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.

Articles by Brad Dell

Am I making excuses or simply explaining my reality with CF?

I’ve been trying to write more. I promise. But my tacrolimus dose is pretty up there, and it’s getting on my nerves. Literally. Nerve pain from the medication, an immunosuppressant used in lung transplant management, has me feeling like I’m driving diabetes lancets into my fingers with every…

How personifying cystic fibrosis made me a monster slayer

Mom raised me to be a hungry reader, so it wasn’t long until I explored one of her favorite genres, Southern Gothic. Tales from this corner of the library are identified by distorted realities, eerie supernaturalism, eccentric characters, and sometimes abrupt violence. These elements are often bound together to critique…

For Me, Fear of the Unknown Is Harder Than Fighting Disease

For two decades, plummeting pulmonary function percentages terrorized me, weight flew from my body, and my diagnoses list stretched longer than a CVS receipt. Trips to the clinic featured grim reports detailing my body’s ruin: estimated organ expiration dates, fistfuls of prescription slips to counteract the destructive side…

Are Emotional Spoon Shortages Driving Your Exhaustion?

I’m beginning to rethink the sources of my fatigue. Yes, sickness and physical activity are still real sources of exhaustion, but I’m realizing I’ve neglected a deeper flavor of struggle.   Many of us sick folk are familiar with the “spoon theory.” The analogy goes…