Dear Friends and Family,
It is that time of year again!! Time to reach out to all our 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 her and those in the CF Community that benefit from this modulator, but there are still so many with CF who don’t benefit from this medication and that is why it’s so important for us to keep fundraising so that every person in the CF community has a life changing medicine. Everyone deserves a fighting chance.
Katie and Jake's twins, Hadley and Hayven are growing up so quickly following in their mama’s path of doing gymnastics and dance. Hayes is going to be 2 and definitely keeps Katie very active. They provide so much joy in their lives. This has been yet another amazing year for Katie, as she has made it a whole year without any hospitalizations. With that being said, Those sweet kids 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 Katie’s life would not have been possible without all 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. We walk for them. Will you join us and support our 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. We will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support us! 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 us reach our 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.