Many label their lives with cystic fibrosis a “battle.” I prefer “war.”* There’s the daily grind: The clinic…
Brad Dell
Brad Dell is Deaf and was diagnosed with cystic fibrosis at 2 months old in 1993. He received a double-lung transplant from UC San Francisco in January 2017, then cochlear implants nine months later. He lives in Hawaii, where he was raised. Usually he’s traveling the world, chugging coffee, or devouring books. He also pastors Restoration Community Church and serves as the director of community content at BioNews, this site’s publisher.
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Articles by Brad Dell
In Appreciation of Siblings
In ancient home videos of the Dell family, there’s shot after shot of my…
7 Tips for Managing Your Pain
I’d been anticipating my bilateral cochlear implant surgery for more than a…
Only 61.8 percent of cystic fibrosis patients comply with their daily respiratory medication and 41.2 percent comply…
You’ll meet legions of doctors throughout your life with cystic fibrosis. You’ll encounter doctors you adore and who…
A Letter to CF Parents
Dear parent, I know you’re afraid. My parents were afraid, too. My mom left a college biology class crying; the…
I fought cystic fibrosis for 15 years before the overwhelming burden collapsed. My family was driving to get…
Most of last summer was spent either in a hospital bed or lying on my couch — the couch I…