Raise Your Voice for HER!
It is hard enough to have a successful pregnancy under normal conditions. Now our hospitals are jammed, chaotic, and operating in a different mode. Yet, there is always hope for moms with HG, and that is why we ask for your support as we work to bring focused education and resources to those women who need it during a highly stressful time. We are here for women regardless of what is going on around the world.
During this uncertain time funding has been very minimal yet our work continues unabated. COVID-19 might push us around a bit, but it won’t keep us DOWN. We can continue our mission with your help. We will Raise Your Voice!
Please help us launch our new mobile-friendly site, continue advocacy and support, and many other educational and research projects. This means more moms will get better care in 2020 and beyond!
Our mission is to find a cure for hyperemesis and its complications through advanced research, offer education and support to those seeking effective management strategies for hyperemesis, and provide information on new resources and treatment options as they become available.
HER Foundation EIN: 71-0912435
HG Mom Stories
Kierstan’s HG Truths
I have been sick in all four of my pregnancies, and my first two ended in first trimester miscarriages. I got pregnant with my first daughter in 2017 and was…Read More
Thank you, Rachel, for sharing your journey with Hyperemesis Gravidarum (HG). There it is. The big blue plus sign. We’re pregnant! We were newlyweds, pregnant for the very first time…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
We hold them in our hearts
October is Pregnancy and Infant Loss (PAIL) Awareness Month, and we want to honor the memories of the little ones we hold in their hearts. October is Pregnancy and Infant Loss (PAIL) Awareness Month, and we want to honor the memories of the little ones we hold in their hearts. We are grateful for the transparency and love shared by members of our loss community.Read More
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…Read More
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,…Read More
Raise Your Voice: Petty
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.Read More
Come Home to HER: Samantha
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…Read More
Struggling with the Unknown of HG: Letitia
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,…Read More
Raise Your Voice: Alana
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…Read More