The Other Side of MS, LLC

08/25/2025

🚨 New Episode of The Other Side of MS 🚨

Ursula didn’t just get diagnosed with MS.
She got diagnosed in the middle of running marathons.

October 2014. Two marathons. One month. And the words no runner, no mother, no woman wants to hear: You have multiple sclerosis.

Since then, Ursula has refused to shrink. She’s run 15 marathons. Raised $150,000 with her family’s race, The Mill Chill. Built Team Mighty Strong. And kept showing up — not as an “inspiration,” but as a woman learning to live with MS on her own terms.

This episode isn’t about medals or finish lines. It’s about what it costs to keep moving when your body betrays you, and why being “mighty strong” doesn’t mean being unbreakable.

🎧 Listen now: https://open.spotify.com/episode/4sOHB38DZcOWCUAblSRmyk?si=0dbc5e4a9e4c4b79

👉 Don’t just scroll by. Like, comment, and share — so more people see the truth behind MS.

The Other Side of MS · Episode

08/18/2025

🚨 New Episode Alert: The Other Side of MS 🎙️

Steve Clayton was just 30 years old when a ski accident uncovered something far more life-changing — multiple sclerosis. As a trauma nurse, he had spent years on the other side of the diagnosis. Now, he faced it himself.

In this episode, Steve shares what it means to live on both sides of MS: as the nurse who explains and the patient who endures. From reshaping his career to leading a Bike MS team that’s raised over one million dollars, his story is raw, real, and unforgettable.

🎧 Listen now on Spotify:
👉 https://open.spotify.com/episode/0x4iZFkMlFWdU5XwiYmUsw?si=4ce98301c05f4997

If Steve’s story resonates with you, please take a moment to like, comment, and share this episode. Every share helps amplify the voices of people living with MS.

The Other Side of MS · Episode

07/07/2025

New Podcast Episode released today:

At 17, Emma thought her life might be over.

She was weeks from high school graduation when everything changed — vomiting daily, sleeping 20 hours, and using a wheelchair without knowing why. Then came the MS diagnosis.

In this raw conversation, Emma shares the truth about missing prom, crawling up stairs, and finishing school from a hospital bed. She opens up about dating with MS, the cost of chasing dreams while chronically fatigued, and why she refuses to let this disease define her.

🎧 Listen to The Other Side of MS now on Spotify:
https://open.spotify.com/episode/76jUgivzgzX4A7nCEUODuV?si=0a1305e1aff74701

The Other Side of MS · Episode

07/02/2025

The Other Side of MS
NEW RELEASE: Episode 14 - The Art of Becoming — Hannah Garrison’s Story

🟠 https://open.spotify.com/episode/5YmIhlADk9SOtHDn1Gt2TG?si=31153935cb5849bd

When Hannah Garrison was diagnosed with MS in 2017, she didn’t just face a disease — she faced herself.

Raised with silence, perfectionism, and the weight of being “the sensitive one,” Hannah opens up about the years she spent dismissed, misunderstood, and quietly falling apart. In this raw and deeply honest conversation, we talk about everything — generational shame, disability acceptance, mental illness in her family, and how her art became a place to survive and finally be seen.

This isn’t a story about overcoming. It’s a story about becoming.
And it might be the most emotionally layered episode we’ve ever released.

The Other Side of MS · Episode

06/17/2025

🎙️ NEW EPISODE JUST DROPPED 🎙️

Allie Ann Marie didn’t just survive her MS diagnosis...she survived silence, shame, and the weight of a lifetime of unspoken trauma.

This is not an easy listen. But it’s a necessary one.

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

Allie’s story is raw, honest, and heartbreakingly human. She talks about divorce, abandonment, and the darkness that followed her diagnosis—and she shares what finally helped her begin to heal.
It’s one of the most emotionally powerful conversations we’ve ever released. I hope it finds the people who need it.

It’s one of the most emotionally powerful conversations we’ve ever released. I hope it finds the people who need it.

🎧 Listen now: https://open.spotify.com/episode/3LseCgCUxQlj2TvKUfg5wq?si=784c81d82d5e4b2f

The Other Side of MS · Episode

06/09/2025

💥 NEW: The Body She Didn’t Recognize
🎧 Listen to Susie Wyss and her story now → https://open.spotify.com/episode/33KXYLjXx7LMXDjmnrw4dE?si=a79da2c2bbbb4304

Before MS, Susie taught spin class. Her body was her identity.
Then one day, she woke up — and couldn’t walk.

This isn’t a story about “staying strong.”
It’s about losing everything you thought made you who you are — and choosing to start over anyway.

🧡 In this episode, Susie shares:
✔️ The truth about invisible symptoms
✔️ The guilt of “looking normal”
✔️ How she built a 44-member Bike MS team from rock bottom
✔️ What faith, fear, and fierce hope sound like when MS rewrites your life

👇 If you’ve ever had to start over — physically, emotionally, spiritually — her voice is the one you need to hear today.

💬 Drop a comment: What part of Susie’s story hits you the hardest?
🔁 Share this with someone who needs real talk about what MS really looks like.

The Other Side of MS · Episode

05/12/2025

Sometimes the person who shows up for MS isn’t the one living with it, but the one still carrying the weight of watching someone they loved struggle in silence.

Dr. Dee is a veterinarian. She treats patients who can’t tell her what hurts. And her husband’s former spouse lives with MS, a truth that changed both their lives forever.

This conversation isn’t about animals.
It’s about how compassion moves beyond diagnosis. How support doesn’t always come in expected ways.
And how the MS community includes not just those who live with it—but those who refuse to look away.

Listen today at: https://open.spotify.com/episode/1CUllXzZEtFltncOxjPAdS?si=4eff90af4af34b44

The Other Side of MS · Episode

04/13/2025

Another solo training ride gearing up for Bike MS in Kentucky mid June followed by Colorado two weeks after. We also have Wisconsin Georgia, and then our home ride here in Florida coming up later in the year.

You can see all of my rides on www.bike–ms.com. You can also listen to our podcasts by clicking the podcast link on the homepage. We have an amazing podcast coming up tomorrow with Zohra Cherif. Probably one of our most raw and most honest interviews we’ve done to date. It’s one you don’t wanna miss.

Check out Casey’s video.

04/07/2025

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’...

04/03/2025

Here’s my interview on The Buzz Daily News Network’s Legacy of Leaders show:
🎥 https://legacyofleaderstv.com/2025/shows/legacy-of-leaders/legacy-of-leaders-with-casey-murphy-of-the-other-side-of-ms-podcast/

Honestly… it wasn’t my best. I missed the chance to spotlight the incredible work of the MS Society the way I wanted. But I showed up, shared from the heart, and stayed true to why we do this. I’m out here sharing and caring — even when it’s not perfect.

Thanks for always having my back.

On "Legacy of Leaders," Morgan Yonge welcomes outstanding leaders to this uplifting and interesting show, filled with practical advice, personal experiences and tips for business leaders and aspiring leaders. This week, Morgan sits down with Casey Murphy of The Other Side Of MS - Podcast

03/31/2025

Becca’s Unfiltered Journey with MS 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 liv...