Thank you so much for clicking on my link for the Great Strides Walk. It's 2024, Lets go big everyone!!!!!!!!
Nicole Dragon was an amazing human being that I had the privilege of calling friend for 17 years. In 2016 she unfortunately succumbed to this awful disease. The life she lived, the smile she had, the impact she left on so many, will forever be remembered by all of her friends and family.
This walk gives some of us an opportunity to see each other and remember and honor Nikki. We are also raising money to fight Cystic Fibrosis. In Nikki's lifetime science has made phenomenal advances in medicine and treatments for people suffering from this disease. Those treatments and medicine are what allowed Nikkii to spend as much time as she did with all of us. Please help me this year raising money for this foundation. I do believe they have a positive impact in this world. Help add many more tomorrows to all of the people suffering with this disease.
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.