We invite our community to take Provider Packets of resources to a hospital, clinic, or practice with your personal story and passion will make a difference.
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The Hyperemesis Education and Research Foundation’s mission is to provide Hyperemesis Gravidarum (HG) support, advocacy, education, and research to improve treatment and outcomes.
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Just like with any trauma, the severity of impact depends on how the individual person experiences HG and any prior history of trauma. This is why preventative care, such as accurate education and support, can make the difference between a woman (or caregiver) resolving and integrating their traumatic experience or developing PTSD (or Complex PTSD)…
Read MoreWe invite our community to take Provider Packets of resources to a hospital, clinic, or practice with your personal story and passion will make a difference.
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This year there is HOPE. Don’t you feel it…the feeling of CHANGE. We have suffered through so many uncertainties and challenges in 2020, and now we can look forward to the end of the year and to a new beginning. Here at HER Foundation, we are ready for a very BIG day in the nonprofit world:…
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Lace Up and #Move4MOMs! All proceeds of our virtual Walk, Run, or Roll go to our new LED Crisis Fund.
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I have two toddlers, ages 2 and 3 1/2. During both HG pregnancies, I was diagnosed with Hyperemesis Gravidarum (HG), which is a pregnancy illness that includes severe nausea, vomiting, weight loss, and electrolyte disturbance. My pregnancy experience with HG caused a lot of mental anguish and resulted in my decision to tie my tubes…
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Hyperemesis gravidarum (HG) affects over a million women across the globe every year meaning at least 2% of pregnant women suffer from the debilitating condition. These statistics are drawn mostly from cases of HG which are diagnosed, treated, or reported – mostly from westernized countries by those with health care. Consistent tracking criteria for HG…
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