Welcome to our personal fundraising page supporting Cole's Champions! To view a short video of Cole's story go to www.colesfight.com or simply watch the video on this page.
There are approximately 30,000 Americans living with cystic fibrosis (CF). They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who can struggle every day just to breathe. One of these children is our 16 year old son Cole and we are asking for your help today to aid us in our fight against CF.
Cole was diagnosed with CF when he was only 1 month old. We really didn't know what to expect for our son. We also didn't know what kind of support was already in place for families like ours and what amazing work had already been taking place for decades before Cole's diagnosis. Because of organizations like the Cystic Fibrosis Foundation we now have an incredible amount of hope for Cole and all those living with CF. More importantly, the research that they have helped to fund has led to a number of advances that are extending the lives of those living with CF while we continue striding towards a cure...today, we're asking you to help us continue this fight.
Will you join us? If you simply want to support our team you can make a donation above and share this page with your friends and families to help us spread the word.
By supporting us, you are joining a growing group of people committed to finding a cure for CF. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure.
Thank you for being one of Cole's Champions!
-Mike, Nicci, Cole, Noah & Sam Brewer
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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.