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!
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.
Just like with any trauma, the severity of impact depends on how the individual person experiences HG and any prior history of trauma. This is why preventative care, such as…
In honor of HG Awareness Month 2021, we are launching a new Patient Treatment Brochure and have expanded our HG treatment algorithm.
Dr. Marlena Fejzo, a geneticist at the University of Southern California and a HER Foundation Board of Directors, presented at the Fetal Medicine Foundation (FMF) about Hyperemesis Gravidarum (HG), its potential causes, and treatment options. Over 5600 medical professionals heard her speak, and the talk is freely available on the FMF’s website in English, Spanish, Russian, and Portuguese.
HER is hosting HG Chats on every continent (except Antarctica). We want HG survivors to have an opportunity to talk, connect, and feel heard. You are welcome to join any of these.
