As a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
Read MoreAs a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
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The HER Foundation has partnered with ASPEN, the American Society for Parenteral and Enteral Nutrition, for ASPEN Malnutrition Awareness Week TM (MAW) on September 19-23, 2022. For more information and…
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I was never diagnosed with HG because of the lack of education and knowledge regarding the illness. As a result, I experienced prenatal and postnatal depression and delivered prematurely.
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The HER Foundation is helping a second generation facing Hyperemesis Gravidarum (HG). If your mother have hyperemesis gravidarum (HG) when pregnant with you or siblings, we want to talk.
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My name is Sally. I have three children: Rachel (born 1988), Timothy (born 1991), and Emilia (born 1997). I suffered from HG with all three pregnancies, before the HER Foundation began.
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Thankful! Thankful is what I am. My babies and I survived Hyperemesis Gravidarum only because of the amazing support we received from the HER Foundation.
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I felt depressed a lot because I was dealing with my sickness by myself, but I was able to find an online support system through the HER Foundation and meet other women experiencing the same difficulties. I did not feel alone.
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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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We invite our community to take Provider Packets of resources to a hospital, clinic, or practice with your personal story and passion will make a difference.
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