As a signature Seafair event, Rock ‘n’ Roll Seattle has proudly kicked-off the annual summer festival in Seattle and its courses showcase the stunning natural beauty of the Emerald City amidst the summer sunshine. Join us on Sunday, June 18th for this challenging and beautiful full and half marathon race, and go the distance to end Duchenne!

Date: June 18, 2017
Time: 7 a.m.
Start Line Location: TBD

Visit the official Rock 'n' Roll Seattle Marathon & Half Marathon website for more race day details.

Run For Our Sons is a program of Parent Project Muscular Dystrophy (PPMD), the largest non-profit organization focused entirely on Duchenne.


Run For Our Sons Requirements

In exchange for a race entry, PPMD requires each marathon & half marathon runner to raise a minimum of $1,000. Your entry fee counts toward that minimum.

To help you reach your fundraising goal, PPMD provides fundraising tips, a personalized webpage and other fundraising tools. Our fundraising minimums are determined on a race-by-race basis in order to recover costs and maximize the funding going directly to help those living with Duchenne.

Fundraising minimum due date: June 9, 2017.

By joining the RFOS team for this race, you are personally pledging to raise the required fundraising minimum. If your minimum has not been met by the date specified above, PPMD staff will contact you to secure your position on the team with a credit card. You will then have four weeks after the date of the race to continue to collect donations, after which time you will be asked to make up the difference between the minimum and what you have raised.

Run For Our Sons Team Benefits

  • Guaranteed entry into the race
  • Official Run For Our Sons technical shirt and T-shirt
  • Personal fundraising web page & fundraising support
  • Social media outlets to connect with other runners
  • Dedicated staff person to answer all of your fundraising and race day questions
  • Training resources such as virtual training links and publications
  • Frequent team email updates
  • Knowledge that you are helping to support PPMD’s work to improve the treatment, quality of life and long-term outlook for all individuals affected by Duchenne muscular dystrophy