Explorez tous les épisodes du podcast The Other Side of MS

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 strong one—and what happens when that strength runs out.

We talk about guilt, body betrayal, and the silent fear of losing momentum. And we ask the questions that rarely get asked: Who sees you when the cape comes off? Are you helping others because it heals you—or because you don’t know how to stop?

This isn’t about overcoming. It’s about truth. And sometimes, the bravest thing you can do is admit how much it hurts.

Brad's Website: https://romptocurems.net/

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 a disease that makes him stronger while slowly wearing him down. And he shares the emotional cost of performing “School Dan” when “Real Dan” is quietly falling apart.

This is a story about vulnerability, not victory. About a man who shows up every day with humor, grit, and quiet dignity—even when it hurts. And a reminder that being strong doesn’t mean pretending you’re fine. Sometimes it just means telling the truth.

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 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

One Rider, One Team, One Million Dollars — Curtis’s Story

Curtis was diagnosed with multiple sclerosis in his twenties. What began as fear quickly turned into action. A chance connection to a support group sparked the creation of Team CCC — a cycling team that would go on to raise nearly $1 million for MS research and support. With every mile, Curtis has redefined what leadership looks like in the face of a chronic illness.

In this episode, Curtis reflects on the moment a fellow rider convinced him to try Bike MS, the early days of hiding his diagnosis, and how polka dot jerseys became a symbol of visibility and community. From forming a nonprofit to building a virtual cycling presence on Zwift, his story is one of purpose, persistence, and the power of showing up.

This is not just a story about reaching a milestone. It’s about choosing to turn a diagnosis into momentum — and inspiring others to do the same.

Help Curtis and Team CCC cross the $1 million finish line.
Donate now — 100% of proceeds support the National MS Society

S3_E15: At 17, Emma Thought Her Life Was Over

Emma Archuletta, from Utah, was diagnosed with multiple sclerosis in 2019 at just 17 years old. One day, she was preparing for high school graduation. The next, she was sleeping 20 hours a day, vomiting without explanation, and using a wheelchair. There was no slow decline—only confusion, fear, and the quiet thought that her life might already be over.

In this episode, Emma talks candidly about the chaos of her early diagnosis: missing senior prom, crawling up stairs, and finishing school from a hospital bed while juggling college-level coursework. She shares how her body became unfamiliar, how people questioned her because she “looked fine,” and how she built a dating rulebook to protect herself from rejection.

Now an elementary school teacher, Emma reflects on what it means to pursue a dream career while managing invisible symptoms. We talk about the fatigue that threatens her work, the cost of treatment, and the moments she’s chosen to live boldly—through surfing, snowboarding, and refusing to let MS define her.

This is not a story of triumph. It’s a story of persistence. A story of living with the unknown, and refusing to let it decide who you get to be.

The Art of Becoming — Hannah Garrison’s Story

Hannah Garrison was diagnosed with multiple sclerosis in 2017, but her journey started long before that; in the silence of being dismissed, the guilt of cultural and religious expectations, and the quiet ache of never quite feeling seen.

In this raw and intimate conversation, Hannah shares how MS forced her to confront not only her body, but her identity. We talk about the years she was misdiagnosed, the weight of family history with mental illness, and the internal battle between acceptance and perceived weakness. Through her art, Hannah found a place to be fully herself... messy, brilliant, and unfiltered.

We explore the clash between generational mindsets, the emotional toll of being “the sensitive one,” and what it really costs to make peace with a future others want you to fight. This is not a story of inspiration. It’s a story of truth, survival, and the kind of healing that begins when you stop trying to be who everyone else needs you to be.

If you’ve ever felt unseen, unheard, or quietly breaking — this episode is for you.

Hanna's Art:

• https://hannahbananashop.clued.xyz
• http://Www.hgarrisonart.com

W.T.F., I Have MS? — Chris Brown’s Story

Content Warning: This episode contains discussion of depression, alcohol misuse, and suicidal thoughts, which may be distressing for some listeners.

Just three months after being diagnosed with multiple sclerosis, Chris Brown sits down with us to talk about the weight of a life that hasn’t let up. He’s faced childhood trauma, infertility, the loss of triplets, depression, and addiction. And now, MS.

In this conversation, Chris shares what it’s like to process a life-changing diagnosis in real time. He speaks openly about fear, identity, fatherhood, and the quiet exhaustion of always having to adapt. He also talks about the choice to speak up, even when the path forward is still uncertain.

“If by hearing my story, it gives someone some hope… I feel like I have an obligation to do that.” — Chris Brown

This episode is not about closure. It’s about what it looks like in the middle of the storm.

Chris' MS Fundraiser: https://events.nationalmssociety.org/index.cfm?fuseaction=donordrive.participant&participantID=741869

Content Warning: This episode contains discussion of childhood trauma, depression, and suicidal ideation, which may be distressing for some listeners.

What happens when you spend your life holding it all together—only to realize it’s been breaking you inside?

In this powerful episode, Allie Schmidl shares what it meant to live in silence after her 2022 MS diagnosis—buried beneath shame, fear, and the weight of a lifetime of unspoken trauma. But MS wasn’t the only battle she was fighting.

