https://www.sophiechapmantalent.com/people/tom-neenan/
https://tomneenanart.etsy.com
https://dice.fm/event/mxlvqk-tom-neenan-wip-4th-mar-the-bill-murray-london-tickets
Fantasy, Sci Fi and speculative fiction podcast, observed through the comedic lens of The Bugle. Hosted by Alice Fraser and friends.
Expect reviews, tropes and hot takes on books, film, games and TV from past, present and future.
Writing. Comedy. Podcasts.
Book: https://newsouthbooks.com.au/books/a-passion-for-passion/
ποΈ: Realms Unknown; The Gargle; AI & The Creative Professional; The Bugle
Join my Writers Meetings: http://buff.ly/3eFIs8x
Enquiries: info@gagreflex.co.uk
I am the host of Behind the Bastards and overlord of podcasts at Cool Zone Media
German, English, Spanish
Sociology, Medicine, General Practice
Living on unceded Gumbaynggirr land. Writing, thinking, learning, swimming, napping. Drinking coffee βοΈ.
Professor of Immunology, Imperial College London. Editor of OUP Oxford Open Immunology. Co-author - Penguin Long Covid Handbook. Discusses: Covid-19, Long Covid, T cells, immunogenetics and HLA, respiratory infection, science policy, arboviruses, C19th lit
Author of "stranger and strangerβ, letter writer, advocate and fundraiser for biomedical ME/CFS research.
Chronically enraged that I've had ME/CFS since 1992.
cfsgraphics.com
Green Party Leader (England & Wales)
London Assembly Member.
Chair of London's Fire Committee.
π³οΈβπ
https://podcasts.apple.com/podcast/id1837201724?i=1000724643828
Independent news for Kent
Join thousands of readers getting local news without the clickbait or ads at https://www.kentcurrent.news/
Greater Govanhill is a FREE, award-winning, multilingual, solutions-focused, community magazine.
Powerful citizen journalism in the East of England | Regulated by IMPRESS
Follow us for national and regional news (Norfolk, Suffolk, Essex, Cambs, Herts, Beds)
Web: https://eastangliabylines.co.uk
Email: editor@eastangliabylines.co.uk
person with ME/CFS
professional slug
Precision medicine for complex diseases. Creating better, more personalized diagnostics & treatments for unmet medical needs.
Join us for world-leading AI-led science, healthcare, diagnostics, & drug development.
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.patreon.com/cw/taylorlorenz
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 Covid are treated with the same belief, respect + kindness as any other serious physical illness
Ich wΓ€hle die Linke π΄
Temporarily embarrassed healthy person
#pwME π seit vor 2010 - Skeets in german and english - still a #Novid
Stuttgart
Green Party Campaigner | Living with Long Covid | Bradford | Shipley Town Councillor 2020-24 |
https://linktr.ee/darrenparkinson
Promoted by D Parkinson (Bradford Green Party) at 88 Hirst Wood Road, Shipley, BD18 4BU.
Guardian columnist and journalist. Commentator of the Year 2024. Author of Who Wants Normal? and Crippled.
E: frances.ryan.freelance@guardian.co.uk
Retired Widow Democrat Politics Trump added 7.8Trillion to debt his 1st term Climate Ukraine Womenβs Rights Justice Truth Me/cfs STRESS KILLSπ«DMβs
Horizontal advocate for #pwME. π³π± in π΄σ §σ ’σ ³σ £σ ΄σ Ώ. Medically Retired Hardware Engineer. FOSS Fan.
Ally. PwME/LC. Volunteer with @meactionscotland.bsky.social. He/Him. #SaveSavannah #BIPOCLivesMatter #EndGenocide #CovidIsAirborne #YallMaskin #CleanTheAir
ME after covid infection Feb'22. Young dad. Bedbound. π #ThereForME #GreatestMEdicalScandal #PEM π¬π§π²π«πͺπ¦π§πͺ
Researching βthe greatest medical scandal of the 21st centuryβ. Infection-Associated Chronic Illness, activism, stigma, medical humanities. Postdoctoral fellow in Sociology.
Immunologist and Head of Department of CIMM at the Amsterdam UMC, Netherlands. My team studies the role of antibodies during infection and autoimmune diseases, with a particular focus on post-acute infection syndromes (PAIS), such as Long-COVID and ME/CFS.
Immunologist and ME/CFS researcher @CharitΓ©
https://cfc.charite.de/
Love crafts, history, stories, natural world & spending time with husband, children, family & friends. When M.E /CFS & POTS doesn't stop me - which is most of the time right now. Usually found in a dressing gown. Devon, UK βΏπΏπ³οΈβππ³οΈββ§οΈπΊπ¦
Poet, latest Grief's Alphabet (Seren, 2024) | Academic | Grief, trauma, and the environment | All the πββ¬! | Foodie | Dem πΊπΈ expat in Bristol, UK | Insta: https://www.instagram.com/carrie__etter
ME. Spouse w LC, ME. Writer, bread baker, daydreamer. Still waiting on fair funding and apology from HHS. Masking like someoneβs life depends on it.
