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.
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.
Hospitalized with a central line, TPN feeding tubes, and multiple medications at 4 weeks, the damage had begun. Four specialists said her liver would fail if she continued her pregnancy, she terminated her much wanted IVF pregnancy.
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’m pregnant with my second baby right now. My first pregnancy was a healthy, and I wasn’t expecting Hyperemesis Gravidarum (HG) at all!
The HER Foundation is thrilled to announce that Emmy-winning and Golden Globe-nominated standup comedian, actress, writer, producer, and director Amy Schumer will join the HER Foundation’s Board of Directors.
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.
