The World Endometriosis Society (WES) was founded in 1998 to promote the exchange of clinical experience, scientific thought, and investigation among gynaecologists, endocrinologists, scientists, biologists and other qualified individuals interested in advancing the field of endometriosis.

Through our e-Journal and the World Congresses on Endometriosis we encourage and support collaboration among national and international societies and individuals interested in endometriosis.

The WES is a scientific Society with no link to the industry. We fund our work from our membership dues and from a share of the inscriptions from the World Congresses on Endometriosis.

January / February eJournal published
In this issue we have our first debate amongst two well known letter writers ....don't miss it! We also have an excellent feature on immunity, exercise and endometriosis.

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Endometriosis Awareness Week 2010
Support groups around the world are preparing national and regional events in many countries to raise awareness of endometriosis during the month of March - support them!

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Research in nerve fibres promising
There is no new diagnostic test for endometriossis - yet. But research in nerve fibres is promising for future less invaise diagnositcs.

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Priorities in endometriosis research
Scientific paper published - and made freely available to WES members - from consensus workshop on research directions in endometriosis

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WERF commences third study
The World Endometriosis Research Foundation launced its 3rd study on 31 August to measure the direct and indirect cost of endometriosis in 11 centres in 10 countries.

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Scientists call for greater transparency in clinical trials
80% of registered endometriosis clinical trials are not published. Researchers now call on investigators to publish results within 12 months of a trial's conclusion.

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