What began as one family’s journey has grown into a community committed to showing up, for children navigating serious illness, for families walking similar paths, and for a future shaped by hope and progress.
When people come together through Salty Jeans, support turns into something tangible, creating moments of comfort for families in the hospital and momentum for continued progress in cystic fibrosis care.
raised for cystic fibrosis research
Salty Jeans was founded by a family navigating life with cystic fibrosis and shaped by one simple belief: no family should walk this journey alone.
We advocate, fundraise, and build community-centered experiences that prioritize courage over illness and people over fear. Our work is rooted in real life, hospital stays, daily treatments, hard conversations, hopeful milestones, and the people who choose to show up again and again.
This movement began with Olivia, and grew alongside countless families navigating cystic fibrosis and complex medical care.
Her experiences have shaped how we see courage: not as something loud or fearless, but as persistence, vulnerability, and the willingness to keep going. That understanding drives how Salty Jeans shows up, through grassroots fundraising, family-centered events, and awareness efforts that connect real stories to real outcomes.
The headline and subheader tells us what you're offering, and the form header closes the deal. Over here you can explain why your offer is so great it's worth filling out a form for.
The name Salty Jeans reflects both science and story.
“Salty” references a common early sign of cystic fibrosis. “Jeans” nods to genetics, and to Olivia’s middle name, Jean. Together, they represent the intersection of diagnosis and identity, medicine and humanity.
It’s a reminder that progress is personal, and that behind every advancement is a family, and a community, that cared enough to act.
Support through Salty Jeans is designed to hold both the present and the future.
Locally, we focus on creating moments of comfort and connection for children and families spending time in the hospital. Nationally, we help advance cystic fibrosis research and care through sustained fundraising and advocacy.
Every event, campaign, and contribution plays a role in strengthening families now while helping shape what comes next.