Young Myles speaking at LU Medical School for the first time...
For those of you who have supported us in the past, sincere thanks for again helping out! For those new to this page, meet Myles. He is an engaging and energetic guy who loves baseball and basketball. In 2022, he became a CF Ambassador, and his parents, Stacy and Rob, have been very involved in the cause. Myles is an AMAZING young man. He has been speaking with Liberty University Medical School students for 10 years now about what it's like to live every day with CF. The pictures show Myles in his first year (age 6) and the latest year (age 15!) with the LU mascot, Sparky the Eagle. Thanks to the research at the CF Foundation, after years of taking Kalydeco, a CF Foundation funded medication, he now takes Trikafta, a new CF Foundation funded medication which targets a much larger population. Your dollars are making a real difference to my great nephew Myles and thousands of CF patients!!! Lets keep the funding going!!! Please help us make CF stand for "Cure Found"!!!
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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.