Hi, I’m Shannon. 

I’m a filmmaker, lawyer and activist. I’m a wife, a mother, and a daughter. 

I’m also a person who has lived with endometriosis most of my life. This means countless doctors and tests. It means debilitating pain. It means multiple drugs, repeated surgeries and devastating miscarriages. 

I searched for answers – for years. When I realized the medical system didn’t have easy answers for endometriosis, I began to investigate more deeply and what I found was astonishing. 

Endometriosis is a perfect, awful storm of so many things – societal taboos, gender bias, uninformed doctors and the undeniable impact of commercial interests on our healthcare. 

The goal of this patient-led, patient-first movement is to change that. From films and widespread awareness campaigns to accurate educational tools for healthcare providers and collaborations with lawmakers to change policy and generate research funding – we are reshaping the status quo.

Together, we can break the cycle.

Shannon

Casey Berna

Casey Berna

Associate Producer

Katie Bormaster

Katie Bormaster

Partnerships

Elizabeth Dollarhide

Elizabeth Dollarhide

Social Impact

Jenneh Rishe

Jenneh Rishe

Advocate

Emily Hatch

Emily Hatch

Advocate

Kyung Jeon-Miranda

Kyung Jeon-Miranda

Advocate

Laura Cone

Laura Cone

Advocate

Hillary Rodham Clinton

Hillary Rodham Clinton

Executive Producer

Orrin Hatch

Orrin Hatch

Corrine Foxx

Corrine Foxx

Executive Producer

Mae Whitman

Mae Whitman

Executive Producer

Senator Elizabeth Warren

Senator Elizabeth Warren

Legislative Partner

Senator Mitt Romney

Senator Mitt Romney

Legislative Partner

Heather Guidone

Heather Guidone

Advisory Committee

Jhumka Gupta, PhD

Jhumka Gupta, PhD

Advisory Committee

Iris Orbuch, MD

Iris Orbuch, MD

Advisory Committee

Nancy Petersen, RN

Nancy Petersen, RN

Advisory Committee

Michael Rogers, PhD

Michael Rogers, PhD

Advisory Committee

Millen Magese

Millen Magese

Advisory Committee

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