This cHanGes Everything shirts

Support HER’s life-saving mission and buy a shirt today! There are six different styles in six different colors! All proceeds support our education, research, and policy efforts.

Read More

HG Impact: Sabrina

I was never diagnosed with HG because of the lack of education and knowledge regarding the illness. As a result, I experienced prenatal and postnatal depression and delivered prematurely.

Read More

HG Impact: Maria and Her Family

Thankful! Thankful is what I am. My babies and I survived Hyperemesis Gravidarum only because of the amazing support we received from the HER Foundation. 

Read More

HER has been making HERstory since 2000

The HER Foundation has been making HG history since 2000. In honor of Women’s History Month, we introduce the four women who have been with HER since the beginning.

Read More

Complications Secondary to Hyperemesis Gravidarum

Hyperemesis Gravidarum (HG) is not self-limiting, and its impact can last a lifetime for mothers and their children. Until there is recognition of this fact and comprehensive, universal, effective treatment for all HG patients, every level of society will continue to face the costs of HG.

Read More

Why we do what we do!

The HER Foundation’s staff, clinicians and referral coordinator volunteer many hours each year to respond to thousands of emails, messages, and calls for help with Hyperemesis Gravidarum (HG). This is core to our mission, and we want to share why we want to expand this service. Enjoy these heartwarming messages and stories.

Read More

HERstory: Amy

In HER Words: Thank you for sharing your Hyperemesis Gravidarum (HG) journey. I had baby fever. I wanted a baby so bad it hurt. I was jealous of others who were…

Read More

HERstory: Saloni

For the second installment of the #HERstory Global Initiative, we spoke with Hyperemesis Gravidarum (HG) survivor Saloni, who is currently residing in India. She shines some light on her personal…

Read More

We’re Celebrating 20 Years of Help and Hope for HG

From 2000 to 2020, we have been building a healthier future for the next generation! Over the past 20 years, we have offered support and resources to over 2,000,000 people across the globe. We hope you enjoy these highlights from our start as a patient-driven organization to our current role as the leading HG research and education organization in the world.

Read More

HERstory: Veronica

This summer, we had the pleasure of interviewing Veronica about her experience with Hyperemesis Gravidarum (HG). Veronica is an HG survivor and native Venezuelan who is currently residing in Toronto,…

Read More