AmazonSmile charitable giving program ends

Amazon’s charitable giving based on your shopping is ending. We rely on those donations for ~$2600 in operating costs covering site fees for about 10 months of the year. Please help us meet this deficit by giving today, creating a monthly donation, or hosting a fundraiser? Our resources and support are free to all in need because of those who gave in the past. Will you help those who come after you? Please give today!

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January 2022 HER Foundation Online HG Support Group

As a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…

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HER Research Surveys

Be a part of finding answers about Hyperemesis Gravidarum (HG). Currently, the HER Foundation has three active research surveys. Please participate!

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Goals for 2023

In 2023, we will continue our support of families across the globe, continue our groundbreaking research, advocate to change policy to improve maternal and fetal outcomes, and launch an exciting new education program!

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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 in the HG Community

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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Best of 2022

The HER Foundation has accomplished a lot in 2022! We are thankful for the support of our donors and community and want to share the highlights that made this HER’s best year yet! This is what 22 years of Helping Generations survive Hyperemesis Gravidarum (HG) looks like.

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newborn

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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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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