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Teagan

@mecfs_with_tea

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Life & community w/ chronic illness:
Long Covid, Moderate MECFS, MCAS, POTS, HEDS, fibromyalgia & reactivated EBV
Art account: @artplaywithtea

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Glow in the dark Art Camp was epic!👻 Might need to do more art raves for kids this winter 💯✨

Thank you, Art Camp Fam! I can't believe this gets to be my job! So grateful for all of you, truly.🖤🤍

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what a sMASHING success!!! I cannot thank everyone enough for coming out to support us ❤️‍🔥 this show gave me an opportunity to really embrace myself and my community and I am moving forward from it feeling so loved and supported! can't wait to see what creativity this cracks open for me next... keep an eye out 👁️‍🗨️

huge thank you to the other artists and their wonderfully creative minds 🧑🏻‍🎨 and also to my girlfriend and mom I could not have pulled this off without their support!!!

check my etsy shop for originals, prints and stickers 🖌️

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Masking doesn’t mean you can’t still develop ME (he was masking), but it does reduce risk. And if more people masked, the world would be safer and more accessible for so many people.

Every time you choose not to mask, you’re sending a message to disabled people that their safety doesn’t matter. Masking is a direct way to show care for your community, even if you don’t think your individual choice matters.

We don’t have to be perfect at it. Practice wearing one around the house. Find masks that work better for you. Work through the discomfort and biases you hold.

And please, stop saying you care about disabled people while refusing to take basic steps to help protect them.

Caring about disabled people requires caring about disabled people when it inconveniences you, too.

(follow the tagged people to learn more directly from those living with ME)

#wearamask #myalgicencephalomyelitis #severeME

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Severe MECFS Awareness Day @runformecfs #mecfs #mecfsawareness #mecfslife #chronicillnessawareness #chronicillnesssupport

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Final part to this series 💫

#myalgicencephalomyelitis #meawareness #caregiver

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💙 💙

Part two 💫

#myalgicencephalomyelitis #meawareness #caretaker

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Today is Myalgic Encephalomyelitis (ME) Awareness day. Read about it. Learn from those with ME. Wear a mask. Please.

To those with ME, I’m so sorry. Validation and compassion aren’t enough. You all deserve so much more.

To those that love someone with ME, I see you. The grief is immense for all involved.

#meawarenessday #myalgicencephalomyelitis

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Loving someone with severe ME has reshaped how I understand privilege, access, and connection. Full slide descriptions are in the comments.

@m.e_and_sophs_ @vaguedistresss @nebulow @mecfs_with_tea @stillmasking @m.e_and_more @therealchronicillnesscrafter @francesha @whitneydafoe @whatdoesntkillyoumovie @the.chthonic.companion @quella_the_dizzy_octopus @living.life.with.m.e @thejournalingrat @lovenrageillustrations @my.liberation.space @misfortunatelyv @samanthahahehe @alexis___me

#mecfs #myalgicencephalomyelitis #longcovid

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