Accessibility doesn't have to come with a complicated price tag or a steep learning curve. Sometimes the most powerful tools are the simplest ones. In this episode, Dawn Campbell, Chief Operating Officer of the TouchPad Pro Foundation, shares the story behind the BrailleDoodle — a tactile learning device that helps blind and low vision children and adults explore braille and independent learning through touch. And here's a bonus: it doesn't require batteries or an internet connection.  Dawn shares how the BrailleDoodle came to life out of a teacher's determination to reach his students during the pandemic, and what happens emotionally when someone picks up a device that lets them create something entirely on their own.  This is for parents who have wondered when to introduce tactile learning, educators looking for tools that actually work in a classroom, and families who want to give their child a foundation for independence. To learn more about BrailleDoodle, explore their resources, or get one into your child's hands, visit brailledoodle.org.  Want to be a guest on the podcast? If you or someone you know has a story to share — whether you've experienced a pediatric retinal condition yourself or are raising a child who has — we'd love to hear from you. Reach out to us at [email protected]. You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast

Most people know that research takes time. Few people understand what that actually means — the decades of experiments, the failed hypotheses, the teams of students, and the quiet persistence that eventually moves something from a lab to a clinical trial. In this episode, Dr. Kenneth Mitton, Director of the Pediatric Retinal Research Laboratory, and Nicole Giudici, MS, PA-C and member of the PRRF Board of Directors, pull back the curtain on what research really looks like. Dr. Mitton traces the decades-long journey from the discovery of the protein at the center of Norrie disease and FEVR to where Retinova Therapeutics stands today, on the cusp of an FDA clinical trial application. Along the way, he explains what it means to train the next generation of scientists and physicians in a lab made possible by PRRF donors and the families who trusted the process. This episode is for anyone who has ever wondered where their donation goes, how long research really takes, or what it means to be part of a community that is genuinely moving the needle. Want to be a guest on the podcast? If you or someone you know has a story to share — whether you've experienced a pediatric retinal condition yourself or are raising a child who has — we'd love to hear from you. Reach out to us at [email protected]. You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast

Breyanna Soper was diagnosed with FEVR at nine years old. By her early twenties, she had lost the majority of her functional vision. What she didn't lose was her determination or, eventually, the partner who would walk every step of that journey with her. In this special Father's Day episode, Breyanna and her husband Matthew join us for an honest conversation about what life, love, and parenthood really look like when one partner has significant vision loss. They share how they met, what it took for Matthew to truly understand what living with low vision meant, how they navigated the decision to start a family knowing their son Leland could carry the FEVR gene, and what the early months of parenthood have looked like for a family that has never been afraid to figure things out as they go. This episode is for every parent, partner, and caregiver who has ever wondered if vision loss changes what's possible. Breyanna's answer is simple: there's always a way. Want to be a guest on the podcast? If you or someone you know has a story to share — whether you've experienced a pediatric retinal condition yourself or are raising a child who has — we'd love to hear from you. Reach out to us at [email protected]. You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast 

Matthew Shifrin was 13 years old when a family friend typed out the first ever set of accessible Lego instructions for him on a braille typewriter. That experience changed everything. A decade later, Matthew founded Bricks for the Blind, a nonprofit that has adapted over 550 Lego sets and now reaches blind and visually impaired builders in more than 120 countries, all for free. In this episode, Matthew shares the story behind Bricks for the Blind and what it really means for a blind child to be able to build a Lego set independently — the confidence, the joy, the learning, and the sense of belonging that comes with it. He walks through how the process works, why sorting pieces is more important than most people realize, and what he has learned from the builders who write to him from all over the world. He also speaks candidly about what companies and organizations consistently get wrong when designing for blind and visually impaired people, and what it would take to do better. To explore free accessible Lego instructions, donate, or get involved as a writer or tester, visit BricksForTheBlind.org or email [email protected]. You can also find Bricks for the Blind on Instagram, Facebook, YouTube, and LinkedIn at @bricks4theblind. Want to be a guest on the podcast? If you or someone you know has a story to share — whether you've experienced a pediatric retinal condition yourself or are raising a child who has — we'd love to hear from you. Reach out to us at [email protected]. You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast

When Mike Mulligan went to get contacts before a high school basketball game, he had no idea that appointment would change the entire trajectory of his life. He was diagnosed with Coats' disease at 18. Mike then built something he never expected: a career dedicated to helping others navigate vision loss with confidence, independence, and possibility. In this episode, Mike shares his journey from diagnosis to becoming both a Certified Orientation and Mobility Specialist and a Certified Vision Rehabilitation Therapist, and the work he does today through Blind On the Move. He breaks down why Braille still matters in a world full of audio technology, how assistive tech is opening doors that didn't exist a decade ago, and what families can do right now to help their child build independence — even when it feels easier to just step in and do it for them. To learn more about Mike's work and find resources for the blind and low vision community, visit BlindOnTheMove.com or reach out to Mike directly at [email protected]. Want to be a guest on the podcast? If you or someone you know has a story to share — whether you've experienced a pediatric retinal condition yourself or are raising a child who has — we'd love to hear from you. Reach out to us at [email protected]. You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast

