Dear Friends and Family,
It is that time of year again!! Time to reach out to all my wonderful friends and family and ask you once again to dig into those pockets to make a small donation.
Katie has been doing so great on Trikafta. This medication has been completely life changing for Katie. However, she had a bit of a setback this year and needed to be hospitalized to receive intensive antibiotics and undergo a few bronchoscopies. But fortunately she seems to be doing great once again.
Katie and Jake's twins, Hadley and Hayven are growing up so quickly. They provide so much joy in their lives. And in June 2022 they welcomed their son Hayes. He is as sweet as can be!
Those sweet babies need to have their mommy around for a long time, so that makes fundraising for a cure even more important.
The incredible medication that has changed Katies life would not have been possible without all of your support in the past, so we thank you immensely!!
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.