National endometriosis research network – sign up

The NECST Network is a collaborative group of clinicians, scientists, endometriosis patients and consumer advocates who have come together to coordinate support for research organisations, and conduct clinical trials for endometriosis treatments and services.

The NECST Network and Jean Hailes are passionate about research that will improve the lives of the one in nine women of reproductive age in Australia living with endometriosis and its often debilitating symptoms.

Visit the NECST website, where you can:

• sign up and become a member of the NECST Network
• browse Jean Hailes’ endometriosis resources for patients & health professionals
• learn more about the NECST Registry, register your interest to be a recruitment site and participate to assist with data collection on patterns of care of those living and diagnosed with endometriosis.

Patients can apply to be members of the NECST Network to be kept up to date with the latest research information and network activities. However, to take part in research, they can only be referred by their gynaecologist.

Patients can ask their gynaecologists to get in touch with the NECST Network if they’re interested in becoming a recruitment site for the NECST Registry.