Es gibt immer noch eine große Lücke zwischen dem, was die Öffentlichkeit über COVID-19 weiß, und dem, was sie wissen sollte. Deshalb hier Infos über COVID-19.

Living an increasingly small life enforced via chronic illness yet striving to embrace snippets of delightfulness wherever and whenever I can #MillionsMission

Spouse, Mom, Nana, #Decentarian. Clean the air! Union Proud! MPLS "There's some good in this world, Mr. Frodo... and it's worth fighting for". - Samwise t

Depleted human. Slowly making photographs about a life with ME/CFS, like Long Covid. https://linktr.ee/andrewgifford.photography Bristol, UK. 335.42 ppm. He/h

Mostly bedbound by severe #ME/CFS #POTS #EDS #MCAS + more. Chronically hopeful for better days. Determined to fight against injustice so people with ME + Long C

Unbeliever (political & religious), Wales rugby, #c4news, porridge, tea, #MEcfs 'Obvious but wrong' Also JTJ on the other place https://johnthejack.com

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

Here to learn

Nature lover🐦, peace seeker, gentle soul. From engineer to psychology graduate. Now more husk than human🐌: Housebound Pw #MECFS #PoTS #CPTSD #Menieres

ME/CFS | Long COVID | IACC

Friend, storyteller, auntie, explorer, cat mom, islander. Pronouns: She, her, aviatrix. FKA ameliaearhart1.

30+ I am trans, chronically ill (Myalgic Encephalomyelitis,) disabled and tired. AUDHD as well. I like anime, video games, plants, yoga, and anatomy. Asexual

Finance & Art. History & Sociology & Fashion History. ME/CFS & LC 🫩

Professor of Human Geography at Uni of Liverpool, research on chronic illness, energy limiting conditions, fat embodiment. Feminist, Fat Activist, Spoonie, PwME

ME. Spouse w LC, ME. Writer, bread baker, daydreamer. Still waiting on fair funding and apology from HHS. Masking like someone’s life depends on it.

Climate crisis, reader, me/cfs, allergies. You DM, I block.

(Dimensional Sliding Chibi Vampire) 🔞+ only MutualAid: dianamutualaidsupp PFP by cyb3rd0ll Header by @KyandyArt on Twitter 30+ Partner: @shadowsfang1.bsky.soc

Animagus. Hearty but not hale. Celebrant of beautiful action. Likes bicycles. Note: The only time I post with my real name is in scientific journals. Kaurna Co

Mom, grandma, retired teacher & secretary. Yellow dog Dem. Every act of kindness is an act of resistance. Nobody has justice until everybody has justice. She/he

🏳️‍⚧️ he/they +18 please (i reskeet NSFW) pfp: cow in pool banner: Communists, Haters, Perverts and Boring Individuals 🇵🇸 donate to Shrouk Al-Qita'a @shro

Housebound by MECFS, mostly bed/ Sofa since 2022 Bildschirm triggert PEM, deshalb selten hier & Energiebudget reicht nur für liken und weiter verbreiten Lebe in

Living with ME/CFS since 1983. An advocate since my diagnosis in 1988.

Demokratie ist schön, macht aber viel Arbeit. 🐲 🚲♥️ Fahrrad * Respect Cyclists Berlin e.V. * ADFC Berlin * abgehärtete Kurzstreckenpendlerin mit Bahn & Bromp

95% of posts on #MyalgicEncephalomyelitis, #LongCovid or #chronicillness. With ME/CFS 37 years, severe ME 32 years. @IrishMECFSAssoc trustee 29 years 26 publ

🍋eugenics leads to fascism🍋LC/ME/MCAS/lupus/endo🍋still with her🍋OG khive🍋smash the motherfucking white supremacist patriarchy on the right AND the left🍋

Medical Gaslighting; Psychologisierung, Stigmatisierung von ME/CFS, PAIS; Kritik an "Psychosomatischer Medizin" Universität Leipzig sie/ihr, they/them

Irish Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Association-for Information, Support & Research NB: Posts ≠ advice. Registered Charity RCN 20100254.