When life leaves us blind, love keeps us kind. (The Messenger) Enjoy The Silence! Austria

Owned by a cat. Refugee from the hell place. ME/CFS for 34 years and counting. "Anti-recovery activist" ( some chance!) Boring.

Subscribe to my tech and online culture newsletter UserMag.co Listen/watch Power User podcast on all platforms!! Support my work on Patreon: https://www.patr

Physiker, Patentingenieur. Blockiere, zB Logikabstinenzler, verdächtige Accounts, InvestierDichReich usw. / (😷+8💉) : 0🦠

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

Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak. I care. Ⓐ💚, (FR/DE/EN, but posts in english) Clinging

Well, it seems I'm still on this plane of existence! Disability rights stuff, fashion history. Cumbria (UK). Autistic. She, for the moment.

Food obsessed traveler. Mountain goat. Professional data nerd. All opinions are mental.

Informed decisions & verifiable facts please, not opinion & belief. UK. 🇬🇧 Mine of occasionally useful information. NHS and healthcare 💙 #Equality #Justbe #I

#CannabisMedizin🥦 #MEcfs🪫😷 #IchBinArmutsbetroffen💣 #GGUltra📎 ᓚᘏᗢᗢᘏᓗ ✨Anne Brorhilker Fan Club✨ I may be sick, but I won't be still.📢 Profilbild, schlafend

ME/CFS, Long Covid & PAIS | science & physiotherapy | #SaubereLuft #CleanAir | 📍Vienna | posts/skeets = personal opinion www.verhac.at de/en

I occasionally try to explain and comment on ME research, or even contribute to it. And I advocate for more and better research.

One of #MillionsMissing since 2002 #MEcfs Diagnose 2021 🐦 @will_ins_Gruene

Surviving MyalgicE aka ME/CFS & AAG to tell the story, pwME & advocate w/ a JD. Into MEdical, Social, Climate Justice & Arts. ME-dical apolide, Human Neutrino,

he/him

Science defender and eco-worrier. (she/her) No DMs please (can't access).

ME-dically gaslit for 10yrs.

I'm Cal, in Toronto 🇨🇦. Doing tool and #gamedev, #film, #writing. Wrangling chronic illness, so I can get back to acting, circus, martial arts. Tech prefs: #M

Covid informed #PlusLife user looking for all the smart people I followed on the other place… #MECFS ally #sisterofpwme #millionsmissing #cleanair #covidisairbo

💛 Österreichische Ges. für #MECFS ⚡ NEWS zu #MECFS #pwME #myalgicE 👇 Informationen, Spenden, Kontakt http://linktr.ee/oeg_mecfs https://mecfs.at/

🦼 #ME/CFS Hungry for life, future, perspective. Instead, stagnation, trapped in MECFS hell "and then you have no choice but to search for life in the ruins

PD Dr. (religion, empirical education research) mother of Mila who suffers from very severe ME/CFS ME/CFS | Disability | Social Justice https://milaandmecfs.fi

Bouwjaar 1964 - woon sinds 15 jaar in het oosten van Vlaams-Brabant, samen met hubby - voorheen druivendorp bij Brussel - geïnteresseerd in mensen, natuur, kuns

Carer for my daughter with very severe ME | ME-Myalgic Encephalomyelitis |

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

Hausarzt, Immer mit Maske, für SaubereLuft, Impfbefürworter und Verfechter evidenzbasierter Medizin, KEINE Homöopathie

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