Gabby is an awesome 6 year old who happens to have cystic fibrosis. She was in the gray area of CRMS for a few years before they changed her diagnosis to full CF about a year ago. Gabby is a busy girl and does not let this diagnosis limit her too much! She plays softball, basketball, and soccer, and dances jazz and hip hop. Her vest and nebulizer treatments take a lot of time out of her day for sure, but she is a trooper!
We are walking in Great Strides because we want to raise funds for the CF Foundation. Gabby's CF mutations are rare and therefore she is not eligible for modulator drugs at this time. We are hopeful that in the future, she will be eligible for one of these life changing medications. There is a lot of research being done right now and much more in the years to come. Thank you for donating any small amount to our Great Strides team which will go towards finding a cure for CF!
Join our team and walk with us, or donate on one of our team members' pages!! THANK YOU!
Join our team to help make a difference in the lives of all people living with CF. To become a member, click the "Join this team" button. From there, you can donate and start fundraising.
As a member of our team, you are joining a growing community of people committed to finding a cure for cystic fibrosis. Together, we can make CF stand for Cure Found.
Connect With Us
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated June 15, 2022. To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials.
To minimize the risk of COVID-19 infection, we ask that attendees at CF Foundation events follow these steps:
FOR YOUR SAFETY AND THE SAFETY OF OTHERS: