Walk with our team to Cure Cystic Fibrosis

J4 And The Breathtakers
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J4 and the Breathtakers

Joe was 7 days old when he was diagnosed with Cystic Fibrosis. Since then we have had regular appointments at the CF clinic in Hasbro Children’s Hospital. We meet with a multidisciplinary team that prevents and controls symptoms related to CF. Joe is growing beautifully thanks to the early management of his Cystic Fibrosis. With the many successful treatments available to his mutation we have no doubt he will live long fulfilling life.

We have learned so much in the past 7 months about the strides made through the CF Foundation in order to find a cure for this disease and we intend to be apart of what the future has in store.

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?

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$715
raised of $1,000 goal
 

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7 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.