Sometimes it’s difficult knowing what to say to HG patients. These lists come from the HER Foundation’s community.
The HER Foundation is the global voice of HG, and we are proud to celebrate the 11th annual HG Awareness Day on May 15th. Throughout the month of May, the international *hyperemesis gravidarum (HG) community is educating about #HGimpact! Together, we are changing the future for the next generation.
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.
