A Family Tradition - a Column by Carlos Briceño

First in a series. My wife, Jill, and I met Christy Dearien last year at a Huntington’s disease (HD) event in Maryland. Like Jill, Dearien’s brother is gene-positive for HD. Dearien had just published a book, “Livable Lives: Conversations with the Huntington’s Disease Community,” exploring how this…

I got home from work the other day and caught a glimpse of a relic on our television set: a 5 p.m. local newscast. Stranger still, my wife, Jill, was actually leaning forward and watching it. On the newscast, some government officials were criticizing diversity, equity, and inclusion, or DEI,…

Huntington’s disease (HD) has cast a long shadow over my wife Jill’s family tree. When she was diagnosed in 2018, we knew we’d be fighting the same enemy that had taken her father and many other relatives on his side of the family. Today, we focus on what gives…

When I received my wife’s recent text, which she wrote in all caps — something she’s morally opposed to — the room seemed to tilt. I felt like dancing like a fool while laughing and crying at the same time. Jill had included a link with the following headline: …

A quiet evening at home recently threw me for a loop. My wife, Jill, and I were relaxing in our living room, watching a reality TV show, when one of the cast members used the term “woke” to insult someone. Without missing a beat, Jill looked at me with genuine…

When my wife, Jill, was diagnosed with Huntington’s disease (HD), our world shifted. HD is a cruel, inherited, neurodegenerative illness that affects movement, cognition, and emotions. It’s a diagnosis that forces you to confront life’s fragility head-on. For us, it also became a wake-up call — a chance to…

My family has a running list of sayings I’m officially banned from using at home. Apparently, tossing out cheesy phrases multiple times a day is grounds for an intervention — at least according to my wife, Jill, and our daughter, Alexus. But for this column, I’m breaking the…

I never thought I’d be driving to work listening to the Kelce brothers interview Taylor Swift about her upcoming “Life of a Showgirl” album on their “New Heights” podcast. At 61, my musical tastes have been pretty set for decades: Give me some Bruce Springsteen or U2, and…

Last in a series. Read part one.  Choosing genetic testing for Huntington’s disease is an act of courage on its own, as I pointed out in my column last week. But as my wife, Jill, discovered, the medical system’s maze can make it feel like an outright ordeal.

First in a series. When people ask my wife, Jill, about her Huntington’s disease, I never expect her reply to reach for a playground metaphor. But she has a way of drawing from everyday life, turning even the hardest subjects into something instantly relatable. “It’s just like a…