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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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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