By Laura Michell
“We maybe don’t have a cure and the meds might be hit and miss, but it is possible for HG sufferers to receive empathy and care – and fluids!”
That desire to ensure women suffering from hyperemesis gravidarum (HG) are taken seriously and receive a standard level of care, regardless of where they live, their background or socio-economic status was one of the driving forces behind Caitlin Kay-Smith’s decision to found the charity Hyperemesis Australia.
Ms Kay-Smith suffered HG for the first time when she was pregnant with her daughter in late 2017-18.
HG is characterised by severe and persistent nausea and vomiting that impacts the daily life of sufferers. It often leads to substantial weight loss and dehydration, with sufferers unable to eat or drink properly.
Ms Kay-Smith…