With a bright, new decade so close, we are reflecting on our history. We began as a site in 2000, became a 501(c)3 nonprofit in 2003, and in 2019, we have over 900 volunteers and an active Board of Directors. We are the voice of HG progress.
Because of your support, HER has achieved many firsts including publishing over thirty ground-breaking research studies INCLUDING THOSE identifying the first genes associated with HG; developing HG assessment tools and protocols; building a comprehensive website; creating the first iOS HG Care App to improve tracking and reporting of symptoms and treatment; and supporting HUNDREDS OF THOUSANDS OF women facing HG.
In 2020, we will continue our support of families across the globe, work to educate providers at conferences and one-to-one, continue our groundbreaking research, and advocate to change policy to improve maternal and fetal outcomes.
- Conferences to education medical professionals
- Meeting with policy leaders
- Partnering with businesses and organizations
- Educating hundreds of thousands on social media
- Leading HG Awareness Month
- HER HG Documentary
- And much much more
We look forward to spreading education, raising awareness, conducting research, and telling YOUR story! 
I am HER! You are HER! We are HER!
Believe in HER!
Together, we are changing
the future for the next generation!
What is HG? HG is hyperemesis gravidarum: a potentially life-threatening pregnancy disease that causes chronic malnutrition, dehydration, and debility due to severe nausea and vomiting, and may cause long-term health issues for mom/baby.
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