Archive for the ‘Szajnuk Family’ Category

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Ava Szajnuk’s Sixth-Year Anniversary: Second Chance at Life

June 15, 2019 12:00 pm

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June 15th marks Ava’s sixth-year anniversary of her first cranial surgery during the summer of 2013. Today, also marks the first day I started to share our journey...

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Announcement: Exciting News for our Family!

May 10, 2019 11:30 pm

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Our family is incredibly grateful to the Miller family, Steve Starks, Dennis Lindsey, Quin Snyder and the entire Utah Jazz organization for this very blessed opportunity for our...

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“Undiagnosed is a Diagnosis” by Gina and Ava Szajnuk

May 29, 2018 3:45 pm

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Welcome to the world of the unknown. My oldest daughter, Ava Szajnuk, is growing up so fast and her voice is so important for the next generation. In...

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Global Gene’s RARE Daily: Learn more about RUN, our Mission and our Family

May 27, 2018 10:29 am

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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...

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Watch #RUNNBA: Utah Jazz National Anthem Buddies

May 5, 2018 10:46 am

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RUN’s #RUNNBA: Utah Jazz National Anthem Buddies Watch our #RUNNBA video and experience what it was like to be on the court of the Utah Jazz! In 2015,...

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RUN’s 2018 Rare Disease Day!

February 28, 2018 9:27 pm

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RUN’s 2018 Rare Disease Day events were incredible! Thank you to the Rare Disease Legislative Advocates and the EveryLife Staff for allowing me to share our journey and...

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Wishing you a Safe and Healthy 2018!

December 31, 2017 11:22 pm

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As 2017 comes to an end, we want to wish you all a safe and healthy 2018!  Thank you to all of our RUN families for continuing to...

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A Dream Come True! The Szajnuks meet Rachel Platten

September 22, 2017 3:20 pm

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We are all  a “Lone Ranger” We all have our own “Fight Song” RUN will “Stand By You” Together we are RUN family We Can Do Hard Things...

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RUN’s Journey

February 22, 2017 10:20 am

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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...

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Happy New Year to my RUN family

January 1, 2017 9:39 pm

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Happy New Year’s Day to all of our family and friends. I went back through our 2016 pictures and landed on this picture this morning. As we are...

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