Thanks for supporting this wonderful cause!

Alia is a joyful, curious 9-year-old who lights up every room she enters. In 2024, Alia was diagnosed with the FOXP1 syndrome—a rare genetic condition that impacts speech, learning, and development. Like many children with rare disorders, her path is full of challenges, but also strength, resilience, and so much love.

With fewer than 600 cases known worldwide, FOXP1 research remains drastically underfunded—and yet holds the key to unlocking clinical trials, communication tools, and support systems that could change lives.

Our goal is to raise $10,000 for critical FOXP1 research—to fuel science that offers real hope to Alia and other neurodiverse children navigating rare genetic conditions.

Every contribution helps us take a step closer to answers, research, and a brighter, more inclusive future.

Walk with us. Support the science. Stand with Alia