Take a moment this holiday season to stop and breathe. Listen to the laughter. The songs. This silence. The stories. A regular segment for our A Couple Takes on MS podcast is “MS in Their Voices.” This segment features the…
Imagine if you stopped learning after you graduated from high school. Or, how about after college? Think of everything you would have missed. See what we did there? We just made you think. Learning is so important, and it never…
One of our regular listeners sent us what seemingly was a simple question: “What keeps you motivated in living with Multiple Sclerosis?” Simple, right? Not necessarily. While it wasn’t necessarily a complex question to answer, it was, shall we say,…
The annual economic burden for the nearly 1 million people living with Multiple Sclerosis in the U.S. is, wait for it … $85.4 billion. That’s billion. With a “b.” The $85.4 billion, according to a report from the National Multiple Sclerosis Society,…
The first day of Fall is Saturday, September 23, 2023. Oh, Fall. Dan and I both love this season. The cooler temperatures, the plethora of football games, the vibrant colors of changing leaves, and the comfort of a cozy sweater…
Sometimes what other people are seeing seem so obvious to them. “How could you not see it?” they ask. Maybe you could see it but just not very clearly. You don’t want to face the truth that your vision is…
There’s more to our relationship than 18 years of marriage and each of us living with Multiple Sclerosis. We also are in a caregiving relationship. Jennifer is my primary caregiver, and I am hers. We were so humbled and honored…
If a bill goes before Congress and you never told members how their actions will impact you, how confident are you that they will vote in your favor? As two people living with Multiple Sclerosis, this isn’t a chance we’re…
It’s challenging enough living with Multiple Sclerosis when you are settled into the comforts of your home, but the stresses compound when you venture out on an overnight trip. Gone is your strategically crafted accessible environment and you find yourself…
A listener recently submitted a question to us through acoupletakesonms@gmail.com wondering, “How does someone just diagnosed with MS (or even someone who has lived with MS for some time) find the courage to ask for help?” What an incredibly insightful…