Evening of HOPE – Hosted by Recursion in honor of Rare Disease Day
Watch our “Evening of HOPE” for Utah Rare Disease Day 2026! It’s our fourth annual event, hosted by Recursion Pharmaceuticals in partnership with the Rare & Undiagnosed Network (RUN). The special evening took place on March 3rd, 2026.
We welcomed speakers from across the rare disease community – physicians, patients, and advocates – to share their stories of hope.
They include:
▪️ Erica 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 Utah
▪️ Justine Case, patient and advocate with Utah Rare Disease Advisory Council (RDAC)
▪️ Aaron Quinlan, professor at University of Utah
▪️ Sally Jo Zuspan, RN, MSN, director of research at University of Utah
▪️ Tracy George, president of ARUP Laboratories
▪️ Stacy Allen, parent and advocate at Intermountain Health
▪️ Januel Gomez-Colon, patient and Utah RDAC Council member
A special thank you to Recursion for hosting the event. A very special thank you to all of our speakers. It’s an evening we will cherish forever.
Thank you all for your continued support of our family, RUN, the Utah RDAC and the entire rare and undiagnosed community.
Much Love,
The Zanik Family
Contact information: Gina Zanik (Szajnuk)
Co-founder and Executive Director, Rare and Undiagnosed Network (RUN)
Chair, Utah Rare Disease Advisory Council (RDAC)
W www.rareundiagnosed.org
E ginaszajnuk@gmail.com P (310) 883-4353
Media:
To Read: RARE Revolution Magazine: Undiagnosed.
To Read: A mother’s unrelenting crusade to help those trapped in the wilderness of the undiagnosed – by Lee Benson
To Read: “What is the hardest part of being undiagnosed?” by Gina Szajnuk
To Read: “Undiagnosed is a Diagnosis” by Ava and Gina Szajnuk
To Read: The Szajnuk Journey
To Read: “Push Through” by Ava Szajnuk
To Listen: RARE Cast by Global Genes: “A Young Rare Disease Advocate Discusses Life with an Undiagnosed Condition”sease Advocate Discusses Life with an Undiagnosed Condition”
To Read: How Utah Jazz GM Justin Zanik found himself fighting for not just his team, but his life – ESPN
To Listen: ESPN Daily: How a Family’s Bond Saved the Jazz GM
To Watch: Fox 13 News “Undiagnosed”
To Watch: RUN’s Two Year Anniversary Video by Small Forces
To Watch: RUN’s One Year Anniversary Video
To Watch: #UndiagnosedDay RUN’s 2016 Video
About
Gina Zanik (Szajnuk) started her career in the entertainment industry. She worked in Hollywood for over ten years. She supported movie directors, producers, actors, literary agents and executives. She entered the world of the NBA and NFL and served as Director of Client Services and Executive Assistant to the CEO at Priority Sports & Entertainment in Chicago. She supported the President of Basketball Operations at U1st Sports, an NBA and European basketball agency. She worked in corporations supporting VP, President, and CEO level executives for five years in Los Angeles and Manhattan. She now serves as the Founder and Executive Director for the Rare and Undiagnosed Network (RUN), a 501©3 nonprofit organization in Salt Lake City formed in 2014. Her three children, each of whom live with a chronic, invisible, and undiagnosed rare disease, continue to inspire, and motivate her to empower patients and their families with genomic information and community through advocacy, networking, and support. Gina is also living with a chronic, invisible and undiagnosed rare disease. She serves as the Chair of the Utah Rare Disease Advisory Council (RDAC). She is a member of the Undiagnosed Disease Network International (UDNI). In 2016, Gina was the Chair of Utah Rare and was on the Executive Committee for four years. Gina continuously works to build a network of rare advocates, geneticists, researchers, specialists, and volunteers who can come together under one platform. In 2016, RUN started the international Undiagnosed Rare Disease Day (Undiagnosed Day) awareness campaign on April 29th. She was a member of the Participant Engagement and Empowerment Resource (PEER) of the Undiagnosed Diseases Network (UDN) for two years. She served as the National Organization for Rare Disorders (NORD) as their Utah State Ambassador and then as their Undiagnosed Advocacy Ambassador for four years. She is a public speaker and published writer. In 2016, Gina won the Rare Voice Award from the EveryLife Foundation for Rare Diseases as well as accepted the Rare Champion of Hope – Advocacy Award from Global Genes. She is married to Justin Zanik, the NBA Utah Jazz General Manager. Gina has brought awareness to the public about the importance of undiagnosed and rare diseases through RUN’s NBA Initiative started in 2015. She was born and raised in Madison, WI. She graduated with a Bachelor of Arts from the University of Wisconsin – Madison.
(Photo by Season Atwater Photography)