Speak with our HG Experts

To contact the HER Foundation for interviews, please email media@hyperemesis.org.

HG women in your area

To find women around the world willing to share their stories to help raise awareness of HG, please email media@hyperemesis.org.

Media Relations Contacts

Please direct media inquiries to media@hyperemesis.org.

Our HG Experts

Dr. Marlena Fejzo, a Harvard-trained women's health researcher, specializing in genetics, an affiliated with the University of Southern California. Dr. Fejzo is credited with discovering the cause of HG and is the world's leading research scientist on HG and a HER Foundation Board member and Research Advisor. Dr. Fejzo endured HG during her pregnancies. Email her at research at hyperemesis.org.

Dr. Aimee Brecht-Doscher is an OBGYN in the Los Angeles area who has personally been affected by HG. She is a HER Foundation Board member and the Medical Advisor for the Foundation. Email her at aimee at hyperemesis.org.

Kimber MacGibbon is a registered nurse (RN) and has helped many thousands of families facing HG across the globe since 2000. She has an extensive understanding of HG from a medical, advocacy, and personal perspective. Kimber is also co-founder of the HER Foundation. She and Dr. Fejzo have co-authored over three dozen publications on HG in collaboration with universities, including USC and UCLA. Kimber had HG in both of her pregnancies and is located in Portland, Oregon. Email her at kimber at hyperemesis.org.

World Breastfeeding Week 2022

July 31, 2022

Each year, the World Alliance for Breastfeeding Action promotes World Breast Feeding Week from August 1-7. The 2022 theme is Step up for Breastfeeding: Educate and Support. While there are benefits for breastfeeding, not all HG survivors are able to breastfeed.

You are not alone!

July 24, 2022

The third Thursday of every month from 12-1 PM/Central, the HER Foundation hosts an Online HG Support Group facilitated by licensed professional who are also HG survivors as a service to people with a current or prior diagnosis of hyperemesis gravidarum (HG). These groups are facilitated by volunteers Sarah Coffman and Elizabeth Lowder, HER Foundation Advisory Council members and HG survivors.

HER wants to talk with the next generation

July 10, 2022

The HER Foundation is helping a second generation facing Hyperemesis Gravidarum (HG). If your mother have hyperemesis gravidarum (HG) when pregnant with you or siblings, we want to talk.

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