Leah Chase

Leah Chase
Adult with CF
Leah-Chase-Headshot

Diagnosed with cystic fibrosis as an infant in 1972, Leah has participated in many clinical trials. She endeavors to perpetuate programs, education, and research about CF until a cure is found. Leah lives in North Carolina with her significant other and his daughter. She also has a 20-year-old son who serves as air crew in the U.S. Air Force. She is unable to work outside the home but does not let that stop her from being productive. She enjoys freelance writing, word games, spending time with family and friends, and is considering starting a blog.

Blog Posts

Leah-Right-Friends-Rectangle

Friendships are an important aspect of life, but they are especially meaningful when you have a disease like cystic fibrosis. By finding a group of people who take the time to understand what I'm going through, I've been able to maintain a strong support system through the ups and downs of life with CF.

 

| 4 min read
Leah-Chase-Water-Rocks-Smile-Featured-Rectangle

Having lived with cystic fibrosis for 47 years, I want to pay it forward and share the life lessons I've learned with new parents of children with CF.

| 4 min read
Leah-Chase-Doctor-Stuff-Care-Teams-Say-Featured-Rectangle

A lot is said during clinic visits. Here's just a few examples of what we've heard that show the range of relationships people with CF have with members of their CF care teams.

| 4 min read