Columns

I Hope Telemedicine Is Here to Stay

As I’m sure most of us can attest, the world is a messy place right now. It is impossible to ignore. While I have never experienced anything as unprecedented as these times, I have experienced the messiness of life with SMA. I’m finding myself leaning on past experiences to help…

Service with a Smile and a Waggly Tail

One month after our baby Jeffrey was diagnosed with spinal muscular atrophy, I met Cindy Schaefer on an SMA message board. Her son, Bionews Services columnist and forums director Kevin Schaefer, was diagnosed with type 2 SMA a couple years before that. During our…

Ella Loves Summer Play, Even with SMA

Ella loves the outdoors. As summer begins in our area, the warm weather follows, with shorts and short-sleeved shirts the preferred attire. But spinal muscular atrophy (SMA) presents some challenges for Ella as she plays outdoors. One challenge is getting herself outside. She has two options.

Welcome to the Launch of SMA My Way

I am officially a baby influencer. I spent the morning tweaking my social media pages. I’ve been doing that a lot lately, ever since I graduated with a master’s degree and found myself with oodles of free time. But this was different. This was purposeful. This was in preparation for…

I Feel Recharged by Fresh Air as Summer Approaches

The long-awaited days of summer have nearly arrived, and I am doing my best to take full advantage of the warmer weather. After so many months of sweaters that make it harder for me to move and sporadic snow flurries late into the year, it’s refreshing to throw open the…

Recent Health Issues Leave Me Guessing

For the past few months, I have been experiencing some debilitating health issues. I’ve spoken with my doctors. I’ve tried different medications. And while as a team, we have figured out ways to give my body some reprieve at times, the root issue has yet to be diagnosed and resolved.