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The HER Foundation is dedicated to helping women survive the many complications and debilitating symptoms of Hyperemesis Gravidarum (HG) to improve their long-term health and avoid pregnancy loss.

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Our mission is to advance HG research through collaboration with leading universities, provide multi-lingual education on effective management to health professionals and families, and support those impacted by HG. The HER Foundation is the voice of support and hope to all who are faced with managing HG.

The HER Foundation is the world's largest grassroots network of hyperemesis gravidarum (HG) survivors and leading site for HG information on the Internet. As one of the only dedicated HG research teams, we are working to find a cause and cure for hyperemesis through genetic research. HER is an advocate and support for over 16,000 women around the world annually on social media, and approximately 250,000 via www.HelpHER.org.