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National Action Plan

Inadequate medical care causing significant harm:

The United States does not invest enough in the health of its citizens who suffer from Endometriosis. Endometriosis is nearly as prevalent as diabetes in women, yet receives only pennies on the dollar in federally-funded spending on research and public health awareness campaigns.  

Lifetime of crippling pain and failed treatments: 

Women, girls, and transgender individuals with endometriosis can face a lifetime of incapacitating pain, organ failure, repeat surgeries, acute abdomen, infertility, diagnostic delays of up to 10 years or more, increased risk for certain cancers, increased risk for cardiovascular disease, and multiple failed treatments that don’t work or cause severe injury from adverse side effects. There is no cure for endometriosis and no known cause.

Something must change:

The millions who suffer from this excruciating, chronic disease deserve better. That’s why you’ll see thousands of endometriosis sufferers and supporters marching in the streets all over the world each year in March for Endometriosis Awareness Month and EndoMarch Day, to get the word out that endometriosis is not just a bad period, but one of the most serious, potentially debilitating diseases women, girls, and transgender individuals can face in their lifetimes.

Still, those suffering from a severe, chronic illness shouldn’t have to march in the streets in the first place to receive basic medical care. 

We need congress to act:

That’s why we can’t wait any longer for change to happen. We need Congress to act. We need Endometriosis Health Care Reforms now. 


Camran Nezhat, M.D.,

Endometriosis Specialist &
Founder, Worldwide EndoMarch & World Endometriosis Day
Palo Alto, California, USA


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