Sean Wilson 🍴☕🍰🍺 @HelloSeanWilson

Scottish boy living in Wiltshire. Independent Financial Adviser on Sabbatical. #ME/CFS patient. Councillor for Lydiard & Freshbrook ward in Swindon. Swindon, England Joined January 2015

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Patrick Maguire @patrickkmaguire

a day ago

Home secretary this morning: we need to change the rules around indefinite leave to remain. Prime minister this morning: Reform are racists for talking about indefinite leave to remain. #comms

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ME/CFS Science @mecfsskeptic

4 days ago

1) During his presentation at the 2025 Fatigatio conference, Prof. Bhupesh Prusty argued that physiologically, ME/CFS patients look similar to healthy individuals until they are put under stress.

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Och. Ming Campbell. He was what politicians used to be - full of integrity, grit and with a good sense of humour. A really lovely man and a good contact who always had time for you. He was one of the only sane people I’d chat to in Westminster. Really sad to see him go.

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Jon Mackenzie @Jon_Mackenzie

4 days ago

This could be a quote about what is happening at Manchester United [HT @markstkhlm]

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The New Statesman @NewStatesman

6 days ago

EXCLUSIVE: ANDY BURNHAM’S PLAN FOR BRITAIN by @TomMcTague Andy Burnham tells me that changing Westminster needs to be the focus of this year’s Labour Party conference. “The issue for the conference is: where is our plan to turn the country around?” Still, it is impossible to…

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Mushy @MusharafAsghar

2 weeks ago

Today I turn 29 years old, which means it’s been 13 YEARS since I was on #EducatingYorkshire. I want to dedicate this post to all the amazing teachers who change a young person’s life for the better. I am privileged to have received the love throughout the years. Thank you

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ME Research UK @MEResearchUK

2 weeks ago

Dysfunction of natural killer cells (immune cells that can destroy infected cells) has frequently been implicated in ME/CFS. The findings of a recent study exploring gene variants (alleles) further support the role of these immune cells in ME/CFS. tinyurl.com/4hyb7cns

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Hannah Davis @ahandvanish

2 weeks ago

New study on PEM! After a mild stress challenge, people with ME had a sharp drop in haptoglobin (Hp), a blood protein that protects the body from damage when red blood cells break down. Low Hp correlated with worse PEM & cognition. …nslational-medicine.biomedcentral.com/articles/10.11… 1/ #LongCovid #pwme

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davidtuller @davidtuller1

2 weeks ago

just figured I'd again post this interview with Columbia's Dr Ian Lipkin, who discusses his team's new paper on immune dysfunctions in ME/CFS and his hopes for treatment options in a few years: youtube.com/watch?v=-_ihsJ…

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Open Medicine Foundation @OpenMedF

2 weeks ago

A new review from Melbourne ME/CFS Collaboration, in collaboration with Collaborative Center at Montreal, highlights the potential of metformin, an antidiabetic agent, as a treatment for #MECFS and #LongCOVID. 👉 Read the full publication: ow.ly/uXQJ50WVZax

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davidtuller @davidtuller1

3 weeks ago

Columbia's Ian Lipkin on innate immunity in ME/CFS and related topics...youtube.com/watch?v=-_ihsJ…

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GC @ThePOTSPostman

4 weeks ago

Living with chronic illness is just a big waiting game. Waiting for the flare to stop. Waiting for the pain to ease. Waiting for the brain fog to lift. Waiting for the fatigue to dissipate. And waiting everyday for life to feel like life again.

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Sacha Lord @Sacha_Lord

4 weeks ago

When the pub dies, more goes with it than just a pint. Pubs are part of British culture. They’re where people meet. Where ideas are shared. Where strangers debate politics, sport, life. Where worldviews get challenged, rightly so, all over a pint. But now? £7 pints at a…

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Derya Unutmaz, MD @DeryaTR_

4 weeks ago

I am one of the 60 researchers who signed this international declaration on ME/CFS & Long COVID, disease that cause suffering for millions of people. A decade ago, when I became involved in ME/CFS, many physicians & scientists didn’t even consider it a real disease, unbelievably!

ME/CFS Research Foundation @MECFSResearch

4 weeks ago

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Stan Collymore @StanCollymore

4 weeks ago

A sad day in Staffordshire and the Black Country today. Banks's brewery has brewed its last pint in over 150 years of making the world's best Mild and Bitter. A local icon, you'll be sadly missed.

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Trevor Noah @Trevornoah

a month ago

United should be proud, there's no shame in losing to a top four team. 🙏🏽 #Grimsby #CarabaoCup

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Erik Niva @ErikNiva

a month ago

Blundell Park, hemmapaln för Grimsby Town. Definitivt facit för hur en fotbollsarena ska vara belägen.

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ME Research UK @MEResearchUK

a month ago

Results from a small study of 24 people with ME/CFS and 24 healthy controls has provided clear justification of the need for researchers to further investigate the role steroid hormones may play in ME/CFS disease mechanisms. Read more here: tinyurl.com/kyceup2y

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Daniel Missailidis, PhD @DanMissailidis

2 months ago

I see a few hundred new followers so thought I’d say hi. I’m a molecular biologist in Australia who has been studying ME/CFS for ten years and Long COVID since the pandemic started. Most of my work has been on abnormal metabolism in immune cells. A few new papers coming up soon.

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John Hansel @JohnHansel77066

2 months ago

My beautiful daughter Emily is celebrating her 23rd birthday today! If you're scrolling by please drop a like and join me in wishing her a Happy Birthday 🎈 🎂 🎁