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

Hannah’s #HGreality

I knew nearly nothing about hyperemesis, even after my ER diagnosis. The HER website helped educate me about symptoms and how to approach medical professionals. HER helped alleviate some concerns about medications.

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Danielle’s HG Journey

Before discovering the HER Foundation, I felt alone and like something was wrong. After discovering a community and support, I knew I wasn’t alone. HER brings together HG sufferers and supports them.

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photo of Hannah and her partner

Words That Trigger

HG isn’t the price to be paid for a healthy baby. It doesn’t have to happen in order for pregnancy to be viable, so it doesn’t have to be “worth it.” 

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Queeneth Shares a Beautiful Message of Thanks

We are glad to inform you of the arrival of our son. He was born weighing 7 pounds and 3 ounces. While we are most grateful to God, we are particularly very thankful and appreciative of all of the support the HER Foundation gave us. 

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Tala Shares #HERstory

The HER Foundation educated me on the website and social media, and I used the HG Care app. When I was scared to take Zofran, they sent me the lastest research. HER understands, and I didn’t feel alone. One day, they will find a cure.

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Tiffany Shares #HERstory

My entire pregnancy was traumatic, and I still suffer from PTSD due to HG. My son is now 3 years old, and we are all happy, healthy, and thriving. My husband and I made the decision early on that our son would be our one and only.

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Candace Renee and Maxwell on HG and Prematurity

Candace Renee, Maxwell’s mom, TV Personality, Actress, and Host and star on Floribama Shore talks with HER about Hyperemesis Gravidarum (HG) and her son’s premature birth.

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HG Impact: Sabrina

I was never diagnosed with HG because of the lack of education and knowledge regarding the illness. As a result, I experienced prenatal and postnatal depression and delivered prematurely.

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HG Impact: choose your words carefully

Hospitalized with a central line, TPN feeding tubes, and multiple medications at 4 weeks, the damage had begun. Four specialists said her liver would fail if she continued her pregnancy, she terminated her much wanted IV pregnancy.

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HG Impact: Sally

My name is Sally. I have three children: Rachel (born 1988), Timothy (born 1991), and Emilia (born 1997). I suffered from HG with all three pregnancies, before the HER Foundation began. 

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