Raise Your Voice for HER!
It is hard enough to have a successful pregnancy under normal conditions. Now our hospitals are jammed, chaotic, and operating in a different mode. Yet, there is always hope for moms with HG, and that is why we ask for your support as we work to bring focused education and resources to those women who need it during a highly stressful time. We are here for women regardless of what is going on around the world.
During this uncertain time funding has been very minimal yet our work continues unabated. COVID-19 might push us around a bit, but it won’t keep us DOWN. We can continue our mission with your help. We will Raise Your Voice!
Please help us launch our new mobile-friendly site, continue advocacy and support, and many other educational and research projects. This means more moms will get better care in 2020 and beyond!
Our mission is to find a cure for hyperemesis and its complications through advanced research, offer education and support to those seeking effective management strategies for hyperemesis, and provide information on new resources and treatment options as they become available.
HG Mom Stories
There exists in California, and other parts of the world regularly inundated by wildfire, a variety of plants called fire followers. The growth and bloom of these species are triggered by different aspects of fire. Some bloom due to the choking smoke. Others, the unbearable heat, but all require the devastation of all consuming flame…Read More
My daughter turned four years old on April 15, which means it has been four years since I have had hyperemesis. When I look around and take in the global health crisis that surrounds us, I find myself having a lot of thoughts, and a lot to say, to the point of wanting to yell…Read More
Most people celebrate finding out they are pregnant but I was terrified. I so badly wanted another baby, but I didn’t want to go through hyperemesis gravidarum (HG) again. I woke feeling strange that Friday. I had a Mother’s Day morning tea for my son’s preschool, but I felt nauseous and off. I suspected I could be…Read More
The HER Foundation began after my first pregnancy. I started having increasing nausea and vomiting a few weeks after our honeymoon that I thought was due to a stomach ulcer or the flu. I was absolutely shocked when the doctors said I was pregnant. While I was not ready to be pregnant because I had…Read More
It was January 1999, and I was 13 weeks pregnant sitting in the Emergency Room hooked to an IV. Since violently vomiting Thanksgiving dinner, I had barely kept anything down. The ER doctors looked at my blood work, and I have never seen a team move so fast. This was my introduction to medical professionals that understood how…Read More
They say when you see those two little lines on your home pregnancy test, your life is forever changed. As I wrestled my 9 month old into his pj’s I can say this is very true. However, sometimes life changes in ways we couldn’t imagine. When you see those two lines you start picturing the future filled…Read More
I had a niggle*. A niggle that remained after all plausible causes for my bouts of sickness and fatigue were eliminated and two whizzy sticks later the niggle was confirmed. There was a bundle of joy! I was brought to my knees – in the bathroom. Repeatedly! “Morning sickness is part of the pregnancy!” “It won’t last.…Read More
“Making the journey across country to meet my fellow HG survivors was something I had to do. Hearing similar survival stories from other HG moms and their supportive HG dads was healing for my soul. Someone FINALLY understood the suffering I endured to have my children. It was quite an emotional day for both my…Read More
The HER Foundation and Ashli Foshee McCall are like old friends — they go way back and have been working together to help HG women around the globe. For many years, Ashli has donated her books to the HER Foundation to help us raise money for awareness, education and research. Ashli has just released a…Read More