1 in 3 HG pregnancies ends in loss. Whether your loss is due to miscarriage, termination, stillbirth, or neonatal, HER is here for you. Pregnancy and Infant Loss Remembrance Day honors the babies we hold in our hearts.
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.
Hyperemesis Gravidarum (HG) as a disease manifests itself in different levels of severity and is not the same for every woman. Understanding the range of different experiences helps with understanding what HG is. Regardless of whether HG is mild, moderate, or severe, the mother is miserable and misses out on the joy of a healthy pregnancy.
HER’s Dr. Fejzo presented at India’s AICC RCOG North Zone Annual Conference 2022. The virtual conference had 1200+ registrations and Dr. Fejzo’s session was viewed by over 400 delegates. The presentation…
What is the best treatment for hyperemesis gravidarum? How do you treat hyperemesis at home What is the first line treatment for hyperemesis gravidarum? What are the drugs of choice for hyperemesis gravidarum?
HER Resource Packet Order a packet with a comprehensive selection of HER Foundation resources for patients and clinicians including information on assessment tools, treatment algorithms and protocols, the HG Care…
What is the best treatment for hyperemesis gravidarum? What is the cause of hyperemesis gravidarum? What is hyperemesis gravidarum and how is it treated? Is hyperemesis a high risk pregnancy? How do you relieve hyperemesis gravidarum?
Each year, the World Alliance for Breastfeeding Action promotes World Breast Feeding Week from August 1-7. The 2022 theme is Step up for Breastfeeding: Educate and Support. While there are benefits for breastfeeding, not all HG survivors are able to breastfeed.
The third Thursday of every month from 12-1 PM/Central, the HER Foundation hosts an Online HG Support Group facilitated by licensed professional who are also HG survivors as a service to people with a current or prior diagnosis of hyperemesis gravidarum (HG). These groups are facilitated by volunteers Sarah Coffman and Elizabeth Lowder, HER Foundation Advisory Council members and HG survivors.
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.
