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Contact The HG Collective for support, guidance, and resources.
HG is common, serious, and still too often dismissed. We're working to change that — through better policy, better clinical standards, and better evidence.
Start the symptom guide→I'm looking for support — find clear information, resources, and real experiences from people living with HG.
Access clinical guidance, assessment tools, and CPD training to help you recognise and treat HG earlier.
Learn how we work with healthcare systems and policymakers to improve HG care standards nationally.
Our interactive HG Symptom Guide can help you get a sense of your situation. Answer a few simple questions about what you're experiencing.
Start the Symptom Guide→Takes about 2 minutes. Not medical advice, based on public domain HG guidelines.
Our approach follows RCOG guidelines so sufferers get care that's timely, appropriate, and consistent — wherever they're treated.
We shape our work around what sufferers actually go through, so care pathways reflect real needs, not assumptions.
We work to improve care and outcomes for everyone affected by HG — sufferers, families, and the healthcare professionals who treat them. That means:
There's a specific kind of sexism society still feels very comfortable with: the kind that disguises female suffering as exaggeration. Hyperemesis Gravidarum sits right in the middle of it.
Reading the Amos investigation into maternity services with one question in mind: what does it tell us about HG? The answer wasn't what I expected.
For women living with serious conditions like Hyperemesis Gravidarum, the Government's plans for a single national formulary could fundamentally change whether treatment is accessible — or not.
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