HER Foundation Online HG Support Group

As a service to moms with a current or prior diagnosis of HG, the HER Foundation will host free, monthly online support groups via Zoom Meeting on the third Thursday of the month from 12:00 – 1:00 PM/CST. Currently, there is a limit of 150 participants. Follow the Facebook event for updates and reminders. The purpose of…

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HER Foundation Online HG Support Group

As a service to moms with a current or prior diagnosis of HG, the HER Foundation will host free, monthly online support groups via Zoom Meeting on the third Thursday of the month from 12:00 – 1:00 PM/CST. Currently, there is a limit of 150 participants. Follow the Facebook event for updates and reminders. The purpose of…

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HG Chat!

Join us for HG Chat on Friday, November 27th, hosted by T and Suzanne. HG Chat is a chance to get together with other HG moms and socialize.

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HER Foundation Online HG Support Group

As a service to moms with a current or prior diagnosis of HG, the HER Foundation will host free, monthly online support groups via Zoom Meeting on the third Thursday of the month from 12:00 – 1:00 PM/CST. Currently, there is a limit of 150 participants. Follow the Facebook event for updates and reminders. The purpose of…

Read More

HER Foundation Online HG Support Group

As a service to moms with a current or prior diagnosis of HG, the HER Foundation will host free, monthly online support groups via Zoom Meeting on the third Thursday of the month from 12:00 – 1:00 PM/CST. Currently, there is a limit of 150 participants. Follow the Facebook event for updates and reminders. The purpose of…

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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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2020 Champions for Change Summit

For the first time ever, you can join us from wherever you are for Champions for Change Summit! Registration for this virtual event gives you access to our live event keynotes and workshops, an opportunity to network with patient engagement opportunities and more!

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We’re Celebrating 20 Years of Help and Hope for HG

From 2000 to 2020, we have been building a healthier future for the next generation! Over the past 20 years, we have offered support and resources to over 2,000,000 people across the globe. We hope you enjoy these highlights from our start as a patient-driven organization to our current role as the leading HG research and education organization in the world.

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HER Foundation Online HG Support Group

As a service to moms with a current or prior diagnosis of HG, the HER Foundation will host free, monthly online support groups via Zoom Meeting on the third Thursday of the month from 12:00 – 1:00 PM/CST. Currently, there is a limit of 150 participants. Follow the Facebook event for updates and reminders. The purpose of…

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HERstory: Veronica

This summer, we had the pleasure of interviewing Veronica about her experience with Hyperemesis Gravidarum (HG). Veronica is an HG survivor and native Venezuelan who is currently residing in Toronto, Canada. Veronica is the first mom we were able to interview in her native language, Spanish, as part of our #HERstory Global Initiative. Below is…

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