I would love for you to join our team and help us on our mission to find a cure for Cystic Fibrosis!
There have been so many amazing medications, therapies and treatments made available to those with a CF diagnosis. Although these are life changing opportunities, there is still no cure for this genetic disease. My family and I will not stop raising money and awareness in an effort to hopefully see a cure for CF happen within our lifetime.
Other advocates, caregivers and CF fighters have paved the way for this generation to take advantage of life changing medications. It's our turn to step in and continue the fight.
We need your help! Please consider making a tax deductible donation to the CF foundation so they can help us find a cure for Cystic Fibrosis.
Thank you for your continued support! It means more to my family than you will ever know.
With love,
The Krause Family
Here is a little bit more about CF....
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. Will you join me? Please consider donating to my Great Strides fundraising campaign today!
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting groundbreaking research and medical progress towards a cure. 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.