she/her ◦ ecology lover ◦ 🍄🟫 ◦
musings from the sickbed ◦ 🌻 ◦
one of the millions missing #myalgicencephalomyelitis ◦ 🛏️ ◦
@abrokenbattery.bsky.social
Severe ME patient currently on a 10% battery, the gas goes out more than I do. I also compile ME/CFS Awareness videos. https://linktr.ee/abrokenbattery
@cozydelaney.standingintheodds.com
they/them | 32 | western australia ♡ shiny hunter | premier ball enthusiast ♡ chronically ill cozy creature ♡ @cozycereza.standingintheodds.com ♡ https://linktr.ee/cozydelaney
@ntisec.bsky.social
Father, creative, thinker, asks questions. Since 1997 mild MEcfs, since early March 2020 rather severe longcovid. Dutch & English
@drinfosec.bsky.social
University prof. on cyber risk & systemic risk | He/him | Posts/RTs lots on #Covid #LongCovid. Covid is significant systemic risk. #COVIDisAirborne #MaskUp #IAQ #AirQ
@alexandrite113.bsky.social
@katieabey.bsky.social
Sunshine-haired creative force🧚🏻 Award winning book illustrator✍🏻 Helping you embrace your weirdness🐛
@wholesomecomic.bsky.social
Instagram: https://www.instagram.com/wholesomecomic/?hl=en Print shop: https://longhighfive.com
@bethdrawsthings.bsky.social
Art and stuff! Etsy, Patreon, and more - https://linktr.ee/bethevans
@positivelypresent.bsky.social
Dani DiPirro • Author / Artist / Optimist 📚 Into the Moment, Out of Your Mind, Grow Through It, & more
@titsay.bsky.social
illustrator • constantly changing • http://patreon.com/titsay • comm info: http://ko-fi.com/titsay/commissions • contact me at: titsay.art@gmail.com • prints at: inprnt.com/gallery/titsay
@anxietyfox.com
A little fox that is spreading love & mental disorder acceptance! Created by @naomiromeroart Inquires: naomiromero4@gmail.com
@sugarhai.com
🩷 cute art, sometimes funny, all original, made by me, a human 🩷 patreon: patreon.com/sugarhai 🩷 shop: sugarhai.com #kindness #cuteness #love #art #support
@sickgirlprobsss.bsky.social
👽I'll be your Disabled alien today🛸 Coping with lifelong chronic illness & pain 🦓 MALRO • EDS • IC • POTS • IBD • C-PTSD • ENDO • MCAS • *and fun No filter here 💅🏼 Theme park & adrenaline obsessed 💖
@chronicillnessfc.bsky.social
An inclusive community, resource hub & mutual support for people w/chronic & invisible illness. Friendship & Digital hangouts! 📍SF #EDS #MCAS #POTS #MECFS #PMDD #AuDHD #PTSD Mental health advocate, indigenous #LGBTQIA+🍉 Sign up at the form below🤍✨
@renegaderesearch.bsky.social
Renegade Research (RR) is a non-profit 501c3 decentralized organization pioneering patient and caregiver led research focused on ME/CFS and LongCovid... Website: https://renegade-research.org 💙 Project: @remissionbiome.bsky.social
@crookedneighbor.bsky.social
Former medical communications professional, current long covid patient and caregiver, mask daddy, scheming for better housing and social services for pwME/LC (she/her) #NoNYMaskBan
@ethyricalartist.bsky.social
Losing my housing pls see links! Disabled artist 🇵🇷🏳️🌈 Create from🛏️when able due to #MyalgicE #POTS #Endo etc🫠 Cats, art, plants, knit & crochet Late diagnosed #Autistic PNW 🇱🇸 #DisabilityJustice Abolitionist Anti-imperialist https://linktr.ee/EthyricalArtist
@somethingchronic.bsky.social
95% bedbound by ME/CFS, POTS, hEDS, MCAS and more. Chronically hopeful for better days. Determined to rise up against injustice for a world where pwME and LC are treated with the same understanding, kindness and belief as any other serious physical illness
@mecfsnanoneedle.bsky.social
Severe #MECFS Patient Bedridden. No energy to speak. #MECFSDiagnosticBiomarkers Drug companies need a #MECFS and #LongCovid diagnostic blood test for successful clinical trials. https://mecfsdiagnosticbiomarkers.substack.com/
@montereybayaquarium.org
How do you do, fellow squids? 🌊 We're your frondly Aquarium with a mission to inspire conservation of the ocean. https://www.montereybayaquarium.org
@thisthingblog.bsky.social
Hi, I’m Jenny! (She/her) ✏️ Chronic illness and disability content. “For when ‘Get Well Soon’ is just a bit shit”. Freelance designer, consultant, small biz owner 🏴 https://www.thisthingtheycallrecovery.com/links
@alilbitofaith.bsky.social
A Lil Bit Of Faith | 🇧🇩🤲🏾🏳️🌈 25 | Chronically ill, Disabled, Neurodivergent
@flashes.blue
