We invite YOU to join us in fundraising for a cure within Gabby's lifetime. Join our team, start your own team, join as an individual or make a donation. Sign up today for Great Strides Putnam- June 1, 2024
Gabby was diagnosed with Cystic Fibrosis in 2006 when she was just 9 months old. She is an active healthy teen who doesn’t let CF hold her back. Since her diagnosis we have made it a priority to do everything in our power to raise funds to find a cure for this disease, so she can live a long and healthy life. Every day Gabby does lung exercises and takes Pulmozyme with a nebulizer to help to keep her lungs healthy. This medication was developed thanks to donations to CFF which supports research and development of CF treatments and eventually a cure. CF is considered an ‘orphan’ disease and receives no federal funding. The Cystic Fibrosis Foundation relies on donations to support its research and treatment centers.
Connect With Us
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.