Honolulu Marathon 2026

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Honolulu Marathon 2026

Set against the breathtaking backdrop of Honolulu, this unforgettable race experience takes you along world-famous beaches, past Diamond Head, and through cheering crowds from around the globe. As one of the largest destination marathons in the world, it's more than a race. It's a celebration of endurance, community, and purpose.
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 and give people living with CF a better chance at living a long, healthy life. While we've made significant progress, we still have a long way to go. We still lose precious lives to CF every day. You can help us accelerate progress.
To have the best experience possible, we ask that every participant takes the time to prepare physically and that you are willing to commit to raising or exceeding the fundraising minimum.

How to join the Breathe Team and register for the Honolulu Marathon:

Step 1:
Please reach out to Jenn Kalker at jkalker@cff.org to receive more information and to complete your fundraising commitment form.

Step 2:
Once you have completed your commitment form, Jenn will send you a private link that will allow you to register with us through this website. This will create a fundraising page for you to begin fundraising through our Breathe Team platform! 

Step 3:
Jenn will also send you a promo code to register for free on the Honolulu Marathon website. Once you complete this process, you are ready to participate in Breathe Team at the 2026 Honolulu Marathon!!
If you have any issues getting signed up or if you have already registered for the Honolulu Marathon but would like to join the Breathe Team, you can contact Jenn Kalker at jkalker@cff.org or 858-452-2873
**All fundraising minimums must be met at least 7 days prior to race day to receive your bib.

Benefits You Will Receive from joining the Breathe Team: 
• CFF Staff support to help you meet and exceed your running and fundraising goals
• Personal fundraising page through Breathe Team website
• Guaranteed race entry
• Training resources
• Breathe Team moisture wicking shirt
 • Other fundraising incentives as you hit different levels
 
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!

Step Up Your Fundraising

Become a 65 Roses Champion

by raising $1,000 or more

Learn 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

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.

View Attendance Policy