Meet Caden ! "Dum spiro spero: While I breathe, I hope."
Meet our special guy Caden! Caden was born with Cystic Fibrosis. This rare genetic disorder affects little Caden's lungs and pancreas. As Caden will fight this for the rest of his life, we hope to engage our community and grow awareness. In his First year of life, he's already fighting hard! It’s been a year of both highs and lows. Here's Caden's CF reality: He needs between 7-8 breathing treatments a day. He wears his inflatable vest hooked up to a machine 3 times a day. In spite of all of that, Caden is a happy, well-adjusted little warrior! Caden’s Parents, Jeff and Gina, and big brother, Cameron, would love to have you join us to Fight for a Cure!
Join our team and help add tomorrows to Caden's life, along with the lives of all affected by Cystic Fibrosis!There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day just to breathe. I walk for them and hope you will support me in my efforts. Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Real progress has been for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Please consider making a donation to my Great Strides fundraising campaign today!
Please support me!
Help me reach my fundraising goal by donating to my Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting groundbreaking research and medical progress. Your gift is 100-percent tax deductible.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: