We are fundraising to raise money for our daughter, Deklyn, who was born with Cystic Fibrosis. She attends her appointments and performs all of her extra treatments/medication/routines like a champ. All money raised will go to the Michigan/Ohio chapter of the Cysytic Fibrosis Foundation to perform research to find a cure for Cystic Fibrosis.
Any help would be truly apprecitaed!
If you would like to join our team: DEKLYN'S DEFENDERS and join us for the walk in person or virtually and raise funds on you own, please sign up under our team page.
The details of our walk are as follows:
Grand Haven Great Strides
Sunday May 19, 2024 @ Lake Shore Middle School
Check in @ 1:00 & Walk begins at 2:00.
We chose Grand Haven because we really wanted to involve my Aunt Jeri in the walk and that is where she lives. She has been a HUGE advocate for Deklyn on her journey and can't wait to enjoy Great Strides together!
Thanks everyone!
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I walk for them. Will you join me and support my fundraising goal?
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
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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.