MS Michigan Man 64 Podcast

Living with MS: David's Journey from Diagnosis at 13. MS Warrior 61

distribution@podgo.io (Brian Wallace) — Wed, 30 Sep 2026 11:20:00 +0000

In this episode, David Velez shares his inspiring journey living with multiple sclerosis since the age of 13, discussing the physical, mental, and emotional challenges, as well as the importance of community and resilience.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

# Luis Greenleaf: A Journey Through MS and Love. MS Warrior #60

distribution@podgo.io (Brian Wallace) — Thu, 24 Sep 2026 12:00:00 +0000

In this episode, Brian interviews Louise Greenleaf and Don Greenleaf about her 47-year journey with multiple sclerosis, sharing insights on living with the disease, love, resilience, and creative expression.

keywords
Multiple Sclerosis, MS, resilience, love, caregiving, writing, mental health, chronic illness, inspiration, medical journey
key topics
Louise Greenleaf's 47-year journey with MS
The impact of MS on daily life and relationships
The role of love and support in managing MS
Creative outlets as mental health therapy
Medical history and treatment evolution for MS
The importance of positivity and resilience

takeaways
Love and support are crucial in managing chronic illness.
Creative expression can be a powerful mental health tool.
MS symptoms can flare up due to stress and other triggers.
Maintaining a positive outlook helps cope with severe disability.
Medical treatments have evolved, but early diagnosis remains key.

We also want to thank our sponsors - including our new sponsor Valiant! Look for merch coming soon and in the meantime you can pick up your 2026 football schedule t-shirts NOW at this link! https://shop.championscircleuofm.com/s/d39620

Knight's Steakhouse is also a sponsor and an Ann Arbor family-owned institution! Hail Media has and will be running events / livestreams at the downtown location at the corner of Liberty and Maynard across from the Michigan Theater! www.knightsrestaurants.com

And of course, ‪ @OLIPOP ! OLIPOP contains a functional ingredient blend and supports digestive health - a New Kind Of Soda!

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops. Listeners can get 20% off of orders at drinkolipop.com/GOBLUE ○ URL: drinkolipop.com/GOBLUE

Like and subscribe 👍 to the channel and join us on:
Facebook: www.facebook.com/hailmediagroup
Instagram: www.instagram.com/hailmediagroup
LinkedIn: www.linkedin.com/company/hail-media-group/
TIkTok: www.tiktok.com/@hailmediagroup
Substack: https://hailmediagroup.substack.com/
X / Twitter: https://x.com/hailmediagroup

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hail 〽️edia.
Our Stories.
Our University.
Our Team.
Go Blue!

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Living With MS: The Hardest Parts No One Talks About

distribution@podgo.io (Brian Wallace) — Thu, 17 Sep 2026 12:00:00 +0000

In this episode, Brian interviews musician Chris Hendricks about living with cerebral palsy, his journey in music, and how embracing vulnerability can lead to personal growth and community connection.

key topics
Living with cerebral palsy and its non-progressive nature
The role of music in personal development and expression
The importance of vulnerability and sharing stories
Building supportive communities through social media, especially TikTok
The significance of the Danny Awards and its impact on disabled artists
The value of embracing one's condition as a source of strength
The story behind the song 'Say Yes' and its message of hope
The influence of early life experiences and societal perceptions on self-identity

And of course, ‪ @OLIPOP ! OLIPOP contains a functional ingredient blend and supports digestive health - a New Kind Of Soda!

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops. Listeners can get 20% off of orders at drinkolipop.com/GOBLUE ○ URL: drinkolipop.com/GOBLUE

Special thanks to our newest sponsor A2 HomeGirl Real Estate Group/ EXP Realty: Sheri Weintraub is one of the top realtors in Ann Arbor. Her primary focus is working with UMICH parents on investment properties for current students

Like and subscribe 👍 to the channel and join us on: Facebook: www.facebook.com/hailmediagroup Instagram: www.instagram.com/hailmediagroup LinkedIn: www.linkedin.com/company/hail-media-group/ TIkTok: www.tiktok.com/@hailmediagroup Substack: https://hailmediagroup.substack.com/ X / Twitter: https://x.com/hailmediagroup

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hail 〽️edia.
Our Stories.
Our University.
Our Team.
Go Blue!

Subscribe to Hail Media for Michigan Football news, analysis, game reactions, Wolverines breakdowns, Michigan Basketball coverage, and more throughout the 2026 season.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Fighting MS Together: Stories of Strength and Resilience

distribution@podgo.io (Brian Wallace) — Wed, 9 Sep 2026 12:00:00 +0000

In this episode, Brian welcomes Tariq, known as Thrax on TikTok, to share his personal journey with multiple sclerosis (MS). Both men, touched by this chronic illness, find strength in their shared experiences, highlighting the importance of community and understanding.

The Diagnosis Journey

Tariq recounts the unsettling moments leading up to his MS diagnosis in 2013 at just 33 years old. He describes the strange symptoms that first alerted him to something being wrong, including a crooked smile and muscle spasms. After a series of misdiagnoses and tests, he faced the sobering reality of living with MS:

"They come back and they like, oh it's so sad, you know, it's like two or three doctor nurse and they clipboards and all that shit with their gowns on. And um, sorry, but you got uh multiple sclerosis..."

The fear of the unknown is palpable in his words, as he reflects on the confusion and anxiety that often accompany such a life-altering diagnosis.

Denial and Acceptance

Both Brian and Tariq share their struggles with denial after their diagnoses. Tariq admits:

"I was in denial for the longest time... I was still working and all of that shit, you know? So it didn't affect me enough to worry about it."

They discuss how the progression of the disease can sometimes lead to a false sense of security, masking the realities of living with MS until it becomes harder to manage.

The Power of Community

A significant theme emerges around the power of community, especially on platforms like TikTok. Tariq reflects on how sharing his story and hearing others’ experiences has been transformative:

"I learned more in the past twelve months on TikTok than I know in the whole thirteen years I had this internet."

Both men emphasize the importance of connecting with others who understand the daily challenges of living with MS, highlighting the support and insights gained through shared stories.

Understanding MS

Brian reflects on his own journey and how critical it is for those outside the MS community to understand the diverse experiences of individuals living with the diseas.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Navigating Life with MS: DJ Morgan's Journey. Ms Warrior #57

distribution@podgo.io (Brian Wallace) — Wed, 26 Aug 2026 12:00:00 +0000

In this heartfelt episode, host Brian welcomes DJ Morgan, a former Notre Dame football player, to share his inspiring journey after being diagnosed with multiple sclerosis (MS).

