Chelsea Miller
We found out our daughter, Chase, had Cystic Fibrosis when she was in-utero. Thanks to breakthroughs in research led by the CF Foundation and our amazing medical team at UAB, Chase was able to start receiving medicine before she was even born. She arrived healthy on August 8, 2024, and will continue to take medication daily for the rest of life until there is a cure for CF.
We are so thankful that Chase was given the opportunity to start receiving treatment as early as she did, and we hope Chase’s story can help other families.
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.
We are so thankful that Chase was given the opportunity to start receiving treatment as early as she did, and we hope Chase’s story can help other families.
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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