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.
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The Ayden Rae Foundation
Provides an Online forum and support resources to families worldwide.
Beyond Morning Sickness
Author Ashli Foshee McCallâ€™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.
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.
Pregnancy Sickness Support
A UK charity supporting sufferers of nausea and vomiting in pregnancy and Hyperemesis Gravidarum.
Disseminating information about Hyperemesis gravidarum.
Established to disseminate information and support mothers with HG.
Ayden Rae Foundation Forum
Beyond Morning Sickness
Hyperemesis Gravidarum Social Network Support Groups
Ayden Rae Foundation HG Support Group
Hyperemesis Gravidarum (HG) UK
Surviving Hyperemesis Gravidarum
Steunpunt Hyperemesis Gravidarum
Ayden Rae Foundation
Hyperemesis Gravidarum Blogs
Knocked Up â€“ Knocked Over-
Heart Break Kids-
Love Makes A Family-
Live, Laugh, Love-
Hyperemesis Gravidarum: A Diary-
The Write Wing Mom-
Nausea, Vomiting and Hyperemesis Gravidarum in Pregnancy-
Strollers and Stilettos – One Mother’s Balancing Act-
The Real Supermum-
A Pregnancy With Hyperemesis Gravidarum
Diary of a First Child
No I Donâ€™t Want a Ginger Biscuit! â€“ My Hyperemesis Hell
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 oneâ€™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.