Walk with our team to Cure Cystic Fibrosis

Evan Noelle
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Evan Noelle

Evan Noelle Veto is a feisty, funny, cuddly and energetic toddler. She was born on March 8, 2022 and has Cystic Fibrosis. She spent 52 days in the NICU and underwent multiple surgeries and procedures. Her favorite things to do are dance, eat chips, splash in the bath, ride her scooter, laugh with her big sissy, put mommy's makeup on, get surprises and keep her parents on their toes. Evan doesn't let having CF slow her down

We're walking for a cure to this life shortening disease for Evan and everyone with CF. They all deserve a chance to dance and laugh throughout long and healthy lives. 

Join our team! 
The walk is at Cedar Crest College at 10 a.m. on April 26!

We invite you to take part in Great Strides by joining our team. We promise, you belong here! This event promises to be a fun-filled day where you can help advance the care and research needed to cure cystic fibrosis. By walking with us, you’ll enjoy not only the natural camaraderie (yes, lots of laughter!), but the important impact we are making together.

While the CF Foundation has made incredible progress, not everyone with CF can benefit from existing therapies and we still need a cure. This will require time, funding, and persistence – but with you on our team – we are ready to go the distance.

Our team is committed to providing every person with CF the opportunity to live a long, healthy life. Will you join us?
FEB
18

Selfie queen!

Join our team! The walk is at Cedar Crest College at 10 a.m. on April 26!

JAN
29

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$1,435
raised of $2,000 goal
 

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16 Participants

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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.