Review evidence and fund addition of Fabry disease to the newborn screening test

Fabry is a rare genetic disease that can cause life-threatening heart, kidney, and nerve damage. It often goes undiagnosed until it’s too late. Early detection at birth can save lives and allow families to access treatment sooner. Some countries and regions already screen newborns for Fabry and we think that we should too. As someone with Fabry, I know how crucial early diagnosis is. This change could transform care for future generations.