Share Your HG Story With Us!

We'd love to hear your story and share it with our community! Please take a moment to fill out our survey.

If you have any pictures you'd like to include, feel free to email them to us at story @ hyperemesis.org.

We appreciate your contribution to spreading awareness. Thank you for sharing your story with us!

Hannah’s #HGreality

March 5, 2023

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.

Danielle’s HG Journey

December 26, 2022

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.

photo of Hannah and her partner

Words That Trigger in the HG Community

December 23, 2022

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.” 

newborn

Queeneth Shares a Beautiful Message of Thanks

December 20, 2022

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. 

picture of mother and newborn

Tala Shares #HERstory

December 18, 2022

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.

Tiffany Shares #HERstory

December 10, 2022

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.

Candace Renee and Maxwell on HG and Prematurity

November 27, 2022

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.

HG Impact: Sabrina

July 10, 2022

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.

HG Impact: choose your words carefully

June 27, 2022

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 IVF pregnancy.

HG Impact: Sally

June 12, 2022

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.