Recovery doesn’t happen in isolation, and when you live with Multiple Sclerosis, even a “routine” surgery can totally upend daily life. In this episode of A Couple Takes on MS, we get real and open up on the weeks following…
In this episode of A Couple Takes on MS, we’re honored to welcome Sarah Locke, founder of Locke’s Promise, a New Hampshire–based nonprofit born from her own lived experience with Multiple Sclerosis. Sarah shares how Locke’s Promise came to life,…
What does it look like to keep showing up year after year and mile after mile for the people you love and the cause you believe in? In this episode of A Couple Takes on MS Podcast, we’re joined by…
As we closed out 2025, we found ourselves reflecting on what it really means to keep showing up while living with Multiple Sclerosis and how, sometimes, the best way to move forward is to look back. In this episode of…
Caregiving is an act of love, but it can also be exhausting, overwhelming, and emotionally heavy. That’s why self-care for caregivers isn’t selfish. It’s essential. In this episode of A Couple Takes on MS, we’re joined by Susanne White, a…
Adaptive fashion matters. It’s about dignity, confidence, creativity, and ensuring people with MS feel seen and supported. In this episode, we share our experiences as runway models at the 2nd Annual MS Focus on Fashion event in Fort Lauderdale, hosted…
In this episode, we’re honored to welcome Professor Robert Motl, a leading researcher whose work has revolutionized the understanding of how exercise and physical activity help manage Multiple Sclerosis. As a professor at the University of Illinois Chicago, Rob (as…
It’s been a busy (and meaningful) stretch for us these past few weeks! In this episode, we take you behind the scenes of our latest adventures across Michigan — from savoring local flavors at the Taste of Generosity event in…
In the epic episode, we welcome legendary blogger, podcaster and fashion icon Ardra Shephard. In our conversation, we celebrate her trailblazing work in the MS and disability communities and get an inside look into her highly anticipated memoir, “Fallosophy: My…
When you are living with Multiple Sclerosis, how do you know when you need to take on fewer activities? To take a break. To say, “Not today.” To give yourself permission and just stop. In this episode, we reflect on…