Sometimes having an mitochondrial condition is hard, especially when you want to draw. Or wash and dry your hair.
Fortunately, my Mum can help with that last one.

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The horrible history of How medical misogyny & decades of medical malfeasance by a faction of psychiatry led to no treatments for & patients in 2021

https://t.co/edMwj4nPXv

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But have you tried…?

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https://t.co/CLzYWlW0Kf

🌈841刺繍マスク再入荷しました❣️

メンズサイズL,M
レディースサイズ(S)

    

https://t.co/CLzYWlW0Kf

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All we have in our heads is the strong desire to get back to life.


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There is an estimated 24 millions patients living with around the world, 25% housebound or bedbound, sometimes for decades, no biomarkers and no approved treatments. We hope that research will look at biological mechanism of

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【筋痛性脳脊髄炎】を知ってください。
患者さんたちは今も病と闘っています。

ブルーフォトチャレンジで応援します💙




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【筋痛性脳脊髄炎】を知ってください。
患者さんたちは今も病と闘っています。



5 16

I love how allows me to draw half decent illustrations while stuck in bed w

dry ink outliner & my handmade watercolour brushes imported from

1 5

Living that life.
Doubly fun when you’re a living that life!
(Shout out to the community on this one - you guys are badass.)

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Share the stories and important information about M.E. & RT the words of others, together we can break the isolation and invisibility sufferers have been forced into for so long.

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患者さんの環境が整い、笑顔になって欲しい。そんな花びら(患者さん)を集めたい😌🌸



… 画像は さん作です。ありがとうございます🙏🏻💗

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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...

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Today Wonder Woman Tabitha began her run.
She’s completing this 1400km challenge through 2020 as she raises money for , raising hope for many of us living with this illness.
To celebrate I drew a puffin.

https://t.co/p3TwywU8Q9

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2009 selfies to 2019 selfies (stopped hiding the bottom of my face, stopped only taking pictures of my hair after it had been pulled straight in a bun all day, recovered from depression, developed some positive self-esteem, and got diagnosed with )

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