a body with a question mark next to it

How Cystic Fibrosis Affects Me

Today I talk about how my cystic fibrosis affects me, from pills and nebulizers to physio and IVs. Here is a brief summary of my personal experience with CF.

 

How does cystic fibrosis affect you?

Can you relate to Kate's personal experience with cystic fibrosis? We would love for you to share your experience with us as well. Share your story on our Stories page or let us know in the comments below!

By providing your email address, you are agreeing to our privacy policy. We never sell or share your email address.

More on this topic

This article represents the opinions, thoughts, and experiences of the author; none of this content has been paid for by any advertiser. The Cystic-Fibrosis.com team does not recommend or endorse any products or treatments discussed herein. Learn more about how we maintain editorial integrity here.

Join the conversation

or create an account to comment.