## A Shared Passion for Football

Brian and DJ bond over their experiences in college football, reminiscing about the thrill of playing at prestigious programs. DJ reflects on his time at Notre Dame, highlighting the incredible coaches and teammates that shaped his career. "My career at Notre Dame was amazing. I wouldn't trade it for anything," he shares. The conversation takes a personal turn as they discuss their diagnoses and the challenges that come with it.

## The Diagnosis Journey

DJ recounts the early signs of his MS, starting with vision issues that he initially dismissed. "I started to experience vision loss. It wasn't necessarily like my vision was gone, but it was like a constant glare in my left eye," he explains. After several consultations and tests, he received his diagnosis, which was a shock for someone so young and active. "When the doctor told me, I thought, okay, how do we fix it?"

## Insights and Support

Both Brian and DJ emphasize the importance of understanding MS and the shared experiences of those affected. DJ shares advice he received from others living with MS, such as the mantra "motion is lotion"—a reminder to stay active and keep moving.

## The Road Ahead

As they conclude their discussion, DJ reflects on his journey since diagnosis and how he remains hopeful and focused on managing his health. Brian and DJ's conversation shines a light on the resilience of those battling chronic illnesses and the importance of community support.

Through their stories, Brian and DJ aim to foster understanding and connection among those dealing with similar challenges. Their narratives remind us that while each person's experience with MS is unique, there is strength in shared stories and support.

---
To dive deeper into DJ's journey and hear more about his inspiring outlook, listen to the full episode of the MS Pishka Man64 Podcast.

@OLIPOP ! OLIPOP contains a functional ingredient blend and supports digestive health, making it an easy go-to when Chris wants something that fits his busy lifestyle.

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops. Listeners can get 20% off of orders at drinkolipop.com/GOBLUE ○ URL: drinkolipop.com/GOBLUE

● OLIPOP is also available in the soda aisle and with the chilled beverages at thousands of retailers nationwide, including Walmart, Target, Costco, Whole Foods, Sprouts, Publix, Meijer and more! FOLLOW US FOR MORE MICHIGAN STORIES!

Like and subscribe 👍 to the channel and join us on: Facebook: www.facebook.com/hailmediagroup Instagram: www.instagram.com/hailmediagroup LinkedIn: www.linkedin.com/company/hail-media-group/ TIkTok: www.tiktok.com/@hailmediagroup Substack: https://hailmediagroup.substack.com/ X / Twitter: https://x.com/hailmediagroup

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hail 〽️edia.
Our Stories.
Our University.
Our Team.
Go Blue!

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

How to Stop MS Flare Anxiety from Spiraling Into Panic. Matt Rowe Interview

distribution@podgo.io (Brian Wallace) — Sat, 22 Aug 2026 12:00:00 +0000

In this episode, Matt Rowe from Optimal Body, Optimal Minds shares practical tools and mental frameworks to manage stress and anxiety during MS flare-ups, emphasizing the power of awareness, breathing, and positive mental shifts.

key topics
The fight-flight-freeze response and its impact on MS symptoms
The importance of awareness and non-judgment of thoughts
Breathing techniques to calm the nervous system
The concept of stepping past despair with small steps
The role of community and support in mental health

takeaways
Becoming aware of negative thoughts can help re-engage the prefrontal cortex.
Deep breathing can quickly reduce fight-flight responses.
Small, incremental mental shifts lead to greater resilience.
Expressing and feeling emotions prevents them from persisting.
Community support lifts individuals and enhances recovery.

And of course, @OLIPOP ! OLIPOP contains a functional ingredient blend and supports digestive health, making it an easy go-to when you want something to fit your busy lifestyle.

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops. Listeners can get 20% off of orders at drinkolipop.com/GOBLUE ○ URL: drinkolipop.com/GOBLUE

● OLIPOP is also available in the soda aisle and with the chilled beverages at thousands of retailers nationwide, including Walmart, Target, Costco, Whole Foods, Sprouts, Publix, Meijer and more!

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hail 〽️edia.
Our Stories.
Our University.
Our Team.
Go Blue!

Subscribe for weekly Michigan basketball breakdowns, and comment below on which player development storyline you want us to cover next.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Navigating Pediatric MS: Erica's Journey with Frankie. MS Warrior #56

distribution@podgo.io (Brian Wallace) — Wed, 19 Aug 2026 12:00:00 +0000

In this episode, Brian interviews Erica, a mother of a pediatric MS patient, to shed light on pediatric multiple sclerosis, diagnosis, treatment, and the importance of community support. They discuss Frankie’s journey, mental health considerations, and how awareness can empower families facing similar challenges.

keywords
pediatric MS, multiple sclerosis, MS diagnosis, chronic illness, mental health, community support, MS awareness, treatment, pediatric neurology, living with MS

key topics
Frankie’s diagnosis at age 9 and his journey living with MS
The importance of early diagnosis and treatment in pediatric MS
Mental health considerations for children with MS and their families
The role of community support and awareness in managing pediatric MS

The medical process from symptoms to diagnosis and treatment options

The impact of MS on a child's life and how they cope
Advocacy and fighting for timely diagnosis and care

The significance of mental health assessments and ongoing support

And of course, @OLIPOP ! OLIPOP contains a functional ingredient blend and supports digestive health, making it an easy go-to when Chris wants something that fits his busy lifestyle.

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops. Listeners can get 20% off of orders at drinkolipop.com/GOBLUE ○ URL: drinkolipop.com/GOBLUE

Like and subscribe 👍 to the channel and join us on: Facebook: www.facebook.com/hailmediagroup Instagram: www.instagram.com/hailmediagroup LinkedIn: www.linkedin.com/company/hail-media-group/ TIkTok: www.tiktok.com/@hailmediagroup Substack: https://hailmediagroup.substack.com/ X / Twitter: https://x.com/hailmediagroup

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hail 〽️edia.
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Running Through MS: Cheryl's Inspiring Marathon Journey

distribution@podgo.io (Brian Wallace) — Tue, 11 Aug 2026 12:00:00 +0000

An inspiring conversation about resilience and advocacy in MS.

Cheryl's story is a powerful testament to resilience in the face of adversity. Diagnosed with Multiple Sclerosis (MS) in 2006, she didn't let the condition define her. Instead, she continued to pursue her passion for running, completing marathons even after her diagnosis.

## The Diagnosis Journey

Cheryl's symptoms began after an impressive marathon performance, with her arm feeling numb and painful. Initially dismissed as a sports injury, it took her ten months and multiple doctors before she received a definitive MS diagnosis. "I wish I didn’t have that whole ten-month span where MS was getting worse. I could have started on DMT ten months prior," she reflects.

## Advocating for Oneself

Navigating the healthcare system can be daunting, especially when faced with a chronic illness. Cheryl emphasizes the importance of self-advocacy, recounting how she pushed to see a specialist after her initial neurologist hesitated to diagnose her. "I'm just one of the hardest things for me is advocating for myself. I always say yes to everything. I don’t want any contradictions," she shared.

