The Other Side of MS – Details, episodes & analysis

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

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.