It was dark inside Finch Field House. Loud cosmic techno music was blaring. Spotlights were shining through the darkness. The stage manager peered beyond the curtain, waved her hand, and whispered, “Go!” That’s exactly what I did. I rolled onto…
Yes, I am married to a model. All of the planning, discussing and fittings are completed, and Jennifer will make her mark on the runway at the 25th Annual Threads Fashion Show this Saturday on the Central Michigan University campus.…
Dan and I often talk about the power music has in helping us through our life with Multiple Sclerosis. From meaningful lyrics, haunting melodies, hard-driving drums or guitar solos, music just gets us and meets us right where we are.…
When things don’t seem to go their way, people often find it’s easier to ignore it, mutter frustrations under their breath, share thoughts with friends, and post opinions on social media. We have been there many times ourselves. But other…
I have experienced firsthand the benefits of working remotely for nearly five years as a senior writer at Ruffalo Noel Levitz. This is why my former colleague Kristi DePaul – now the CEO of Founders – didn’t have to ask…
Dan and I often say that we are one in a million. This tongue-in-cheek statement loosely refers to the fact that there are nearly one million Americans living with Multiple Sclerosis, and each one of us is one of that…
When is the last time you weighed yourself? How did you do it? For most people, it’s a matter of stepping on a scale and looking at the number. But for Jennifer, who no longer can stand on her own,…
There is exciting research happening at the University of Pennsylvania addressing ways to slow Multiple Sclerosis progression through precision medicine. Dan and I had the opportunity last month to interact with a lead researcher on this project. We, along with…
Each of our podcasts opens and closes with the same responsive phrase: Dan: “We’re A Couple Takes on MS. I’m walking.” Jennifer: “And I’m rolling.” Dan: “But together, we’re moving forward.” One of the ways we keep moving forward together…
Jennifer and I have shared personal stories about our life with Multiple Sclerosis for more than 20 years. They’re what we know. But it’s always humbling when other people connect with us because they want to know more about our…