When Amber Bobnar's son Ivan was diagnosed with Leber's Congenital Amaurosis at just a few months old, she found herself searching for answers, resources, and most of all, connection. What she found instead was a private email listserv full of invaluable information that no one outside of it could access. So she decided to change that. In this episode, Amber shares the story behind WonderBaby.org — the resource she built that has grown into a meaningful home for parents of children with visual impairments and multiple disabilities. She opens up about the early days of Ivan's diagnosis, the unexpected challenges of advocating for a medically complex child in a place with limited resources, and the hard-won lesson she wishes she had learned sooner: that love and connection matter more than any resource she could gather. To explore WonderBaby's library of resources, articles, and community for families raising children with visual impairments, visit the website: WonderBaby.org Follow WonderBaby on Facebook: https://www.facebook.com/wonderbaby.org/  You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast

Dr. Antonio Capone has spent his career changing what is possible for children with retinal diseases. In this episode, he shares the journey from his early start in psychiatry to finding his calling in pediatric retina, where precision surgery meets long-term impact.  You'll hear how the field evolved over decades, why severe ROP cases declined, and how training specialists around the world helped bring sight-saving care closer to home for families. Dr. Capone also explains how PRRF expanded beyond research to support parents raising children with rare retinal disease, and why the greatest challenge today is not always medical, but helping young adults move from education to independent, employed lives.  Read Jeanne McClellan's blog post with Dr. Capone on our website: https://prrf.org/a-conversation-with-dr-tony-capone/  Join us April 17-19, 2026 for a powerful weekend that educates, inspires, and unites. Saturday's Family Connection Conference brings education and resources to families affected by pediatric retinal diseases, while Sunday's Hope for Vision Walk brings together our community to fund critical research and programs. Participate in one or both events, either virtually or in person at Oakland University in Rochester, MI: https://prrf.org/upcoming-events/united-in-hope/ You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast 

What does it actually take to get a toddler to wear an eye patch every day for five years? According to Cathy Thompson, founder of Patch Pals, it takes routine, distraction, flexibility, celebration — and a patch that a child actually wants to wear. In this episode, Cathy and her daughter Mackenzie share the story behind Patch Pals: how a cataract diagnosis led to a daily patching battle, how Cathy's homemade solution changed everything, and how that idea grew into a business that has quietly reshaped how families and doctors approach amblyopia treatment. Now in her thirties, Mackenzie reflects on her patching years and offers a message directly to the kids and parents who are in the thick of it today. Whether you're just starting the patching journey or struggling to stay consistent, this episode is the encouragement and practical guidance you deserve to hear. To explore the Patch Pals collection of patches, resources, activity ideas, and their community of happy patchers, visit PatchPals.com.  Join us April 17-19, 2026 for a powerful weekend that educates, inspires, and unites. Saturday's Family Connection Conference brings education and resources to families affected by pediatric retinal diseases, while Sunday's Hope for Vision Walk brings together our community to fund critical research and programs. Participate in one or both events, either virtually or in person at Oakland University in Rochester, MI: https://prrf.org/upcoming-events/united-in-hope/ You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast

Jule Ann Lieberman's path into assistive technology grew out of curiosity, persistence, and a desire to stay independent. What began as an interest in learning more about technology evolved into graduate study, professional certification, and a career dedicated to helping blind and low vision individuals access the tools that support school, work, and daily life. In this episode, Jule Ann shares her journey as both a low vision professional and someone living with vision loss. She reflects on teaching future specialists, supporting clients of all ages, navigating public transportation with a guide dog, and evaluating emerging tools like smart glasses and AI. This conversation centers on adjustment, advocacy, and the practical ways technology can strengthen confidence and independence. Learn more about TechOWL here: https://techowlpa.org/ Join us April 17-19, 2026 for a powerful weekend that educates, inspires, and unites. Saturday's Family Connection Conference brings education and resources to families affected by pediatric retinal diseases, while Sunday's Hope for Vision Walk brings together our community to fund critical research and programs. Participate in one or both events, either virtually or in person at Oakland University in Rochester, MI: https://prrf.org/upcoming-events/united-in-hope/ You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast   

As the founder of the Children's Low Vision Resource Center, Paula Korelitz spent decades turning advocacy into action for children with visual impairments and their families. In this conversation, she walks through the early days of meeting families in the NICU, building resources that did not exist, and connecting education, research, and real-life learning in meaningful ways. Paula shares why active learning changed her practice, how the Resource Center introduced families to tools, teaching strategies, and community support, and what she believes parents, educators, and young adults need to hear today. This episode highlights the power of early advocacy, thoughtful education, and one voice willing to build what systems had not yet created. Join PRRF April 17-19, 2026 for a powerful weekend that educates, inspires, and unites. Saturday's Family Connection Conference brings education and resources to families affected by pediatric retinal diseases, while Sunday's Hope for Vision Walk brings together our community to fund critical research and programs. Participate in one or both events, either virtually or in person at Oakland University in Rochester, MI: https://prrf.org/upcoming-events/united-in-hope/ You can find more episodes and ways to get involved with the Pediatric Retinal Research Foundation here: https://linktr.ee/throughoureyespodcast