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My Great Strides Story

Evelyn Waters

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Evelyn Waters

Evelyn Waters has Cystic Fibrosis. It's a genetic disease causing extra thick mucus to form in her body making her more likely to get sick and requiring her to take medicines to digest food. 

We were devastated with her diagnosis but have been so excited with all the technological advances she has seen in her lifetime. Thanks to support from the Cystic Fibrosis Foundation (CFF) Evelyn has been able to start many new medicines and treatments. Now she is 5 years old and thriving. 

This year Evelyn even got the okay to stop 40 minutes worth of respiratory treatments because she is doing so well. We are so thankful! We are hopeful for a cure but know God is using her mightily. 

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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.