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International HG Support Search

Hyperemesis Gravidarum affects families worldwide. Families impacted by HG have expressed that having support from family, friends and medical professionals was crucial. 

Below is a list that we have compiled to help families find current HG information and support networks. There are many great HG related foundations worldwide that provide the necessary support to help mothers through pregnancies that are complicated by Hyperemesis Gravidarum.
Quick jump to a section of this page:

United States HG Support

The Ayden Rae Foundation  
Provides an Online forum and support resources to families worldwide.

Beyond Morning Sickness  
Author Ashli Foshee McCall’s website provides current HG information and support.
Ashli Foshee McCall battled severe Hyperemesis Gravidarum four times, loosing two children to the condition.

Provides online and phone support for women who have high-risk pregnancies. International HG Support


SOS Morning Sickness
Educating visitors about hyperemesis gravidarum, nausea and vomiting during pregnancy.

Motherisk counselors speak to hundreds of women and their healthcare providers each day, providing guidance, support and peace of mind.

United Kingdom

Pregnancy Sickness Support
A UK charity supporting sufferers of nausea and vomiting in pregnancy and Hyperemesis Gravidarum.


Frauen Informationen zum Thema Hyperemesis
Disseminating information about Hyperemesis Gravidarum.


Steunpunt HG
Established to disseminate information and support mothers with HG. Online Discussions & Social Networks

Motherisk Forum

Hyperemesis Gravidarum Social Network Support Groups


Ayden Rae Foundation Fan Page

Ayden Rae Foundation HG Support Group

Hyperemesis Gravidarum (HG) UK

Surviving Hyperemesis Gravidarum

Steunpunt Hyperemesis Gravidarum


Ayden Rae Foundation


Hyperemesis Gravidarum Blogs:

Spewing Mummy

Knocked Up Knocked Over

Hyperemesis Heroine

Heart Break Kids

Love Makes A Family

Live, Laugh, Love

Hyperemesis Gravidarum: A Diary

Alternative Mama

Are They All Yours

A Pregnancy With Hyperemesis Gravidarum

Diary of a First Child

Multiple Mummy

The health related information found on the Ayden Rae Foundation website is provided to help families become educated about Hyperemesis Gravidarum, discover their options concerning HG, and gain the support necessary to survive HG.
The information found on the website is not intended to replace, change, and/or substitute the advice of one’s healthcare provider. The information is provided for educational purposes only. It is vital to remember that every patient presents with their own distinctive circumstances and each patient should be treated as a unique individual and advice should be given on a case by case basis. 

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