Late last month I turned 28 years old, the age my brother, Isaac, was when he passed away from Duchenne muscular dystrophy (DMD). I have the same disease, and it’s put me through many exhausting battles. But each time, I’ve emerged stronger. In fact, I graduated with a…
Columns
Siblings are the greatest thing I have given my children. They are built-in friends who share the earliest memories, parents, and everything else. As my kids have gotten older, they have many “remember that time” stories they love to laugh about as they reminisce. Duchenne muscular dystrophy (DMD)…
I’m looking out our patio doors at our backyard. I can hear the not-so-gentle Nebraska gales blowing around the wind chimes this morning as I watch leaves drift through the air. I’ve just come in from a fast-paced walk; sweat is sticking to my neck, and my heart rate is…
I’ll admit that I was a support group cynic in my younger days. My attitude was that I’d figure things out on my own. I just couldn’t see the benefit of sitting around a table and talking to others about my struggle with facioscapulohumeral muscular dystrophy (FSHD). In retrospect,…
It’s no secret that I love the holidays. If you look through my past columns, you’ll find some about Christmas, Thanksgiving, and birthdays. I derive so much joy from creating a celebration for my family. Halloween is no exception. I am the queen of a good…
I always assumed my three sons with Duchenne muscular dystrophy (DMD) wouldn’t get to experience college. I knew it would depend on their health, disease progression, and openness to making it happen, as well as all the typical things like good grades and test scores. However, as my…
When I moved to Pittsburgh in January to be closer to my children and grandchildren, we were aware that we’d have to make modifications to our new home. Finding an accessible home in that city was impossible, especially during the pandemic real estate boom, when houses were selling…
My oldest son, Max, is graduating from high school this year. I know I’ve shared that repeatedly, but the long list of lasts he’s experiencing as a senior continue to inspire my writing. I have three sons with Duchenne muscular dystrophy (DMD): Max, 17, Rowen, 14, and Charlie,…
I was mad at my husband, Jason, for spending the night in the recliner. He’d been there because he’d been snoring loudly enough at night that I hadn’t been sleeping well, and he wanted to ensure I got a good night’s sleep. But I was in no mood to recognize…
Getting surprise help when you have facioscapulohumeral muscular dystrophy (FSHD) isn’t considered newsworthy. But maybe it should be. These days, it seems that most, if not all, of the news on television and social media is bad. These negatives aren’t limited to reports on wars, hurricanes, inflation, pandemics, and…
Recent Posts
- MDA Engage: Event sessions highlight community, hope
- The benefits of my son becoming a caregiver for his brothers with DMD
- MDA Engage: The right assistive equipment can aid independence
- I found a new FSHD life hack to respond to my worsening leg weakness
- Gene therapy restores key protein in models of rare muscular dystrophy