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#Faith4ACure

Until CF Stands for "Cure Found"

We are a non-profit organization dedicated to raising awareness for cystic fibrosis (CF), sharing our journey, and funding research for a cure. Our mission is deeply personal—our daughter, Olivia Jean, battles CF every day, and we won’t stop until a cure is found for her and everyone living with this disease.

See How You Can Get Involved
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Join our fight against cystic fibrosis

Fundraise With Us
Join our Great Strides walk in the spring or Xtreme Hike in the fall.
Participate in Our Events
Participate in our local, regional, and national events.
Give Direct Donation
Make a direct donation to support our mission.
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What is Cystic Fibrosis?

A Chronic, Progressive, and Life-Altering Genetic Disease

Cystic fibrosis is a relentless, life-shortening genetic disease that affects the lungs, digestive system, and other organs. While medical advancements have come far, there is still no cure for CF patients, including Olivia.

Learn More about Cystic Fibrosis

Living with cystic fibrosis

Nearly 40,000 children and adults in the U.S. (and about 105,000 worldwide) live with CF, with over 1,000 new cases diagnosed each year.

Cystic fibrosis impacts everyone differently, and for Olivia, that means managing both respiratory and digestive symptoms every single day. Here's what CF looks like in our world:

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Salty-tasting skin

Due to the body’s inability to properly regulate salt levels, Olivia loses excess sodium through sweat, putting her at risk for dehydration—especially in warmer months.

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Persistent coughing

Thick mucus builds up in her lungs, triggering daily coughing as her body works to clear her airways.

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Frequent lung infections

That same mucus creates a perfect place for bacteria to grow, leading to chronic infections that can damage the lungs over time.

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Shortness of breath

Inflamed, congested airways make breathing a struggle—especially when she’s tired or sick.

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Poor growth despite a healthy appetite

Even though Olivia eats well, her body can’t absorb nutrients properly without digestive enzymes, affecting her growth and weight gain.

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Chronic sinus infections

Just like in her lungs, mucus collects in the sinuses, causing congestion, inflammation, and frequent infections.

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Chronic constipation & belly pain

Olivia deals with uncomfortable GI symptoms like constipation and stomach aches daily—requiring a consistent mix of medications and Miralax.

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Dehydration risk

Because she loses so much salt in her sweat, Olivia is more prone to dehydration, especially during physical activity or heat.

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Fatigue & energy dips

Between early-morning treatments, digestive struggles, and respiratory flare-ups, Olivia often tires easily—especially during activity-heavy days.

Want to see what daily life with CF really looks like?

Watch this short video of Olivia using her chest vibration vest—a key part of her twice-daily airway clearance routine.

 

HOW WE HELP

Raising Awareness and Vital Funds

We host and participate in fundraising events to support research, drug development, and high-quality CF care. Every contribution helps move us closer to a cure.

Total Funds Raised for 2025 (last updated July 2025)

Raised: $3,496.25
Goal: $10,000
Donate Now Get Involved
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We Need Your Help

Featured Campaigns

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Local Fundraising
65 Roses Field Games

The event is family-friendly and for all ages, featuring classic field games reimagined with cystic fibrosis (CF) awareness themes. Participants will enjoy fun challenges, a scavenger hunt, and opportunities to learn more about life with CF – all while raising critical funds for research.

$0

Fund Goal

$1000

Raised

$0

Status

Open
Register to Play
Participate in Salty Jeans Super Bowl Squares
National Fundraising
Super Bowl Squares

Score big for a great cause! Purchase your Super Bowl Squares, cheer on your team, and get a chance to win cash prizes—all while supporting the Cystic Fibrosis Foundation. This 50/50 fundraiser is a fun and easy way to make an impact. Every square brings us closer to a cure!

$1560

Fund Goal

$2000

Raised

$1560

Status

Closed
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Local Fundraising
Salty Jeans Egg Drop

Make Easter extra special while supporting a great cause! Order pre-filled eggs to be hidden in your yard or delivered to your door for a fun-filled hunt. You can also donate eggs to bring joy to children at Children’s Mercy Hospital. Every egg makes a difference!

$923.57

Fund Goal

$1000

Progress

$923.57

Status

Closed

Since 2019, our family has been dedicated to raising funds and awareness for the Cystic Fibrosis Foundation—what began with simple donation asks has grown into a full calendar of heartfelt events that bring our community together in the fight for a cure.

Today, Salty Jeans leads several creative fundraisers throughout the year:

  • Super Bowl Squares
    A fun way to give back while cheering on your favorite team
  • Salty Jeans Egg Drop
    Spreading Easter joy to families locally and to kids at Children’s Mercy Hospital
  • 65 Roses Field Games (Launching Fall 2025)
    A family-friendly event filled with competition, connection, and purpose

Every event is a chance to build community, raise vital research funds, and help us get closer to a day when CF stands for Cure Found. Join us in any way you can—we truly can’t do this without you.

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About Us

Meet Team Salty Jeans

Behind every great cause is a team of dedicated people—and Team Salty Jeans is no exception. We’re a family-driven community, united by love, resilience, and a deep commitment to fighting cystic fibrosis alongside our daughter, Olivia.

Each year, we proudly participate in two major events through the Cystic Fibrosis Foundation: the Great Strides Walk in Kansas City (Spring) and the Xtreme Hike in Missouri (Fall). By joining our team, you’ll be part of something bigger—raising critical funds for research, spreading awareness, and helping add more tomorrows for everyone living with CF.

 

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Sarah & Kevin Logan
Team Leaders & Olivia’s Parents
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Christine Hays
Aunt & All-In Teammate
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Amy Roether
Aunt & Supportive Host
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Alayna & Alyssa Hays
Cousins & Young Advocates
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Tricia Cobb & Heather Bagby
Friends Who Hike With Heart
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Amanda Hamilton
Aunt & Consistent Supporter
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Marlene Roether
Grandma & Everyday Helper
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Nathan Roether
Uncle & Always-There Volunteer
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Scott Logan
Grandpa & Steady Supporter
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Twynnin Brown
Longtime Friend & Loyal Teammate
#Faith4ACure

A Family’s Journey

Our blog, Faith4ACure: A Family’s Journey, is where we share the heart and soul of Team Salty Jeans. Here, you'll find real stories of resilience, hope, and advocacy—from Olivia’s journey and our family’s experiences to the latest in cystic fibrosis research, fundraising efforts, and community impact.

Stay current with upcoming events, inspiring CF warrior spotlights, and practical insights on CF care and awareness. Whether you're a supporter, a fellow CF family, or just learning about the cause, we invite you to follow along, get involved, and help us turn CF into Cure Found.

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The Hidden Battle of Cystic Fibrosis: Managing an Invisible Illness

One of the most challenging aspects of living with cystic fibrosis (CF) is that many of its...

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Olivia’s Bright Spring: A Cystic Fibrosis Story of Hope, Healing, and Easter Giving

This season has been one we’ll never forget. It’s been full of growth, gratitude, and a few...

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Navigating Tough Choices: A Family's Journey of Hope and Heartbreak

Life Isn’t Always Clear-Cut: Life brings us to crossroads more often than we’d like—moments where...

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