Our mission is to increase endometriosis awareness, fund landmark research, provide advocacy and support for patients, and educate the public and medical community.
Founders: Padma Lakshmi, Tamer Seckin, MD
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Patient Day

Every year, the Endometriosis Foundation of America hosts a patient conference designed to equip patients with all the tools and information they need to live their best lives with endometriosis. 

The virtual conference will include panels by experts in fields ranging from extrapelvic endometriosis and fertility to mental health and nutrition. We believe that living with endometriosis requires a collaborative and interdisciplinary effort that prioritizes the patient's voice. We are excited to continue spotlighting patients who will take the virtual stage to tell their stories and share their toolkits for advocacy, management, and support. This year, we're delighted to host not one, but three days of this empowering and educational event for the endometriosis community. 

Patient Day was created for and inspired by endometriosis patients and we invite you to share this day with your loved ones and support network. Together we can seek the information and support that the endo community deserves.