MM’s HG Story: Discovering HG at 15

I was 15 years old when I first discovered I was a victim of Hyperemesis Gravidarum (HG). I remember being so sick that I couldn’t go to school, take a…

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You are not alone!

The third Thursday of every month from 12-1 PM/Central, the HER Foundation hosts an Online HG Support Group facilitated by licensed professional who are also HG survivors as a service to people with a current or prior diagnosis of hyperemesis gravidarum (HG). These groups are facilitated by volunteers Sarah Coffman and Elizabeth Lowder, HER Foundation Advisory Council members and HG survivors.

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