We talk about the weight of vulnerability, the fear of being seen as broken, and what happens when even your body starts telling the story you’ve tried to silence. Allie opens up about surviving divorce, the ache of parental abandonment, and the quiet devastation of feeling invisible in your own pain.

“I was beating myself up a little bit over how I got to where I am… I felt like this was my fault.” — Allie Schmidl

But this isn’t just a story of darkness—it’s one of reckoning, healing, and choosing to be heard.

If you’ve ever felt unseen, unheard, or afraid no one would stay if they knew the truth—this episode is for you.

Before MS, Susie Wyss’s body was her job — a fitness instructor, powered by movement and strength. Then one morning, everything stopped. She woke up unable to walk. What followed was a long, painful journey through misdiagnosis, grief, and a complete redefinition of identity.

In this episode, Susie opens up about the moment she felt like a stranger in her own body, the invisible symptoms that linger even now, and the hard truth about how others see her — or don’t. We talk about the guilt of looking “normal,” the ache of feeling misunderstood, and what it really means to fight for hope when your body won’t cooperate.

Susie didn’t just build herself back — she built a 44-member Bike MS team that’s raised nearly $100,000. But this isn’t a story about fundraising. It’s about rebuilding. About letting go of who you were. About choosing to lead anyway.

Will Anthony Talk MS - A Podcast about Perseverance and Positivity

Before MS, Will Anthony built a life behind the chair — salon owner, jingle writer, entrepreneur. But MS didn’t just take his livelihood; it tested his faith, reshaped his identity, and led him to a new calling.

Diagnosed in 2008 after two years of believing he’d had a stroke, Will faced a reality he couldn’t pray or push away. And yet, he didn’t fold. In this episode, we talk about what it means to be a “positive person” when positivity isn’t always enough. We explore faith as an anchor — not a shield — and how Will’s relationship with God deepened through diagnosis, isolation, and loss.

Will is now an MS Ambassador out of Cleveland, Ohio, and the host of his own podcast, Will Anthony Talk MS, where he creates space for others to share their truth. His story is one of vulnerability, resilience, and spiritual clarity.

He doesn’t charge MS a dime for the empathy it never gave him — he offers it freely, just as he does in this episode.

🎧 Listen to Will Anthony Talk MS on YouTube: https://www.youtube.com/@WilliamSteward-m7y

Troy Mitchell spent 22 years as a U.S. Marine Corps officer—leading combat units, earning a doctorate, teaching graduate school, and chasing the next finish line.

Then came progressive MS. The goals changed. The gear changed. The silence got louder.

In this episode, Troy opens up about what it means to lose function but still lead, to be admired for your story while feeling invisible in your truth, and to carry the weight of independence when asking for help feels like failure. He talks about the collapse of his marriage, the conversations he doesn’t have with his son, and why pain in a combat zone was easier than pain that comes for no reason at all.

We cover the kind of ground that doesn’t fit in a résumé — the terrain of identity, masculinity, MS, and what it means to build a future from a life that’s already unraveled.

🎧 Listen now: Follow, like, and leave a review to help elevate voices like Troy’s.

💬 Share: Send this episode to someone who needs to hear it.

🚴‍♂️ Support Troy’s MS fundraiser: He’s riding in the Bluegrass Bourbon Ride to raise money for MS research and support.

Donate here:
 https://events.nationalmssociety.org/index.cfm?fuseaction=donate.participant&participantID=595746

Katie Heckert: mother, former litigator, top fundraiser—and MS warrior.

What happens when a sharp legal mind faces a disease that refuses to follow rules? In this episode of The Other Side of MS, Katie Heckert shares what it’s like to live with multiple sclerosis after having to step away from her career in litigation—not by choice, but by necessity.

She opens up about the relentless ache, the misdiagnoses, the frustration of being dismissed—and the resilience required to keep showing up as a mother, a wife, and a powerful voice in the MS fundraising community. Katie doesn’t sugarcoat her journey. But she doesn’t let it silence her either.

If you’ve ever wondered what MS really feels like—or what strength sounds like when it has nothing left to prove—this conversation is for you.

💛 If Katie’s story moves you, please consider supporting her personal Bike MS fundraiser for the PGA Tour: Bike to the Shore ride. Click here to donate directly. 100% of contributions go to the National MS Society.

As mentioned on the podcast: 

First Descents is a nonprofit organization that provides life-changing outdoor adventures for young adults impacted by serious health conditions, including cancer and multiple sclerosis. Their programs are specifically designed for people aged 18 to 39 (though they also have offerings for healthcare workers and older adults), and focus on using adventure-based experiences—like rock climbing, kayaking, and surfing—to build community, confidence, and emotional healing.

Most people wouldn’t expect a veterinarian to be deeply involved in the MS community—but that’s exactly what makes Dr. Deanna “Dee” Greer’s story worth hearing.

Dr. Dee, owner and Medical Director of Birch Island Veterinary Center in Jacksonville, Florida, has spent her career listening to those who can’t speak—animals in pain, suffering in silence. But it’s her personal connection through her husband’s former spouse, who lives with MS, that led her to become an annual donor to the National Multiple Sclerosis Society.

Her sponsorship of this episode isn’t advertising. It’s personal. Her contributions go directly to the MS Society—not this podcast—and her story is a reminder that compassion doesn’t have to come from shared diagnosis. Sometimes, it’s a choice.

