Hi friends,
There are approximately 30,000 Americans who were born with and are living with cystic fibrosis and my husband, Drew, is one of them. He is a more fortunate CF patient, whose health has been greatly improved by the amazing medications developed by scientists in the last 5+ years and partially funded by the CF Foundation.
Many other people, most of them children, aren't as fortunate, and end up needing a lung transplant, or worse.
The life expectancy of CF patients has doubled in the last 30 years - let's continue the progress! There are more senior dogs we need to adopt! :)
We’ve come so far, but there’s still so much work to do - please walk with us, donate to help others with CF, or both!
THANK YOU!!
Erin & Drew
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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.