My name is Ethan I'm 14 years old and I am very energetic and love to play. I'm just a normal 14 year old except for one gene mutation that gives me CF (Cystic Fibrosis). You would never know just by looking at me but if you spent a day in my shoes you would experience breathing treatments, lung therapy, and a whole lot of pills. CF doesn't stop me from doing the things that I love like playing football, basketball, and swimming with my brother. I started 8th grade this year and I love playing with all my friends. My teachers are so nice and helpful giving me my medicine before snacks and lunch everyday. Please help me find a cure by donating to Team Leurquin.
My name is Jaxson and I am Ethan's brother and I am 8 years old and started 3rd grade this year and like my brother Ethan I also have CF(Cystic Fibrosis).I am always happy and enjoy listening to music and playing basketball and football with my big brother. Please help Team Leurquin find a cure.
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease. By walking today, I am helping add tomorrows to the lives of people living with cystic fibrosis. Will you join me? Support me by making a donation to my Great Strides fundraising campaign today!
Join our team and help add tomorrows!
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. We walk for them. Will you join us? All we need you to do to become a member of our team is click on the "Join our Team" button. From there you can make a donation and start your fundraising.
By becoming a member of our team and making a donation, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure.
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
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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.