In this episode, we also explore the science of empathy through the lens of veterinary medicine, including Dr. Dee’s reflections on the book Compassionomics, which examines how just 15 seconds of human connection can change clinical outcomes.

To learn more—or to match Dr. Dee’s generosity with a donation of your own—visit www.bike-ms.com and click the “Donate” button. 100% of all funds go directly to the National MS Society.

In this powerful episode of The Other Side of MS, Cori — a mother, advocate, and MS warrior — opens up about the grief, faith, anger, and invisible struggles that come with living two decades with multiple sclerosis.

She shares how her perspective has evolved over the years, the lessons her children are learning by watching her fight, and the moments she’s felt abandoned — by her body, by faith, and by those who just “don’t get it.”

Cori doesn’t sugarcoat the truth. She talks about the exhaustion of constantly having to explain herself, the vulnerability of visible disability, and the heartbreak of being seen only as a diagnosis.

If you’ve ever felt unseen in your MS journey — or want to understand what it really feels like — this is the conversation we need to have.

💬 Support Cori’s Walk MS Fundraising in Fort Wayne, Indiana:
Click here to donate or learn more

In this episode, we sit down with Zohra — a Korean and Algerian, first-generation American woman living with MS — to talk about the truth that doesn’t fit in a brochure.

This isn’t a highlight reel. It’s what it feels like to be praised for your strength while silently drowning in exhaustion. It’s the fear that if you open up, they’ll just call it complaining. It’s what happens when your body starts forcing you to step down from leadership—and you have no say in it.

Zohra has spent nearly two decades in education. She understands what empathy is supposed to look like—and what it feels like when it’s withheld. From the night she met the MS community for the first time in a piano bar… to the moments she keeps spare clothes at work in case her body won’t cooperate… Zohra doesn’t hold back.

This is the side of MS we don’t talk about enough. The invisible weight. The slow losses. The kids who notice more than adults. The humor that saves us.

If you’ve ever had to smile through something unspeakable—this episode will feel like a hand on your shoulder.

Moved by Zohra’s story?

Diagnosed with MS on her 10th wedding anniversary, Pam Grimes has spent the last three decades not just living with the disease—but showing up anyway. From raising three young kids while adapting to life in a wheelchair, to turning her entire neighborhood into a grassroots fundraising walk, Pam’s story is one of quiet resilience, fierce love, and unwavering purpose.

She doesn’t call herself a hero. But after listening to this conversation, you just might.

Pam also creates hand-embossed greeting cards—thoughtfully designed, dry embossed by hand, and bundled to raise funds for the National MS Society.

📬 Text Pam at 812-236-6233 to order 5 cards for a $25 donation. Every dollar supports MS research and services through the National MS Society.

She’s also hosting her own version of Walk MS on April 12th in her Indiana neighborhood—an inspiring local effort that brings friends, family, and neighbors together for a cause that’s deeply personal.

Want to support Pam’s MS fundraising? Text her directly to learn how you can donate or participate in this powerful community event.

What happens when your body betrays you—but you still show up like nothing’s wrong? In this unforgettable episode of The Other Side of MS, host Casey Murphy sits down with Becca, a Nashville nonprofit leader, yoga-lover, and corporate change maker who’s lived the invisible chaos of MS for the past two years.

But this isn’t your average “inspiring story.”

Becca talks about the diagnosis she never saw coming, the moments that broke her, and the parts of MS no one wants to say out loud—including how it’s reshaped her identity, her sex life, and her relationship with herself.

She shares what it’s like to run meetings while quietly negotiating with her bladder, why “you’re so strong” can feel like a slap, and what she would say if MS were a person sitting in front of her.

If you’ve ever wondered what resilience really looks like—or felt alone in your struggle—this episode will stay with you long after it ends.

🎙 Tap in. Listen close. You won’t forget Becca’s story.

🎁 Support Becca’s Bike MS fundraiser:
https://events.nationalmssociety.org/index.cfm?fuseaction=donate.participant&participantID=620049

A masterclass in storytelling and emotional depth, this episode of The Other Side of MS featuring Amber is a raw, unfiltered look at the realities of living with multiple sclerosis. Host Casey Murphy expertly guides the conversation, creating an environment where Amber shares her truth in a way that is both deeply personal and universally relatable.

The episode doesn’t just scratch the surface—it dives into the emotional complexities of **motherhood, resilience, and the unseen battles of MS**. Amber’s honesty, paired with Casey’s ability to ask the tough, thought-provoking questions, makes for an unforgettable conversation. This discussion is as powerful as it is necessary, challenging the listener to rethink their understanding of chronic illness and the human spirit.

What sets this episode apart is its balance—there’s vulnerability, but also strength; hardship, but also hope. And just when you think you know where the conversation is going, it takes a turn that forces both Amber and the audience to reflect on the deeper layers of **what it means to adapt, to fight, and to redefine true strength.**

This isn’t just another MS story—this is a conversation that will stay with you long after the episode ends. A must-listen for anyone who wants to understand MS beyond the diagnosis, beyond the medical jargon, and straight into the heart of what it means to live with it.

