The Voices of MED13L

In this episode of Growing Up With MED13L, we go back to the very beginning with Belen Fernandez Crespo, mother to 18-year-old Nacho, joining us from Spain. Belen knew something was different when Nacho was still a baby, long before anyone would listen. He went undiagnosed for eleven years, and when the name MED13L finally arrived, it brought her something unexpected: relief. In this honest and moving conversation, she shares what those early years were really like, from a little boy who was "locked in his body" and could not point, nod, or shake his head, to the small, hard-won moments that changed everything. She talks about the therapies that helped and the ones that were nothing more than false hope, the optician who finally gave Nacho glasses and opened up the world to him, and the communication device he now uses to build sentences of his own. Nacho is loving and charming, quick to greet you with a hug and a kiss on the cheek. He adores his books, his toys, and climbing steep trails with the parents who go at his pace and never rush him. Belen is just as honest about the uncertainty of what comes next as Nacho ages out of school, and about the fear she carried on her own for far too long. Her advice to other families is simple and hard-earned: never give up, hold on to the small victories, and do not keep your pain to yourself. Wherever you are in your own MED13L story, we hope you feel a little less alone after spending this time with Belen and Nacho. Sign up for our newsletter, fill out the family census at med13l.org, and catch up on any surveys waiting for you. When you are rare, everyone counts, and every family's voice helps move research forward. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

In this special research update episode of Voices of MED13L , Rowan Dias opens with reflections from the World Orphan Drug Congress and the MED13L Foundation’s first year participating in the Million Dollar Bike Ride before introducing a recorded community update with Dr. Ricardo Ramirez, Chief Scientific Officer of The MED13L Foundation. Dr. Ramirez walks families through the Foundation’s current research priorities, including natural history studies, adult outcomes, community surveys, biomarkers, drug repurposing, gene therapy, and the path toward future observational studies. He also addresses questions from the MED13L community about speech development, treatment timing, variant types, long-term care, sleep, the gut-brain connection, and how families can participate in research. This episode offers an accessible overview of where MED13L research stands today, why community participation matters, and how the Foundation is working to move science forward with urgency, safety, and the voices of families at the center. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

An Honest Look at MED13L, Our Community, and the Foundation Behind It MED13L Awareness Month Special | May 2026 This Awareness Month, host Vanessa Dias gets honest — about the spectrum of MED13L, the families the foundation hasn't yet heard from, and what it actually looks like to run a rare disease foundation as a volunteer parent doing the work between therapy drop-offs and bedtime. She also pulls back the curtain on the foundation itself: a small group of volunteer parents, most of them mothers, all of them living a version of the same life you are — and what it would mean for the whole community to lean in just a little more. In this episode: Updates on the patient census, genetic report uploads, and the Million Dollar Bike Ride in Philadelphia on June 13th Why those "me too" threads on Facebook need to make their way to the registry The full spectrum of MED13L — medically, developmentally, and across families An honest look at who runs this foundation and how the work actually gets done The hiring of a Chief Scientific Officer and what that means for research Connect & Get Involved: Want to be featured on the podcast? Or host your own episode? Email vdias@med13l.org 🔬 Research opportunities: med13l.org/research-hub/join-med13l-research-opportunities 📄 Latest publications: med13l.org/research-hub/publications 📧 Reach the team: info@med13l.org 🚴 J oin the Million Dollar Bike Ride team: June 13th, Philadelphia Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Growing Up with MED13L: Life at 14 In this episode of Voices of MED13L , we continue our Growing Up with MED13L series with an honest look at the teenage years. Host Vanessa Dias is joined by Chelsea and Vern Klassen, who share what life looks like today for their 14-year-old daughter, Caitlynn. They offer a candid glimpse into Caitlynn’s world—from her communication journey with AAC and experiences in school to friendships, family dynamics, and increasing independence. Chelsea and Vern also speak openly about the realities of raising a teen with complex needs, including balancing support with autonomy, navigating puberty, and thinking ahead to the future—while celebrating the joy, personality, and strengths that define who Caitlynn is. For families earlier in their MED13L journey, this episode provides something invaluable: perspective on what the teenage years can look like, along with reassurance and hope for the road ahead. 💬 In this episode, we discuss: Communication challenges and breakthroughs with AAC School supports and learning in a modified curriculum Social development, friendships, and sibling relationships Independence in daily living and life skills Navigating puberty and healthcare decisions Long-term planning and redefining expectations 💛 A powerful conversation about growth, grief, resilience, and the beauty of meeting your child exactly where they are. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

In this episode of Voices of MED13L , we continue our series Growing Up with MED13L with a powerful, in-depth look at the teenage years. Host Vanessa Dias is joined by fellow MED13L parent Michelle Seaver , who shares what life looks like for her 16-year-old daughter today — from communication and learning to socialization, independence, and daily routines. Many families wonder what adolescence might hold for their child with MED13L. Michelle offers an honest and hopeful look at the realities of life at 16: How her daughter communicates and advocates for herself What school, friendships, and confidence look like Where she needs support — and where she shines How boarding school has helped her grow socially and academically What independence can look like for teens with MED13L Why progress is real, just on a different timeline This conversation is grounded, encouraging, and deeply relatable for any family thinking about the road ahead. Michelle also shares insights on therapies, life skills, reading development, and the importance of community — along with a glimpse into future possibilities through programs like Riverview and beyond. Growing Up with MED13L: Life at 16 is part of our ongoing series highlighting lived experiences across childhood and adolescence. For newly diagnosed families or anyone wondering what the future may look like, this episode offers reassurance, perspective, and real stories of growth. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Why the MIND Study Matters: Building Clinical Trial Readiness for MED13L In this powerful and informative episode of Voices of MED13L , Vanessa sits down with Abigail Sveden, MS, CGC , a genetic counselor at the Boston Children's Hospital and member of the Rosamund Stone Zander Translational Neuroscience Center (TNC) . Together, they unpack the critical importance of the MIND Study — MED13L Syndrome Investigation of Natural History and Development — and what it means for families today and for the future of therapeutics. 🧬 What You'll Learn in This Episode: What translational neuroscience really means — and how lab discoveries move toward real-world treatments Why natural history studies are essential for clinical trial readiness How longitudinal data helps researchers understand development over time The role of neurobehavioral assessments (including the Vineland) in FDA-approved outcome measures Why standardized data collection is critical for future therapeutics New clinical observations emerging from the MED13L cohort How participation today helps prevent future families from facing a “Google search diagnosis” Abigail shares how the TNC brings together experts in genetics, neurodevelopment, EEG, regulatory science, and basic research — all working toward one goal: improving outcomes for individuals with rare neurodevelopmental disorders like MED13L. Vanessa also speaks candidly about the parent experience — the emotional weight of surveys, the importance of being heard, and why documenting your child’s story is one of the most powerful contributions you can make to the community. 📊 MIND Study Snapshot 🎯 Goal enrollment: 30 participants ✅ 27 fully enrolled 📈 24 have completed Year One components 🔁 Annual follow-up is critical for longitudinal data 📍 In-person visits at Boston Children’s Hospital prioritized (virtual options available) Participation includes: Interview-style visits with the study team Neurobehavioral assessments Standardized questionnaires (including the Vineland) Medical record review Optional photo and biospecimen contribution This data builds the foundation for: Clinical trial readiness FDA-accepted outcome measures Published research to educate physicians worldwide Future therapeutic development 💛 Why It Matters Every story matters — especially in rare disease. Participation helps: Define what MED13L looks like across the lifespan Identify patterns in development, seizures, puberty, motor differences, and more Inform physicians so families are no longer handed a Google printout Build the roadmap toward future treatments Hope is built on data. Data is built by families. 🔬 Additional Research Opportunities If the MIND Study is full, there are other ways to participate: MED13L Census (homepage of med13l.org) Simons Searchlight Rare-X Citizen Health (5-minute registration that helps collect medical records) Links are available on the MED13L Foundation research page and below. 