//=time() ?>
Twitter is over capacity, well join the #pwME club. Time for a rest.
Feasgar math
Good afternoon
Guid efternuin
Tráthnóna maith
Tha mi an dòchas gum bi latha sgoinneil agad
I hope you have a great day
I hiner ye hae a stoatin day
Tá súil agam go bhfuil lá iontach agat
Diary comics from today that have, as always, ended up being about my illness
#HourlyComicDay #HourlyComicDay2023 #pwME
The imaging showed an extensive meningeal lymphatic network around the cavernous sinus in the back of the skull - where people with #LongCovid and #pwME often have severe headaches....
3/
UK Health Secretary, @sajidjavid, has promised radical changes for ME patients and posts a tweet saying the disease has received too little attention and therefore he will develop a cross-govt plan to improve outcomes.
May other countries follow his lead. #pwME #MEcfs
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
1/n
Want to buy a cute card to raise funds for @theslowlane_ME's Tea Party for M.E.?💙
I got you covered!☕️
The cards come with their own individual envelopes & are from a professional printer 💌
You can find them on my Etsy shop: https://t.co/MN3VZN77Ji
#pwME
#MillionsMissing
Thank you to everyone who bought a card to raise funds for @theslowlane_ME's Tea Party for M.E.💙
The first batch has just been sent this morning!☕️💌
If you want to grab one, you can find them on my shop: https://t.co/MN3VZN77Ji
#pwME
#MillionsMissing
I'm a caregiver for a #pwME one of the #MillionsMissing Our lifestyle has become everyone's norm. Housebound. Unable to find answers in modern medicine. Zoom appointments. Myalgic Encephalomyelitis cases will increase with COVID-19 so this could remain your norm. See @MEActNet
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
No.2 “but you don’t look sick” 👀
#pwme #meawareness
ME Awarness themed illustrations✨
No.1 “not just tired”
#pwme #MEawareness
@HeelGezondeMama And here’s the second cartoon. Sadly this is a true story. I changed her name for privacy. Her husband found her collapsed on the way to bed and autopsy report read as below in speech bubble 🙄 There’s nothing natural about dying at age 39!!! 💔😢 #pwME #MEawarenesshour
Living that #period life.
Doubly fun when you’re a #Spoonie living that #ChronicIllness #Disabled life!
(Shout out to the #endometriosis community on this one - you guys are badass.)
#artwork #illustration #PeriodProblems #mecfs #pwme #disability #spooniehumor #spoonieartist
@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
Wishful thinking didn't work. Went to bed hoping for a good day to draw. But it's a high pain, low movement, tears overspilling sort of day. I want to remain hopeful, but for how long can hope fight against this relentless assault on my body and psyche?
#MEcfs #pwME #ChronicPain
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
It can be difficult for children to understand the impact of #MECFS. If you are struggling to explain the condition to them we have a number of children's stories available to help.
-My sister has M.E.
-I have M.E.
-My Mummy has M.E.
https://t.co/CdwB9SwLrj #pwME #Spoonie