Living with cystic fibrosis has been a defining aspect of my life since infancy. Diagnosed at just three months old, I quickly became accustomed to a routine of countless pills morning and night, enzymes every meal, vest and nebulizer treatments, lab draws, hospital stays, and everything else that comes with having CF. My health journey has been a roller coaster, filled with ups and downs, but through it all, I've remained resilient and determined. Despite facing numerous battles, I take pride in the accomplishments I've achieved and the life I've built for myself.
Throughout the years, I've refused to let CF hold me back from pursuing my dreams. I successfully graduated from college and secured a fulfilling full-time job in the marketing field—a career path I've always been passionate about. One of the most monumental moments in my life was discovering that I was pregnant with my incredible little girl. For so long, I doubted whether I'd ever be healthy enough to experience motherhood, making her arrival the highlight of my existence. Each milestone reached serves as a testament to my strength and resilience in the face of adversity.
The loss of my sister to CF in 2021 was a devastating blow, reminding me of the urgency of the fight against this relentless disease. As I walk in her honor and in support of the thousands battling CF, including myself, I am fueled by a determination to make a difference. With every step, I carry her memory in my heart, motivated to advocate for research, raise awareness, and ultimately, find a cure for cystic fibrosis.
Juliann
Achievements:
Juliann Davis
Event: Valley of the Sun
| Team: Salty Sisters
Juliann's Fundraising Goal: $500.00
| Amount Raised: $720.00
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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.