5 things I learned from BreatheCon

BreatheCon, held this past weekend, was an online conference for CF patients from around the country to come together to be able to share life experiences, ideas, and give inspiration to each other in battling this disease.
I attended, and it was an incredible experience. Hearing from keynote speakers who have faced such adversity and have come out of it stronger and more motivated than before, was so uplifting to hear. I believe it created a lot of hope and courage for those that still have our toughest challenges to face.

I want to share the top 5 things that I now understand better about life with Cystic Fibrosis: Continue reading 5 things I learned from BreatheCon

Announcing BreatheCon, a space by and for CF adults

For the first time, over 50 percent of those of us living with CF are over the age of 18. Our community has a wealth of knowledge and a great desire to connect, but little ability to interact face-to-face.
Continue reading Announcing BreatheCon, a space by and for CF adults