Craniocervical Instability (CCI) and Spinal Stenosis are two conditions that have been associated with ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) and Fibromyalgia, and can affect the symptoms experienced by individuals with these diseases.

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Did you know that Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) affects an estimated 17-24 million people worldwide?
It's time for more research and understanding of this exhausting illness.

Join to help spread awareness for

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You suffer from ME/CFS at we help you, did you know that: May 12 is International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Awareness Day😴 we recognize and support millions of people who have ME/CFS by raising awareness and providing education.#TiredAF

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I'm thrilled to be part of - raising awareness for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (MECFS).

We spread the word and support our fantastic artist, , who suffers from this debilitating illness.

💤

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Millions worldwide suffer from Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

It's a debilitating illness that deserves more attention, research, and support from society.

Let's raise awareness and work towards new understanding and treatments for

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My Bloodborne PC, Percy. Poor dude is out here, anemic, has like, myalgic encephalomyelitis, needs a cane for some mobility issues, and his bright idea is that there is absolutely nothing wrong with going to Yharnam for treatment.

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The last of my artworks is about Very Severe Myalgic Encephalomyelitis which has been described as a living death.

My artwork represents the darkness Very Severe M.E patients live in. Cut off from the world and hidden behind the four walls of their room.

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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 /


1/n

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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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There are 17 card left on my Etsy shop to raise funds for '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 🛀🥧


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Drew this 👉🏻👈🏻

ME* & Me

*(Myalgic encephalomyelitis. Aka Chronic Fatigue. Yes, I had to google that.)

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Being believed is more rare an occurrence than seeing a unicorn in your bathtub.

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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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I'm a caregiver for a one of the 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

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Non-classical MHC class II chaperone HLA-DO/H2-O controls CD4 T cell thymic selection; its loss leads to susceptibility to 2 murine diseases, collagen-induced & experimental autoimmune https://t.co/M2Iv3qckiM

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

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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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Via the newsletter of EMERGE Australia

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