S3_E17: Teresa, Jax Bourbon Social: The Power Behind the Pour and MS
Release Date: 07/18/2025
The Other Side of MS
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...
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"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...
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“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...
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This is the MS story people are not ready for. And that is exactly why you need to hear it. Tiffany opens up about the diagnosis that broke her plans, the marriage that had to be rebuilt, the faith that almost collapsed, and the moment she hit the floor and wondered if her family would be better off without her. This is not a polished MS story. This is the real one. Where to Find Tiffany Official Website: TikTok:
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In this Season 4 premiere, clinician and MS patient Selena shares her powerful story of navigating multiple sclerosis from both sides of care. She opens up about the early symptoms she hid, the fear and uncertainty of diagnosis, the grief of losing her former self, and the daily reality behind the phrase “no two days are alike.” Listeners will hear what MS looks like through the eyes of a medical provider, how cycling and community support her healing, and why talking openly about the “new normal” is essential for anyone living with MS. This episode offers real insight, real emotion,...
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Running Into MS with Ursula Forrester Ursula has always been a runner - marathons, half-marathons, and miles that measured more than distance. But in October 2014, after years of unexplained symptoms, she was diagnosed with multiple sclerosis. Suddenly, endurance meant something entirely different. She is a wife, a mother of two, and a professional in advertising who still chooses to see the glass half full. But behind that optimism lies the daily reality of MS modifying, compensating, and sometimes surrendering to the fatigue that doesn’t show up on finish line photos. Ursula and her family...
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Steve: From Trauma Nurse to MS Warrior Steve was 30 years old, working as a travel nurse in Idaho, when numbness crept up his leg and refused to go away. A ski accident had rattled his body, but what scans revealed was something else entirely: lesions on his brain and spine. In 2002, Steve entered a world he had once only witnessed from the other side of the hospital bed, the world of multiple sclerosis. As a trauma nurse, Steve knew the language of medicine. But living it was different. He walked away from graduate school, leaned on his family in Colorado, and began reshaping his life around...
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What Strength Really Looks Like Brad was diagnosed with MS at 45. Now 64, he’s a speaker, a cyclist, and a face of strength for others living with the disease. But behind the workouts, the travel, and the public optimism is a more complex truth—one that doesn’t always fit into a social media caption or a feel-good campaign. In this episode, Brad sits down for a different kind of conversation. One that doesn’t ask him to inspire, perform, or push through. Instead, we talk about the days he can’t move. The pressure to keep showing up. The identity that forms around always being the...
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School Dan - I do What I Can, When I Can, While I Can Dan has been a teacher for over 20 years, a school spirit leader, a cyclist, and a quiet force in his Florida community. His energy is infectious. His optimism is constant. But behind the vibrant classroom persona is a man living with relentless, invisible pain—and the pressure to never let it show. In this episode, Dan opens up about how MS has shaped every part of his identity, from the walking stick he once felt ashamed of to the pride that makes asking for help harder than it should be. He talks about the dual realities of living with...
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Teresa, Jax Bourbon Social: The Power Behind the Pour and MS Teresa Eichner is more than the co-founder of Jax Bourbon Social—she’s the relentless force behind one of Jacksonville’s most impactful fundraising events for the National MS Society. After a sudden MS diagnosis in 2016, Teresa’s world shifted. But instead of retreating, she channeled her decades of experience in PR and politics into advocacy, community-building, and bold visibility. In this raw, deeply honest conversation, Teresa opens up about the private cost of public recognition, the invisible weight of fatigue, and...
info_outlineTeresa, Jax Bourbon Social: The Power Behind the Pour and MS
Teresa Eichner is more than the co-founder of Jax Bourbon Social—she’s the relentless force behind one of Jacksonville’s most impactful fundraising events for the National MS Society. After a sudden MS diagnosis in 2016, Teresa’s world shifted. But instead of retreating, she channeled her decades of experience in PR and politics into advocacy, community-building, and bold visibility.
In this raw, deeply honest conversation, Teresa opens up about the private cost of public recognition, the invisible weight of fatigue, and what it really means to be the “well-spoken face” of MS. We talk about her diagnosis story—one of the fastest we’ve heard on this show—and how it unexpectedly brought her full circle to the MS Society. She also shares what it’s like to carry her symptoms quietly through a packed, sold-out fundraiser… all while smiling, organizing, and holding a DeWalt fan like it’s her fourth child.
We also ask a harder question: do glamorized events risk minimizing the brutal reality of MS? Teresa doesn’t flinch. And neither do we.
Whether you’re here for bourbon, boldness, or the bare truth—this one stays with you.
🎟️ Learn more or support the mission:
https://www.jaxbourbonsocial.com/event-details