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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My brainfog is very bad atm. I wish people knew, how widely limitting these cognitive impairments can be! It feels, as if i had lost half of my IQ, thinking & speeking slowed down to snail's pace, ongoing memory-loss, trouble finding words or finishing sentences!

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


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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!!! 💔😢

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Nice to see my illustrations circulating each week during - I’m yet to wake up early enough to post at that time. It’s quite early here in Australia 🥱😴 here’s a clearer image. 😊💙

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I've had ME since I was 10. Relapsing, remitting and getting worse with every relapse. That is a total of 36 years of battling with doctors who think you're a hysteric. Being yelled at, even. And accused of wasting time and money. Like we're in it for the fun 😒

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A friendly reminder that this is tonight, Wednesday, 8.0-9.0pm U.K. time. Do join in if you can, to spread the awareness, the companionship and your own ME story. Use the hashtag.

WE ARE STRONGER TOGETHER. 🤗

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How a body with myalgic encephalomyelitis feels like ?
It's a torturing disease ..

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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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Here’s a plain pumpkin in case anyone wants to doodle a spooky face on this instead of carving with weak, clumsy fingers!

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Here's a random unicorn I doodled for everyone affected by 💙🦄 We need magic.

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