Independent publisher.
fitzcarraldoeditions.com
27 I ME/CFS seit 2021 I WING UniversitΓ€t Augsburg I DE II EN
https://www.mecfs.de/was-ist-me-cfs/
Feralcatbox.com/store - painter, tattooer, stuff maker, dream eater.
RWJF ClinicalScholars Alum, School Nurse, Scientific Diver/ocean lover bedridden by severe #LongCovid 3/2020 & #MECFS, #POTS, #MCAS #hEDS #Chiari. #healthequity
Disabled. Living with severe M.E. Watching the world from the window while bedbound. Excuse typos etc, sometimes the cognitive bits donβt work. Also posting on endometriosis and a little on mental illness too π΄σ §σ ’σ ³σ £σ ΄σ Ώ
Hello, welcome :)
Slowly making a documentary photography project about living with ME/CFS, a complex and challenging biological disease - like Long Covid.
https://linktr.ee/andrewgifford.photography
Bristol, UK. 335.42 ppm. He/him/oi.
Uhm, yes hello! ππ»
31 y/o Norwegian coke zero drinking PS5 gamer and a Twitter migrant cursed with ME. Currently learning Spanish and love painting/drawing. Recently started sewing π§΅πͺ‘
Trying to survive this crazy timeline Iβm forced to exist in.
A platform for projects related to David Graeberβs legacy, developing his ideas and projects that will take on a life of their own, continuing and contributing to his work.
https://davidgraeber.institute
π³οΈβππpw/ME #LwiththeT arty activist MyalgicE -Still Masking π·
(I have left the other place permanently, please interact with me here!)
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
Bespoke critical deep dives. JUST KING THINGS. HOMESTUCK MADE THIS WORLD. GAME STUDIES STUDY BUDDIES. other stuff. @ckunzelman.bsky.social @ztul.bsky.social and Danni too. www.rangedtouch.com
ME researcher at the University of Edinburgh.
Daily quotes from the author of Wide Sargasso Sea, Good Morning, Midnight etc. "If I could choose, I would rather be happy than write." Dead since 1979.
"End Times Fascism" book coming September 2026.
Doppelganger. This Changes Everything. The Shock Doctrine. No Logo. On Fire.
UBC Professor of Climate Justice.
π naomiklein.org
π¬ news.naomiklein.org/newsletter
I used to be a person, now Iβm a ghost, lingering on in the world of the living. ME/CFS since 2011, severe since 2021.
stand-up comedian / podcaster
dark prince of glasgow
https://linktr.ee/macarthurboyd
Comedian, Cricket Statistician, Podcaster. Host of The Bugle podcast and BBC Radio 4's The News Quiz. Taskmaster champion. Test Match Special statsmonger. Live shows: andyzaltzman.co.uk
ME/CFS | Long COVID | IACC | Stand with Minnesota
Livestreams: twitch.tv/Limmy
Blog: https://brianlimond.substack.com/
I make @hyperfixedpod.bsky.social I used to make Reply All. One day I will be in the ground hopefully flowers will grow out of me
Music:
Slowfawns.bandcamp.com
Western kabuki (the official podcast of Bluesky):
patreon.com/weste
β #ForgottenPoets & #ForgottenPrints β Pre-1930s poetry & art β Edited by Dick Whyte #dwpoems β https://forgottenpoets.substack.com
β Poetry New Zealand β
#PoetryAotearoa
β Forgotten Press β
https://linktr.ee/forgottenpoets
Solve M.E. is a non-profit organization that serves as a catalyst for critical research into diagnostics, treatments, and cures for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), Long Covid, and other infection-associated chronic conditions.
Researching the cell biology of ME/CFS since 2016, now also Long COVID and PD. Papers: https://scholars.latrobe.edu.au/d2missailidi/publications
Books: Is A River Alive? (May β25), Underland, The Lost Words, The Old Ways etc | Films: River, Mountain, Upstream | Music: The Moon Also Rises, Lost In The Cedar Wood, etc
Nature, climate, people.
Prof at Cambridge.
https://linktr.ee/robmacfarlane
Unconditional / Universal Basic Income (UBI) knowledge resource
Founder & CEO of UBI-focused nonprofit ITSAfoundation.org
My channel: youtube.com/scottsantens
My #UBI FAQ: scottsantens.com
Contact me: linktr.ee/scottsantens
Disabled by very Severe Post-COVID ME/CFS. Not always able to use phone. Bedridden. Unable to Speak.
I care.
βΆπ, (FR/DE/EN, but posts in english)
Clinging onto the ledge above the abyss.
A number of years ago the interest in glass, vintage and antiques began, with this our collection has grown and interest has increased, we have also seen an increased interest in our surroundings in this area, so for this reason we create this account.
Foxy features every day!
All credit goes to real owner.
Previously a psychotherapist.
Bedridden #ME 32years
Daughter severe ME, eldest son MS.
I like art, nature, books, people, music, poetry and podcasts!
