Cover image of show The Other Side of MS

The Other Side of MS

Podcast by Casey Murphy

English

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About The Other Side of MS

The Other Side of MS isn't here to inspire you—it's here to tell the truth. This podcast gives voice to the raw, unfiltered stories of people living with multiple sclerosis—the ones you rarely hear. Hosted by longtime MS advocate Casey Murphy, each episode pulls back the curtain on the emotional, invisible, and often uncomfortable realities of MS. From navigating public spaces with incontinence, to losing careers, marriages, or mobility, these aren't just stories of strength—they're stories of being human. We don't chase silver linings. We hold space for pain, for humor, for grief, for resilience—and for the voices that deserve to be heard without being sanitized or simplified. If you're ready for a podcast that doesn't sugarcoat the experience of living with MS, this is it. This is The Other Side of MS.

All episodes

82 episodes

episode S4_E6: Rachael Fenich - Facing MS Together artwork

S4_E6: Rachael Fenich - Facing MS Together

Rachael has seen multiple sclerosis from more than one angle. Her husband lives with it. So do other members of her family. Over time, what she thought she understood about MS has changed in ways she didn't expect. In this conversation, Rachael talks about what MS actually looks like inside a marriage. The parts you don't see. The things that don't get said. What happens when one person is "house planting" and the other is trying to understand how to respond. They talk about communication, frustration, and the quiet ways both people hold things back to protect each other. Rachael also shares what changed when she faced her own autoimmune diagnosis, and how that shifted the way she understood what her husband had been carrying all along. This is not a story about inspiration. It's about learning how to live inside something you didn't choose, together. Rachael Fenich serves as the Executive Director of the Georgia Chapter of the National Multiple Sclerosis Society. Helpful Links * Donate to the Bike MS Georgia Ride [https://events.nationalmssociety.org/2748/donate] * Learn more about the Bike MS Passport Program [https://events.nationalmssociety.org/pages/6788] * Join Bike MS. Find a Ride Near You [https://events.nationalmssociety.org/pages/1230?language=en]

14 May 2026 - 27 min
episode S4_E5: Mark Morabito | "You Didn't Sign Up for This" artwork

S4_E5: Mark Morabito | "You Didn't Sign Up for This"

Mark Morabito looked at his wife in a hospital room and told her she could leave. He had just been diagnosed with MS. And in his mind, he already knew how it would end. In this episode, Mark doesn't hold back. He talks about growing up watching his mom live with MS, believing it was a slow decline you couldn't escape. He shares the fear of becoming her, the regret of what he wishes he had known sooner, and the moment everything shifted. We push on the idea of "mind over matter." Because for some, that mindset feels empowering. For others, it feels like a lie. This is not a clean story. It's tension, contradiction, and truth in real time. What does it mean to fight a disease you can't control? And where is the line between strength and reality? Listen in. Support Mark in Walk MS: https://events.nationalmssociety.org/participants/890235 [https://events.nationalmssociety.org/participants/890235]

30 Apr 2026 - 41 min
episode S4_E4: Justin Yuhaze - Some Days Are Tougher Than Others artwork

S4_E4: Justin Yuhaze - Some Days Are Tougher Than Others

"Some days are tougher than others." Justin Yuhaze was diagnosed with MS just days before the birth of his second daughter. In this episode, he talks about the months that followed, the symptoms he tried to hide, the depression he did not always want to name, and the moments that pushed him toward deeper conversations instead of avoiding them. Justin also shares what it has meant to raise two daughters who have only ever known him with MS and the choices he makes to stay active and present in their lives. Donate to Justin's Bike MS Fundraiser: Justin is riding in Bike MS: City to Shore Ride 2026 as the team captain of Muggles on a Mission. Help him reach his goal of raising $5,000 for the National MS Society. Support his fundraiser here: https://events.nationalmssociety.org/participants/784914 [https://events.nationalmssociety.org/participants/784914?referrer=mf%3A784914%3Afundraise-share-you]

23 Apr 2026 - 25 min
episode S4_E3: Tyler Saldutti - Define Me By This artwork

S4_E3: Tyler Saldutti - Define Me By This

"People will abandon you. They will come up with whatever they need to justify it." Tyler was diagnosed with primary progressive MS in 2013, and the impact reshaped every part of his life. His marriage ended, relationships shifted, and the identity he built as a Division I athlete began to fall away. In this episode, Tyler talks about nine years of denial, the people who stepped back when MS became too heavy for them to hold, and the isolation that comes from realizing you do not get MS alone. He also shares what it is like to have two young daughters who now listen closely when an Ocrevus commercial comes on, trying to understand what the medication might mean for their dad. This is not a story about silver linings. This is a story about truth.

16 Apr 2026 - 32 min
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