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.
Support another 20 years of helping mothers and babies thrive. HER is the global voice and leader for HG research and education.
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.
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…
For the second installment of the #HERstory Global Initiative, we spoke with Hyperemesis Gravidarum (HG) survivor Saloni, who is currently residing in India. She shines some light on her personal…
This summer, we had the pleasure of interviewing Veronica about her experience with Hyperemesis Gravidarum (HG). Veronica is an HG survivor and native Venezuelan who is currently residing in Toronto,…
Petty, co-founder of HG Indonesia, shares about her HG pregnancy, the support she received from HER Foundation volunteers, and how she now suppports others.
When we saw the two pink lines on the pregnancy test for our third child, I could already picture the moment when our boys would meet their sibling: the five…
I have two toddlers, ages 2 and 3 1/2. During both HG pregnancies, I was diagnosed with Hyperemesis Gravidarum (HG), which is a pregnancy illness that includes severe nausea, vomiting,…
Along with many other women, I dreamt of starting a family one day and experiencing the joys of pregnancy. In the spring of 1998, I became pregnant with my first…
