Our Cystic Fibrosis Journey

In 2012 my daughter Lauren was diagnosed with Cystic Fibrosis.

Throughout this journey, the CF community has brought about understanding, inspiration, passion, gratefulness, and optimism for our future. 

The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for CF and supports a broad range of research initiatives to tackle the disease from all angles.  

When the Cystic Fibrosis Foundation was established in 1955, people born with the disease weren't expected to live to attend elementary school. Today, because of the Cystic Fibrosis Foundation's efforts, people with CF are living into their 30s, 40s, and beyond!