🌍 Amber’s Mission: We Are Illmatic Amber is a major supporter of We Are Illmatic, a movement dedicated to empowering those living with MS through awareness, advocacy, and community support. Focused on breaking stigmas and amplifying diverse voices in the MS space, We Are Illmatic serves as a powerful platform for education and inspiration.

📸 Follow Amber: Instagram: @weareillmatic

💰 Support Amber’s MS Fundraising:

• 👉 Donate to Team Illmatic
• 👉 Donate to Amber’s Personal Fundraiser

Welcome to Season 3 of The Other Side of MS podcast! In this episode, host Casey Murphy sits down with Jasmine Hanna, who was diagnosed with Multiple Sclerosis at 25.

Jasmine shares her raw and unfiltered story—from the terrifying first signs of MS to the daily realities of living with an unpredictable disease. Through resilience and advocacy, she has transformed her diagnosis into a mission to support others, connect with the MS community, and raise awareness through Bike MS.

This conversation explores the unseen struggles, the victories, and the unwavering determination that defines life with MS. Tune in for an inspiring discussion that redefines what it means to live boldly with a chronic illness.

In this inspiring episode of 'The Other Side of MS', Casey Murphy sits down with Carmen Lucia Gonzalez, a remarkable chef, author, and advocate who has been living with multiple sclerosis since her diagnosis at the age of 17. Carmen shares her powerful story of resilience, from overcoming childhood trauma to navigating the challenges of MS while pursuing a successful career in the culinary arts.

Carmen’s culinary journey has taken her through Michelin-starred kitchens, where she honed her skills before transitioning to developing allergy-friendly menus that continue to impact thousands of children today. Her book, Allergy Menus, Recipes, and Techniques, is a testament to her expertise and her passion for creating inclusive culinary experiences. Despite the obstacles she faces, Carmen continues to thrive, raising awareness about both multiple sclerosis and food allergies with a spirit of determination and hope.

This episode delves deep into Carmen’s life, exploring her courage, adaptability, and the lessons she’s learned along the way. It’s a must-listen for anyone seeking inspiration from someone who refuses to let MS define her.

Order her book on Amazon: Allergy Menus, Recipes, and Techniques

Join host Casey Murphy on 'The Other Side of MS' as we dive into a powerful and uplifting story of a relentless individual whose journey with multiple sclerosis inspires many. This episode features heartfelt interviews and testimonies from friends, family, and community members who celebrate our special guest's strength and determination.

Listen in to discover who our 'beacon of inspiration' is and witness a story that exemplifies courage, community, and the unwavering dream of a world free from MS. Don't miss this touching tribute that showcases true heroism and the impact one person can have on many.

To learn more about Karyn, please listen to her episode S2 / E7

Donate to Karyn's Bike MS Fundraiser 

Donate to Eric's Bike MS Fundraiser

Join host Casey Murphy on 'The Other Side of MS' as we delve into the inspiring journey of Joanne and Eric. Diagnosed with multiple sclerosis 16 years ago, Joanne's story is a testament to resilience, faith, and determination, supported unwaveringly by her husband Eric. As a passionate advocate and cyclist for Bike MS, Eric has raised significant funds for MS research. Together, they share their experiences, the challenges of living with MS, and the strength of their community. Listen in for heartfelt interviews, valuable insights, and the powerful message of hope and advocacy for a world free of MS.

In this deeply moving episode of 'The Other Side of MS', Casey Murphy engages in a heartfelt conversation with Kim, a source of inspiration and motivation for the Bike MS cause. Kim, who has been battling multiple sclerosis since her diagnosis shortly after high school, shares the profound impact of the disease on her life—from abrupt symptoms leading to severe physical challenges to the eventual stabilization of her condition through relentless determination and medical intervention.

Kim's journey is a powerful narrative of resilience, underscored by her marriage to Jim, who has been an unwavering support through the peaks and valleys of her MS journey. She reflects on the abrupt onset of her symptoms, the challenges of navigating life with a disability, and her commitment to advocacy and support for others facing similar battles. Kim's story is not just about the struggles; it's about the joys and triumphs, the strength of relationships, and the enduring hope for a cure. This episode encapsulates the spirit of those fighting MS, making it an essential listen for anyone touched by the disease or involved in the quest for its cure.

In this episode of 'The Other Side of MS', we are joined by the remarkable Daisy, who shares her deeply personal journey with multiple sclerosis (MS), which began in her early childhood. From her initial denial and fear of the diagnosis to embracing her challenges head-on, Daisy's story is one of courage and resilience. Despite the daunting relapses and the isolation felt from her peers and educators, she has risen above to advocate for understanding and support for those living with MS. Now pursuing a degree in communications, Daisy aims to be a voice for the disabled community, championing change and fostering hope. Her narrative isn't just about the struggles of living with MS but also about finding strength in adversity and the importance of community support. This episode is a testament to the human spirit's capacity to overcome and inspire, making it a must-listen for anyone seeking a dose of real-world courage and inspiration.

In the inaugural episode of 'The Other Side of MS', we talk with Dr. Vanessa Marion Collazo, a neurologist specializing in multiple sclerosis. Dr. Vanessa discusses the nature and types of MS, her journey into the field, and the ways she supports patients and caregivers. The episode also delves into the personal and societal impacts of the disease and offers valuable resources and advice for those affected by MS. Learn more about the complexities of MS and the latest advancements in treatment, along with heartfelt insights into the caregiving experience.

