Our Mission:

The Ayden Rae Foundation is a worldwide awareness organization dedicated to advocacy for Hyperemesis Gravidarum (HG) sufferers as well as expanding outreach for education, research, and an eventual cure. 

Kate Middleton Diagnosed with HG
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Welcome to Our New Website!
We've been hard at work redesigning our website, and we're excited to finally unveil it.
We're proud of our new look, and we hope you'll like it, too. Our goal is to make it easier for you to find and use important information.

Some of the new features include:

  • Simplified design

  • Improved navigation

  • Sharing

Hyperemesis Gravidarum in the News
This is Hyperemesis Gravidarum Awareness at its BEST!!! We made the front page of the paper. Thank you Puddle Pirate Productions for all that you do for our cause and to help families worldwide know that they are not alone. Together we are making a difference one family at a time.  Read article
Pregnant & Starving Surviving HG
Many families have stated, "If only there were a documentary film following an HG family from the beginning of pregnancy to the end then the world would truly understand our suffering!"  The Ayden Rae Foundation and Puddle Pirates Productions heard your pleas and now we are doing our best to capture the true suffering of HG Survivors worldwide. This wouldn't be possible without the courageous families that are allowing film crews to invade their lives during a time when most just want to give up and we want to thank them. 

HG documentary 

Puddle Pirate Productions 


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