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The Library · Cancer Journeys
The Zebra Diagnosis: Neuroendocrine Tumor Stories
$21.99 USDDigital edition · PDF + EPUB
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From the Introduction
A retired school secretary in Leeds kept a hot water bottle in her desk drawer and a map in her head of every toilet in town, through twelve years of being told it was IBS. Others were treated for asthma, ulcers or a rash blamed on a spinning-class seat. The writers here describe the long search for a rare name, and the ordinary years of scans that followed.
FormatPDF + EPUB
Testimonies50 first-person accounts
Length237 pages
PublisherHealing Stories Network
CollectionCancer Journeys
DeliveryInstant download + emailed to you
A note before you read
This book is a collection of personal, first-person testimonials offered as companion reading. It is not medical advice. Always consult a qualified healthcare provider regarding any medical condition or decision.
About this volume
Inside this volume
Fifty first-person accounts describe neuroendocrine tumours, the rare growths once called carcinoids that can start in the bowel, pancreas, lung, stomach, appendix and beyond. Some were found by accident, after an appendix operation, a kidney stone scan, a colonoscopy a sister insisted on, a heartburn scope or a cesarean delivery. Others took years: a receptionist who kept fainting from low blood sugar, a cough that never answered to an inhaler, ulcers three times in four years, a face that flushed at an insurance desk every few days. Writers include a bank manager in Bengaluru, a truck driver in Monterrey, a calligraphy teacher in Osaka, a pastry chef relearning to eat, a market vendor in Quezon City, a fifteen-year-old goalkeeper's mother and a man who started a support group in his garage. They write from Lagos and Algiers to Christchurch and Calgary. The book covers monthly injections, tablets with mouth sores and sore feet, radioactive PRRT, liver embolization, a Whipple operation, a liver transplant list, carcinoid heart disease, MEN1 in the family, a clinical trial, costs counted in rupees, Ramadan and travel. Many live with stable scans for years, one for twenty. Others do not: a twenty-six-year-old has a fast-growing carcinoma, one woman's cancer reached her bones, and a seventy-eight-year-old chose comfort over more treatment.
Who it's for
For anyone newly told they have a neuroendocrine tumour or still searching for an explanation of flushing, diarrhoea or low blood sugar, and for the partners and parents who come to the scans.
Format · Instant download · PDF & EPUB · Fifty first-person accounts · PDF: 237 pages
A collection of personal testimony, offered as companion reading — not medical advice.
What's inside
- 50 single-author testimonies from real people
- A short, plain-language introduction to the topic
- Editor's note, contents page, and curated resource list
- Professional interior typesetting and an original cover
Formats & reading
Every purchase includes a print-quality PDF (best for desktop, tablet, and printing) and a reflowable EPUB (best for Kindle, Apple Books, Kobo, and phones). Files are DRM-free. You can download both instantly from the order-confirmation screen, and we email them to your inbox as well, so your books are always within reach.
Related reading
What you get
Inside this volume: 50 Neuroendocrine Tumor stories
50
first-person testimonies
8
thematic parts
PDF + EPUB
both formats included
Instant
download + emailed to you
Fifty real people, in their own words — honest, unhurried companion reading, never a substitute for medical advice. Every order arrives two ways the moment you pay: an instant download and a copy emailed to your inbox.
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