After starting our journey in Central Oregon and participating in 3 Great Strides walks surrounded by friends and family we have moved to Texas. Family will still be participating in Oregon so we have taken our team National. Help support us in Portland, Oregon as well as San Antonio, TX and New Barunfels, TX.
CF is a disease in which you can look fine on the outside but inside you could be falling apart. You never know when your child may become ill and that illness can cause irreversible damage to their lungs. One tiny cold that may not be a big deal to others could cause a hospital admission for our children. We fight everyday to keep them as healthy as possible.
Please support us by making a donation in any amount possible. Even the smallest amounts add up, be it $5, $20 or even $50. If you cannot spare even a small amount please support us by sharing our story and spreading awareness.
Great things are in the works that could drastically extend our children's lives so they may hopefully outlive us. Help us give Neila and Von every opportunity to our live us.
Help us reach our fundraising goal by donating to our Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. Your gift is 100-percent tax deductible.
Neila and Von make up only 2 of the 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 and hope you will support us in our efforts.
Great Strides is a fun, family-friendly event that raises awareness and support for people with CF and their families.
Please support us!
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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.