Our sweet baby, Dane, entered the world on February 14th, 2016. Dane was 7 pounds 12 ounces, 19.5 inches long, and unbeknownst to us at the time . . . born with Cystic Fibrosis. As new parents, our world was rocked when at just over two weeks old we received the news that our newborn baby was just a little bit more special than we were originally expecting. Fast forward a few years to June 2018 and our world was once again shaken with the arrival of our little spitfire, Hollis, and yet another CF diagnosis. Our family has vowed to become advocates for both Dane and Hollis and for the countless others around the world who suffer from Cystic Fibrosis.
As a family, we hope you will support us in our efforts to raise awareness. Our goal is that through our participation, we will be able to add to the number of tomorrows available for our sweet babies. We are eternally grateful for your support and generosity.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.