Maya turns two today! So grateful for her and the joy she brings!
Sweet Maya was born with a rare genetic disorder called cystic fibrosis. The Cystic Fibrosis Foundation has made many advancements in the care of CF. I have seen Maya and her family benefit from the support of this foundation and the huge impact it has had on their lives. In honor of her birthday we are participating in a fundraiser through the Cystic Fibrosis Foundation!
If you would like to donate to the continued research of CF please follow the link below!
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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.