top of page

Art by Caitlin Smits

About

5CA885FE-3B2A-41B0-B666-9161D87BE1D5.png

A MUSEUM ON INVISIBLE ILLNESSES AND DISABILITIES. WHY?

The Lyme Museum is an independent museum with an education hub, a digital platform, a physical collection and an international community, hosted at the Documentary Media Centre in Leicester (UK). We are the first museum dedicated to exploring the lived experiences of invisible illnesses and disabilities through materiality and storytelling. We collect objects, stories, flat lays and artworks with one aim: making the invisible visible, one flat lay and one story at a time.

We are really, really interested in stuff! The everyday mundane objects that become part of our identity as chronically ill and/or disabled people. Those are not always the objects that museums display, and yet they are the ones that make the invisible visible.

In museums, we call this materiality, but really, it's stuff! And stuff is great! From mobility aids, to pills, to objects of comfort, there is so much to talk about, and that's why we are here. Changing the narrative on disability and chronic illness through objects and first-person narratives.

316421042_10160087165474185_621356750317421705_n.jpg

Angela Stienne

Founder

(she/her/hers)

Angela Stienne is the founder of The Lyme Museum. She is a museum researcher (PhD) and storyteller from Paris, with over ten years of experience in the cultural sector in the United Kingdom. She works at the intersection of medical humanities, museum studies and science communication, with a track record in leading engagement on complex issues related to bioethics and the human body. Angela has worked extensively on storytelling, building projects around collections of displaced human remains, giving a voice to refugees and asylum seekers and exploring alternative narratives around museum objects and people. She has chronic Lyme disease and hypermobility syndrome.

www.angelastienne.com

bottom of page