This book is my gift to the endometriosis community, who have supported me so much over the last 3 years. Fuelled by own my 22 year struggle for a diagnosis, this book contains everything we currently know about endometriosis and how to live with it. It is packed with expert insights, experiences from the community, tips from clinicians, and voices that we don’t often get to hear from. It is everything that I wish I had when struggling for that diagnosis, and everything that I wish every clinician involved in endometriosis care will read. Because the current system is failing us. It’s time to truly work together to provide patients with the care they desperately need and deserve.