📩 Interested in the MIND Study? To learn more or inquire about participation, contact: Abigail Sveden, MS, CGC 📧 abigail.sveden@childrens.harvard.edu Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Growing Up with MED13L: Life at 11 (with Anna Fracalossi) Welcome back to The Voices of MED13L , the official podcast of the MED13L Foundation. I’m Inon Shampanier—dad to a child with MED13L and your host for today’s episode, as we continue our Growing Up with MED13L series, where families share what daily life looks like at different ages and stages. In this episode, we’re joined by MED13L parent Anna Fracalossi , mom to Elisa (11) . Anna shares their long diagnostic journey—first noticing developmental delays around six months, moving from Brazil to the United States, navigating years of therapies and specialist visits, and finally receiving an MED13L diagnosis through exome sequencing when Alisa was seven. Anna then brings us into Alisa’s life today at age 11: her routines, therapies, and the joys she’s found through movement and community—swimming, tennis, and Miracle League baseball. We also talk candidly about behavioral rigidity, emotional regulation, and how ABA has helped Alisa build tools to communicate feelings, shorten the intensity of tantrums, and navigate frustration. A highlight of the conversation is Alisa’s transition to middle school , where she participates in a more inclusive academic setting alongside typically developing peers—with thoughtful supports in place. Anna shares what that transition has looked like socially and academically, and why peer role models have mattered so much for Alisa’s growth and independence. This episode is also filled with hope: Anna reflects on Alisa’s steady progress in communication (from no words to full sentences), her love of the arts—music, ballet, opera, and visual art—and the new developmental milestones of preteen life: growing independence, shifting interests, and emerging self-advocacy. Above all, Anna offers a powerful message to families who are new to MED13L: be gentle with yourself , allow space for grief and change, and trust that over time you can rebuild expectations into something grounded in joy, connection Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Growing Up With MED13L: Life at Age 12 In this episode of The Voices of MED13L , we launch our new Growing Up With MED13L series with a powerful and honest conversation titled “Life at 12.” Host Vanessa is joined by fellow MED13L parent Katie Johnston , mom to Addie, a bright, confident 12-year-old living with MED13L syndrome. Katie shares Addie’s journey to diagnosis at age nine and reflects on what life looks like today—academically, socially, emotionally, and at home. From navigating special education services and IEP advocacy, to communication challenges, puberty, independence, friendships, and sibling dynamics, this episode offers a real-world look at the joys and complexities of raising a preteen with MED13L. Listeners will hear how receiving a diagnosis brought clarity, community, and renewed strength for advocacy, as well as practical insights on therapies, AAC use, school placement, routines, and fostering independence. Katie also speaks candidly about acceptance, hope, and what she envisions for Addie’s future. This episode is especially meaningful for families wondering what the MED13L journey can look like beyond early childhood—and a reminder that while every child’s path is different, none of us walk it alone. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Welcome to The Voices of MED13L, the official podcast of the MED13L Foundation. In this special trailer, host Vanessa Dias introduces Growing Up with MED13L — a new ongoing series that explores what life looks like for individuals with MED13L at every age and stage. Each episode features a family from our global community, sharing their lived experiences — from early diagnosis to daily routines, school transitions, therapy progress, and life as a teen or young adult. The series isn’t chronological, because our journeys are not the same. Whether you’re hearing from a family whose child is close in age to yours or several years ahead, these conversations offer connection, perspective, and hope. Together, we’ll highlight the incredible resilience, progress, and love that define growing up with MED13L — and remind every listener that they are not alone. 🎧 This is Growing Up with MED13L: Life at Every Age. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Mini Episode: 13 Minutes with MED13L Host: Katie Boychuck, Chair of the MED13L Foundation In this first-ever 13 Minutes with MED13L mini-episode, Foundation Chair Katie Boychuck walks families step-by-step through Citizen Health —a secure, easy-to-use platform the Foundation is recommending to help parents centralize their child’s medical information. Katie shares openly as both a leader and a MED13L parent, explaining why organizing records in one place can make care coordination, appointments, and day-to-day decision-making far more manageable. She also highlights the importance of the MED13L Census, touches on Rare-X enrollment progress, and shows exactly how simple it is to create a Citizen Health account using your child’s CRID. If you’ve been meaning to sign up but haven’t found the time, this episode offers a clear, supportive walkthrough you can follow in real life—right from your phone, your car, or wherever you are in the middle of your busy day. Together, we are not so rare. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

