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Rare Awareness Radio

Rare Awareness Radio

By: Rare Awareness Radio
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About this listen

 Shedding light on underrepresented diseases and the efforts of non-profit foundations working tirelessly to support those affected.All rights reserved Economics
Episodes
  • EP 19 Nicole Legro

    EP 19 Nicole Legro
    Jun 28 2025
    A Voice for the Undiagnosed: Dr. Nikki Legro on FAM177A1, Genetic Advocacy, and Reimagining Maternal-Fetal Medicine - In this powerful episode of Rare Awareness Radio, we sit down with Dr. Nicole “Nikki” Legro—a physician, researcher, and rising leader in the rare disease space. Currently a third-year OB/GYN resident at Georgetown University, Nikki reflects on the long and winding path that led to her groundbreaking work helping to define the FAM177A1-related disorder through the NIH’s Undiagnosed Diseases Network and Stanford University. She shares her early inspirations, the challenges and triumphs of co-authoring a multi-year publication in Genetics in Medicine, and what it means to advocate for families navigating life with an undiagnosed or rare genetic condition. Nikki also discusses the future of maternal-fetal medicine, the growing role of AI in genetic diagnostics, and the deep human connections that drive her work forward. This episode is a must-listen for anyone passionate about the intersection of research, advocacy, and patient-centered care in the world of rare disease. Topics Include: The origin story of Nikki’s interest in rare genetic conditions Her work with the Hawkins family and the FAM177A1 research fund Challenges in publishing rare disease findings Evolving approaches to prenatal genetic screening The future of OB/GYN and gene therapy Building trust and trauma-informed care with patients and families 📣 Subscribe and share to support awareness, research, and advocacy for the rare disease community. #RareDiseaseAwareness #GeneticAdvocacy #WomenInMedicine #MaternalFetalMedicine #FAM177A1
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    37 mins
  • EP 18 Clement Chow

    EP 18 Clement Chow
    Jun 3 2025
    In this episode of Rare Awareness Radio, host Richard Juknavorian speaks with Dr. Clement Chow, Associate Professor of Human Genetics at the University of Utah School of Medicine. Dr. Chow and his team are doing groundbreaking work in rare disease research using an unexpected but powerful model: the fruit fly. We dive into Clement’s recent drug repurposing screen focused on FAM177A1 deficiency, a rare neurodevelopmental disorder. Hear how his team screened over 1,500 FDA-approved drugs using a fly model exhibiting a lethal phenotype—an innovative, cost-effective approach that could fast-track treatments for rare disease communities. Clement shares how his lab collaborates closely with patient foundations like the FAM177A1 Research Fund, how symptom management can be a gateway to deeper understanding, and what the future holds for applying discoveries across genetically linked rare diseases. Whether you're a scientist, advocate, or rare disease family member, this episode offers hope, insight, and a look at the power of creative research partnerships. 🎧 Listen now and learn how a tiny fly could make a world of difference. Special thanks to Jill Hawkins and the FAM177A1 Research Fund for making this episode possible. Link to Jill's episode: https://on.soundcloud.com/Xj9lYExwMcDxLJRj9f #RareDisease #FAM177A1 #ClementChow #DrugRepurposing #FruitFlyResearch #TranslationalScience #RareAwarenessRadio
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    28 mins
  • EP 17 Saquib Lakhani

    EP 17 Saquib Lakhani
    May 24 2025
    🔬 “From ICU to Genome: Dr. Saquib Lakhani on CRELD1, Early Detection & Rare Disease Advocacy” | Rare Awareness Radio 🎧 In this powerful episode of Rare Awareness Radio, we sit down with Dr. Saquib Lakhani, Director of the Early Detection Program at Cedars-Sinai Guerin Children’s and a leading pediatric critical care physician. Dr. Lakhani shares how a single ICU case launched a global collaboration that uncovered the link between CRELD1 and a new spectrum of rare genetic disorders involving seizures, developmental delay, and cardiac irregularities. We explore the diagnostic odyssey faced by families, the promise of genomic sequencing, the impact of early detection, and the inspiring role of patient communities like CRELD1 Warriors. 💡 Whether you're a researcher, clinician, advocate, or parent — this episode highlights how science, empathy, and global teamwork are transforming the future of rare disease care. 🧬 Topics covered: Understanding CRELD1 and its clinical implications The importance of early molecular diagnosis Collaborating across labs, hospitals, and continents Supporting families through the diagnostic journey The role of AI and emerging technologies in rare disease research 📍 Listen now and help us raise awareness — because every rare story deserves to be heard. #RareDisease #CRELD1 #Genomics #PediatricCare #EarlyDetection #RareAwarenessRadio #GeneticResearch #PatientAdvocacy #SaquibLakhani #CedarsSinai #PrecisionMedicine
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    33 mins
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