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.
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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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The Hyperemesis Education and Research Foundation’s mission is to provide Hyperemesis Gravidarum (HG) support, advocacy, education, and research to improve treatment and outcomes.
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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…
Read MoreWe 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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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…
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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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I have two toddlers, ages 2 and 3 1/2. During both HG pregnancies, I was diagnosed with Hyperemesis Gravidarum (HG), which is a pregnancy illness that includes severe nausea, vomiting,…
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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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