Welcome to Salty Sisters, a team dedicated to raising funds for the Cystic Fibrosis Foundation in honor of Juliann and her late sister Jessica. As sisters both living with cystic fibrosis, they shared a bond that goes beyond words. Our team name, Salty Sisters, reflects their shared experiences with CF – from the salt air of the beach that helps CFers get out mucus from their lungs, to the need for extra salt on our food, and the literal saltiness of our skin due to excessive sweating, a common symptom of CF.
Jessica's journey with CF was marked by both resilience and struggle. Despite facing numerous challenges, she remained determined and optimistic, especially after receiving a life-changing lung transplant. Her spirit and ambition inspired us all as she embraced her newfound freedom to breathe better. Sadly, Jessica's battle with CF came to an end in 2021, leaving a void in our lives that can never be filled.
Despite the heartache of losing Jessica, we are committed to continuing her legacy by participating in the CFF Great Strides walk. This year marks our team's first step back into fundraising after her passing, and though it's been difficult, we know that Jessica would want us to carry on the fight against CF.
Support Us!
Every dollar we raise brings us closer to a cure for cystic fibrosis, a disease that affects thousands of individuals.
By supporting our team, you are not only honoring Jessica's memory but also helping to improve the lives of CF patients everywhere, including Juliann. Join us as we walk, fundraise, and advocate for a future free from cystic fibrosis. Together, we can make CF stand for Cure Found.
How do I join?
To become a member and walk with us in-person or virtually, click “Join this Team” button and start fundraising and tracking your miles walked now!
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.