A photo viewing client for u from the creator of @skeetsapp.com & @bluescreen.blue iOS: https://t1p.de/b3o4x Android: Not available yet ❓ FAQS: https://t1p.de/24kj0 🐞 Bug Reports: https://t1p.de/phwii 💡 Feature Requests: https://t1p.de/8tmnc
@wanderingkayli.bsky.social
@wandering on Instagram ✍🏻 Disabled with Long Covid 38+ months Long COVID Researcher @sfu-fhs.bsky.social Master’s Student @sfucmns.bsky.social writing on biopolitics & Long COVID https://beacons.ai/wanderingkayli
@edyong209.bsky.social
Writer, journalist. Science, health. Pandemics, animals. Birder, photographer. Many words, some awards. AN IMMENSE WORLD, I CONTAIN MULTITUDES. Married to Liz Neeley, parent to Typo. he/him 📷 Canon R6mkii + RF 800mm Edyong.me
@imjustkate.bsky.social
☆ Recently entered the world of chronic illness & disability with #ME/CFS. ☆ Personal & professional coach. ☆ Writer. ☆ Observer & listener. ☆ Lover of the magic of the universe, space & nature. ☆ Eternal optimistic realist. ☆ We're all connected 💜🕉
@swastrosarah.bsky.social
Speaking up for everyone affected by severe/very severe #ME. Medical science has everything to learn about human biology from the post infection disease ME. #MEKills backstory https://x.com/swastrosarah?lang=en-GB
@jayletay.bsky.social
Author of A Girl Behind Dark Glasses, A Girl in One Room and A Girl Beyond Closed Doors. Casual artist and public speaker too
@piengreta.bsky.social
a small chronically ill creature (moderate-severe ME/CFS) from finland, known as piengreta.
@viralpersistence.bsky.social
fund research and clinical trials for infection associated chronic illnesses now, and furthermore provide clean energy-powered hotel cold on demand for free. medicaid, not medicare, for all. aspiring #burquesky member.
@aiyawylde.bsky.social
passionate + fragmentary girl writer / queer / sensual / poly / ghost / decolonizing 🍉 leo sun•cap moon+rising severe ME • Lyme+co • CW mental health
@jesshoneybadger.bsky.social
Chaotic good writer and scientist with severe, bed bound MECFS. Writing wholesome stories, science stuff, and funny anecdotes from bed. Lover of memes. jesshoneybadger.substack.com
@diatoma.bsky.social
Ella/she/her. I write, I read, I draw plants. Chronically ill en la Ciudad de México. #ME #MECFS #POTS
@sabinehermisson.bsky.social
PD Dr. (religion, empirical education research) mother of Mila who suffers from very severe ME/CFS (Bell 0) https://milaandmecfs.files.wordpress.com/2022/05/mila-spiegel.pdf Vienna, Austria #CleanAir
@whitneydafoe.bsky.social
Severe ME/CFS patient and advocate. Writer, photographer, filmmaker. artist, activist, creative. Bedridden since 2013 sick since 2004. Never. Giving. Up. ✊
@katybrc.bsky.social
Myalgic Encephalomyelitis - M.E + POTS for 38 years Donor to the UK MEcfs Biobank for 10 years & @DecodeMEstudy Please watch http://dialogues-mecfs.co.uk/videos/ London, UK No DMs please #pwME
@adarkenedroom.bsky.social
One of the #millionsmissing || Raising awareness of the most severe form of #MyalgicEncephalomyelitis
@thisiscfsart.bsky.social
An online exhibit of creative expressions by people suffering from ME/CFS. Visit the exhibit at www.thisiscfs.art.
@louise-fox.bsky.social
She/her also comfortable with they/them. Former art therapist. Proud chili pepper parent. Living with severe ME and POTS. Giant nerd. From Berlin.
@naomidharvey.bsky.social
Zoologist & veterinary research. She/her. 22yrs with #MEcfs Pro-vax but vaccine injured. Life on pause due to moderate/severe ME/CFS ♿️ Patient Expert in ME/CFS, POTS and syndromic Long Covid. Please excuse my typos.
@paulaknight.bsky.social
Author, illustrator, comics memoir THE FACTS OF LIFE (Myriad) Kidlit Books x3 Writing illustration comics poetry photography Disabled nonambulatory bedbased 6yr #pwME No DMs pls https://linktr.ee/paulajknight https://ko-fi.com/bedscape She/Her
@itswhitneywitch.bsky.social
Disability Justice Living with ME, EDS, POTS, MCAS, vascular compressions, spinal comorbidities & more Ambulatory wheelchair user Cozy gamer, lazy gardener, hopeful baker
@janetdafoe.bsky.social
ME/CFS patient advocate and caregiver. Mom to Whitney. Spouse of Ron Davis. Child Psychologist.
@danwyke.bsky.social
M.E. inactivist, person-centred counsellor, recovering poet (Rack & Waterloo Press)
@exceedhergrasp1.bsky.social
Scientific Director, #MEAction Stanford Med Université de Montréal TIME100 Health 2024 #ME, #EDS, #POTS, #LongCOVID Views my own exceedhergrasp1 on Twitter