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The burden of endometriosis is enormous, with one in ten women suffering from this painful and debilitating condition. It is estimated to affect 1.5 million women in the UK and 190 million women globally. Despite its prevalence, it is currently taking an average of eight years for women to receive a formal diagnosis, with 27 being the average age at which a diagnosis is made. This can have a significant impact on the physical and mental health of those living with the condition, with 30-40% experiencing infertility.
An early, accurate diagnosis in a primary care setting can have a crucial impact on the care a patient with endometriosis receives, providing the opportunity for timely referral, advice on managing the condition and connecting the sufferer with wider support networks. This timely, practical book brings together clear and concise information for GPs and primary health care teams on how this can be achieved quickly, accurately and effectively.
About the Editor
List of Contributors
Foreword by Gaity Ahmad
Foreword by Pete Gibson
Foreword by Kay Marshall
Preface
Acknowledgements
1. Definition and types
2. Staging and classification
3. Prevalence
4. Causes and risk factors
5. Symptoms
6. Investigations
7. Pharmacological management
8. Pelvic physiotherapy in the management of endometriosis
9. Other non-pharmacological management options
10. Surgical management: Introduction
10A. Surgical management I
Shatha Al-Attili, Jamel Tahar Aissa and Gaity Ahmad
10B. Surgical management II
Hannah Draper and Andrew Horne
11. Tertiary care: The Specialist Endometriosis Centre
12. Delayed diagnosis: How to reduce the risks
13. Living with endometriosis: Stories from patients and their families
Courtney Ormrod’s story
Courtney Ormrod and Paul Ormrod
Lucy Bowker’s story
Lucy Bowker and Tony Bowker
Siobhan Kennett’s story
Siobhan Kennett and James Kennett
Patient stories: Summary from the Editor, Anita Sharma
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