Lisa Kelley is a passionate advocate for the Fragile X community whose connection to Fragile X spans three generations. Her 33-year-old son has full-mutation Fragile X syndrome, her father recently passed away from FXTAS, and she and her sisters are carriers affected by FXPOI. The impact of FX has profoundly shaped her life and inspired her commitment to health, nutrition, and wellness. Through her work in healthy food, education, and community building, Lisa strives to help individuals and families live healthier, more connected lives while creating opportunities for inclusion, resilience, and hope.