Tré LaRosa,  —

Tré LaRosa is a scientific project manager, patient advocate, and writer. He has cystic fibrosis (CF) and carries two copies of the F508del mutation. He's been on Trikafta since 2019. He writes about science, living with CF, grief, family, and everything in between in an effort to get you thinking about what it means to be human. He lives in Arlington, Virginia with his fiancée Jessica and their two wonderful, lazy dogs, Duncan and Leo. He enjoys playing sports, being outdoors, and reading — and especially buying more books.

Articles by Tré LaRosa

Searching for Motivation as I Struggle With Depression

When I took Advanced Placement psychology in high school, a few subjects stuck out to me as being intuitive. I was weirded out by this because the majority of school lessons were not intuitive. Math, chemistry, and biology are logical and scientific, but I don’t naturally understand cells, or how…

Surveys Play a Critical Role in Improving the Patient Experience

I used to dislike surveys, polls, and questionnaires. I understood why they existed — customer or patient feedback is important — but I never really saw anything change once I took a survey. I hadn’t considered that perhaps my feedback was unrealistic or didn’t represent the entire community. It wasn’t…

How I’ve Learned to Use My Insecurity to My Advantage

I recently saw a meme in which a person is smiling or laughing in the first panel, then looks utterly dismayed in the second. The second panel’s overlay reads: “Tfw [that feeling when] I realize I’m being perceived by everybody else who ever interacts with me.” This meme is one…

The Long Journey of Learning to Love My Own Body

I used to be ashamed about my insecurities. I believed that as a man, I was supposed to be strong. I was supposed to silently hate myself, my appearance, and my body, while projecting an immutable air of confidence. That was the “manly” way. My masculinity, my…

Yes, I Will Get the COVID-19 Vaccine

I can’t remember when I first fell in love with science. I loved learning about it and going on field trips, but I didn’t enjoy science fairs because I missed hanging out with my friends (although I did place second at a science fair with some assistance from my dad).

My Experience With COVID-19

Life would be much easier if every complicated disease or disorder weren’t so complicated. COVID-19, cystic fibrosis, depression — if they all manifested uniformly and could be treated the same across the afflicted population, the world would be much simpler. As always, life just isn’t that simple. About two weeks…