About the project
I would be here if I could, has grown into the UK’s largest collaborative social art project, co-created with individuals living with ME and Long Covid.
What began as a single question from a bed has evolved into a nationwide movement, inviting hundreds of people to take part.
This is social art at scale — a space for many to express their creative voices and be heard beyond physical boundaries.
Through stories and memories, these messages tell of special times and places, amplifying the absence from the lives they once lived.
Every message can be seen and heard on the message map, and the journey of the Mirrorbox has now begun. Over the next few years, it will travel to message locations across the UK.
Our mission is to enable people with ME and Long Covid to be seen and heard through the shared love, memory, and experience of place; so we all feel connected to a wider sense of belonging.

About the artist
Alison Larkman is a Bristol-based artist living with life-altering M.E. She created the project after months of being housebound and dreaming about where she would be if she could. Her work explores themes of invisibility, fragility and the unseen. A former international rower, Alison studied at Chelsea College of Art, Newlyn Art School and Spike Island. In between those times, she has run businesses, worked with Hell’s Angels and retreated with M.E.
You can find more about Alison’s artwork at alisonlarkman.com.

About the team.
We are a small team running a big project. Over 60% of the team are living with ME and Long Covid. We come from lived experience and as such a place of deep understanding.
So many people living with chronic illness and disability have experience and great skills but cannot commit to traditional working patterns due to the fluctuating nature of their conditions. We are looking to challenge that.
We have created role-sharing processes to enable and support multiple people to be part of our team (some of our team work as little as 2 hrs a week but still make valuable contributions). For every role, applicants must have the skills and experience we are looking for but the time they are able to work is flexible and open to discussion.
If this is you, and your skills and experience match any roles we are advertising (current vacancies are posted in project updates), please get in contact, we want to hear from you.
Our supporters
As well as individual donations, Arts Council England has awarded I would be here if I could two project grants to develop and start the project and we have recently received a grant from the National Lottery Community Fund.
Special thanks to Action for M.E., which has offered time and expert advice on fundraising, and the charities Long Covid SOS, Long Covid Support and 25% M.E. Group for their encouragement.
We are continually fundraising for the Mirrorbox journey and are happy to talk to businesses and organisations interested in getting involved and supporting us.
Further information
About M.E.
ME – Myalgic encephalomyelitis (also known as ME/CFS) is a neurological condition which affects more than 250,000 people in the UK and has a major impact on individuals’ health and life. At any one time, one in four of those with ME. are affected so profoundly that they are housebound or bedbound.
ME can be caused by glandular fever, COVID-19 and other viral infections, but the precise trigger isn’t always identifiable. It leads to debilitating fatigue and pain, amongst other symptoms, and people with the condition are often unable to recover from the slightest exertion.
While some people with ME can make good progress, others battle illness for many years and sometimes never recover. Severe ME may lead to cognitive impairments. People may depend on a wheelchair for all movement and be unable to tolerate dim lighting or soft sounds. At the most severe end of the spectrum, people are unable to swallow and must be tube fed.
For more information on ME, visit Action for M.E. and 25% M.E. Group.
About Long Covid
Long Covid is a rapidly emerging condition caused by COVID-19 that is increasingly seen as a post-viral fatigue syndrome akin to ME. In 2024, it was estimated that 1.3 million people in the UK – over 2% of the population – were living with Long Covid symptoms.
Long Covid has a wide range of symptoms that may arise due to virus-induced organ infection. Many of these symptoms align with those experienced by people with ME
For more information on Long Covid, visit Long COVID SOS and Long COVID Support.
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