Sweet Delilah
Hi Friends,
We may have shared with some of you that our niece Delilah was born with Cystic Fibrosis. She spent many months in the hospital, but after great care in Houston, she is home and doing well. She is beautiful and thriving, but the battle is not over.
Forty thousand people in the United States have cystic fibrosis: a progressive genetic disease that affects the lungs, pancreas, and other organs. They are family and friends who face the sobering prospect of a shortened lifespan. But we can change that!
You can support Delilah and others!
By supporting our goal in fundraising, you have an opportunity to be part of ending this disease. Please consider supporting us and our commitment to ensuring Delilah has a bright, healthy, and happy life!
Join Mark and me in supporting a cause dear to us and our family. Your support means more to our family than you could ever imagine!
With love,
T&M
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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.