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

HERstory: Amy

I had baby fever. I wanted a baby so bad it hurt. I was jealous of others who were pregnant. When I saw pregnant women, they looked so happy waddling around, picking out baby stuff, and always talking about how great it was. When I got pregnant with my daughter in the fall of 2010, I was…

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HERstory: Lindsey

At the end of November 2020, I found out I was pregnant with our third child. The day after my doctor called me to confirm I was indeed pregnant, the sickness started with a vengeance. I couldn’t eat even though I felt hunger, and the nausea was so strong I felt like I couldn’t take…

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We all love a happy ending: update from Rachel

We did it! My daughter, Dakota Aoibhinn, and I survived Hyperemesis Gravidarum. She is a thriving, smiley, giggly four month old, and we couldn’t be more in love with her.  My husband and I had always wanted a big family, but the thought of surviving another HG pregnancy sends waves of nausea through my body…

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HG Truths: HG and Primary Hyperparathyroidism

When two things don’t mix well… A memoir about HG and Primary Hyperparathyroidism by Nikki Reaching a diagnosis of Hyperemesis Gravidarum (HG) was a long journey for us, but as Thomas Fuller put it, “A disease known is half cured.” We went through three difficult pregnancies with the usual runaround of “its morning sickness,” “it…

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Takiyah’s HG Truth

I was first diagnosed with Hyperemesis Gravidarum (HG) in 2007-2008 with my first pregnancy. Unfortunately, I didn’t have all the resources I do now or the knowledge of what to expect. Due to HG and ptyalism, I couldn’t keep food nor water down. I suffered from heart palpitations throughout the pregnancy due to a heart…

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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 sick days after conception. I didn’t understand why I wasn’t feeling well and ended up taking a test at 4.5 weeks. I just kept getting…

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HERstory: Rachel

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 with our first baby, and life couldn’t have been any more perfect. I was on a cloud of happiness. I was already thinking of cute…

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Losing Quinn

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 space for those expectant parents who lost their babies. Three days later, I started bleeding and was devastated to learn that my 7 week embryo…

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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.

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HERstory: Saloni

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 HG journey, which she is still undergoing to this day as she continues to recover. Because she believes that there is little HG awareness in…

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