Endometriosis - by Jen Moore (Paperback)

About the Book

Have you struggled to get diagnosed, be believed or get the right treatment for endometriosis? This book is for you.

Book Synopsis

'Everything you need to empower yourself about endometriosis ... highly recommend this.'
Dr Nighat Arif, author, GP, broadcaster

Have you struggled to get diagnosed, be believed or get the right treatment for endometriosis? This book is for you.

We still don't know what causes endometriosis, and we don't know how to cure it either. What we do know is that it can cause debilitating pain and seriously affect mental health. Endometriosis is not 'just a bad period'; it is a whole-body disease which is as common as asthma or diabetes, affecting 1 in 10 women. Yet it is barely covered in medical school, leaving sufferers repeatedly dismissed when trying to access care.

Backed with up-to-date scientific knowledge and interviews with endometriosis specialists and those affected by the condition, Jen Moore gives you all the tools you need to:

- Understand what endometriosis is (and what it is not)
- Deal with the system and get a diagnosis
- Navigate the ins and outs of surgery
- Cope with physical and mental pain
- Fight for better endometriosis care

This beacon of hope is your go-to guide to endometriosis, getting the care you deserve and finally feeling seen and heard.

Review Quotes

"Everything you need to empower yourself about endometriosis, from how to manage the symptoms, even what to pack in the hospital bag, to managing lifelong symptoms - highly recommend this." --Dr Nighat Arif, author, GP, broadcaster

"A refreshing read from lived experiences. This is a useful overview on endometriosis and the challenges it creates. I love that it's inclusive and highlights inequities that exist too. It's a helpful guide everyone needs to read." --Dr Aziza Sesay, Vice Chair and Creative Director of Black Female Doctors UK

"Jen is an amazing advocate, campaigner and educator within the community. She always conveys her message and information with empathy, accuracy and relatability. Having people like Jen doing the work she does makes a difference to the lives of so many." --Gabz Pearson, Co-founder of Menstrual Health Project

"An essential book that will help all women feel less alone on their endometriosis journey, and help educate and inform those who don't understand what endometriosis is and all its complexities. This book will change so many women's experiences, thank you Jen for writing it." --Clare Bourne, author of 'Strong Foundations'

"As a thoracic surgeon who dared to speak out, I'm heartened to see the reality of endometriosis starting to gain the attention it deserves." --Dr Francesco Di Chiara, thoracic surgeon

"A must-read for patients, families, and doctors - a perfect blend of personal stories and expert insights." --Mr Mikey Adamczyk MD MRCOG, endometriosis specialist

"I'd prescribe this book for all GPs to read - we have been painfully slow and dismissive in the diagnosis and treatment of endometriosis for too long. I can see this book changing that and I really hope it does." --Dr Ellie Cannon, resident 'Mail on Sunday' GP

"Got endo? You need this book." --Maisie Hill, author of 'Period Power'

"A brilliant transparent guide on how to navigate life, relationships and symptoms when it comes to endometriosis. It really offers practical nuggets and I think it will be helpful for those struggling with endometriosis but also for those who have family members, partners or friends with the condition." --Dr Raj Arora, GP, TV medic and endometriosis sufferer

About the Author

Jen Moore is a highly respected educator, speaker and campaigner specialising in endometriosis and adenomyosis. The co-founder of The Endometriosis Action Alliance, she also consults for organisations such as the NHS, sits on the All Party Parliamentary Group for endometriosis, and is committed to overhauling clinical education at medical schools. Through her work she has amplified the voices of thousands of endometriosis sufferers and promoted change at an institutional level. @jen.dometriosis