Our Team is named after our son Keldan Pablo, we are one of the founding Teams for this event to raise funds for the cure for Cystic Fibrosis. We are extremely proud that the Tulalip Fundraising Events has succeeded in raising funds each year.
Working along sides of other teams and local business has been rewarding to us and now to all those of you that have joined us in donating to this even. We join with the other teams and hope you will join with us to find a cure for Cystic Fibrosis and get us one step closer to a cure for Cure for Cystic Fibrosis, a rare, genetic, life-shortening disease that makes it difficult to breath.
With supporters like you by our side, the Cystic Fibrosis Foundation continues to lead the way in the fight against CF, fueling extraordinary medical and scientific progress. The life expectancy of someone born with CF has doubled in the last 30 years. Despite this progress, many people with CF do not benefit from existing therapies either because their disease is too advanced or because their specific genetic mutations will not respond. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day in the face of this devastating disease.
We participate in Tulalip Great Strides for them.
Will you join us?
Tulalip Great Strides is a fun event that provides a fantastic opportunity for family, friends, students, and colleagues to come together to make a difference in the lives of people with CF.
To participate, just click on the "Join our Team" button. From there, you can make a donation and start fundraising.
By joining our Tulalip Great Strides team and making a donation, you will be part of a tenacious and passionate group of people committed to ending this disease. Together, let’s make CF stand for Cure Found!
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.