Our Board of Directors

DLG4 SHINE Foundation was formed to represent and fight for the global DLG4 Synaptopathy community. The board has worked hard to organize medical resources and plan with researchers, develop patient registries, raise funding for research, and drive awareness of DLG4 SHINE among the medical community as well as in the general public.  Aside from DLG4 SHINE activities, our board members balance caring for their SHINE children and families, professional lives, and other responsibilities. Take a minute to learn about each of our dedicated members, and reach out or look for us on social media.