Patient Impact

Our work transforms the diagnosis and care of people living with congenital hyperinsulinism worldwide, turning genetic discovery into clinical change.

For families, a genetic diagnosis can end years of uncertainty and guide life-changing clinical decisions.

Improving Equity: The Open Hyperinsulinism Genes Project

Through the Open Hyperinsulinism Genes project, a partnership between our The Exeter Centre for Hyperinsulinism Genetics and Congenital Hyperinsulinism International, we are removing financial barriers to genetic testing, ensuring that families worldwide can access accurate diagnosis regardless of location or income. So far, over 1137 children from 63 countries around the world have benefited from this project.

Learn more about the impact of this project

Family Testimonials

Thank you, we really appreciate your and the CHI Association’s kindness – Mum, Israel

Thank you for agreeing to our request, in my country there are very few possibilities of accessing more health services. – Mum, Peru