For the second installment of the #HERstory Global Initiative, we spoke with Hyperemesis Gravidarum (HG) survivor Saloni, who is currently residing in India. She shines some light on her personal…
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For the first time ever, you can join us from wherever you are for Champions for Change Summit! Registration for this virtual event gives you access to our live event keynotes and workshops, an opportunity to network with patient engagement opportunities and more!
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Petty, co-founder of HG Indonesia, shares about her HG pregnancy, the support she received from HER Foundation volunteers, and how she now suppports others.
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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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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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Along with many other women, I dreamt of starting a family one day and experiencing the joys of pregnancy. In the spring of 1998, I became pregnant with my first…
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I struggled with PTSD and Postpartum Anxiety following my first HG pregnancy. It took years of therapy, communication with other HG survivors, and HER Foundation resources and support to find…
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I have always been fiercely proud of my self-reliance; in fact, I have always been fiercely proud, period. But when you suddenly cannot brush your own hair, cannot shower, cannot get dressed without vomiting, vanity and pride quickly disappear.
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May 15th is International HG Awareness Day, and we will be celebrating all month! The 2020 international HG community theme is Raise Your Voice! You can help spread awareness about Hyperemesis…
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