The third Thursday of every month from 12-1 PM/Central, the HER Foundation hosts an Online HG Support Group facilitated by licensed professional who are also HG survivors as a service to people with a current or prior diagnosis of hyperemesis gravidarum (HG). These groups are facilitated by volunteers Sarah Coffman and Elizabeth Lowder, HER Foundation Advisory Council members and HG survivors.
Read MoreMeet Kathryn Romine at 5 PM/PST on Sunday, October 24th, where she will share her HG journey with Kimber and explain why she is part of the HER Ambassador Council.…
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Trauma from Hyperemesis Gravidarum (HG) cannot be prevented. The HER team believes the following tips will give you the best chance of being prepared for HG in a subsequent pregnancy.…
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Just like with any trauma, the severity of impact depends on how the individual person experiences HG and any prior history of trauma. This is why preventative care, such as…
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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…
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When we saw the two pink lines on the pregnancy test for our third child, I could already picture the moment when our boys would meet their sibling: the five…
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Our daughter, Liora Elle, was born on January 1, 2020. That New Year’s Day, we finally triumphed over a nearly year-long fight against hyperemesis gravidarum (HG).
Read MoreJune is PTSD Awareness Month! Up to 18% of HG survivors are diagnosed with full criteria PTSD while others suffer with symptoms and still more go undiagnosed. Here at the HER Foundation, our goal is that no mother suffers alone. We want to empower you and share our research and resources to help you advocate for your mental and physical health.
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