Please consider donating $5, $10, $15, $20 + to the CF Foundation on the behalf of my two babies, Brantley & Hattie, and the countless other children and adults affected by this LIFE THREATENING disease! You may see my babies playing soccer and baseball, or at dance & swim lessons... that doesn't mean they are playing with ease! They are giving it EVERYTHING their little bodies have to play these sports! We do these activities to help improve lung function! Playing one inning takes them double or even triple the recovery time than it takes a child not living with CF. But you wouldn't know that by looking at Brantley and Hattie. They don't know how hard they are fighting to breath, because they have never had the opportunity to "Breathe Easy"! Your donation can and WILL change that!!!!
That change in your cup holder puts EVERY CF patient one breath closer to a CURE!! Be that Breath!!!
**Team Lowe shirts are available for PREORDER until April 18, 2023!
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.
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today!
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
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 life-saving research and medical progress. Your gift is 100-percent tax deductible.
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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.