## Support from Loved Ones

Cheryl's journey was also shaped by her supportive husband, Brian, who learned alongside her and encouraged her to pursue her passion for running despite her diagnosis. "He supported me through all of my crazy ideas running these marathons," she said.

## The Role of Exercise

When discussing treatment options, Cheryl highlighted the importance of staying active. "I felt like I needed to take the daily injection because at least I'm doing something every day. I'm helping my body every day." Her experience underscores the evolving understanding of exercise as a critical part of living well with MS.

## Closing Thoughts

Cheryl's story exemplifies the strength and perseverance of those living with chronic illnesses. She reminds us that while the journey may be filled with challenges, it is possible to continue pursuing our passions and advocating for ourselves. To hear more about Cheryl’s inspiring journey and insights on living with MS, listen to the full episode of the MS Michigan Man64 Podcast.

And of course, @OLIPOP !

OLIPOP contains a functional ingredient blend and supports digestive health, making it an easy go-to when Chris wants something that fits his busy lifestyle.

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops.

Listeners can get 20% off of orders at drinkolipop.com/GOBLUE
○ URL: drinkolipop.com/GOBLUE
● OLIPOP is also available in the soda aisle and with the chilled beverages at
thousands of retailers nationwide, including Walmart, Target, Costco, Whole Foods, Sprouts, Publix, Meijer and more!

FOLLOW US FOR MORE MICHIGAN STORIES!
Like and subscribe 👍 to the channel and join us on:
Facebook: www.facebook.com/hailmediagroup
Instagram: www.instagram.com/hailmediagroup
LinkedIn: www.linkedin.com/company/hail-media-group/
TIkTok: www.tiktok.com/@hailmediagroup
Substack: https://hailmediagroup.substack.com/
X / Twitter: https://x.com/hailmediagroup

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hail 〽️edia.
Our Stories.
Our University.
Our Team.

Go Blue!
Subscribe for more Michigan football interviews, recruiting coverage, player stories, and conversations from around the Wolverines program.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Living with MS at 20: Gianna's Journey. Ms Warrior #54

distribution@podgo.io (Brian Wallace) — Tue, 4 Aug 2026 12:00:00 +0000

In this episode, Brian talks with Gianna, a 20-year-old recently diagnosed with MS, about her journey, treatment options, and the importance of community and mental health support.

key topics
Gianna's MS diagnosis at age 20
The journey from symptoms to diagnosis
Treatment options and early intervention
The role of family and community support
Mental health and coping strategies for young adults

takeaways
Early diagnosis can significantly impact treatment outcomes.
Community support, especially online, provides vital emotional aid.
Understanding MS helps reduce fear and stigma.
Living with MS requires adaptability and resilience.
Open conversations about mental health are crucial for chronic illness management.

This episode is also supported by OLIPOP.

OLIPOP contains a functional ingredient blend and supports digestive health, making it an easy go-to when Chris wants something that fits his busy lifestyle.

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops.

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hail 〽️edia.
Our Stories.
Our University.
Our Team.
Go Blue!

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

From MS Diagnosis to Stage Triumph: Kristin’s Inspiring Journey. MS Warrior 53

distribution@podgo.io (Brian Wallace) — Tue, 28 Jul 2026 12:00:00 +0000

Kristin shares her remarkable journey of living with multiple sclerosis, battling breast cancer, and returning to the stage as a professional opera singer. Her story highlights resilience, adaptation, and overcoming life's toughest challenges.

key topics
Kristin’s military service and MS diagnosis
Impact of MS on daily life and career
Breast cancer diagnosis and treatment decisions
The role of community and support networks
Adapting to physical limitations and returning to stage
The importance of healthcare choices and quality of life
The emotional and mental resilience required
Kristin’s future plans and ongoing journey

This episode is sponsored by Knight's Steakhouse with multiple locations in Michigan including the future home of Hail Media events, including livestreams from the downtown location at Liberty and Maynard across from the Michigan Theater! www.knightsrestaurants.com

This episode is also supported by OLIPOP.

OLIPOP contains a functional ingredient blend and supports digestive health, making it an easy go-to when Chris wants something that fits his busy lifestyle.

Grab an OLIPOP, settle in, and enjoy this episode of Go Blue Hoops.

You can also support us directly on our Patreon which will help us to continue to bring the best Michigan content your way! Not required, certainly appreciated. www.patreon.com/hailmediagroup

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Living with MS: Terry’s Journey from Diagnosis to Resilience

distribution@podgo.io (Brian Wallace) — Tue, 21 Jul 2026 12:00:00 +0000

In this episode, Terry shares his journey with MS from diagnosis to living with the disease, highlighting the importance of community, mental health, and resilience. Tune in to learn about the challenges and triumphs of managing MS and how support networks can make a difference.

drinkolipop.com/goblue for 20% off.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

How Brianna and Justin Navigate MS Together. Ms Warrior 51

distribution@podgo.io (Brian Wallace) — Tue, 14 Jul 2026 12:00:00 +0000

In this episode, Brianna shares her journey with MS, from diagnosis to managing symptoms and supporting her partner Justin. They discuss treatment options, mental health, and the importance of community and hope.

key topics
MS diagnosis and symptoms
Treatment options and medication journey
Mental health and therapy importance
Impact on careers and relationships
Role of community and social support
Hope and future outlook for MS patients

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Allie McGuire – The Reality Nobody Talks About. Ms Warrior 50

distribution@podgo.io (Brian Wallace) — Tue, 7 Jul 2026 12:00:00 +0000

In this episode, Brian interviews Allie, founder of Aware Now Media, about her journey living with MS, the importance of mental health, and her efforts to raise awareness through storytelling and media.

key topics
Allie's MS diagnosis story
The role of family and community support
The importance of mental health in chronic illness
The impact of storytelling and media in awareness
Building resilience and finding new purpose

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Living with MS: Marielle Dacquel’s Journey of Resilience. Ms Warrior 49

distribution@podgo.io (Brian Wallace) — Wed, 1 Jul 2026 12:00:00 +0000

In this episode, Marielle Dacquel shares her inspiring journey living with MS, the mental health challenges, and how she uses social media to raise awareness and support others. Discover practical insights and motivational stories that highlight resilience and community strength.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Danielle McNair Breaks Down Her Hardest Moment. Ms Warrior #48

distribution@podgo.io (Brian Wallace) — Wed, 24 Jun 2026 12:00:00 +0000

This episode features a heartfelt discussion on living with MS, the importance of community support, and the impact of trauma on autoimmune diseases. Guest Danielle shares her journey from diagnosis to managing MS while balancing family and mental health.

