Founded in 2024 as a 501(c)(3), The Isaacson Family Foundation raises awareness and makes strategic charitable investments in support of medical institutions whom are working tirelessly towards treating and curing Glut1 Deficiency Syndrome. Their youngest of four children, Hannah, suffers from this genetic disorder. Glut1 DS is a brain energy failure syndrome caused by impaired glucose transport across brain tissue barriers, causing symptoms such as eye‐head movement abnormalities, seizures, neurodevelopmental impairment, deceleration of head growth, and movement disorders. Currently, there is no cure. Raising awareness and raising funds go hand in hand when it comes to providing a better quality of life for those patients and families who are suffering. Together, we will aim to make Glut1 DS a disease of the past.