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My CF Cycle for Life Story

Mary Ann Wilson

Fundraising for Pittsburgh CF Cycle for Life 2026

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Mary Ann Wilson

On Saturday September 12th Ray and I will be riding in the Cycle for Life for Cystic Fibrosis. We have participated in this event every year since our beautiful granddaughter Natalie was born with this disease. Natalie is 13 years old and in 8th grade. She is quite an athlete and is busy hiking, running Cross Country and Soccer. She has participated in MANY group runs, 5Ks and other events. She has quite a collection of medals from these events!. Her parents have done everything possible to keep her healthy. Natalie is also an AMAZING artist and spends a lot of time creating beautiful drawings 🥰.

There is currently no cure for cystic fibrosis. I’m cycling to help change that reality. We are getting closer and closer to a cure! We've come SO FAR since Natalie was born and we are getting close to the finish line. This has all been possible because of donations from people like you💕



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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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.

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