Supporting sufferers of
pregnancy sickness
WHAT SUPPORT DO YOU NEED?
Support our work
Hyperemesis Australia is a not-for-profit organisation that relies on public support in order to operate. Help us continue our important work.
You are not alone
Whether you’re currently suffering, a survivor, or have terminated a pregnancy due to HG we have a support group ready and waiting for you.
Got a question?
Read our FAQ guides on life with HG, preparing for a future pregnancy, supporting a loved one with HG and common medications.
SURVIVOR TESTIMONIALS
Lauren
HG is a very dark and lonely place, at a time when you should be feeling excited and positive. Without the ongoing support, advice and advocacy of Hyperemesis Australia, I’m not sure where I’d be. During my pregnancy when no care provider would listen and understand my unique, real needs, HG Australia was there offering support and resources to help me through this tough time. I’m forever grateful for discovering this much-needed space.
Alanna
Hyperemesis Australia offered me a huge amount of support throughout my HG pregnancy. HG can be a very lonely place and I don’t know what I would have done without the sharing of research, suggested treatment options, advice and the overall emotional support that was provided by HGA. Having someone to talk to who knew exactly what I was going through really helped get me through those dark days. I will be forever grateful for this.
Chanté
Hyperemesis Australia has been a wonderful support on the other side of my HG pregnancy. Unfortunately, it was only founded after my baby was born but has since been an ongoing support and place to share thoughts and feelings and always allowing my feeling to be heard. I have visited the website numerous times for information to pass on to friends and family.
Caitlin is an outstanding HG activist and I am truly grateful for this organisation.
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