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Our Great Strides Story

Katie Roberts

Fundraising for Tulsa Great Strides 2026

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Katie Roberts

There is currently no cure for cystic fibrosis and too many people with CF die young. I’m walking for my daughter, Kollins, and to help change that reality.


Meet Kollins — our strong, beautiful, and incredibly brave 2-year-old.

Kollins was diagnosed with Cystic Fibrosis, a life-shortening genetic disease that affects the lungs and digestive system. Every day, she fights battles most people never see—treatments, medications, and the constant challenge of simply breathing.

But if you met her, you’d see so much more than CF. You’d see her smile, her strength, and her unstoppable spirit.

This May, we’re walking in Great Strides to fight for Kollins—for better treatments, longer lives, and ultimately, a cure. Because the truth is, Cystic Fibrosis is still a devastating disease, and too many families face a future filled with uncertainty.

We walk so Kollins can have the future she deserves.

Thank you for supporting Team Kollins and being part of her fight.


Will you help us end cystic fibrosis?

By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward – a cure for everyone with CF.

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$50
raised of $500 goal
 

Achievements

Leader

Team Salty Herd for Hope - Team Kollins

$150
$3,500

Recent Donations

Attendance Policy

The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.