Always believe in the power of your voice and your story to influence change. Whether it’s at the local, state or national level, your experiences are valuable in making things better for you and many others dealing with the same…
We’ve never met Sarah Kirwan and Carl Deriso as a married couple, let alone had a shared conversation with the two of them. But less than two minutes into our chat with the Arizona couple, it was like we were…
This episode released on Valentine’s Day so of course it embraces a theme related to maintaining loving relationships when you or your significant other are living with Multiple Sclerosis. Just think about it: all committed relationships present their share of…
We all know Multiple Sclerosis is a relentless, unpredictable, frustrating disease. It can make living with it seem impossible, but we can regain some control in how we manage our MS. Shortly after she was diagnosed more than 26 years…
When people ask who in the MS community inspires us, Jenn Powell is always among the top names on our list. For real. Seriously. Jenn is for real. She is living with Secondary Progressive MS and truly speaks our language:…
It’s one thing to not be included in social activities, but the perceived intention shifts for people who are living with visible or invisible disabilities. Questions like, “How much did my disability play into me being excluded?” or “Do my…
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…
More than 50 million people across the United States live with the primary responsibility of caring for a loved one, such as a spouse. A parent. A child. A sibling. A close relative. A friend. They are the family caregivers…
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,…