As a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
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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.
Read MoreAs a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
Read MoreAs a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
Read MoreAs a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
Read More
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.
Read MoreAs a service to moms with a current or prior diagnosis of HG, the HER Foundation hosts free, online support groups via Zoom on the third Thursday of the month…
Read More
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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