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Via @MEAssociation It's ME Awareness Week from 9th to 15th May 2022
#pwME #MECFS #MyalgicE #MEAwarenessWeek20222 #MEAW2022 #JustOneWish
A talented individual (WantedAlive) thought up these cartoons and employed Rick Menard to illustrate them. They said they can be freely shared around to raise awareness and understanding of #MyalgicEncephalomyelitis / #ChronicFatigueSyndrome
#MEcfs #CFS #MyalgicE #PwME #MyE
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The horrible history of #MyalgicEncephalomyelitis How medical misogyny & decades of medical malfeasance by a faction of psychiatry led to no treatments for #MECFS & #LongCovid patients in 2021
https://t.co/edMwj4nPXv #meawarenesshour
There are 17 card left on my Etsy shop to raise funds for @theslowlane_ME's Tea Party for M.E. ☕️💙
https://t.co/MN3VZN77Ji
And here's a a little animation I made to get you in the Blue Sunday mood - happening on Sunday 16th May 🛀🥧
#MyalgicEncephalomyelitis
#TeaPartyForME
Being believed is more rare an occurrence than seeing a unicorn in your bathtub.
#MyalgicEncephalomyelitis
There is an estimated 24 millions patients living with #MyalgicEncephalomyelitis #mecfs around the world, 25% housebound or bedbound, sometimes for decades, no biomarkers and no approved treatments. We hope that #COVID19 research will look at biological mechanism of #LongCovid
PLEASE LIKE AND RETWEET ❤️ @MEActNet #MillionsMissing #shareyourart @mermhart @jenbrea Depicting my 15 year #lockdown with #verysevereme #bedbound in my ‘cell’ yet still desiring the technicolour of a normal life - bursting from my heart. #MyalgicE #pwme
@abcnews Thank you ABC for writing this story and Tony (& wife) for sharing your experience. Very relatable, 'like you're wading through wet cement' & that's on a good day... #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #MECFS #pwME #MyalgicE #CFS
Dr. Koroshetz doesn't get it!
@NINDSdirector
refuses to fund research to end the #MyalgicE health crisis. This is #NotEnough4ME & we won't stop fighting until our demands are met! Sign/share
@meactnet
petition: https://t.co/ETqJ5ukVph
#MyalgicEncephalomyelitis #Spoonie
Via the newsletter of EMERGE Australia
New blog 'Illustrator Interrupted' currently on break from illustrating children's books #kidlitart #mecfs #me #cfs #pwME #MyalgicEncephalomyelitis #Fibromyalgia
#autoimmunedisease #hashimotosdisease https://t.co/iBqjmDEu5E
I’ve been feeling like Kaneki Ken in the first 3 episodes of Tokyo Ghoul...sick af and puking everything TF UP.💦
That’s the real reason why I did this cosplay 4yrs ago.🖤🔪✨
#cfs #chronicillness #Fibromyalgia ME/CFS #myalgicencephalomyelitis
Some dark humour for #MECFS awareness week. Sadly, my inspiration to draw this was from a true story... https://t.co/FYfzA0Y62P #MillionsMissing #may12 #mecfs #me #cfs #MyalgicEncephalomyelitis #ChronicFatigueSyndrome #fm #Fibromyalgia #meAction #pwME #pwMECFS @MyalgicE
I’m honoured that my ‘Elephant & ME’ illustration is to be displayed in Belgium Art Expo ME in Words & Pictures #May12 #MECFS International Awareness Day. Full article & stories of 2 inspiring people #pwME here… https://t.co/SGSdARPQiN #MyalgicE #MyalgicEncephalomyelitis #CFS
Today's feels #mecfs #chronicillness #myalgicencephalomyelitis @MEActNetUK @MEAssociation
Here’s a plain pumpkin in case anyone wants to doodle a spooky face on this instead of carving with weak, clumsy fingers! #meawarenesshour #MEfriendly #pwme #myalgicE
Still recovering from #MillionsMissing #MEawarenessDay
#mecfs #spoonies #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
My 2016 image depicted that although people with #MyalgicEncephalomyelitis can appear well, under the skin the ME is affecting the muscles. Last years image depicted how ME takes a hold of your body and is always there whether you can see it or not. #millionsmissing #MEawareness
💙 Tomorrow, #May12 is Awareness Day for #MyalgicEncephalomyelitis and #ChronicFatigueSyndrome #MECFS and #Fibromyalgia #FM 💜 For me, this is personal. continue reading... https://t.co/KrNbYNxlKQ @jenbrea @MEActNetAu @MEActNet #MillionsMissing #MEAction