Giving Tuesday: Give HOPE

This year there is HOPE. Don’t you feel it…the feeling of CHANGE. We have suffered through so many uncertainties and challenges in 2020, and now we can look forward to the end of the year and to a new beginning. Here at HER Foundation, we are ready for a very BIG day in the nonprofit world:…

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HER Foundation Featured on the Connect Kindness Podcast

Calling all podcast lovers! HER Foundation’s very own Co-founder and Executive Director Kimber MacGibbon, RN, was interviewed about Hyperemesis Gravidarum (HG) and HER’s mission and work on the October 2, 2020, episode of the Connect Kindness Podcast.

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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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Stella Escobedo Reports on Hyperemesis Gravidarum and HER Foundation

Stella Inger Escobedo reports on hyperemesis gravidarum (HG) and the HER Foundation on The CW San Diego. The piece features Escobedo’s diagnosis with HG in first trimester and interviews with Marlena Fejzo, PhD., geneticist and member of the HER Board of Directors, and Dominique Albrecht, HER leader. The story highlights our new collaborative campaign, 1MomIs2Many.…

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About HG for Indonesian Moms

Kimber MacGibbon, RN, Co-founder and Executive Director of HER Foundation is presenting for Indonesian moms about hyperemesis gravidarum (HG), treatment options, HG care, and ways to support women with HG.

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Prematurity Awareness Month

November is Prematurity Awareness Month. Hyperemesis Gravidarum (HG) is one of the leading causes of prematurity. Women with HG are up to 4-fold increased risk are premature birth and are more likely to deliver babies that are small for gestational age and growth restricted likely due to malnutrition and stress.  Support HER Foundation’s efforts to…

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Losing Quinn

This time last year, I noticed Facebook friends posting about National Pregnancy and Infant Loss Awareness Day, a day I’d never heard of, and I made a note to hold space for those expectant parents who lost their babies. Three days later, I started bleeding and was devastated to learn that my 7 week embryo…

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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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Pregnancy and Infant Loss Awareness Day

1 in 3 HG pregnancies ends in loss. Whether the loss is miscarriage, termination, stillbirth, or neonatal loss, we remember the babies we hold in our hearts. Pregnancy and Infant Loss Awareness Day honors our lost little ones. We invite you to add your HG baby to our memorial page.

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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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