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.

HERstory: Amy

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…

© HER Foundation 2022. No part of the materials available through the hyperemesis.org site may be copied, photocopied, reproduced, translated or reduced to any electronic medium or machine-readable form, in whole or in part, without prior written consent of the HER Foundation. Any other reproduction in any form without the permission of the HER Foundation is prohibited. All materials contained on this site are protected by United States copyright law and may not be reproduced, distributed, transmitted, displayed, published or broadcast without the prior written permission of the HER Foundation.

volunteer in action

You are not alone!

HERstory: Amy

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