Invisible Illness

Reading About Chronic and Invisible Illness: Where to Start

A guide to our Chronic & Invisible Illnesses shelf — ten anthologies of first-person testimony, from long COVID and POTS to Lyme, histamine intolerance, and chronic illness in relationships.

· By Shashank Bhosale

Reading About Chronic and Invisible Illness: Where to Start

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Invisible illness asks its sufferers to do two jobs: be sick, and prove it. The conditions on this shelf — long COVID, POTS, Lyme, histamine intolerance — share contested edges, long diagnostic odysseys, and the exhausting work of being believed. The fifty voices in each volume have done that work, and reading them is, for many people, the first time their own experience appears on a page.

Here is the Chronic & Invisible Illnesses shelf, mapped.

The post-viral era

The contested diagnoses

Living around illness

From the Reading Room

Companion pieces include living with invisible illness, long COVID, POTS, and medical gaslighting.

The whole shelf lives in our Chronic & Invisible Illnesses collection.

These books are companion reading, not diagnostic guidance. Some conditions on this shelf are medically contested, and the accounts reflect personal experience rather than settled science; your own path deserves a clinician who investigates rather than dismisses.

The Reading Room publishes personal stories and editorial notes from our press. Everything here is companion reading — never medical advice, diagnosis, or treatment. For guidance about your own health, please speak with a qualified clinician. Read how we collect and edit patient testimony in our Editorial Standards, or meet the press at The Masthead.

From the Library
Fifty first-person accounts of chronic & invisible illnesses

If this piece was useful, the volumes below hold fifty full-length accounts from people who have been through it — the part an article can only summarise.

Browse all 13 volumes in Chronic & Invisible Illnesses →