Resources
Endometriosis resources including support groups, self-help books, articles, coping, and a glossary

FACTS about endometriosis to aid journalists, medical writers, bloggers, etc, who wish to ensure their publications about endometriosis are correct.

The James Lind Alliance on Research Priorities in Endometriosis has published the top ten priorities for research into the treatment and effect of endometriosis on millions of women with the disease.

“Endometriosis: the experts’ guide to treat, manage and live well with your symptoms” is an easy to read book, which covers most aspects of what endometriosis is, how it is diagnosed and treated – and how to live life despite persistent symptoms.

Well-known physicians from around the world, who have a special interest in endometriosis, share their opinions about endometriosis and justify their proposed diagnostic and treatment strategies.

This film is a documentary created by two women with endometriosis to show other women what they can expect when they get endometriosis. Now available for all to watch.

The Colour Atlas of the laparoscopic appearance of endometriosis has been re-issued and is now available for free download from the Internet.

Diagnostic delay and hit and miss treatments in endometriosis are often due to myths and mis-conceptions about the disease – get the FACTS here.

The James Lind Alliance (JLA) Priority Setting Partnership for Endometriosis Steering Group members.

Background and mission of the JLA PSP for endometriosis: what we are trying to achieve with this project.

“Endometriosis and pelvic pain”, by Susan Evans and Deborah Bush, is a practical book for women with pain. It is written in an easy-to-read style with information on how to alleviate a wide range of pains.