Hello family and friends,
We are so excited to be walking again this year as Carter’s Crew!
CF has been a part of our lives for eight years now. There are still really hard days with CF , but there are also moments where we are struck with complete gratitude, thankfulness and an abundance of hope. This is because we have seen how hard the CF community fights and we have seen how much love we are surrounded with. Carter has so many people in his corner cheering him on and this is truly what keeps us going. This boy is the most resilient and tough 8 year old. He really does not let anything get him down.
Carter is tough and we have no doubt that he is an incredible CF fighter, but we walk because we know that here is more in store for all of those with CF. Real progress has been made in the search for a cure. The new modulator, Trikafta, was a huge stride in the right direction and is a great placeholder until we get that cure. We are in the fight until it is done. By walking alongside us in our journey you are helping provide hope for us, Carter and all those with CF. We have every reason to believe that the cure is within reach and we are excited to be a part of it!
Please consider joining Carter's Crew by walking with us or making a donation to our team. We appreciate all of the love and support!
Brandon, Allie, Carter, Addie, Ava and Aubrey
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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.