Andy

Dear cystic fibrosis, Forty-six plus years ago, you entered my life. I never knew life without you and it’s likely I never will. You have… Read More »Dear Cystic Fibrosis – My open letter to CF

Sitting at home yesterday, the phone rang and I recognized the number. In that moment, I knew I had lived up to the words of… Read More »Life-Changing moment- My Trikafta Approval

Most of you have heard by now that Trikafta has gained FDA approval and will soon become avalible to CF paitents in the US. It’s been a… Read More »Trikafta- Preparing for a life-changing​ drug!

When I was little, I didn’t know how to talk about my cystic fibrosis. To be honest, I didn’t even know what CF was. I… Read More »How to Tell People You Have Cystic Fibrosis

Working out has impacted my life greatly and I’m not just referring to my appearance. Getting fit has provided me confidence. It’s a confidence I… Read More »5 Keys To success – Staying Fit with CF

Wish For Wendy Foundation looking to the future and for a cure for cystic fibrosis. Nearly three years before I was born, my mom gave… Read More »The Wish For Wendy Foundation – Looking To The Future

Three Tips for Traveling With Your CF Treatment Equipment When you have cystic fibrosis, traveling requires a little advance planning due to the number of… Read More »3 Tips for Traveling with Cystic Fibrosis

Mental Health Awareness in 2019 Imagine being trapped in a well and the higher you climb, the further away you get from your escape. In… Read More »Mental Health Awareness​

You may have heard a CF patient or two talk about pills. Pills, Pills, Pills am I right?? So what kind of pills might a… Read More »How Many Pills Do You Take? – A day of pills as a CF patient.

Did you know that one of the symptoms of having cystic fibrosis is malnutrition? Yup, you heard it! Individuals with CF (like me) don’t absorb… Read More »What Does Diet Have to do With Cystic Fibrosis?