Are you as excited as we are about the international Hyperemesis Gravidarum (HG) conference being in the United States for the first time? ICHG 2024 happens every other year, and…
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The HER Foundation is the global voice of HG, and we are proud to celebrate the 11th annual HG Awareness Day on May 15th. Throughout the month of May, the international *hyperemesis gravidarum (HG) community is educating about #HGimpact! Together, we are changing the future for the next generation.
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My doctor said I could afford to lose weight with being fat. The mental struggle of watching my body deteriorate and wondering if me or my baby would die was traumatic.
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Along with good medical care, surviving Hyperemesis Gravidarum (HG) means finding others who understand. Here are some ways to make connections. Facebook Support Groups The HER Foundation offers multiple support…
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The Hyperemesis Education and Research Foundation’s mission is to provide Hyperemesis Gravidarum (HG) support, advocacy, education, and research to improve treatment and outcomes.
Read MoreThe Champions for Change Summit is dedicated to empowering our community with the education, training, and resources needed to make necessary changes in maternal health, hosted by MoMMA’s Voices. This…
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We’re shining a light on HG Truths! May 15th is International HG Awareness Day (HGAD), and we’re shining a light on HG Truths all month! The HER Foundation is the…
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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…
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