

Miss Diagnosis is part memoir, part field manual, and part patient-advocacy guide. Drawing from PJ Pape’s long journey through invisible illness, wrong diagnoses, disability, questions around MS and Lyme disease, bodywork, and self-advocacy, the book helps readers prepare for appointments, organize symptoms, ask better questions, and stop apologizing for what their body knows.
Miss Diagnosis is based on lived experience and practical self-advocacy. It is not a substitute for
medical advice, diagnosis, or treatment.
Author and patient advocate