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 Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Episode Highlights 1️⃣ Seek Support from Specialists – Learn which specialists to see: cardiologist, neurologist, developmental pediatrician, orthopedist, speech, occupational & physical therapists, and feeding specialists. – Contact your local school district early for early intervention services. – Visit our Glossary for common medical and therapy terms: med13l.org/resources – Ensure all providers use the MED13L ICD-10 Code (Q87.85) to correctly document and track care. 2️⃣ Be Counted in the 2025 MED13L Census Visit med13l.org and click Register to be counted. Every registration helps researchers and clinicians see the true scope of MED13L and adds your family to the global map. 3️⃣ Stay Informed — Sign Up for the Newsletter Join the mailing list for updates, research news, and family stories. Catch up on past issues in our Newsletter Archive. 4️⃣ Learn the Basics — Start with the FAQ Page Get trusted answers to the most common questions: New to MED13L? Visit our FAQ. 5️⃣ Join the MED13L Registries — Turn Stories Into Science – Apply for your Clinical Research ID (CRID): thecrid.org – Enroll with RARE-X (caregiver surveys): rare-x.org/med13l – Upload records securely via Citizen: citizen.health/partners/med13l-foundation 6️⃣ Connect With the Community Join our social spaces for connection and support: – Register with the Foundation – Facebook Family Group – Instagram @med13lfoundation – Slack Group Signup 🌐 Visit: www.MED13L.org 📬 Contact: info@med13l.org 💙 Together, we’re turning stories into science — and science into treatments. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Episode 1: Welcome & Where We’re Headed Hosted by Vanessa Dias & Katie Boychuck In this trailer episode, we introduce the hosts and The MED13L Foundation—how it started, what drives us, and why this podcast exists. Whether you're navigating a new diagnosis, supporting a loved one, or working in research or medicine, this episode offers a personal and accessible introduction to MED13L Syndrome and the global community coming together around it. We share the story of how the Foundation began, our mission and values, and what success looks like as we push toward earlier diagnoses, stronger family support, and meaningful progress in research. What you’ll hear in this episode: – Meet your hosts – How the MED13L Foundation came to be – Our mission, values, and goals – How we’re building connection, support, and hope – What to expect from future episodes Resources Register with the Foundation’s Census: HERE Access the Community Checklist: HERE Citizen Health: https://www.citizen.health/partners/med13l-foundation Rare-X: https://rare-x.org/med13l/ Website: www.med13l.org Facebook: https://www.facebook.com/med13lfoundation/ Instagram: https://www.instagram.com/med13lfoundation/# Next up: Updates and the Foundation’s most pressing needs. Submit topics you'd like to hear covered HERE 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. Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...

Officially Launching in October 2025! Welcome to The Voices of MED13L The Voices of MED13L Podcast is brought to you by The MED13L Foundation and co-hosted by Katie Boychuck , Chair, and Vanessa Dias , Vice Chair. Both are parents of children with MED13L, and their personal journeys have set them on a path to push for research, create change for a better future, foster connection within the community, and continue the search for treatments and ultimately a cure. In this podcast, you’ll hear: Updates on the latest research and therapeutic discovery Stories from families living with MED13L around the world Insights from clinicians and researchers working to unlock new possibilities Together, Katie and Vanessa bring the voices of science, family, and community into one space — helping fuel hope for tomorrow while strengthening the bonds of today. ✨ Subscribe today and join us for The Voices of MED13L — where connection, discovery, and hope meet. This trailer episode is hosted by Rowan Dias , a student at Deerfield Academy in the Class of 2027 and sibling of a child with MED13L Syndrome, who, with the help of a generous grant from Deerfield Academy's Center for Service and Global Citizenship , helped set up the podcast during a summer internship to expand the Foundation’s reach to families, researchers, and supporters. Visit our website at www.med13l.org & follow us on social media @med13lfoundation Support the show Resources MED13L Awareness Campaign: https://secure.qgiv.com/event/med13lfoundationp2p/ Profile Frame for Socials: https://twb.nz/med13lfoundation Be Counted in the 2025 Census: https://med13l.org/patient-registry-genetic-report-stubmission/ Million Dollar Bike Ride: https://charity.pledgeit.org/MillionDollarBikeRide/teams/@med13l Community Checklist: Google Drive Link CRID: thecrid.org Citizen Health: citizen.health/partners/med13l-foundation Simons Searchlight: https://research.simonssearchlight.org/account/create Rare-X: rare-x.org/med13l Website: med13l.org Facebook: facebook.com/med13lfoundation Instagram: instagram.com/med...