About Us

The Endometriosis Foundation of America strives to increase disease recognition, provide advocacy, facilitate expert surgical training, and fund landmark endometriosis research. Engaged in a robust campaign to inform both the medical community and the public, the EFA places particular emphasis on the critical importance of early diagnosis and effective intervention while simultaneously providing education to the next generation of medical professionals and their patients.

 

The Endometriosis Foundation of America is a 501(c)3 non-profit organization. EIN number 20-4904437

 

 

 

Get in Touch!

Get in Touch!

Questions? Comments? Concerns? Please contact us at:

Our Supporters

Our Supporters

  Did you know all that you accomplished this year? Through your support, you   increased disease recognition among the general public and medical communities, advocated for patients, provided expert surgical training to physicians,…

EFA Executive Board of Directors

EFA Executive Board of Directors

Piraye Yurttas Beim, PhD Dr. Piraye Yurttas Beim founded Celmatix in 2009 to empower women to be more proactive and informed about their fertility through better data, including genomics. She was on the front lines of the personalized medicine…

Endofound Staff

Endofound Staff

Leslie Wolf-Creutzfeldt, Executive Director Leslie Wolf-Creutzfeldt has held leadership positions in healthcare and Foundation public relations and advocacy for over 30 years. She has spent her career communicating to a wide audience complex…

Resource Materials

Resource Materials

YOU can help us raise endometriosis awareness! Please click on individual links below to download free copies of outreach and education materials. For information and materials about how to host an EndoWalk, please email generaladmin@endofound.org.…

Video Gallery

Video Gallery

Endometriosis Foundation of America Video Gallery