Columns

Teacup Rides and Wheelchair-spinning, Oh My!

When I was younger, I enjoyed the hyperactive nature of the teacup ride at Disney World. My mom hated it, but my dad was willing to accompany my siblings and me on this headache-inducing extravaganza. Spinning around inside a giant teacup from “Alice in Wonderland” was enough to entertain…

What It Means to Stay Healthy While Living With SMA

One glance at my medical records will very clearly tell you that I’m not exactly healthy. The information contained within my chart includes a primary diagnosis of spinal muscular atrophy type 1 and a list of medications prescribed to treat that disease and manage its…

SMA Is Part of My Identity, and I’m Proud of It

I came close to starting my first-ever Facebook war recently. Well, not exactly. My conscience quickly kicked in and my mother became my sounding board instead. After reading a comment from a stranger on the internet, I had a lot to say. Sadly, I’m almost immune to the negative…

Appreciating the Spunk and Optimism of a 7-year-Old

“I haven’t had cancer since I was 11 months old!” our cheery granddaughter recently proclaimed. Clara turned 7 at the end of December. She’s witty, imaginative, spunky, highly entertaining, candid, cute, and sharp. Sometimes, though, her facts are a bit skewed. She’s never had cancer. …

Why 2023 Will Be My Year of Resurrection

I have been waiting my entire life. Waiting for someone to love me. Waiting for the snow to melt. Waiting for my skin to clear so I could leave the house without feeling like an embarrassment of a human being. Years ago, in 2019, I wrote a column about…

Children’s Breathing Problems at Night Tied to Zolgensma Use

Despite its well-reported benefits in motor function, the gene therapy Zolgensma (onasemnogene abeparvovec-xioi) may not be as effective at preventing or easing breathing problems at night in young children with spinal muscular atrophy (SMA), according to a small real-world study. Nighttime breathing problems were found to occur in…