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…
Read MoreAs 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…
Read MoreAs 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…
Read MoreAs 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…
Read MoreAs 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…
Read More
The Hyperemesis Education and Research Foundation’s mission is to provide Hyperemesis Gravidarum (HG) support, advocacy, education, and research to improve treatment and outcomes.
Read MoreHER 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.
Read More
Support another 20 years of helping mothers and babies thrive. HER is the global voice and leader for HG research and education.
Read More
Kimber MacGibbon, RN, Co-founder and Executive Director of HER Foundation is presenting for Indonesian moms about hyperemesis gravidarum (HG), treatment options, HG care, and ways to support women with HG.
Read More
This time last year, I noticed Facebook friends posting about National Pregnancy and Infant Loss Awareness Day, a day I’d never heard of, and I made a note to hold…
Read More- « Previous
- 1
- 2
- 3
- Next »
