As a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, HG online support group via Zoom on the third Thursday of the…
As a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, HG online support group via Zoom on the third Thursday of the…
This Giving Tuesday, December 3rd, join a global movement to bring hope to families affected by Hyperemesis Gravidarum (HG)*. Your support fuels research, advocacy, and essential resources for those facing…
Overcoming the Silent Suffering of Hyperemesis Gravidarum (HG) Trigger Warning: Mentions of Loss & Termination My Early Battle with Hyperemesis Gravidarum I suffered severe Hyperemesis Gravidarum (HG) 25 years ago…
Celebrate 24 years of making a difference with us this October! The HER Foundation has helped about 3 million people in over 200 countries since 2000. HER is dedicated to…
The HER Foundation is dedicated to supporting individuals and families affected by Hyperemesis Gravidarum (HG), a debilitating pregnancy complication. By fundraising for the HER Foundation, you can help provide vital…
As a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, HG online support group via Zoom on the third Thursday of the…
The HER Foundation is thrilled to have the groundbreaking research on hyperemesis gravidarum (HG) and pregnancy sickness shortlisted for the Falling Walls Science Breakthrough of the Year 2024 title in…
As a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, HG online support group via Zoom on the third Thursday of the…
Are you as excited as we are about the international Hyperemesis Gravidarum (HG) conference being in the United States for the first time? ICHG 2024 happens every other year, and…
