Endometriosis UK is the leading UK charity championing the rights and needs of those with endometriosis.
Endometriosis impacts on the physical and mental health of 1 in 10 women and those assigned female at birth in the UK from puberty to menopause, although the impact may be felt for life. That’s over 1.5 million who desperately need support and information to help them understand this chronic condition which takes an average of 8 years and 10 months to diagnose in the UK.
We are determined to ensure that everyone gets prompt diagnosis and the best treatment and support. We work to break down barriers to access – whether information, treatment or support. We lead collaboratively across our community, acting to inform, empower and advocate for all those affected by the disease. The endometriosis community is at the heart of all we do, and we strive to support and represent all experiences. We strive to make change happen for everyone with endometriosis, to end chronic menstrual related pain being brushed off as normal and raise awareness of endometriosis with the wider public. We’re here to provide vital support services, reliable information and a community for those affected by endometriosis.