HYPEREMESIS EDUCATION & RESEARCH FOUNDATION
Hyperemesis Education & Research (HER) Foundation provides education & support for mothers suffering from hyperemesis gravidarum and those who care for them. The HER Foundation is the world's largest network of HG survivors and the leading resource for HG information. In 2003, HER became the global voice of hope and understanding for women with HG. Our mission is to find a cure through research, to provide education and support for those seeking effective management strategies, and to provide them with clinical resources. Goals: 1. Minimize suffering & complications. 2. Eradicate morbidity & mortality. 3. Improve outcomes. 4. Promote a universal protocol. 5. Raise public awareness & improve policies. 6. Educate practitioners & caregivers. 7. Expand clinician education & awareness. 8. Publish clinically relevant research. 9. Fundraise for research, awareness, and educational projects. 10. Develop tools to improve diagnosis & management.
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Want to know more about hyperemesis (HG)? Your voice for HG awareness support and research Our Mission Each year millions around the world experience trauma financial strain debility andor incredible misery due to severe nausea and vomiting of pregnancy Hyperemesis Gravidarum or HG. HER Foundation has empowered millions of people managing HG with information and support to minimize suffering longterm health complications and pregnancy loss. Next year marks 25 years of HELP and HOPE for families across the globe thanks to supporters like you. Help sustain our programs by making your 2024 donation TODAY.
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