Abigail McLain, 6, was diagnosed with cystic fibrosis at 5 weeks old. However, because of her two rare CF mutations, she is not eligible for any existing CFTR modulators. Her parents, Adrienne and Jordan McLain, share their dreams for their daughter and what gives them hope for the future.
This video was featured in Plenary 1 of the 2022 North American Cystic Fibrosis Conference.
Негізгі бет CF Foundation | Abigail McLain's Cystic Fibrosis Story
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