Our Great Strides Story
As many of you know, supporting research into a cure for Cystic Fibrosis (CF) is critically important to me and the Cystic Fibrosis Foundation (CFF) is a phenomenal organization making great strides towards this every day.
My wife Rebecca not only suffers from CF but came very close to losing her battle with it in 2015. After respiratory failure from end stage CF, the better part of a year on a ventilator, and a double lung transplant, and especially now while she’s facing a kidney transplant…we’re even more determined to ensure this doesn’t happen to someone else’s loved one!
Every year we fundraise for a cure to this terrible disease through one event or another (or multiple). If you choose to donate, and I hope you do, it will be not only appreciated…but impactful. Please consider following the link and reading more of our story.
Thanks!
Ray
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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.