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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
It’s M.E. Awareness Week. A condition often misunderstood. M.E is individual to the person who has it. To our M.E pals, we see you, we got you and we want you to continue to share your stories. #mecfs #cfs #chronicfatiguesyndrome #chronicpain #chronicillness #MillionsMissing2019
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
@theandrewgurza I'm loving this thread full of talent. Illustrator here https://t.co/4JkCDjSdz0 I love illustrating children's books when I'm able to... #mecfs #pwme #autoimmunity #rheumaticarthritis #UCTD #fibromyalgia #connectivetissuedisease
Dear Universe,
This was Sunday, a wonderful few hours with my good friend, we (re)discovered @StoryhouseLive with @matthaig1 talking all things mentally significant.
But it’s now Thursday & I’d just like my body to calm down so I can do some more nice things.
Diolch,
Yvie
#MEcfs
This is how my heart is feeling today. Wish my body would keep up! 😂... Huge thank you to all who helped support us 🦋💕 We raised over $2000 for @EmergeAus & as promised, given our own $2000 to biomedical research for #MECFS #NCNED https://t.co/49716d4cRg #pwME #cfs @ #GCM19
One of the symptoms of #mecfs is extreme sensitivity to stimulation. For me sound and vibration were especially challenging though that is slowly improving. This #symptomatology #embroidery represents how sensitive my neurology was at the time. #SciArt #SciArtTweetStorm
Today's feels #mecfs #chronicillness #myalgicencephalomyelitis @MEActNetUK @MEAssociation
Still recovering from #MillionsMissing #MEawarenessDay
#mecfs #spoonies #MyalgicEncephalomyelitis #ChronicFatigueSyndrome
💙 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
Building on progress of #EMERG taking #MECFS further forward #BRMEC6 & #IIMEC11 June 2016 http://t.co/ln2oNhzf88
Sinceretks @sixwaylymie
4 all contributions 2
#lymedisease #lyme #biowarfare #ms #als #mecfs #cfs #fms
RIP dear soul