In this episode of 'The Other Side of MS', we talk with Leo Kreisel, a Navy veteran and devoted spouse of Heidi, the president of the North Florida chapter of the MS Society. Leo shares his experiences from his 24-year naval career, his supportive role within the MS Society, and his insights on managing both personal and professional sacrifices. Throughout the conversation, Leo reflects on his approach to volunteering, his admiration for Heidi's work, and the vital importance of community in dealing with MS. Highlights include Leo's thoughts on emotional resilience, family dynamics, and addressing misconceptions surrounding MS.

In this episode of 'The Other Side of MS', we talk with Shannon Abney, who was diagnosed with multiple sclerosis in 2006. Shannon shares her journey of navigating life with MS, from initial symptoms and misdiagnoses to finding the right treatment and support. Despite experiencing severe pain and challenges like trigeminal neuralgia, Shannon discusses her resilience, the support from her family, and her involvement in Bike MS. The episode underscores the importance of community, advocacy, and understanding in the fight against MS.

Donate to Maddi's Bike MS Fundraiser

In this heartfelt episode, Maddie, a second-grade teacher and single mom, shares her inspiring journey of living with multiple sclerosis (MS) since her diagnosis right before her 21st birthday. Maddie recounts how she transitioned from nursing school to teaching and managed the challenges of MS while still living a fulfilling life. She touches on the support she's received from friends and family, the significance of the Bike MS events where she found strength and community, and how she balances being a parent with the demands of MS. Drawing from her experiences, Maddie offers insights into setting personal boundaries, dealing with misconceptions, and maintaining a positive outlook despite her condition.

In this powerful episode of The Other Side of MS, we honor Linda Bushong-Reid — the extraordinary woman behind the Big Bananas Cycling Team, which has raised nearly $1.7 million for the National MS Society.

Alongside her husband Bruce, Linda has spent over a decade leading one of the top fundraising teams in the country — with relentless dedication, creative vision, and an unwavering heart for the cause. Known for her humility, strength, and quiet leadership, Linda proves that impact doesn’t always need a microphone to be heard.

This conversation takes you behind the scenes of the Bananas’ incredible legacy, from 150-mile bike rides to the annual silent auction that’s become a community institution.

Hosted by: The Big Bananas Cycling Team

Date: Monday, May 5, 2025

Time: 5:30 p.m. – 8:30 p.m.

Location: Mr. Chubby's Wings, 150 Valley Circle, Ponte Vedra Beach, FL

Over 250 incredible items from local merchants, restaurants, artists, and service providers — plus a 50/50 drawing! 100% of proceeds benefit the National Multiple Sclerosis Society, North Florida Chapter.

💬 Support Linda’s Mission:
Click here to donate to her fundraising page

• Linda’s evolution from rider to leader of a nationally recognized fundraising team.
• The origins of the Big Bananas and their nearly $1.7 million raised for MS research and support.
• Creative fundraising methods that blend joy, purpose, and community impact.
• Personal reflections on what drives Linda to keep going — and why she won’t stop until there’s a cure.

Get ready for an electrifying journey as we delve into the world of Bike MS with three dynamic National MS Society heroes! In this episode, Erika from the majestic mountains of Colorado, Sydney from the sunny beaches of Florida, and Ashley from the historic landscapes of Virginia, open up about the magic and mayhem behind organizing these monumental rides. Experience the powerful stories, personal connections, and unique regional flavors that make each Bike MS event a life-changing adventure. From overcoming obstacles to celebrating victories, our guests share their heartfelt passion for creating a world without MS. Whether you're a dedicated cyclist, an enthusiastic supporter, or simply curious, this episode will captivate and inspire you to join the movement. Hop on and ride with us as we pedal towards a future free from multiple sclerosis!

Join us for a special bonus episode of "The Other Side of MS," captured live amidst the exhilarating energy of the Bike MS Colorado event on June 29th and 30th. This unique installment features raw, brief interviews with four inspiring individuals directly from the route—sounds of the ride and all. Our guests include both "I Ride with MS" cyclists and supporters whose lives have been touched by MS, sharing their compelling reasons for riding and the impact of their efforts.

First, we meet Meg Stenson McCormick, a ten-time participant riding in memory of her late husband. Next, Andi Lewis discusses the significant personal and community support fueling his ride. Joey Maestas shares his emotional connection to the event, riding for both a family member and a friend's father who passed away during last year's ride. Finally, Gretchen Mitterer, a veteran of the MS community, reflects on the evolution of MS treatments and the powerful sense of community at these events.

Though each interview lasts only between 1-3 minutes, their stories are profound—highlighting the strength, hope, and solidarity of the MS community. Tune in to hear these voices of courage, resonating with the spirit of Bike MS and the collective stride towards a cure

• Donate to Meg Stenson McCormick
• Donate to Andi Lewis
• Donate to Joey Maestas
• Donate to Gretchen Mitterer

Resilience and Transformation: Deanna's Journey with MS

Explore the inspiring journey of Deanna, a long-time MS warrior whose life was reshaped by her diagnosis. From her early days as a competitive diver to confronting the life-altering challenges of MS while raising young children, Deanna’s story unfolds as a remarkable testament to resilience and transformation.

