My story
I was diagnosed with Cystic Fibrosis at the young age of 6 weeks old.
My family & friends have been joining me in the Great Strides walk since I can remember. Every year it is so much fun getting together with friends and family in an effort to raise money to find a cure for Cystic Fibrosis. I am so thankful for the wonderful support each and every one of them gives me. This year we have a fundraising goal of $1,000. So please help the cause by giving a donation to our team... or even better yet joining us in our walk for a cure!
The basics
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.
Breathe Easy ~ Kori Jo Maier
Achievements:
Wendy Tradewell
Event: Milwaukee
| Team: Wendy's Walkers
Wendy's Fundraising Goal: $1,000.00
| Amount Raised: $0.00
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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.