Liam was born with a disease called Cystic Fibrosis. Cystic Fibrosis is a sickness that can make it hard for people to breathe and digest food. People with CF have a problem within their bodies that makes sticky mucus, which can block many passageways but mainly the tubes that carry air in and out of their lungs.
Ever since Liam was one month old, his health has required multiple doctors appointments, specialists, medications, hours of breathing treatments and respiratory therapy.
People with Cystic Fibrosis need special help from doctors to stay healthy and strong, but with the right care, they can still play, laugh, and have fun like any other kid.
Please walk with our team MILES4LIAM at this years Great Strides event in support of finding a cure for Liam.
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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.