Posts tagged ‘rare and undiagnosed Network RUN’
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RUN’s NBA Initiative: NBA Teams Hosted Rare and Undiagnosed Families!
The Utah Jazz honored 30 rare and undiagnosed children and their siblings on the court as National Anthem Buddies on March 17th, 2018! Ricky Rubio and Alec Burks...
#RUN2U Program: University of Utah School of Medicine’s Pediatric Medicine Interest Group
Do you know what it is like to live with a rare or an undiagnosed rare disease? Please join the University of Utah School of Medicine’s Pediatric Medicine...
Global Gene’s RARE Daily: Learn more about RUN, our Mission and our Family
Rare Leader: Gina Szajnuk, Co-founder and Executive Director of Rare and Undiagnosed Network Written by Daniel Levine on the Global Gene’s RARE Daily on March 5, 2018 Photo...
RUN & S1LY: The Connect for Hope Project
When you have a rare or undiagnosed condition, finding someone who gets it is a game changer. Introducing The Connect for Hope Project: Our new partnership with S1LY!...
#RUNNBA: Meet our Utah Jazz National Anthem Buddies!
In 2015, we started RUN’s NBA Initiative through the generosity of the Utah Jazz and the Larry H. Miller family. We were so excited to continue our initiative...
April 29th is #UndiagnosedDay: Undiagnosed Rare Disease Day!
All rare diseases were once undiagnosed. Please help us raise awareness for #UndiagnosedDay. Thank you to Governor Gary Herbert for his declaration. This coming April 29th is officially...
RARE Carousel of Possible Dreams! Help Us Fundraise!
Please consider joining our team and help us power up our fundraising efforts! Dear Friends and Family, The Rare and Undiagnosed Network (RUN) is participating in the...
National Ability Center: Saluting Our Heroes
Thank you to the National Ability Center (NAC) for including RUN at your Saluting Our Heroes luncheon. It is always such an honor to be a part of the...
Rare Disease Day
The Szajnuk’s celebrated #RareDiseaseDay with a tea party planned by Lucy! She even drew on the white napkins the Undiagnosed awareness ribbon:) Priceless! However, we are missing our...
RUN’s Journey
My name is Gina Szajnuk and I am the mother of three children with an undiagnosed genetic dysfunction. I am also undiagnosed. We live in a diagnostic odyssey...