The HER Foundation is thankful for our business partners who support our mission.
HER Board members, Marlena Fejzo, PhD, and Patrick Mullen, MD, are running the first study of GDF15 in HG patients in the United States.
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.
Join us in honoring Maria and her twins on Thursday, November 25th. Maria’s voice was silenced due to preventable complications of Hyperemesis Gravidarum (HG), and we all must be a voice for her. No mother should be silenced by HG!
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…
At the end of November 2020, I found out I was pregnant with our third child. The day after my doctor called me to confirm I was indeed pregnant, the…
Marlena Fejzo, PhD, HER Board Member and Research Advisor, presents at the American Society of Human Genetics Annual Meeting on the genetics of Hyperemesis Gravidarum (HG).
Read the latest research on the safety of ondansetron (Zofran) in an HG pregnancy.
The Hyperemesis Education and Research Foundation’s mission is to provide Hyperemesis Gravidarum (HG) support, advocacy, education, and research to improve treatment and outcomes.
