02/27/2026
Tomorrow is Rare Disease Day – an important reminder of just how prevalent rare diseases remain and how critical it is that we continue to leverage all of our tech tools and AI advances to find new treatments.
Rare diseases impact more than 300 million people worldwide – and 30 million in the U.S. – and just 5% of rare diseases have a treatment. Better approaches are needed.
🔹 On Tues., March 3, Recursion will host Utah Rare Disease Day at our Salt Lake City headquarters. We’ll welcome speakers from across the rare disease community – physicians, patients, and advocates – to share their stories of hope.
They include:
▪️ Erika Fox, Chief People and Impact Officer at Recursion
▪️ Oskar & Ava Szajnuk, rare disease patients with Rare and Undiagnosed Network (RUN)
▪️ Kelvyn Cullimore, President and CEO, BioUtah
▪️ Andy Roberston, executive director, BioHive
▪️ Justine Case, patient and advocate with Utah Rare Disease Advisory Council (RDAC)
▪️ Aaron Quinlin, professor at University of Utah
▪️ Sally Jo Zuspan, RN, MSN, director of research at University of Utah
▪️ Dr. Tracy George, president of ARUP Labs
▪️ Stacy Allen, parent and advocate at Intermountain Children’s Health
▪️ Januel Gomez, patient and Utah RDAC Council member
🤗 We’re looking forward to hearing from so many community members who are dedicated to raising awareness around rare diseases – and helping us to support patients and new treatments.