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.
We invite our community to take Provider Packets of resources to a hospital, clinic, or practice with your personal story and passion will make a difference.
Join the HER Foundation as we raise awareness about HG’s Impact during HG Awareness Month, May 2022.
Hyperemesis gravidarum (HG) does not look the same for every patient. Learn about the severity levels.
Dr. Marlena Fejzo, geneticist and HER’s Research Advisor and member of the Board of Directors, was featured in the Inverse article, “When morning sickness kills: doctors have dismissed hyperemesis gravidarum for decades, but new research could undo this harmful legacy.”
The HER Foundation’s breakthrough psychosocial study shows that Hyperemesis Gravidarum (HG) is not self limiting and has societal implications.
We created this tool to help guide HG patients through the steps of self advocacy.
Hyperemesis Gravidarum (HG) is a risk factor for premature birth. On Prematurity Awareness Day, meet Crew and Tru.
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…
21 years of Help & Hope! From 2000 to 2021, we have been building a healthier future for the next generation! We have offered research, support, advocacy, and education resources…
