #magicbeans #mitochondria #supplements #spoonie #forty #choosetolivealifeyoulove #life #meawarenessmonth #fibromyalgia

[chronicallyhopefulblog]

Get Your Own Personalised Millions Missing Poster For ME Awareness Month

Get Your Own Personalised #MillionsMissing Poster For ME Awareness Month! Share your story, raise awareness, show others they're not alone. Can be anon. #pwME #MyalgicE #SevereME #CanYouSeeMEnow #SpoonieBloggers #BloggingBed

#MEAwarenessMonth is coming up in May and I thought, since many of us cannot go to the live events in person, I’d like to help my fellow people with ME (pwME) to raise awareness online​ by offering you personalised Millions Missing posters​!

​I know ​you ​are an incredibly creative and driven group of people, but I also know that many are too ill to use their skills and talents as they would like…

[cherylbenson]

#Repost @jomoss1975 with @get_repost ・・・ Jess wants to be believed. #MillionsMissing London. @MEActNet #Ajourneythroughthefog #chronicillness #MECFS #MEaction #spoonies #chronicpain #MEAwarenessMonth #myalgicE #PwME #MEAwarenessDay #MEAwarenessWeek (at London, United Kingdom)

[chronicallycraftykatie-blog]

Was so great to wake up to my #spoonie jewellery from @100birdiesforME #MEawarenessmonth #mecfs #fibro #chronicillness

[myalgicencephalomyelitiscfstom]

Day 29 part #1 (3 minutes 6 seconds) Daughter tries to raise awareness and understanding of M.E., which her mother suffers from, with a film she made, "Sleeping Beauty". August 7 piece from a UK local TV station (ITV Meridian)                                                                                                                                                                                                                                

[lanakilamiller]

🙋🏼I do - #Repost @myillnessmythoughts ・・・ #mecfs painful truths 🔵 Liking & reposting these posts helps raise awareness for much needed understanding & research so one day we might get to be able to LIVE instead of EXIST. 💙THANK YOU💙 #MEawarenessweek #MEawarenessmonth #MEadvocacy #BelieveME

[jenicorn88]

No filter. No touch ups. Just me. With ME. Had a pretty ok day, rested until it was time to get ready to go to the theatre to see a contemporary ballet of rumplestiltskin with Mum. The hoke to watch an episode of castle and listen to an audiobook while I settle down to sleep. #meawarenessmonth #meawareness #cfsme #spoonie #invisibleillness