On February 28, 2025, a powerful force gathered in Seattle: scientists, clinicians, patient advocates, rare disease families, students, and supporters—all united by a common goal: accelerating discovery together for rare diseases.
Rare Genetic Disease Research in Seattle and Beyond, the inaugural Rare Disease Day event in Seattle, co-hosted by PNRI and Seattle Children’s Research Institute, was more than just a meeting—it was a milestone. From the moment the doors opened, the energy was undeniable. Ideas were exchanged, collaborations took shape, and throughout the day, one message rang loud and clear: rare disease research is advancing faster than ever, fueled by science, advocacy and collaboration.
“Seattle has a thriving rare disease research ecosystem, with incredible resources developed by researchers, clinicians, and family foundations,” said Cláudia Carvalho, PhD, PNRI Assistant Investigator and event co-organizer. “This symposium was designed to bring these groups together to share their work, build bridges, and move research forward in a way that benefits the entire community.”
