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Summer's Great Strides Story

Shanann Bragg

Fundraising for Spokane Great Strides 2026

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Shanann Bragg

                      WELCOME TO TEAM STEPS FOR SUMMER 2026!
 

Thank you for visiting our Great Strides 2026 fundraising page! Our team was created in honor of our youngest daughter, Summer, who was born with Cystic Fibrosis (CF) in 2009. CF is a genetic disorder that affects the lungs and digestive system, causing persistent lung infections and limiting the ability to breathe over time.
 

Despite the daily challenges CF brings, Summer exudes energy and a positive outlook.  Many have shared with us that "you would never know that she has CF."  This chapter of being a teenager in high school and playing school and club volleyball have been challenging to fit in the daily care that is so important to manage Summer's health.  Her routine includes daily breathing treatments, pancreatic enzymes with every meal, and occasional antibiotics to help fight off secondary infections like pseudomonas.  We remain dedicated as a family to guide her and to emphasize the commitment that is needed. 
 

For the past 16 years, our family has proudly participated in Great Strides in Spokane, raising awareness and funds for the Cystic Fibrosis Foundation. For personal and family reasons, we missed our first Great Strides ever last year in 2025.  We are excited to be back and can't wait to walk together on June 6th!  We hope that you can join us to support Team Steps for Summer and continue our mission of helping make CF stand for Cure Found.
 

We appreciate your continued support and look forward to Great Strides 2026!
 

With gratitude,
Team Steps for Summer & Family 💜


 

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$100
raised of $100 goal
 

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Team Steps for Summer

$100
$3,500

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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.