Savannah’s spirit will forever live on in the hearts of all who had the honor of knowing and loving her!
The LGS Foundation and our entire community are deeply saddened by the news of the passing of Savannah, the beloved daughter of our Executive Director, Tracy Dixon-Salazar. Savannah’s spirit will forever live on in the hearts of all who had the honor of knowing and loving her. She brought immense joy to everyone around her, and her memory will continue to inspire the work we do every day.
This is an incredibly difficult time for Tracy, Ruben, and their entire family. Our hearts are with them as they navigate this unimaginable loss. We kindly ask that you keep Tracy and her family in your thoughts, offering them love, comfort, and strength as they face this heartbreaking moment. We are grateful for your kindness and compassion!
Savannah Raine Salazar Memorial Research Fund
Established in loving memory of Savannah Raine Salazar, this fund honors the lives of all those lost too soon to Lennox-Gastaut Syndrome (LGS). Inspired by Savannah’s enduring light, the Salazar family has dedicated their lives to advancing research and hope for the LGS community. From Dr. Tracy Dixon-Salazar’s journey into scientific research to the family’s ongoing commitment, this fund fuels the fight for better treatments and, one day, cures. Savannah’s legacy lives on in every step we take toward a brighter future for those living with LGS.
Updated 04/03/25 (AM)