🌟 Brace yourselves for a groundbreaking event! 🧬 Join us on December 17th, 9am PT, as we unveil the latest developments in NDF’s very own Gene Therapy Effort for GNE Myopathy! 🙌✨

🔍 Dr. Angela Lek,  NDF’s Scientific Consultant and VP of Research at the Muscular Dystrophy Association with Rich Horgan, NDF’s Biotechnology Consultant and CEO/Founder of Cure Rare Disease, will dive into the cutting-edge progress we’ve made towards a brighter future. 🌈🔬

Ever wondered how gene therapy works? Curious about the potential impact on GNE Myopathy? 🤔 Now’s your chance to learn and engage! Stick around for a live Q&A session after the presentation, where your burning questions will be answered by the experts themselves. 🎙️🔗

Don’t miss out on this exclusive opportunity to be part of the future of GNE Myopathy treatment. Mark your calendars for December 17th at 9am PT – your curiosity and questions will shape the conversation! 🕘👀

#GeneTherapyBreakthrough #GNEMyopathyWebinar