Research on HG's short- and long-term effects is desperately needed and needed now. We need to do more to find a cure for this disease that has such devastating effects on a growing number of soon-to-be mothers.

Congressman Xavier Becerra (CA)

HG forces women to make difficult decisions... the H.E.R. web site is the most comprehensice location to educatte oneself to make the best decisions.

Marlena S. Fejzo, PhD USA

HG is a devastating illness and yet so little research has been undertaken into causes and therapies.

Dr. Matthes Seeling, MD

HG is a termendously debilitating disease that can have life long consequences. This Web site will provide much needed support to mothers suffering from this disease.

TM Goodwin, MD USA

HG has a devastating personal and family impact and effective management is most important.

Ron Taylor, MD UK

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How to Help HER Foundation

Hyperemesis gravidarum (HG) has an incredible impact on the lives of those who experience it, as well as those around them. Many feel a desire to help others survive this very difficult time in life. If you want to help our organization and support our mission, there are several ways you can do that. You have taken the first step by educating yourself on HG so you can increase other's awareness and effectively support those you know with HG.

Other Ways You Can Help:

Refer others, including health professionals to our site for up-to-date, reliable HG information and research.
Print out our online brochures and/or survival guide for distribution to health professionals and hospitals in your area. New brochures are added periodically.
If you have any special skills that you could offer on a volunteer basis, please e-mail us at volunteer@hyperemesis.org.
Contact those you know and refer them to our site to help increase awareness and interest. See our Activism page for more.
Network with service-oriented companies. We are looking for businesses willing to offer discounts on their services for families facing HG to ease their financial burden.
Participate in our HG Surveys, current poll, and other available research studies. See our home page or Research Page for more links.
Support our efforts for publication, research and education. If you have contacts in these areas, or know of opportunities, please refer them to our site or have them contact us directly.
Contact your local media such as TV health reporters, pregnancy and parenting publications, and radio talk shows. Tell them about your experience with HG and refer them to our site for more infomation. See our Activism page for more.
Participate in our online discussion areas and offer support to others or share your story. See our Hyperemesis Discussion Area.
Volunteer to visit and/or offer support to another family in your area facing HG. If you are interested, see our Volunteer section.
Check our site quarterly for the updates and the latest information on HG. E-mail us at volunteer@hyperemesis.org if you would like to be contacted when we have special events or special site updates.

Updated on: Mar. 24, 2010