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My CF Climb Story

Erin Carty

Fundraising for Philadelphia CF Climb

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Erin Carty

Elliotte-Ellie-Chickie!!!! What a journey she has had in just the first couple years of life! And none of it would be possible without the amazing support from her village of family and friends, as well as her team at CHOP. So, thank you to everyone who has been there for every step of the way! We love you more than you know.


Ellie was diagnosed with CF at 2 weeks old. She was admitted to the hospital at 5 months old with a CF exacerbation for 2 weeks, where she was on a ventilator for 4 days in the NICU for part of that stay. Since then, Ellie has been making AMAZING strides in her journey and is growing up with an even more amazing personality.


The Chickie's Climbers team is here to represent more than supporting Ellie. We're here for those who fight this fight day in and day out, and for all of those families who are right there with them. Let's do this! UNTIL IT'S DONE!



There is currently no cure for cystic fibrosis and too many people with CF die young. I'm walking to help change that reality.

CF is a genetic, life-shortening disease that devastates the lungs, pancreas, and other vital organs. CF 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.

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.

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raised of $350 goal
 

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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.