Support line 0800 733 277
'Endometriosis - the brave face disease of women'
History
Endometriosis New Zealand began as a support group in 1985 in Palmerston North, New Zealand and was known as the NZ Endometriosis Support Group. The three founding members Deborah Bush, Margaret McKenzie and the late Joan Moultrie, began the group because of a desire to improve information, educate and support women with endometriosis.
The support group became a registered charitable trust in January 1994, known as the New Zealand Endometriosis Foundation Incorporated (NZEF). A Board of trustees was appointed to act in a governance role. The organisation is now known as Endometriosis New Zealand (ENZ).
Tens of thousands of women and girls throughout New Zealand and abroad have contacted ENZ over the years - many desperate for information and support. The passion and drive to change the course of history of endometriosis, has relied on the unique skills and talents from within the organisation setting global standards of excellence in developing and delivering initiatives, providing services, fostering research and actively lobbying. ENZ has been a major player in contributing to facilitate the wellness of women.

