Rapid City Great Strides 2026

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Rapid City Great Strides 2026

Welcome,
We are so glad you are here! Ready to lace up and join us for our annual walk to cure cystic fibrosis? By participating, you have the power to change thousands of lives. Your support helps the Cystic Fibrosis Foundation fund the research and care needed to help advance a cure for this disease. While we’ve made significant progress, we still have a long way to go. We still lose precious lives to CF every year.  You can help us accelerate progress. Now is the time to act.


Get Ready to Walk

Register: Join us for a day of celebration, community and fun! Let's unite to bring hope and joy to those affected by CF and work towards a future where everyone can breathe easier. Click the “Register” button. 

Recruit: Invite friends, family, and colleagues to join you. Together, we can make a bigger impact.

Fundraise: Fundraising is easy. Use the participant center, the CFF mobile app, or fundraise on Facebook to reach your goal. You can also host a passion fundraising event and check if your employer offers a matching gift program to increase the impact of your efforts. 

Share your story: Your story matters! Share why you’re participating in Great Strides and inspire others to join. Use the tools in the participant center and on the mobile app to easily tell your story!

 
Thank you for your efforts to raise awareness and funds so that we can get one step closer to curing cystic fibrosis. Your participation is critical to advance our mission, and now is the time to act. Sign up today to take steps towards a cure for cystic fibrosis!
Find a Walker
Connie and Bob Templeton
Rapid City Great Strides 2026
Parker Loll
Rapid City Great Strides 2026
Sarah Abrams
Rapid City Great Strides 2026
Victoria Blankenship
Rapid City Great Strides 2026
Lisa Aguilar
Rapid City Great Strides 2026
Arron Frank
Rapid City Great Strides 2026
Zoe Aguilar
Rapid City Great Strides 2026
Ava Aguilar
Rapid City Great Strides 2026
Monique Johnson
Rapid City Great Strides 2026
Marissa Trosen
Rapid City Great Strides 2026
Mary Caropino
Rapid City Great Strides 2026
Alyssa Loll
Rapid City Great Strides 2026
Brandon Loll
Rapid City Great Strides 2026
Holden Loll
Rapid City Great Strides 2026
Elizabeth Baartman
Rapid City Great Strides 2026
Cami Kaubisch
Rapid City Great Strides 2026
Easton Kaubisch
Rapid City Great Strides 2026
Miken Kaubisch
Rapid City Great Strides 2026
Casey Kaubisch
Rapid City Great Strides 2026
Melinda Nalley
Rapid City Great Strides 2026
Gina Haiwick
Rapid City Great Strides 2026
Abby Wortman
Rapid City Great Strides 2026
Find a Team
Team Fischer
Rapid City Great Strides 2026
Parker's Pals
Rapid City Great Strides 2026
Walking For Wesley
Rapid City Great Strides 2026
Arron’s Team
Rapid City Great Strides 2026
Dakotas Strong
Rapid City Great Strides 2026
South Dakota Society for Respiratory Care
Rapid City Great Strides 2026
Team Baartman
Rapid City Great Strides 2026
Valley Climbers
Rapid City Great Strides 2026
Create a Team
Congratulations to our 65 Roses Champions!

2026 Local Ambassador

Meet our 2026 Local Ambassador!

Parker

Parker

Parker’s cystic fibrosis journey began early. At just two weeks old, his newborn screening indicated a high likelihood of CF. His family traveled six hours to Sioux Falls to meet with Dr. Wallace, where Parker underwent a sweat test to confirm the diagnosis. He began taking enzymes immediately; Parker finally began gaining weight and growing stronger. Today, Parker is an energetic three-year-old with a big personality. He is the proud little brother of Holden, 6, and the youngest of three siblings, including his big sister Jasmine, 21, who lives in Washington. Parker also adores his family dog, Buster, who prefers relaxing and taking life a little slower. Parker, however, is always happy to sneak him cookies whenever he can. Parker’s days are full of imagination and adventure, especially when he’s playing with his toy cars, trucks, and trailers. He loves fruit snacks, protein shakes, and his all-time favorite cartoon characters—Paw Patrol. One of the things that makes Parker especially proud is that he’s been swallowing his enzymes whole since he was about 1½ years old—an impressive milestone that shows just how strong he is. Parker wants people to know that there is no cure for cystic fibrosis—yet. But he dreams of a day when there will be. With modern medicine, dedicated researchers, and the unwavering support of his community, Parker believes that together we can make CF stand for Cure Found.

Step Up Your Fundraising

Become a 65 Roses Champion

by raising $1,000 or more

Create a National Team

Join up with friends, family, and colleagues across the country and locally to participate in multiple events, make sub-teams, and get fundraising support to grow your impact.

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Donations and Event Logistics

Events may be subject to change based on health or safety concerns. If an event is moved to virtual, sponsorship benefits may be adjusted to fit that format. If an event is cancelled, your local contact will reach out to discuss options.

Diversity, Equity, and Inclusion

At the Cystic Fibrosis Foundation, we commit to equity, racial justice, diversity, and inclusion as core principles guiding our efforts to provide all people with CF the opportunity to live long, fulfilling lives. We strive to host inclusive and accessible events that enable all individuals to engage fully. Please be aware that a 3-week notice is requested as some accommodations may require time for the Foundation to arrange. If you have a disability and require accommodations to fully participate in this activity, please contact the chapter for assistance.

Contact this Chapter

Thank you to our National Sponsors!

National Peer to Peer Sponsor

National Great Strides Sponsors

Outstanding Corporate Supporter

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.