Meet Our Team‎ > ‎


Meet Kaitlyn McGuire, our personal CFer. Kaitlyn was diagnosed with Cystic Fibrosis when she was 18 months old, which followed with her first of many hospitalizations. In the beginning, we did not understand the battle facing us. We did not understand the questions that will come and may never have answers. Now, at age 12, she is still fighting this battle every day. She faces hospitalizations every 2-3 months and takes medications and treatments daily, but her hope never dims. She has a strong support team made up of her parents, her brothers, dozens of aunts/uncles/cousins, and many friends she has met along the way. 

Kaitlyn's dream is finding a cure for Cystic Fibrosis.

Rachael McGuire, SFAC Founder and Kaitlyn's Mom


Here's some photos of Kaitlyn being a regular little girl despite living her life with Cystic Fibrosis.

Kaitlyn CF Story from 2010

Kaitlyn's CF Story from 2015