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My Great Strides Story

Caleb Remington

Fundraising for Portland Great Strides

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Caleb Remington

As a dad of two, I can’t help but feel an overwhelming sense of gratitude for the advancements in medicine that have made it possible for me to live out my dreams and raise a family. When I was first diagnosed with cystic fibrosis, the outlook for people with my condition was uncertain at best. But thanks to the incredible progress in research and treatment, I’m able to experience the joys of fatherhood that I once feared might never be possible.

However, there is currently no cure for cystic fibrosis, and far too many people with CF die young. That’s why I’m walking today—to help change that reality.

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. It makes it difficult to breathe and fight life-threatening infections, often leading to extensive lung damage and respiratory failure. Every person born with cystic fibrosis is on a unique journey and experiences this challenging disease differently. While progress has been made, a long road lies ahead for far too many people fighting this terrible disease.

We need a cure so that everyone with CF has a better chance to live a long, healthy life.

I am deeply grateful for the scientists, doctors, and researchers who continue to push the boundaries of what’s possible and develop life-changing treatments. But there’s still so much work to be done, especially for the individuals who aren’t candidates for the current treatments. We are all in this fight together, and I’m proud to stand alongside so many others who are working tirelessly for a future where cystic fibrosis no longer defines us.

Will you help us end cystic fibrosis?

By donating to my fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward—a cure for everyone with CF.

Thank you for your generosity and support.

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$530
raised of $2,000 goal
 

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Team Caleb

$530
$2,000

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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.