Miller is a 13 month old baby girl born with an ultra-rare ZMYND8 gene mutation which has caused refractory infantile spasms, developmental delays, and movement disorders.

Miller’s Miracle aims to develop and implement a treatment for Miller while advancing therapies for neurodevelopmental disorders caused by ultra-rare genetic mutations, particularly those associated with refractory epilepsy.

Our mission is to accelerate the development of life-changing treatments through scientific innovation, support affected families, and foster a collaborative community that empowers every child living with these challenging conditions to reach their fullest potential.