Discover how cycling brought rejuvenation to her life, the profound impact of community support, and the vital role of humor in navigating her darkest moments. This episode offers a deep dive into living fully despite chronic illness, providing hope and valuable insights for anyone affected by MS or interested in the resilience of the human spirit.

Navigating Life's Challenges: Schone's Journey with MS

In this heartfelt episode, we dive into the life of Schone, a biracial woman, single mother, and proud member of the LGBTQ+ community, who was diagnosed with MS in 2022.

Schone's journey is a testament to resilience and adaptability. From managing her MS symptoms to navigating her various identities, Schone opens up about the complexities and strengths that define her. She discusses her daily life, the emotional challenges of caregiving, and how she maintains a positive outlook despite the obstacles she faces.

Through candid conversations, Schone sheds light on the misconceptions and biases she encounters and shares her strategies for staying strong for herself and her daughter. This episode is a powerful reminder that while everyone's journey with MS is unique, the shared goal remains the same: to make MS a thing of the past.

Join us for an inspiring and eye-opening discussion that amplifies the voices of those living with MS and the communities that support them. Together, let's work towards a world where MS is nothing but a part of history.

Donate to Curtis: Bike MS Fundraiser

Curtis's Determined Path: Transforming an MS Diagnosis into a Mission

Join us as we explore the extraordinary journey of Curt, who turned his MS diagnosis into a powerful force for change. Discover how Curt's determination and passion led him to raise nearly $1 million for MS research through his team, CCC. From overcoming fears and misconceptions to building a vibrant community of support, Curt’s story is a testament to resilience and hope.

Tune in to hear heartfelt conversations, unexpected twists, and the relentless spirit that drives us all towards a world free from MS. Don't miss this episode – it's a story that will motivate and uplift you!

Donate to Debbie's Bike MS Event

Debbie Hamm, an MS advocate whose story is woven with threads of joy, challenge, love, and loss. As Debbie opens up about her life's tapestry, she shares poignant memories and heartfelt anecdotes that highlight her resilience and unwavering spirit. From her unexpected diagnosis shortly after the birth of her third child to her inspiring journey as a top fundraiser for MS, Debbie's narrative is a testament to the power of human connection and the indomitable will to make a difference.

Listeners will be deeply moved by Debbie's account of meeting Danielle, a fellow MS warrior whose legacy she promised to carry forward. The emotional weight of fulfilling this promise and the profound connections Debbie has formed along the way create a narrative that is both inspiring and heart-wrenching. Debbie's story is a powerful reminder that while MS may disrupt the body's internal connections, it cannot sever the meaningful relationships and communities that provide strength and support.

Tune in to hear how Debbie's advocacy has not only shaped her own life but has also had a lasting impact on those she meets. This episode is a celebration of courage, community, and the relentless pursuit of momentum in the face of adversity.

 Donate to Megan Weigel

Find an Integrative Health Practitioner

Get ready for a fun and insightful episode as we dive into the world of integrative medicine with Megan Weigel. Megan is a vibrant nurse practitioner and the founder of First Coast Integrative Medicine, bringing over 23 years of expertise in neurology and MS care.

In this episode, Megan takes us on her journey from conventional neurology to becoming a trailblazer in holistic health. She reveals how blending Eastern and Western medical practices can offer a comprehensive approach to managing multiple sclerosis. Learn about the latest research on anti-inflammatory diets, discover innovative lifestyle changes, and hear how Megan collaborates with other healthcare professionals to provide the best care for her patients.

But wait, there's more! Megan is also an avid cyclist with Team Spanish Beer, riding in Bike MS events to raise funds and awareness. Her passion for life and dedication to service shine through in every story she shares.

Join us for an engaging and enlightening conversation that challenges conventional thinking and showcases the transformative power of integrative medicine. Don't miss this special episode with the incredible Megan Weigel!

Tune in to an inspiring conversation with Duncan, a key figure at Bike the U.S. for MS. In this must-listen episode, Duncan recounts his transformative journey from casual cyclist to driving force behind cross-country rides that raise crucial funds and awareness for multiple sclerosis (MS). He shares compelling stories of the physical challenges and deep camaraderie experienced on the road, as well as the impactful community service projects that directly support those affected by MS. Duncan's dedication illuminates the powerful intersection of adventure and altruism, making this episode a profound testament to the human spirit’s capacity to inspire and enact change. Join us to hear a story of endurance, community, and hope.

• Bike the US for MS Website
• Donate to Bike the US for MS
• Bike the US for MS Instagram
• Bike the US for MS Facebook

Jill Eisenberg's Bike MS Fundraiser || Mike Tomlin's Bike MS Fundraiser

In this episode, we delve into the remarkable journey of Jill Eisenberg and Mike Tomlin, two pivotal figures in the Bike MS community whose dedication and efforts have been instrumental in the fight against multiple sclerosis.

Mike, a Navy veteran diagnosed with MS in 2007, shares his story of resilience and advocacy, while Jill, a top fundraiser, discusses her unwavering support and the profound impact of their friendship. Together, they've raised significant funds for MS research and support, highlighting the power of community and perseverance.