Author and podcaster #ActuallyAutistic
I'm a wildlife and nature photographer just trying to enjoy life:) Who mucked with the timeline and got it all twisted into this messππ
New Brunswick & Ontario π¨π¦
501(c)3 transforming how #LongCovid, #ME/CFS & Lyme+ are studied, diagnosed, and treated. Leading the #LongCovid Research Consortium.
This page contains moon pics.DM for credit removal. Some Photoshop image posted .
Patient-Led Research for #LongCovid! http://patientledresearch.com
OMF is fundraising to support open, collaborative research to find effective treatments and a cure for ME/CFS, Long COVID, and related diseases.
Retired maths teacher. ME/CFS 35 years. Volunteer staff member on Science for ME international forum, www.s4me.info
Living in London with a Hungarian, two Russian Blue cats, #MEcfs and a healthy obsession with the art of Keith Haring. π¬π§πͺπΊπ³οΈβππΊπ¦β₯οΈ
Psychologist, lifelong activist for womenβs issues, peace and social justice, 40 yrs with ME from Incline Village, fight the good fight and make good trouble, here to create the Beloved Community, San Francisco East Bay transplant from MN.
Providing support & holistic healthcare services to people of all ages affected by #MECFS. Charity number: 1036419 / SC040452
𧬠The worldβs biggest study of genetic causes of #MECFS. Launched September 2022. 𧬠decodeme.ed.ac.uk
Prof of Public Engagement in Science, Uni of Birmingham; anatomist, author, broadcaster; vice President of Humanists UK. All views my own.
Award winning landscape photographer.
Based in Oxfordshire, England.
Shoot with Sony with Sigma Glass & DJI.
https://www.etsy.com/uk/listing/4395675965/2026-britain-photography-calendar-from
https://www.instagram.com/charrison.photography
editor/co-founder @thesicktimes.org | journalist covering Long COVID & related crises | she/her/π³οΈβπ
email: betsy@thesicktimes.org | signal: betsyladyzhets.25 | https://thesicktimes.org/
Scottish photographer with a cat, 8 dogs and 3 wonderful kids :)
Kit bag: Nikon Z8 I 85mm f1.2 | 100 - 400 VR S | 105mm Macro | 40mm f2 | Gitzo Carbon Fibre with Benro S8 Pro Fluid Head
Fujifilm X100VI
Sci Fi obsessed.
Research, algorithmic art & music, machine learning, anti-bias in AI data. #LongCovid research & advocacy @patientled.bsky.social.
Pillow Writers is a free international online writing group for the ME/CFS community. All welcome.
Was: Facilitation & organisational culture nerd for do-gooders; climate & sustainability. Healthy, athletic; MTB, ski, mountaineering, outdoors. Everything on pause: Long Covid is brutal.
A lot funnier IRL
Lancaster, North West England (Plague Island) β₯π¨π
Artist and tea drinker living on a hillside in Wales.
Learning to live a gentle creative life and encouraging others to do the same.
Diagnosed with #MECFS in 1997.
www.patreon.com/gogently
https://linktr.ee/michaelnobbs
βοΈπ§Ά
Calling for an NHS that's there for Long Covid & Myalgic Encephalomyelitis (ME) | www.thereforme.uk
Donate to Justice For ME here if you can please π ππ¦
https://shorturl.at/x1Vyx
Bookworm, British, Lefty. βΏπ¦πͺπΎ π·π
They/them | 28 | ME/CFS since 2016, very/severe since 2022 after covid | Severe hyperacusis
Mostly post about ME but will share things relating to disability justice, leftist & queer issues and Palestine π΅πΈ
In "Australia" on Wurundjeri Country
Former surfer and scuba diver. Lover of the ocean and environment.
24yrs ME, POTS, TN
#pwME #millionsmissing #MEScience
Location: Australia
Caring for loved one with complex infection-associated chronic illness incl. #MEcfs. Decades-late biomedical research funding means no end in sight.
#Calgary #YYC, #Alberta. #Treaty7.
Enlightenment fan and Open Society friend - Pimlico & Exeter.
Not well but naturally this pale.
βπͺπΊβοΈπΊπ¦βΏοΈπβπΏπͺπ
Environmentalist. Scientist. Love to travel. Born and bred in Sheffield.
Migrated to bluer friendlier skies.
#MECFS
NYT bestselling author of the Southern Reach series, including Absolution. Repped by Joe Veltre at Gersh. PNW. he/him
Broadcaster & environmental campaigner
chrispackh.am/links
Co-founder #ThereForME | Calling for an NHS thatβs there for ME & Long Covid | www.thereforme.uk
Independent researcher & policy analyst | Migration & displacement | Projects with @odi-global.bsky.social | www.linkedin.com/in/karen-hargrave
creator of longcovidstudies.net, member of the Patient-Led Research Collaborative, and freelancer.
I occasionally try to explain and comment on ME researchh, or even contribute to it. And I advocate for more and better research.
Disease genomics & molecular mechanisms; ME/cfs: http://decodeme.org.uk, SequenceME @ Edinburgh University. Views - my own. He/him.
