Every year we get closer to a cure for cystic fibrosis. Every year the treatments for it improve. And every year the life expectancy for kids born with CF improves. We are getting there.
Most of the advancements are because of research funded by the Cystic Fibrosis Foundation. They target their money where the research is working.
That's why I donate every year. That's why I walk every year. And that's why I ask my friends for donations.
Every dollar helps. So if you are willing and able to help please go to the link that I'll hopefully remember to include and donate ten or twenty bucks.
My niece and nephew Julie and Michael are amazing people and there are 30,000 kids like them (but not as cool) that deserve to live their best, fullest lives. Let's help give them a chance.
Thanks.
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.