Support HER’s life-saving mission and buy a shirt today! There are six different styles in six different colors! All proceeds support our education, research, and policy efforts.
We’ve reached a huge milestone! The HER Foundation has been Helping Generations for 22 years! Since 2000, we’ve helped over 2.2 million people in 95% of countries through our support, research, resources, and advocacy.
Whether the loss is miscarriage, termination, stillbirth, or neonatal, we remember. Pregnancy and Infant Loss Remembrance Day honors the babies we hold in our hearts. We invite you to add…
Whether the loss is miscarriage, termination, stillbirth, or neonatal, we remember the babies we hold in our hearts. Pregnancy and Infant Loss Awareness Month honors our lost little ones. We…
The HER Foundation has partnered with ASPEN, the American Society for Parenteral and Enteral Nutrition, for ASPEN Malnutrition Awareness Week TM (MAW) on September 19-23, 2022. For more information and…
I was never diagnosed with HG because of the lack of education and knowledge regarding the illness. As a result, I experienced prenatal and postnatal depression and delivered prematurely.
The HER Foundation is helping a second generation facing Hyperemesis Gravidarum (HG). If your mother have hyperemesis gravidarum (HG) when pregnant with you or siblings, we want to talk.
My name is Sally. I have three children: Rachel (born 1988), Timothy (born 1991), and Emilia (born 1997). I suffered from HG with all three pregnancies, before the HER Foundation began.
Thankful! Thankful is what I am. My babies and I survived Hyperemesis Gravidarum only because of the amazing support we received from the HER Foundation.
I felt depressed a lot because I was dealing with my sickness by myself, but I was able to find an online support system through the HER Foundation and meet other women experiencing the same difficulties. I did not feel alone.
