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About us

In 1981 a self-help group for women with endometriosis was set up and in 1982 it became a registered charity - The National Endometriosis Society (registered charity no 1035810) .

As a membership organisation representing the views and needs of women with endometriosis, we are now the UK’s leading provider of support and information on endometriosis.

In 2006, thanks to free consultancy from Weber Shandwick, we were able to undertake a review of our brand with our members to ensure we had a strong identity to which we could all relate. The result was our relaunch as Endometriosis UK in November 2006.

Rebrand Questions and Answers

Endometriosis UK provides services that enable those with endometriosis to understand their disease and to take control of their condition. These services include Local Groups and a free UK Helpline, both of which are staffed by trained volunteers.

Endometriosis affects approximately two million women in the UK, often physically, personally and financially.  The impact of the disease varies with each individual. The role of Endometriosis UK is to improve the lives of people affected and work towards a future where it has the least possible impact on those living with the condition.

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Endometriosis UK launches Manifesto
To read about our commitment to women with endometriosis

Read about our commitment with endometriosis

 

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