A 501(C)3Tax-Exempt, Tax-Deductible Organization

Endometriosis Research Center
World Headquarters
630 Ibis Drive
Delray Beach, FL 33444 USA


Toll Free: 800/239-7280
Phone: 561/274-7442
Fax: 561/274-0931
Contact Us Via Email

"What is Endometriosis?"
 

Endometriosis from Endometriosis.org on Vimeo.

 


NEWS:

We were very sad to recently announce to the retirement of our friend, mentor and advisor, Dr. David Redwine, known the world over for his pioneering works in endometriosis. We wish him well!  

NEW: Concerned about endometriosis of the lungs? Candice F. shares this educational fact sheet here.  Want to learn about her story? Click here.  Also, join her dedicated discussion group to learn more about this uncommon form of endometriosis from others who understand.

Are you ages 18-49, diagnosed with endometriosis, and would like to participate in a study? Click here for more information on the Violet Petal Study.

Looking for our Girl Talk(tm) Program for young women aged 25 and under? We've got a new home on Facebook. Join us there today!

A critical article, new to our Women2Women Program: "Endometriosis: Considerations of LGBT Patients” by A. Dance, MAWH

Abortions Cause Endometriosis?? NO!  Read the facts here!

Dr. David Redwine's new book, "Googling Endometriosis: the Lost Centuries" is now available!  Click to get your copy today

ERC Board Member honored for lifetime acheivements in endometriosis by National Women's Health Foundation

On Facebook? Though our Group Discussion page is clsoed, don't miss all the news and links/info/education on our main wall!

Be sure to check out the latest from Nancy's Nook, musings on endometriosis

The National Office on Women's Health recognizes endometriosis through this insightful spotlight.  If you've been with us over the past 16 years, then you know this woman. But did you know her story?

Have you ever read or shared the Endometriosis Letter from Survivors? Get your copy here

Looking for original MENDO group (Men who Love Women with Endometriosis), founded in 1999 by John Blondin & Carey Lewis? Click here (please note that the MENDO name is property of John Blondin for the ERC and may not be used in any other context without permission; for men only - female partners, please join us here or request our Women2Women materials)

First-ever Endometriosis Legislative ToolKit Launches in DC; ERC a strong contributor to landmark effort

This website is dedicated to the memory of Kristi An Rose.  "So no one else will suffer": Click here to learn more

Order Educational Materials

BRIDGING THE GAP BETWEEN SCIENCE & SUPPORT

Endometriosis is a reproductive illness affecting an estimated 176 million women and girls around the world (WERF).  Mistakenly stigmatized as merely "painful periods", the disease is far more than just simple "killer cramps".  The far-reaching effects of endometriosis negatively impact all of society - indeed, staggering costs associated with the illness soar near an estimated $110 billion annually.  We strive to make a positive difference in the lives of all those affected by the disease.  For almost two decades, ERC has been an international leader in endometriosis awareness, education, encouragement and empowerment, and is involved in a  number of global endometriosis research and collaborative efforts. Unlike other organizations,  however, we are unique in that we are not fee-based.  There is never a cost to be involved in or benefit from the ERC’s many programs.  There are many ways in which the ERC can help you, whether you are a women or girl with endometriosis, a loved one, physician, researcher or media contact.  We are dedicated not only to improving the quality of life for those with the disease, but to continuing our important work with clinicians and researchers all over the world as well in order to find more effective treatments for the disease - and ultimately, to find the cure.  It has been our mission since early 1997 to bridge the gap between patients and professionals.  Come join our efforts...we’re glad you’re here.

We are the Proud Founders of Girl Talk(tm), the First-Ever
Education & Support Program for Young Women

 
Order endometriosis books by clicking
above to support the ERC!

:: Patients, Family & Friends :: Researchers :: Legislative & Public Awareness
At the ERC, our first priority is meeting the needs of the women with Endometriosis and their loved ones.  Through our many diverse programs, the ERC strives to empower, educate and encourage Endometriosis patients from all over the world.  If you are a patient or loved one of someone with Endometriosis, you have come to the right place - the ERC is here to help any way we can...ENTER

The ERC is committed to making sure that the research community continues to be aware of this often misdiagnosed disease. Researchers: please contact us today.

The ERC is a pioneer and continued leader in the efforts to increase recognition of this disease specifically among local, state and federal policymakers.  Through our work, the United State Congress unanimously passed the country's first-ever National Endometriosis Awareness Resolution, H. Con. Res. 291...ENTER