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This fundraiser ended on 01/26/11

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This site is dedicated to our daughter Ava Scott Waltz. She was diagnosed with Cystic Fibrosis at the young age of 4 weeks old.

Ava was born on June 25th, 2010. She was diagnosed 4 weeks after birth with a fatal genetic disease called cystic fibrosis. Aside from the diagnosis she is a very happy and seemingly healthy little girl. We are very blessed to have her in our life and we vow to do EVERYTHING we can to raise her in a positive and uplifting environment. We will fight this!

Our goal is to raise money that will go towards her medical expenses. All proceeds will be used towards giving Ava the best treatment possible including the best medicine, better formula, breathing treatments, and any other medical challenges we face during her journey.

We have a seperate and more important fundraising goal which is to FIND A CURE!!! Please visit that page if your interested in reading more about this disease and how you can help raise and spread awareness.

Most importantly. Please do not feel obligated to donate monetarily. We will graciously accept your continued prayers for Ava's health, strength, and courage. Although she is most important don't forget about us....Dave and I also need your prayers and support so we can be warriors and remain positive and hopeful that our family too can live as happy as our neighbors. God is in the healing business and miracles happen every day.

All of our Love,

Ava, April, Dave Waltz

“The Important thing is this: to be able at any moment to sacrifice what we are; For what we could become”

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