​The MYT1L Project is a parent-led, scientist-supported foundation established in 2025 to advance research into evidence-based interventions for MYT1L Neurodevelopmental Syndrome, a rare genetic condition marked by developmental disabilities, behavioral challenges, and obesity. Our mission is to foster collaboration between families, patients, and researchers to develop effective treatments that improve the quality of life for individuals and their families.

 

In addition to promoting and funding critical research, we support families through regular virtual meetups, active social media forums, and an annual in-person scientific and family conference that shares the latest research and discoveries. Together, we aim to provide guidance, build community, and drive innovation to create a better future for those affected by MYT1L Neurodevelopmental Syndrome.