We're Here to Make a Change

Many people in the US alone live with chronic pelvic and/or menstrual pain, but there are few resources to turn to. Because this pain is often associated with sexual stigma, it can feel isolating. It's also difficult to describe to providers, which can lead to misdiagnosis. We are your Oregon resource for support. Click around the site or send us an email at oregonendometriosis@gmail.com with any questions. We're here to help, and we're here to make a change. 

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Who We Are

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Elle Hurley is a 27 year-old Oregon State graduate and patient navigator who has worked with chronic illness communities including Pacific Northwest Bleeding Disorders, the Valley AIDS Information Network, and the National Psoriasis Foundation. She has written for the Endometriosis Foundation of America and is dedicated to creating a support network for endo and pelvic pain patients throughout Oregon.  

Elle is passionate about mental health and sexual education. She has spoken for national and local organizations from SheBop to Mental Health America about the realities of living with chronic pain. As a member of the LGBTQIA community, she is committed to reducing barriers to care for underserved populations throughout the country. She understands firsthand that being a patient can be overwhelming and isolating. She is committed to providing others with the resources necessary to access care and to feel less alone during their healthcare journeys.