When Serena Lawrence, the late Bionews senior columns editor, responded to my email about potentially writing for Cystic…
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.
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Articles by Tré LaRosa
If you keep up with CF research, you may have seen the news about Phase 3 of the triple…
The period between Halloween and New Year’s — what I usually call “the Holidays” — is the time of year…
As I’ve grown older, I’ve become a self-advocate, taking initiative when possible. I’ve developed a close relationship with my…
I’ve been on Orkambi (lumacaftor/ivacaftor), a cystic fibrosis transmembrane conductance regulator (CFTR) modulator, for just over three years now. My…
Last in a series. Read part one and part two. The poster sessions at the North American Cystic…
Second in a series. Read part one. The poster sessions at the North American Cystic Fibrosis Conference (NACFC)…
First in a series. The poster sessions at the North American Cystic Fibrosis Conference (NACFC) in Denver this month…
As much as we resist the idea, cystic fibrosis can become a defining part of identity; a lifestyle that we’re…
If you read my column last week, you know I care a lot about the interpretation of words. The…