There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers—people who face daily challenges just to breathe. CF doesn’t define who they are, but it is something they courageously battle every single day.
 

Oliver Gregory was diagnosed with cystic fibrosis just three weeks after birth. Our family was devastated—but that moment also ignited a journey of learning, advocacy, hope, and determination.
 

Today, Oliver is 9 years old, THRIVING, GROWING, and doing really well with his health and weight. He is a kind, loving, joyful, energetic, happy guy, even with everything he manages daily behind the scenes. His strength inspires us constantly! We are so PROUD of Ollie!
 

Oliver’s routine includes multiple daily treatments:

💙An inhaler to open his airways

💙CPT (chest compressions) using The Vest machine for 30 minutes TWICE a day to help loosen mucus in his lungs

💙Nebulizer treatments, often done while wearing the Vest, to further break up that mucus
 

In addition, Ollie takes enzymes every day so his body can properly digest food. As he grows and his calorie needs increase, so does his enzyme dosage. Right now, that’s about 16 pills a day—over 5,840 pills every year—just so he can eat, grow, and stay healthy. In addition to those enzymes, he takes probiotics and vitamins daily - another 730 pills ever year!
 

Because of YOU and generous donations from supporters around the world, Oliver is now able to take KALYDECO, a life-changing medication for one of his two CF mutations. He takes it twice daily with a high-fat meal, and it has made a meaningful difference in his journey.

💙 This is why we walk.
💙 This is why we fundraise.
💙 This is why we ask you to join us.
💙 We won't stop until there's a CURE for Ollie!
 

We will walk for Oliver.
Will you walk with us? Will you walk with Ollie to help find a cure? Come on friends, LET's WALK!
 

Becoming part of Team Ollie Ollie CF Free is easy:

💙Click “Join Our Team” to register and start fundraising

💙Or, if you’d prefer, click “Donate to a Team Member” to make a direct donation
 

By joining our team or donating, you become part of a growing community committed to finding a cure for cystic fibrosis. Together, we are truly adding tomorrows—for Oliver and for everyone living with CF.
 

Great Strides is a fun, family-friendly event filled with hope, love, and community. We would love for you to come out, show your support, and walk hand-in-hand with Oliver and our family.
 

🌈 Tie-dye shirts are encouraged!
If you’d like to order one, please reach out to Jenette Mitchell—100% of proceeds go directly toward Ollie’s fundraising goal.
 

Thank you for loving and supporting our Ollie and believing in his future, and walking beside us.
 

With gratitude and hope,
Zach, Jenette & Oliver 💙