Kia ora and welcome!
If you want to know more about endometriosis, you have come to the right place. On this website, you can find out more about the disease, and evidence based best practice treatment and management. You will also find information about self-management – the things you can do for yourself that guide you on nutrition, coping and general well-being. You may be looking for support or advice through ENDO HELP, or a place where you can share your story with others or read about others’ experiences. You’ll find useful links to other websites, blogs and the latest in research.
Endometriosis New Zealand represents the tens of thousands of girls, women, and those assigned female at birth, with endometriosis and persistent pelvic pain in New Zealand, their whānau and we work with those who treat the condition. We have an advisory group of doctors and health professionals known as ESIG or the Endometriosis Special Interest Group. You can ASK ESIG questions on our social media sites so make sure you like our Facebook page, and Instagram. Endometriosis New Zealand is unique in that it provides specialised and professional services and programmes to communities, the workplace and GP and Specialist education. You can donate here.
Our motto is Strength through support Mā te tautoko, ka whai kaha, ka ora. We hope you find strength in the information offered on our website and feel supported in your quest to live well with endometriosis. Nga mihi.