Steven Shorrock

@stevenshorrock.bsky.social

Psychologist & transdisciplinary humanistic, systems & design practitioner | Work, organisations, complexity, risk, justice | Autism, long covid, ME/CFS | FBPsS CPsychol CErgHF PhD 🐝🇫🇷🏴󠁧󠁢󠁳󠁣󠁴󠁿 humanisticsystems.com

Congrats to James Frith MP, newly appointed as the Minister for Health Innovation, with responsibility for ME. I’ve written to him on ME emphasising that given the numbers, and the length and extent of suffering, ME represents a significant burden at personal level, to society and to our economy.

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The Reality of Calculating Exposure and Energy: Geasa and Tynged This is the second of seven realities in this series on living with chronic conditions and dynamic disability, explored through language, concepts and images from Celtic folklore. humanisticsystems.com/2026/06/03/t...

The Reality of Calculating Exposure and Energy: Geasa and Tynged

This is the second of seven realities in this series on living with chronic conditions and dynamic disability, explored through language, concepts and images from Celtic folklore.Many chr…

humanisticsystems.com

The Reality of Calculating Exposure and Energy: Geasa and Tynged This is the second of seven realities in this series on living with chronic conditions and dynamic disability, explored through language, concepts and images from Celtic folklore. humanisticsystems.com/2026/06/03/t...

The Reality of Calculating Exposure and Energy: Geasa and Tynged

This is the second of seven realities in this series on living with chronic conditions and dynamic disability, explored through language, concepts and images from Celtic folklore.Many chr…

humanisticsystems.com

About a decade ago I spent a merry 24 hours trying to work out what Farage’s cultural interests were. It was fascinating because it turned out he had none. Literally none. Someone who knows him very well later confirmed to me that he was completely uninterested in music "apart from military bands"

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#ME/CFS is the neuro-immuno-metabolic illness that takes away your whole body’s ability to function and live. And the more you push through your energy envelope, the more it takes away and disables you. It is also still the most misunderstood, mischaracterized, neglected and underfunded disease.

Seems ludicrous now a couple of years ago I’d not realised the reason why overdoing things on the day after I appeared to have gotten away with overdoing it the day before; wasn’t just doubling the impact of the delayed PEM but creating a situation of rolling PEM 🤦🏻‍♀️

Steven Shorrock@stevenshorrock.bsky.social · 3mo ago

I Crash: Texts from M.E. This post uses my own text messages to give a first-person documentary account of an experience of Long Covid and ME/CFS. humanisticsystems.com/2026/05/17/i...

“The fatigue of ME/CFS is so unlike the ordinary use of the term, that it feels like far too small a word.” Yes! Excellent post. I have mild #longcovid. I can work and live a paced life. Many others cannot. It is cruel. Quality of life plummets. Your life changes. You adapt. You have no choice.

Steven Shorrock@stevenshorrock.bsky.social · 3mo ago

I Crash: Texts from M.E. This post uses my own text messages to give a first-person documentary account of an experience of Long Covid and ME/CFS. humanisticsystems.com/2026/05/17/i...

My hunch is that non-autistic people do not spend months/years reading books about autism, following accounts of autistic people, paying for assessments, or feel the need for a formal process. And if you pass the test…you have a label that non-autistic people would not want.

The school system we have is designed to produce professors, not the vast majority of life paths that people go on to take and the skills they need. Little about the planned secondary school experience, in particular, prepares children for what they are about to encounter on leaving education.

Dr @binitakane.bsky.social explains how a theory that #MECFS is caused by deconditioning and a fear of exercise permeated medicine and framed the illness as psychological. This led to the patients being neglected, gaslit, and some would say abused. Causing huge trauma for the community.

Adam@abrokenbattery.bsky.social · 6mo ago

Clip: Dr @binitakane.bsky.social explains how ME is an energy-limiting illness. The hallmark symptom, Post-Exertional Malaise (PEM), means even normal activities can trigger a worsening of symptoms. Some of her patients have to choose between a shower or preparing a meal that day.