It was International Women’s Day 2023 when I found out the gender of my third child – a girl. We already had two daughters, a 3-year-old and a 21-month-old. We…
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Parenthood transforms with joy, challenges, and unexpected twists. When HG enters the picture, it adds an extra complexity for both moms and their partners. Coping with severe nausea and vomiting…
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Hyperemesis Gravidarum (HG) is not self-limiting, and its impact can last a lifetime for mothers and their children. Until there is recognition of this fact and comprehensive, universal, effective treatment for all HG patients, every level of society will continue to face the costs of HG.
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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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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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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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The HER Foundation has been making HG history since 2000. In honor of Women’s History Month, we introduce the four women who have been with HER since the beginning.
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The HER Foundation’s staff, clinicians and referral coordinator volunteer many hours each year to respond to thousands of emails, messages, and calls for help with Hyperemesis Gravidarum (HG). This is core to our mission, and we want to share why we want to expand this service. Enjoy these heartwarming messages and stories.
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In HER Words: Thank you for sharing your Hyperemesis Gravidarum (HG) journey. I had baby fever. I wanted a baby so bad it hurt. I was jealous of others who were…
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