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My Great Strides Story

Sarah Stone

Fundraising for Harrisonburg Great Strides 2026

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Sarah Stone

Our son, Parker, was born prematurely and was diagnosed with Cystic Fibrosis just a couple weeks later. Not only were we navigating having a newborn in the NICU, but now we were learning about having a child with CF. With the help of the Cystic Fibrosis Foundation we have felt tremendously supported and comforted to know that Parker will have such a great life! We are walking to help find a cure for the life-changing disease that our son is living with and support other families who are learning about raising a child with CF.

CF is a genetic, life-shortening disease that impacts 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 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 our fundraising goal, you have the power to advance the research and science needed to drive our shared dream forward - a cure for everyone with Cystic Fibrosis.

Thank you so much for your support, 
Aaron, Sarah, and Parker Stone

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$250
raised of $250 goal
 

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Team Stone Family

$450
$3,500

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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.