My Tribune piece on Bologna is now online! You can read it here —

My copy of this arrived today and it’s so, so nice! Haven’t actually been able to look at it properly yet though as my partner, an engineer, has decided he needs to read it first ‘for professional purposes’ 🤨

Proud to have got this one listed when I was at C20 Society. Similarities w. his work at Murray Mews, but bigger & more spatially complex - it gets overlooked because it's right next to Alexandra Road, but it's so clever. Love the cascading profile of the art studio block (right)

Extremely chuffed to have been gifted this crested plate from the County Hall members restaurant, by the inimitable Paul Powlesland. Going to eat a celebratory meal off it when the PhD is done. Thanks Paul!

this was the news piece about chronic UTIs. so many people were fobbed off for years with a nonsense diagnosis because the tests used were practically useless. in many cases "real need" is constructed by medical infrastructure, ideological practices etc inews.co.uk/news/chronic-u…

An Oral History of British Architectural Historians is a new oral history project, recorded by SAHGB and recently deposited with us. You can find it at sami.bl.uk by searching C1804... Or you can find out more in this blog! blogs.bl.uk/sound-and-visi…

It's only taken us over 200 years of modern medicine to consider this. Good job 👍👍👍👍

My wonderful friend Tessa Pinto has been extremely unwell for many years now. She last walked in July 2023. ME/CFS is a largely misunderstood and invisible condition, leaving many to suffer in silence with little access to treatment or support. gofundme.com/f/support-our-… (1)

my amazing friends are meeting on the 9th December at 8pm to watch Unrest, an award winning documentary about ME/CFS by ME patient and advocate Jennifer Brea🦒. we invite everyone to join and watch along, then or at any time convenient for you - it's available for free on youtube

thank god for george monbiot. to finally have a respected journalist with a big platform shedding light on the ongoing and monumental suffering and injustice that ME patients continue to face is so affirming and so desperately needed

Today we've sent a #ThereForME letter, co-signed by 28 organisations and smaller initiatives, to Layla Moran 🔶🕊️ Health and Social Care Committee The letter points to inadequacies, present and historic, in care for people with ME and Long Covid, and calls on the committee to undertake an inquiry.

A year ago today I was diagnosed with FND by a neurologist who knew nothing about long covid. Reasoning: no blood test abnormalities I now have blood tests showing I have raised Arginase 1, HIF1a, PINK1, and Activin B Amazing what shows when you actually test relevant pathways