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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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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For the second installment of the #HERstory Global Initiative, we spoke with Hyperemesis Gravidarum (HG) survivor Saloni, who is currently residing in India. She shed 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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We are proud to announce that the HER Foundation has joined ASPEN, the American Society for Parenteral and Enteral Nutrition, as an Ambassador for ASPEN Malnutrition Awareness Week on October 5-9, 2020. It’s a week filled with valuable educational webinars and sharing of informational materials. The goal of Malnutrition Awareness Week is to educate healthcare…
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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…
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Words can’t describe the total shock and awe I felt at the Champions for Change Summit I attended on behalf of the HER Foundation, October 18-20, 2019. For years, I believed that women were either sick like me, specifically with Hyperemesis Gravidarum (HG), or that they must have had a wonderful pregnancy. My time at the Summit…
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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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Lace Up and #Move4MOMs! All proceeds of our virtual Walk, Run, or Roll go to our new LED Crisis Fund.
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AmazonSmile is now available on your mobile app! Every time you shop online, a portion of your purchase can support our work to help families facing HG.
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