Yes, it’s been 10 months since our last podcast, but we didn’t stop moving forward. Rather, we stepped away to give ourselves time. Dealing with Jennifer’s dad’s illness and coping with his passing on October 5, 2024, revealed realities no…
To complement our recent blog post – From love at first sight to a focus on in-home care – about our love story getting featured by the IMPART Alliance at Michigan State University, here is an encore post of one…
Looking for a way to overcome your chronic illness? Fuggedaboutit! Seriously. Forget about it. Easier said than done, right? Jennifer recently reflected on this when she wrote: “I am aware of my Multiple Sclerosis every single day. The disease cannot…
Tyler Susko, Ph.D., knows a thing or two about walking a mile in the shoes of people with walking difficulties. So much so, he is making their experiences better… one step at a time. Tyler is the Chief Technology Officer…
Continuing our focus on Disability Pride Month, I started thinking that we all are different, but is disability just another form of different? It’s one thing for an adult to stare at me in my power wheelchair and make unintentionally…
Disability Pride Month is celebrated every July. Pride in disability? For real? Yes, for real. As A Couple Takes on MS, Dan and I are proud, but it is complicated. Am I proud that I no longer can walk and the…
In Episode 77, Dan (and he admits it) was struggling cognitively. But was his scatteredness because he was tired? Age? Doing too much? Living with Multiple Sclerosis? In response to these questions, we can answer potentially, maybe, possibly and perhaps.…
Not every person could seamlessly tie together the concepts of Step Therapy Reform and the Crap Gap. You just need to leave it to A Couple. Because to us it makes perfect sense to connect: • A bill in the…
So often it seems the more you do, the harder it is to keep your head above water. You tell yourself you just need to get through this task. This morning. This day. Phrases like, “It can wait until tomorrow,”…
Since her MS diagnosis in September 2019, Brittany Quiroz—also known as a “A Hot MS”— has been a powerful voice in the Multiple Sclerosis community. Brittany is an author, speaker, MS activist and a talented singer Whew! Did we say she’s…