Join us as we explore their inspiring narratives, the challenges they've faced, and the passion that drives their commitment to making MS a thing of the past. Whether you're a seasoned cyclist, a family member, or anyone who shares the dream of a world without MS, this episode is sure to resonate with you.

Don't miss out on their insights, the upcoming Bike MS Chesapeake Challenge, and how you can support their efforts. Tune in for an uplifting conversation that underscores the importance of continued support and advocacy in the fight against MS.

Donate to Rob Farthing's Bike MS Fundraiser

In this episode, we are thrilled to feature Rob Farthing, a true beacon of hope and relentless fighter in the quest to end Multiple Sclerosis. Rob’s journey began unexpectedly when a search for a local bike ride turned into a profound commitment to Bike MS, ignited by his cousin Sharon Hundley's battle with the disease. Sharon, once wheelchair-bound by MS, now thrives in remission, fueling Rob’s passion to drive forward research and community support.

Rob shares his heartening story from cycling across scenic routes to mowing lawns for a cause. Yes, you heard it right—his unique fundraising initiative, Mowing for MS, showcases his creative and spirited approach to support the fight against MS. Over 17 years, Rob has not only pedaled with purpose but has also raised his fundraising goals to new heights, aiming for $20,000 this year, thanks to the unwavering support of his community.

Join us as Rob discusses the transformation of the Bike MS event format, his role as a self-appointed 'Ride Evangelist,' and the personal stories of resilience that motivate him every day. This episode isn’t just about a fight against a disease; it’s about the power of community, the strength found in personal connections, and the incredible impact of one man’s resolve to make a difference. Ride along with us and be inspired by a story where every pedal and every blade of grass cut brings us closer to a world free from MS.

Donate to William (Bill) Fitzgerald's Bike MS Fundraiser

In this episode, we delve into the story of Bill Fitzgerald, a renowned news anchor at WTVR CBS 6 in Richmond, Virginia, whose experience with his mother-in-law’s battle against Multiple Sclerosis propelled him into the heart of the MS advocacy movement. Since 2013, Bill has been an active participant in Bike MS, using his influence to raise awareness and support for the cause. As the annual emcee for the Bike MS: Colonial Cross Roads event and a host for the 2020 virtual year, he has played a crucial role in rallying the community and driving fundraising efforts. Bill shares insights into how his journey with MS advocacy began, the impact of his mother-in-law’s resilience on his commitment to the cause, and his unwavering resolve to contribute to finding a cure for MS, reflecting on the powerful legacy of love and determination she left behind.

Join Karyn's Team | Donate to Karyn's Bike MS Fundraiser

Get ready for an inspiring episode as we welcome Karyn Laterza, a phenomenal force in the MS community and the number one fundraiser for last year's Georgia Bike MS event. Karyn's journey with MS is a testament to her incredible resilience and dedication. Diagnosed in 2021, she didn't just face her challenges head-on; she soared above them, becoming a top 1% fundraiser nationally. Her story isn’t just about battling MS; it’s about leading the way in fundraising and advocacy, inspiring hope, and driving change. Today, Karyn continues to champion the cause, and you have the chance to be part of her journey.

Donate to MS Society | What is MS | Donate to Team Spanish Beer

Step into an extraordinary episode as we unveil the untold story of Jennifer Lee, a luminary in the MS community with 34 years at the National MS Society. This episode takes you behind the scenes with an insider's view, revealing the passion, challenges, and triumphs of a journey dedicated to conquering Multiple Sclerosis. Jennifer’s narrative offers a unique perspective, highlighting her ascent from an enthusiastic event coordinator to the influential role of Executive Vice President of Development. Get ready for an enlightening experience filled with inspiring tales, strategic insights, and the relentless pursuit of a world free of MS. This isn’t just any story; it’s a rare glimpse into the soul of the MS movement, shared by one of its most dedicated architects. Tune in to be moved, inspired, and connected to the heart of MS advocacy like never before.

Donate to Natasha's Walk MS Fundraiser

Join us for an uplifting journey with Natasha Acoff, an emblem of resilience and a dedicated MS advocate. In this episode, Natasha shares her life touched by MS, her triumphs as a mother and IT consultant, and her tireless advocacy efforts. Despite the unseen battles of fatigue and muscle spasms, her spirit remains unyielding. Natasha’s story goes beyond personal strength; it’s a tale of community upliftment and hope that resonates across her hometown of Tallahassee and beyond. Tune in for a heartfelt narrative that celebrates courage, fosters awareness, and envisions a future free from MS.

Check out WCTV Coverage, you may see someone you know! 🧡

Donate to Team Andy Panda's Bike MS Fundraiser

Andy's Story of Why he rode for MS

🎙️ Join us for a deeply moving episode as we honor the remarkable life and legacy of Andy Schmit, a beloved figure in the cycling community and a passionate advocate for those living with multiple sclerosis (MS). In this heartfelt conversation with Dawn, Andy's partner, we delve into Andy's extraordinary journey, his unwavering commitment to fundraising for MS, and the profound impact he had on everyone around him.

From his love for cycling to his dedication to supporting individuals with MS, Andy's story is one of resilience, compassion, and boundless generosity. Dawn shares intimate details of their life together, painting a vivid picture of Andy's vibrant spirit and enduring legacy.

