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.
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Trauma from Hyperemesis Gravidarum (HG) cannot be prevented. The HER team believes the following tips will give you the best chance of being prepared for HG in a subsequent pregnancy.…
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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…
Read MorePTSD after an HG pregnancy is treatable. You are not alone. Be patient with yourself. The Hyperemesis Education and Research (HER) Foundation is here to support you and offer resources.
Read MoreJune is PTSD Awareness Month! Up to 18% of HG survivors are diagnosed with full criteria PTSD while others suffer with symptoms and still more go undiagnosed. Here at the HER Foundation, our goal is that no mother suffers alone. We want to empower you and share our research and resources to help you advocate for your mental and physical health.
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