“Evening of HOPE” agenda out now for our Utah Rare Disease Day event on March 3rd, 2026!

February 5, 2026 8:00 am No Comments 0

“Evening of HOPE” agenda for our Utah Rare Disease Day event! Please join us on Tuesday, March 3rd, for our fourth annual event, hosted by Recursion Pharmaceuticals in partnership with the Rare & Undiagnosed Network RUN.

The event will kick off with refreshments and social time, followed by speakers from our Utah rare disease stakeholders, rare and undiagnosed patients, caregivers and patient advocates sharing their powerful stories.

We hope to see you there!

RSVP: https://luma.com/rare-disease

Details: Tuesday, March 3rd

5:00p – 8:00p MT (Doors open at 4:30p)

Recursion

41 S 400 W, Salt Lake City, UT 84101

Virtual Link to Rare Disease Day:
Google Meet joining info
Video call link: https://meet.google.com/stg-uvxi-fjm
Or dial: ‪(US) +1 502-694-4429‬ PIN: ‪258 211 178‬#
More phone numbers: https://tel.meet/stg-uvxi-fjm?pin=8273596141575

Much Love,

Gina Zanik (Szajnuk) (Co-Founder/Executive Director of RUN & Chair, Utah Rare Disease Advisory Council (RDAC), Ryan Kelly (Chief Communications Officer at Recursion) & the organizing committee



Contact information: Gina Zanik (Szajnuk)
Co-founder and Executive Director, Rare and Undiagnosed Network (RUN)
Chair, Utah Rare Disease Advisory Council (RDAC)
www.rareundiagnosed.org 
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

RUN’s GuideStar Profile

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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)