Living with ARG1-D

This video shares the powerful personal stories of two families navigating life with Arginase 1 Deficiency.
Meet Willow, Leo and Thiago, all living with ARG1-D. Through their voices, and those of their parents, you’ll hear about the early signs of the condition, the challenges of getting a diagnosis, and the everyday realities of managing a rare, progressive metabolic disorder.

Their stories shed light on the early symptoms that were often misunderstood or misdiagnosed but most importantly the resilience and hope that comes with better understanding and support.