My entire pregnancy was traumatic, and I still suffer from PTSD due to HG. My son is now 3 years old, and we are all happy, healthy, and thriving. My husband and I made the decision early on that our son would be our one and only.
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Support HER’s life-saving mission and buy a shirt today! There are six different styles in six different colors! All proceeds support our education, research, and policy efforts.
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We’ve reached a huge milestone! The HER Foundation has been Helping Generations for 22 years! Since 2000, we’ve helped over 2.2 million people in 95% of countries through our support, research, resources, and advocacy.
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Whether the loss is miscarriage, termination, stillbirth, or neonatal, we remember. Pregnancy and Infant Loss Remembrance Day honors the babies we hold in our hearts. We invite you to add…
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Whether the loss is miscarriage, termination, stillbirth, or neonatal, we remember the babies we hold in our hearts. Pregnancy and Infant Loss Awareness Month honors our lost little ones. We…
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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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