MED13L Syndrome: The impact on speech development
Speech challenges are one of the most significant hurdles for individuals with MED13L. Many experience severe motor impairments that make communication difficult. By focusing on speech development, we aim to raise awareness, share effective tools, and support families—so that every voice has the chance to be heard.
The Power of Yet
With the right support, persistence, and understanding, children with apraxia related to MED13L syndrome can make meaningful progress. Every sound, every sign, every attempt is a step forward. “Yet” reminds us that communication is a journey—and with the right tools and community behind them, that journey can lead to incredible breakthroughs.
Celebrate the “inchstones”
Knowledge is Power
Through partnerships with clinicians and researchers specializing in speech and language, the MED13L Foundation delivers expert knowledge shaped by real-world experience with MED13L patients.
MED13L-related disorder characterized by severe motor speech impairment
This publication helps parents, clinicians, and therapists better understand and support what is perhaps one of the biggest challenges individuals with MED13L face: Speech
Connecting with the Community
August 2025, The MED13L Foundation Research & Family Meetup in Waltham, Massachusetts, Marissa Mitchell, MS, CCC-SLP and Dr. Cora Taylor conducted research and connected with the MED13L community.
Early Intervention is Key to Development
When speech development is delayed, early intervention provides critical windows of opportunity. The younger the child, the more their brain is primed for learning new speech patterns, building neural connections, and adapting motor planning for communication. Early support can shift a child’s developmental path and open doors to greater ability and connection.
