Our Story
On January 10, 2008, the diagnosis of Rett Syndrome for Ella Foard changed everything. The heartache was profound, yet it ignited a fierce determination to advocate for Ella and others facing similar challenges. The Ella Foard Foundation for Rett Syndrome was born from a commitment to make a difference in the lives of families enduring this rare condition. With a focus on hope and resilience, the foundation strives to raise awareness and funds for critical research.