The Voices of MED13L
"The Voices of MED13L" is a podcast dedicated to raising awareness, sharing stories, and building community around MED13L syndrome—a rare genetic disorder that affects development and communication. Each episode highlights the voices of families, experts, and advocates working to understand and navigate life with MED13L. From personal journeys and medical insights to educational tools and research updates, the podcast offers hope, support, and connection for anyone impacted by this rare condition. Whether you're a parent, professional, or simply curious, "The Voices of MED13L" is a space to listen, learn, and stand together in the face of the unknown.
Visit us at www.med13l.org
Follow us on Instagram & Facebook: @med13lfoundation
X: @med13l_fdn
The Voices of MED13L
Introducing Phil Buta & The Importance of Surveys
Episode 2: Introducing Phil Buta & Why Surveys Matter
In this episode, we welcome Phil Buta, the newest leadership voice at The MED13L Foundation. With nearly 20 years in nonprofit work, Phil shares what inspired him to join our community and how he hopes to support fundraising, research, and long-term strategy.
We also break down one of the most important topics for every MED13L family: why surveys and data collection are essential for advancing research. Katie, Inon, and Vanessa explain how caregiver surveys, medical record uploads, and CRI numbers directly shape what scientists can study and how clinicians understand our children.
Topics include:
• Phil’s background and what brought him to the Foundation
• The role of Citizen, RareX, and the CRI in research
• How caregiver-reported data becomes the backbone of scientific progress
• New Citizen incentives and the AI Advocates tool
• Why the ORTA Toileting Study may become a key biomarker
• How publications influence clinical care—and why our community’s data is needed
This episode offers a clear, practical guide to the steps that help move MED13L research forward. Every family’s participation matters, and every story strengthens the path toward future treatments.
Questions or need guidance?
📧 info@med13l.org
Resources
Be Counted in the 2025 Census: med13l.org/research-hub/join-med13l-research-opportunities/med13l-registry-enrollment
Community Checklist: Google Drive Link
CRID: thecrid.org
Citizen Health: citizen.health/partners/med13l-foundation
Rare-X: rare-x.org/med13l
Website: med13l.org
Facebook: facebook.com/med13lfoundation
Instagram: instagram.com/med13lfoundation
YouTube: youtube.com/@med13lfoundation/videos
Glossary: med13l.org/knowledge-base/glossary
Music Credit:
Intro and outro music for the Voices of MED13L Foundation podcast was composed and performed by Sophie Seaver, sibling of an individual with MED13L syndrome. We thank Sophie for sharing her talent with our community.
Kathleen Boychuck, Chair of The MED13L Foundation
Co-host
Vanessa Dias, Vice Chair of The MED13L Foundation
Co-host
Inon Shampanier, Board Member of The MED13L Foundation
Guest
Phil Buta, Executive Director of The MED13L Foundation
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