As some may not know, I am a carrier of the Cystic Fibrosis gene.
My oldest brother Ryan was born with Cystic Fibrosis. After receiving a double lung transplant and a lifelong battle of severe sickness, he passed away in 2007.
By helping fundraise, the Cystic Fibrosis Foundation can help prolong and strengthen the lives of current and future Cystic Fibrosis patients. Finding out a close friend has Cystic Fibrosis was heartbreaking.
As you can imagine, this hits so close to home. Please help our team fundraise to create more tomorrows!
Although I am extremely honored to join his team.....
Team Wicked Fab for life.
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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.