Don't miss this poignant episode as we celebrate the life of Andy Schmit and the indelible mark he left on the world. Tune in for an unforgettable conversation filled with inspiration, love, and the enduring power of human connection.

Donate to Ted Corby's Bike MS Fundraiser

In this episode, Ted, a husband, father, pastor, and passionate MS advocate, shares his deeply personal experiences. Explore the impact of Ted's enduring friendship with Charlie, who faced an MS diagnosis, and how it influenced his understanding of spirituality, faith, and purpose. Discover the dedication Ted brings to MS advocacy through cycling and the significant role of music in his life. This thought-provoking conversation offers insights into resilience, camaraderie within Team Spanish Beer, and the inspirational narratives that unfold on the journey of living with MS. Tune in for a compelling exploration of spirituality and resilience with Ted Corby on The Other Side of MS.

Barbara Ungerman: Redefining Roots in MS Advocacy

• Donate to Barbara's 2024 Bike MS

As you immerse yourself in Barbara's story, you're not merely a listener, you're invited to join a movement. A movement fueled by the shared commitment to a world where MS no longer casts its shadows. Find inspiration in the unwavering determination of Barbara Ungerman and become part of a community dedicated to transforming the narrative surrounding MS.  In a world often marked by challenges, Barbara stands as a testament to the power of purpose and the indomitable spirit that can turn personal adversity into a force for global change. Join us in honoring Barbara Ungerman, a beacon of hope, resilience, and inspiration in the fight against MS.

Donate to Jessica's Bike MS Fundraiser: https://events.nationalmssociety.org/participant/Jessica-Nevens

Dive into an extraordinary narrative as Jessica opens up about her profound journey with multiple sclerosis (MS). This episode unravels the deep, untold story of Jessica's resilience, taking you through the intricacies of her life with MS.

Experience the raw and authentic challenges she confronts, from managing intrusive thoughts to reshaping relationships amidst a global pandemic. Jessica's candid reflections provide a unique perspective, unlike anything you've heard before.

Celebrate with her as she recounts transformative moments, including a solo trip to Disney and conquering a century ride in Bike MS. These victories exemplify Jessica's unwavering spirit, proving that life with MS is about triumphs as much as challenges.

As Jessica shares the evolution of her relationships, especially with her supportive husband, Martin, listeners gain profound insights into the emotional complexities introduced by MS.

This episode is a deep dive into Jessica's life, a testament to resilience, triumphs, and the unyielding spirit that propels her beyond the conventional MS narrative. Tune in for an intimate and unparalleled exploration of the human experience within the MS community

Welcome to a profoundly inspiring episode of "The Other Side of MS," where we explore the incredible journeys of Jill Eisenberg and Mike Tomlin—two indomitable spirits whose dedication to overcoming Multiple Sclerosis through cycling has not only transformed their lives but also inspired a community.

In this episode, Jill and Mike share their remarkable stories from the front lines of the Southeast Tour of Champions and delve into the emotional and physical challenges they've conquered. From the scenic routes of the Chesapeake Challenge to the heartfelt moments of camaraderie and triumph, their tales are a testament to the power of friendship and the human spirit in the face of adversity.

Join us as we uncover the depth of their experiences and the passion that fuels their commitment to the fight against MS. This isn’t just a conversation; it’s an invitation to witness the extraordinary impact of two people who refuse to let a diagnosis define their lives. Their journey is a beacon of hope and strength for everyone facing their own battles.

My Why

In this special episode, I step out from behind the curtain to share a deeply personal journey that led to the creation of this podcast dedicated to multiple sclerosis (MS). Join me as I reflect on the profound inspiration behind my passionate commitment to the cause and how it all started with a powerful connection to those affected by MS.

Donate to my Bike MS Fundraiser

On this remarkable episode, we introduce you to Jim and Carol Montgomery, two extraordinary individuals whose lives have been profoundly impacted by multiple sclerosis (MS). In a powerful narrative, Jim, a former Chicago Cubs draftee turned passionate MS advocate, shares his journey from the world of sports to becoming a tireless champion for MS awareness and public policy change. Alongside him is Carol, a multifaceted soul with a background in arts and finance, who brings a unique perspective to the advocacy landscape.

Their story unfolds as they discuss the challenges, fears, and the unexpected turns their lives took when MS entered the picture. But beyond personal trials, Jim and Carol are fervent advocates, tirelessly working to improve support, awareness, and access to treatment for the MS community. They candidly explore the hurdles they've faced in their advocacy journey and shed light on the ethical dilemmas they've encountered. Most importantly, they share their unwavering vision of a world where MS is conquered and the promise of groundbreaking treatments.

In this gripping episode, you'll witness the unbreakable spirit of two individuals who have dedicated their lives to making a difference in the realm of MS advocacy. Their story is a testament to the power of hope, resilience, and the pursuit of positive change.

• National Library of Medicine Article (2020 April; 37 [Suppl 1]: S18-S23):The Multiple Sclerosis Surveilance Registry: A Novel Interactive Database Within the Veterans Health Administration
• Science Tech Daily Article:  New Vaccine Can Completely Reverse Autoimmune Diseases like Multiple Sclerosis, Type 1 Diabetes, and Cron's Disease