Meet Bre!
Hi there my name is Breanna Setzer and welcome to our team page. I was diagnosed with cystic fibrosis at age 6 weeks and have been fighting my whole life, a little about cf! Cf is a genetic mutation that affects the whole body but it’s different for every person diagnosed, I have the 3rd rarest form of cf! There are only 13 others in the world with the same genetic mutations as me! A little about me! I am 24 and a mother and wife, I am half blind and deaf because of my cf among a lot of other issues but theres to much to explain, and I’m on the short side at a whopping 5ft. I’m very excited for you to join my team and to have ur support! I’ll see u at the walk!
IT AINT EASY BEIN WHEEZY!
If you’d like to learn more about me and my cf don’t be afraid to ask at the event!
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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.