MS diagnosis journey
Impact of trauma on autoimmune diseases
Role of community support in chronic illness

Share your MS journey to raise awareness
Connect with supportive communities online
Prioritize mental health and seek support when needed

#MultipleSclerosis #MSAwareness #LivingWithMS #ChronicIllness #AutoimmuneDisease #MentalHealth #MSCommunity #InvisibleIllness #Resilience

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

From Diagnosis to Resilience: Joel's MS Journey. MS Warrior #47

distribution@podgo.io (Brian Wallace) — Tue, 16 Jun 2026 12:00:00 +0000

In this episode, Brian interviews Joel, a recent MS diagnosis recipient, sharing his journey from symptoms to diagnosis, mental health challenges, and strategies for coping and staying positive. They discuss the importance of community, mental health, and maintaining a fighting spirit.
keywords
MS, Multiple Sclerosis, mental health, diagnosis journey, coping strategies, community support, MS awareness, chronic illness, resilience, mental health therapy
key topics
MS diagnosis journey
Mental health and coping strategies
Importance of community and support networks

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Ms Warrior 46: Robert Anderson navigating the Hardest Days

distribution@podgo.io (Brian Wallace) — Wed, 10 Jun 2026 12:00:00 +0000

A Multiple Sclerosis diagnosis can change everything—but it doesn't have to define your future.

In this episode, Robert Anderson shares his journey following a recent MS diagnosis, discussing the symptoms that first raised concerns, the challenges of navigating uncertainty, and how he's choosing to fight back through exercise, mental resilience, advocacy, and community support.

Robert opens up about the emotional impact of hearing the words "You have Multiple Sclerosis," the importance of protecting your mental health, and why staying physically active has become a critical part of his strategy for living well with MS. He also discusses the role the online MS community has played in his journey, particularly through TikTok, where people living with MS share information, encouragement, and hope.

This powerful conversation explores what it means to take control after diagnosis, build a support system, and approach treatment with purpose and determination.

🔹 Robert's journey from symptoms to diagnosis
🔹 The mental health challenges of living with MS
🔹 Why exercise remains a key part of his strategy
🔹 The power of the TikTok MS community
🔹 Building a proactive and aggressive treatment plan
🔹 Finding purpose, resilience, and hope after diagnosis

Whether you're newly diagnosed, supporting a loved one with MS, or looking for inspiration from someone refusing to let adversity define his future, this episode offers valuable insight, encouragement, and perspective.

#MultipleSclerosis #MS #MSWarrior #MSJourney #MSCommunity #ChronicIllness #MentalHealth #Exercise #Advocacy #MSAwareness #HealthPodcast

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

What happens when you're diagnosed with Multiple Sclerosis at just 26 years old? Ms Warrior #45

distribution@podgo.io (Brian Wallace) — Tue, 2 Jun 2026 12:00:00 +0000

In this powerful episode, Brian sits down with Celiya Houston, an inspiring MS warrior from Alabama, to discuss her journey from diagnosis to building a meaningful, fulfilling life while living with Multiple Sclerosis. Celiya opens up about the early symptoms that changed everything, the emotional challenges that followed, and how she learned to navigate uncertainty with strength, resilience, and purpose.

This conversation goes beyond MS treatment and medication management. It's about mental health, finding your support system, adapting to life's unexpected turns, and refusing to let a diagnosis define who you are. Celiya shares how community support became a lifeline, why positivity is a daily choice, and how sharing personal stories can help break the stigma surrounding chronic illness.

Whether you're living with MS, supporting a loved one, or simply looking for an inspiring story of perseverance, this episode offers valuable insights, hope, and practical perspective.

What has helped you overcome life's biggest challenges? Let us know in the comments below.

👉 Subscribe for more conversations about Multiple Sclerosis, health, resilience, advocacy, and living life beyond a diagnosis.

KEY TOPICS:
00:00 Introduction
MS diagnosis and early symptoms
Mental health and emotional resilience
Community support and social connection
Treatment options and medication management
Personal growth and advocacy
Living a full life with MS

KEY TAKEAWAYS:
• MS doesn't define your future
• Community support is critical for mental wellness
• Resilience is built through adaptation and perspective
• Sharing stories helps reduce stigma and isolation
• Personalized treatment plans matter

#MultipleSclerosis #MSAwareness #LivingWithMS

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Finding Humor in MS: Eric Gile's Journey and Insights

distribution@podgo.io (Brian Wallace) — Tue, 26 May 2026 12:00:00 +0000

Living with MS, not dying with MS. 💙

In this powerful episode of MS Michigan Man 64, Brian sits down with stand-up comedian Eric to talk about life after an MS diagnosis at 49, the role humor plays in surviving difficult days, and how community can completely change the experience of living with chronic illness.

Eric opens up about his diagnosis journey, navigating treatment options, mental health struggles, resilience, and why creating content online became a form of therapy and connection for thousands living with Multiple Sclerosis.

“This TikTok is therapy for me.”

This conversation is honest, emotional, funny, and deeply human — showing how laughter, support, and perspective can help people keep moving forward even through uncertainty.

If you or someone you love is living with MS, this episode is a reminder that community matters, awareness matters, and hope matters.

🔔 Subscribe for more conversations about Multiple Sclerosis, health, resilience, and real stories from people navigating life with chronic illness.

👇 Share your experience in the comments:
How has community, humor, or support helped you through difficult health challenges?

#MultipleSclerosis #MSAwareness #ChronicIllness

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

How Listening Skills Can Transform Patient Care and Build Trust. MS Michigan Man Podcast

distribution@podgo.io (Brian Wallace) — Tue, 19 May 2026 12:00:00 +0000

Could your MS diagnosis be more manageable than you think? Discover how early intervention, personalized treatment choices, and lifestyle habits can dramatically slow disease progression—and improve quality of life. This episode with neurologist Dr. Brendan Bauer reveals the latest advances in MS care, including the groundbreaking drug Mavenclad, and explains why catching MS early is more critical than ever.

Brace yourself for a deep dive into the evolution of MS treatments over the past 30 years. Dr. Bauer shares insider knowledge on how turning points like MRI technology, early diagnosis, and high-efficacy therapies are transforming what it means to live with MS. You'll learn why innovative drugs are now achieving no evidence of disease activity in half of patients, and how new strategies aim to get even better results.

You'll discover:
How early diagnosis and aggressive treatment can reshape your MS journey
The role of diet, vitamin D, and lifestyle in managing autoimmune activity
Why the location and activity of lesions determine disability, not just lesion count
The importance of patient-doctor collaboration and listening in treatment success
How emerging therapies targeting specific immune cells are pushing the boundaries of MS care

If you're living with MS—active or progressive—or caring for someone who is, this episode offers hope and practical insights. Dr. Bauer emphasizes that catching MS early, staying active, avoiding harmful habits like smoking, and adjusting therapy based on personal response are the keys to a healthier, more active future.

Perfect for MS warriors, caregivers, healthcare providers, and anyone eager to understand the cutting-edge of neurological care. Don’t miss this chance to learn how the fight against MS is evolving—and how you can stay ahead of the disease.

Dr. Brendan Bauer is a neurologist at Mercy Health in Ohio, known for his patient-centered approach and expertise in MS management, with over 25 years of experience and a passion rooted in his family’s neurological legacy.
Get inspired to take control of your MS today—because the future of treatment is brighter than ever.

Be sure to like, share, comment and subscribe

#MultipleSclerosisAwareness
#MSTreatment
#EarlyDiagnosis
#NeurologyInsights
#ChronicIllnessSupport

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

My Most Honest Conversation About Living With MS.

distribution@podgo.io (Brian Wallace) — Wed, 13 May 2026 12:00:00 +0000

Former University of Michigan football player Brian Wallace shares his most honest conversation yet about living with Multiple Sclerosis (MS) for more than 20 years. In this powerful episode of MS Michigan Man 64, Brian opens up about the daily realities of MS, disability advocacy, accessibility challenges, mental health, and life after football.

Joined by advocate Christine Venrick, this conversation explores what people with disabilities experience every day — from mobility barriers and systemic inequality to the fight for dignity, inclusion, and policy change.

Brian’s story is about resilience, fear, strength, faith, perseverance, and learning how to keep moving forward even when life changes completely.

Whether you live with MS, know someone battling chronic illness, care about disability rights, or simply want to hear an honest conversation about overcoming adversity, this episode delivers a raw and emotional perspective that needs to be heard.

🏈 Topics Covered:
• Living with Multiple Sclerosis for 20+ years
• Former Michigan football player life after sports
• Disability advocacy and accessibility awareness
• Mental health and chronic illness
• Mobility rights and inclusion
• Systemic barriers facing people with disabilities
• Why representation and awareness matter
• Using sports mentality to fight through adversity

💬 Powerful Moments:
“Treat me the same as I was treated in football.”
“Mobility is a right, not a privilege.”

Time stamps and chapter titles:

[00:00] – The show opens with a poignant song about the confusion and desire for a "redo" that often accompanies a life-altering diagnosis.

[01:08] – Flipping the Script
Brian introduces the special episode, explaining that he is handing the reins over to Christine, an Alabama-based MS long-hauler he met on TikTok.

[04:19] – What Keeps You Going?
Brian shares that his passion for helping people—whether his kids, his fans during his Michigan football days, or inmates during his career in social work—is what fuels his drive to stay alive and positive.

[06:29] – Identity Beyond the Diagnosis
Brian emphasizes that MS does not define him. He is the same person who played for the University of Michigan & won four Big 10 championships; the diagnosis only changed how he has to live his life.

[08:27] – Resilience and the Michigan Mindset
Reflecting on his upbringing & his time in Ann Arbor, Brian discusses how the discipline and perseverance he learned on the football field prepared him for the physical & mental hurdles of MS.

[12:00] – The Power of the TikTok Community
Brian talks about how his daughter introduced him to the online MS community, which broke his isolation & taught him that everyone's journey with the disease is unique.

[14:53] – Aging with Comorbidities & Advocacy
A discussion on the challenges of aging with MS & the importance of being your own "team captain" & advocate when dealing with doctors.

[20:04] – The Mistake of Privacy
Brian reflects on his early years with the disease, admitting he initially tried to ignore it & hide it from others, a decision he now regrets & tries to correct through his podcast.

[24:26] – Facing the Fear of the Unknown
Brian & Christine discuss the inherent fears of the disease—like losing vision or mobility—& the mental strategies they use to prepare for "what ifs" without letting them consume the present.

[27:05] – Trauma & the "Activation" of MS
Brian looks back on how physical trauma (a car accident at 23) & the emotional stress of planning a wedding at 27 acted as the catalysts that brought his MS to the surface.

[34:21] – Pet Peeves: "You Don't Look That Bad"
Brian shares his frustration with people who dismiss the severity of the disease based on physical appearance, highlighting the many "invisible" symptoms like neuropathy & internal pain.

[37:08] – Deconstructing Disability
A frank talk about the 10-yr process Brian went through to accept mobility aids (canes, rollators, & wheelchairs) & how he eventually stopped caring about the stigma of using them.

[41:19] – Advice for the Newly Diagnosed: Prioritize Mental Health
Brian’s biggest piece of advice is to seek counseling or therapy immediately, as the mental toll of a chronic diagnosis is often more taxing than the physical symptoms.

[45:52] – The Gift of Empathy
Brian concludes that 29 yrs with MS has given him a deeper sense of compassion & empathy for others, teaching him to judge people by their hearts rather than their abilities.

[50:18] – The Final Question: A Life Well Lived
Closing with a reflection on what he hopes to hear at the "pearly gates," Brian expresses pride in his family, his career, & his time as a Wolverine.

Subscribe to Hail Media for athlete-led conversations, Michigan football stories, powerful interviews, and authentic discussions that matter.

#MultipleSclerosis #MSAwareness #MichiganFootball #DisabilityAdvocacy #UniversityOfMichigan #MSWarrior #ChronicIllness #MentalHealth #DisabilityRights #HailMedia

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

The Fight for Mobility Rights: A Conversation with Carmen Lucia Gonzalez.

distribution@podgo.io (Brian Wallace) — Wed, 6 May 2026 12:00:00 +0000

Accessibility, MS advocacy, mobility rights, and systemic inequality are at the center of this powerful conversation as Brian sits down with Carmen Lucia Gonzalez to discuss what everyday life looks like for people living with disabilities — and why real change starts with visibility, data, and action.

Please stay for the interview with David Lyons as well from Optimal Body / Optimal Mind who discusses commitment to getting started and continuing in the gym after you've been diagnosed with a chronic disease! https://optimalbody-optimalmind.com/

From navigating inaccessible spaces to pushing for policy reform, Carmen shares how disability advocacy is about more than awareness — it’s about dignity, independence, and equal access. This episode dives into the hidden barriers faced by people with MS and disabilities, the importance of collecting real-world accessibility data, and how community activism can drive meaningful infrastructure and policy change.

“Treat me the same as I was treated in football.”

“Mobility is a right, not a privilege.”

Those words frame a deeper conversation about inclusion, respect, and why accessibility impacts everyone — not just those living with disabilities today.

Brian and Carmen also explore:
• Accessibility challenges for people with MS
• Why data collection matters in disability advocacy
• How policy change happens through community pressure
• Mobility rights and systemic inequality
• Nonprofit initiatives creating real impact
• Building a more inclusive society through awareness and action

Here are your chapter time stamps and titles:

[00:00] – Opening & Introduction
The episode begins with the show's theme and Brian's personal story of being diagnosed with MS in 1997, just five years after playing for Michigan in the 1992 Rose Bowl.

[01:45] – Welcoming Back Carmen Lucia Gonzalez
Brian introduces Carmen, a fellow "MS Warrior" from Arizona, to discuss the major accessibility and mobility barriers they both face.

[03:11] – Accessibility Realities: NY vs. Arizona
Carmen describes the "culture shock" of moving from New York City to Tucson and the lack of respect and infrastructure for disabled individuals in her new home.

[04:52] – Introducing Project S.A.I.D.
Carmen details her new nonprofit, Systemic Accessibility Inequality Documentation (Project S.A.I.D.), which is collecting a year’s worth of data to present in Washington D.C. on July 26, 2030.

[07:08] – Real-World Barriers: Snow Mounds & Grocery Carts
Brian and Carmen discuss everyday frustrations, such as handicap spots being blocked by 12-foot snow mounds and the lack of motorized carts in stores.

[10:35] – Infrastructure & Policy Goals
A look at how Project S.A.I.D. aims to influence future architecture and city planning to ensure ADA standards are treated as a right, not a "bare minimum."

[16:25] – Miss Wheelchair USA & Global Advocacy
Carmen explains how she is using the Miss Wheelchair USA platform to expose mobility barriers and her plans to write a book on the least accessible cities in America.

[23:03] – The "Same Person": Identity Beyond Diagnosis
Brian reflects on the difference in how he was treated as a Michigan football player versus how he is treated now with a disability, emphasizing the need for simple human respect.

[26:44] – Special Feature: David Lyons on Fitness Mindset
David Lyons (Optimal Body Optimal Mind) joins the show to discuss the difference between "fleeting motivation" and "life-saving commitment" when starting a gym routine with a chronic disease.

[31:35] – Making Fitness a Necessity
The episode wraps up with a discussion on treating exercise like essential medication and how to build habits that stick for long-term health.

If you care about accessibility, disability rights, MS awareness, advocacy, public policy, inclusivity, or creating a society where everyone can move freely and safely, this conversation is essential viewing.

What changes do YOU believe would make society more accessible for everyone?

Subscribe for more conversations centered around leadership, advocacy, resilience, and impactful storytelling.

#Accessibility #MSAwareness #disabilityadvocacy

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #42 - Jen - MS BADASS

distribution@podgo.io (Brian Wallace) — Tue, 28 Apr 2026 12:00:00 +0000

Welcome to Hail Media I'm Brian Wallace, MS Michigan Man 64, Left Tackle for Michigan Wolverines 1988-1991. This is where a former Wolverine gets real about life after football - battles you don't see coming and training that prepares us to take everything on!

Ever felt like your life changed overnight? Here’s how I navigated a chronic illness diagnosis and why mental health matters.

Tag someone who needs to hear this! 💪

Living with multiple sclerosis has been a journey of ups and downs. After my diagnosis, everything I thought I knew about my life flipped. From being an athlete to navigating daily challenges, it’s been tough.

But here’s the thing: mental health is often overlooked in chronic illness discussions. It’s not just about the physical symptoms; the emotional toll can be just as heavy.

I wish someone had emphasized this when I first got diagnosed. It's crucial to find support, whether it's a therapist, a support group, or simply connecting with others who understand. You don’t have to go through this alone.

What’s your experience with mental health in chronic illness?

Let’s keep the conversation going. Check out the full episode in my bio for more insights on living with MS and the importance of mental wellness!

#ChronicIllness #MentalHealthMatters #MultipleSclerosis #MSWarrior #MindOverMatter

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Connect with Jen on TikTok:

https://www.tiktok.com/@_86_jen_86_?_r=1&_t=ZP-95v1NML1qdL

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

We also want to call your attention to Football Alumni of Michigan - an organization that we care deeply about. Follow them here at ‪‪‪ ⁨@michiganfootballalumni⁩ . FAM is a 501c3 nonprofit dedicated to mental health and assisting former Michigan team members with life's struggles after football, whether they are mental or physical. Division 1 football at the level we played it is brutal, and not all players come out of it in one piece. Visit www.michiganfootballalumni.org for more info and to make a tax-deductible donation.

#mswarriors #multiplesclerosis #chronicpain #chronicpainwarrior #chronicpainawareness #chronicpainsupport #chronicpain #multiplesclerosisawareness #multiplesclerosiswarrior #multiplesclerosisfighter #inspiration #inspirational #goblue #michigan #michiganfootball #michiganwolverines #universityofmichigan #wolverines #hailmedia #MentalHealth #mentalhealthawareness

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

Living with MS: MS Warrior #41 Quanta Dunn Is Building a Powerful Support Community

distribution@podgo.io (Brian Wallace) — Wed, 22 Apr 2026 12:00:00 +0000

Living with Multiple Sclerosis (MS) can feel isolating—but what if community is the key to navigating it?

In this episode of MS Michigan Man, host Brian Wallace sits down with Qunta Dunn to discuss his journey living with MS, the emotional toll of a chronic illness, and how building a strong MS support community can change everything.

This episode explores Multiple Sclerosis support, living with MS, MS mental health, MS awareness, and building a community for those navigating chronic illness.

Q shares how being diagnosed with MS at a young age shaped his life—and how it led him to create a 501(c)(7) social club designed to empower MS warriors through connection and shared experiences.

If you’re living with MS or supporting someone who is, this conversation is for you.

“You’re not in this alone.”

🔑 What You’ll Learn:
What it’s like living with Multiple Sclerosis
How MS impacts mental health
Why support networks are critical for MS patients
The power of shared experiences in chronic illness
How to build a community around MS
💬 Join the Conversation:

What has helped you most in your MS journey? Drop a comment below.

🔔 Subscribe for more:

Real conversations around MS, chronic illness, and mental health.

🔍 Keywords:

Multiple Sclerosis, MS support, living with MS, MS awareness, MS community, chronic illness support, MS journey, MS mental health, autoimmune disease support, invisible illness, MS advocacy

#MultipleSclerosis #MSAwareness #chronicillness

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

He’s Lived With MS for 20+ Years… and Still Rides 100 Miles

distribution@podgo.io (Brian Wallace) — Tue, 14 Apr 2026 12:00:00 +0000

Bradley Romp shares how he’s lived with multiple sclerosis for over 20 years while completing 100-mile cycling events and building a movement around resilience.

In this powerful multiple sclerosis interview, MS Michigan Man 64 host Brian Wallace sits down with Bradley Romp—founder of Romp to Cure MS—to break down what it really takes to live, train, and thrive with MS.

This episode dives into Bradley Romp’s journey living with MS, how he manages symptoms through fitness and discipline, and why he refuses to let multiple sclerosis define his life. From endurance cycling to daily mindset, this is a real conversation about overcoming adversity and pushing past limits.

👉 Check the pinned comment for the biggest takeaway from this conversation.

🔍 WHAT YOU’LL LEARN IN THIS VIDEO:
Bradley Romp’s multiple sclerosis diagnosis story
What it’s like living with MS for 20+ years
How fitness and cycling help manage MS symptoms
The mindset behind: “I define MS. MS does not define me”
His mission with Romp to Cure MS
Advice for anyone navigating multiple sclerosis
🎯 JOIN THE CONVERSATION

What’s the biggest challenge you’ve faced when dealing with adversity or health setbacks?
Drop your story in the comments 👇

📈 WHY THIS MATTERS

Multiple sclerosis impacts nearly 1 million people in the U.S. This conversation highlights how living with MS doesn’t mean giving up—it means adapting, fighting, and finding purpose through resilience and community.

🎙️ ABOUT THIS EPISODE

This is a podcast-style interview episode of MS Michigan Man 64, a Hail Media original series hosted by Brian Wallace, focused on real stories, awareness, and inspiration from those living with multiple sclerosis.

📌 SOFT KEYWORD STACK (SEO BOOST)

This MS Michigan Man 64 episode covers multiple sclerosis awareness, Bradley Romp interview, living with MS, MS motivation, MS fitness journey, Bike MS cycling story, overcoming multiple sclerosis, and managing MS symptoms through lifestyle and mindset.

🔗 RESOURCES & LINKS

Learn more about Bradley Romp: https://romptocurems.com/

National MS Society: https://www.nationalmssociety.org/

👍 SUPPORT THE CHANNEL

If you believe in stories like this:
👍 Like the video
💬 Comment your thoughts
🔔 Subscribe for more real conversations

📢 HASHTAGS

#MultipleSclerosis #MSAwareness #BradleyRomp

#LivingWithMS #MSJourney #MSMotivation #BikeMS #ChronicIllness #HailMedia

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #39 - Jenn - MS BADASS & discussion with Matt Rowe about Fight or Flight reaction to MS!

distribution@podgo.io (Brian Wallace) — Tue, 7 Apr 2026 12:00:00 +0000

Most newly diagnosed with multiple sclerosis feel overwhelmed by the diagnosis—until they hear the inspiring stories of those who refuse to give up. What if your mental resilience is just as critical as your medicine?
In this powerful episode, discover how Jenn, freshly diagnosed in 2025, turned her fear into strength by building an online community, embracing hope, and refusing to let MS define her.

Brian then welcomes Matt Rowe of Optimal Body Optimal Mind (https://optimalbody-optimalmind.com/) to discuss the mental side of the response to an MS diagnoses. Emphasizing the importance of not slipping into fear initially. Psychological support, consistent advocacy, and staying motivated despite setbacks. These raw stories highlight the often-overlooked mental health challenges that come with a chronic illness—and how addressing them especially at the moment of diagnoses can be a game-changer and an opportunity for the medical community.

You’ll uncover:
The critical first steps to manage the mental shock after diagnosis
Practical strategies for maintaining hope and motivation when life changes suddenly.

How community, whether online or offline, becomes a lifeline for resilience
Why mental health support is essential—even when medication is prescribed
The importance of proactive self-care, exercise, and mindset shifts for enduring the fight.

Now more than ever, understanding the mental side of MS is vital; neglecting it risks prolonging pain and losing hope. This episode is perfect for newly diagnosed patients, caregivers, or anyone seeking encouragement to turn setbacks into strength.

Whether you're just starting your journey or looking for that extra push, you'll find actionable insights and hope here. Never fight alone—your strongest weapon is your mindset.

#MSAwareness #MentalHealth #ChronicPain #Michigan #mswarrior

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find Brian on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

We also want to call your attention to Football Alumni of Michigan - an organization that we care deeply about. Follow them here at @michiganfootballalumni . FAM is a 501c3 nonprofit dedicated to mental health and assisting former Michigan team members with life's struggles after football, whether they are mental or physical. Division 1 football at the level we played it is brutal, and not all players come out of it in one piece. Visit www.michiganfootballalumni.org for more info and to make a tax-deductible donation.

#mswarriors #multiplesclerosis #michigan #hailmedia #mentalhealthawareness

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

MS Michigan Man 64 Announcement: Partnership w/David Lyons & Matt Rowe of Optimal Body Optimal Mind!

distribution@podgo.io (Brian Wallace) — Wed, 1 Apr 2026 12:00:00 +0000

Join Host Brian Wallace, MS Michigan Man 64, Left Tackle for Michigan Wolverines 1988-1991. This is where a former Wolverine gets real about life after football - battles you don't see coming and training that prepares us to take everything on!

Ever felt like your MS diagnosis is a dead end? 🚫 It doesn’t have to be! Here’s how we’re rewriting the narrative:

Tag someone who needs to hear this!

We’re thrilled to announce our partnership with Optimal Body, Optimal Mind! 💪 Together, we’re on a mission to empower those with MS. Visit David Lyons and Matt Rowe at https://optimalbody-optimalmind.com/

It’s not just about exercising; it’s about creating new neural pathways and training your mind and body to work together.

If you’re feeling stuck, remember: it’s never too late to start. Whether you’re in a wheelchair or just starting your journey, small improvements are possible every single day!

Here are your chapter time stamps and titles:

[00:00] – Intro & Expansion of the Mission
Host Brian Wallace shares his journey from starting the podcast to his upcoming speaking engagement at an MS Summit in Louisville this May.

[00:38] – New Schedule: Moving to One Episode per Week
To balance his increasing public speaking and community work, Brian announces that the podcast will now release one high-quality episode weekly.

[01:05] – Partnering with David Lyons & Matt Rowe
Introducing the founders of Optimal Body Optimal Mind, two fellow athletes living with MS who are joining forces with Hail Media.

[02:24] – Beyond Basic Exercise: Training the Nervous System
David Lyons explains why traditional exercise isn't enough for MS; the focus must shift to creating neural pathways that allow the body to overcome physical limitations.

[03:19] – From Paralysis to Squatting 500 lbs
David shares his incredible recovery story and explains the "winning combination" of mindset and specific muscle-nerve connection training.

[04:02] – The Science of Rewiring Neural Pathways
Mindset expert Matt Rowe breaks down the biology of "rerouting" signals around brain lesions using consistency, focus, and repetition.

[05:40] – Leading Your Nervous System
A deep dive into why training the brain to communicate with the muscles is like fixing the wiring in a house to restore mobility.

[07:32] – The Athlete’s Mentality vs. MS Training
Brian reflects on his time playing football and how he had to shift his "Michigan weight room" mentality to a more specialized approach for his health.

[08:33] – Built by the MS Community, for the Community
The partners discuss their shared "fact of hope" and why being athletes who actually live with MS makes their approach different from traditional physical therapy.

[10:20] – Better or Worse: The Michigan Coaching Philosophy
Applying a classic Bo Schembechler-era question to health: "Did you get better today or did you get worse?"

[11:13] – Accessibility: Training from a Wheelchair or Walker
Addressing the fear of being "too disabled" to start, David and Matt explain how their methods adapt to any level of progression.

[12:12] – Monthly Collaboration Announcement & Outro
Brian reveals that Optimal Body Optimal Mind will now feature in monthly video segments to help spread awareness and support.

Let’s keep pushing forward and supporting each other.

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

#mswarriors #multiplesclerosis #chronicpain #multiplesclerosiswarrior #goblue #michigan

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #38 - Amanda- MS BADASS

distribution@podgo.io (Brian Wallace) — Sun, 29 Mar 2026 12:00:00 +0000

Ever wondered how one diagnosis can lead to another? Meet Amanda, from Kentucky, a cancer survivor navigating life with MS and NMO.

Tag someone who needs to hear this! 💪

Amanda's journey is a testament to resilience. Diagnosed with cancer, she faced immense challenges, only to discover that her health issues were far from over. From panic attacks to numbness, she fought through doctors’ doubts and misdiagnoses to finally receive the clarity she needed. Her story sheds light on the hidden complexities of autoimmune disorders, and how trauma can reveal deeper health issues.

Let’s remember: our bodies are resilient, but they need our understanding and attention.

What’s your experience with health challenges? Share below!

Full episode - link in bio.

#MSAwareness #CancerSurvivor #AutoimmuneJourney #NMO #HealthAwareness

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Connect with Amanda on TikTok:

https://www.tiktok.com/@dickinsonamanda83?_r=1&_t=ZP-9562VZtJBa3

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #37 - Dan and Jennifer - MS COUPLE

distribution@podgo.io (Brian Wallace) — Wed, 25 Mar 2026 12:00:00 +0000

Jennifer and Dan, from Michigan, share their powerful journeys with MS. From diagnoses that shook their worlds to finding love and support in the community, they inspire us to keep going.

Living with a chronic illness isn't easy, but it’s about resilience, support, and advocating for yourself. Jennifer's story of battling MS since 1997 and Dan's journey since 2000 show us that even amidst struggles, there's hope and strength to be found.

Remember, you're not alone in this fight. Surround yourself with support and keep pushing forward.

Want to dive deeper into their stories? Full episode link in bio!

#MSWarriors #ChronicIllness #MultipleSclerosis #LoveAndSupport #GoBlue

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Connect with Dan and Jennifer on their social media:

https://www.facebook.com/share/18BV8j3RTq/?mibextid=wwXIfr

https://acoupletakesonms.com/?fbclid=IwVERDUAQvw-hleHRuA2FlbQIxMABzcnRjBmFwcF9pZAo2NjI4NTY4Mzc5AAEesSpcOMK2X0i8ibgE1V4tIFsk895zR1IXaFevXy2wr8_FdVQGa6jVDuc3D6g_aem_oRMN1eYAJ2eb30znwSDt-A

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #36 - Karen - MS BADASS

distribution@podgo.io (Brian Wallace) — Sun, 22 Mar 2026 12:00:00 +0000

Karen, from Florida, was diagnosed with MS in 2008 after experiencing numbness in her face and leg weakness.

When Karen was diagnosed with MS, she felt a whirlwind of emotions. Karen had been aware of MS through my mom's work with the MS Society, but hearing it for herself was surreal. Instead of letting it defeat her, Karen asked: "What does this mean for me?"

It's easy to get caught up in the physical challenges, but the mental battle is just as crucial. I learned that every morning is a new chance—some days are harder than others, but I choose to make each day count!

Finding support, whether from family or communities like MS Together We Help Each Other, has been a lifeline. We need to talk about mental health as much as our physical health. It’s a journey, and we’re not alone in this.

What’s your take on navigating these challenges? Let’s chat below!

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Connect with Karen on her FaceBook group MS-Together We Help Each Other

https://www.facebook.com/share/g/1CdzR9ktru/?mibextid=wwXIfr

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #35 - Kelly - MS BADASS

distribution@podgo.io (Brian Wallace) — Tue, 17 Mar 2026 12:00:00 +0000

Kelly, from Florida, shares her long road to an MS diagnosis in 2010 and the relief that came with it. After years of battling symptoms and visiting countless doctors, she finally found clarity with a diagnosis. It wasn’t just about understanding her physical symptoms; it was about reclaiming her life.

Kelly’s journey took a pivotal turn when she learned about low-dose naltrexone (LDN) from a nurse during a visit. LDN acts as an immune modulator and pain management solution, which intrigued her.

This story highlights the importance of advocacy in healthcare. Kelly's experience shows how crucial it is to keep pushing for answers and to not settle for vague explanations.

Sometimes, the path to understanding our health can feel overwhelming, but it’s a journey worth taking. What’s your experience with seeking a diagnosis?

#MultipleSclerosis #ChronicIllnessWarrior #MSAwareness #HealthAdvocacy #Podcast

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Connect with Kelly on her social media:

https://www.facebook.com/share/16coFfQ49f/?mibextid=wwXIfr

https://www.facebook.com/share/1ApXAKbq3c/?mibextid=wwXIfr

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #34 - Sunshine - MS BADASS

distribution@podgo.io (Brian Wallace) — Mon, 16 Mar 2026 12:00:00 +0000

In this episode, Sunshine, from California, shares her raw experience of being diagnosed with MS at a young age, 20, and how she faced the unknown in 1995. The struggles of understanding a chronic illness while juggling life as a young mom are real and relatable.

Her story highlights the importance of mental strength and the power of community support.

Join us as we dive deep into the emotional and mental health aspects of living with MS. Remember, you’re not alone in this fight.

#MultipleSclerosis #ChronicIllness #MSAwareness #HealthJourney #Inspiration

Connect with Sunshine on TikTok :

https://www.tiktok.com/@msunmuted.official?_r=1&_t=ZP-94i5Nza6j30

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #33 - Vik - MS BADASS

distribution@podgo.io (Brian Wallace) — Tue, 10 Mar 2026 12:00:00 +0000

Today I'm talking with Vik, an MS warrior from the UK. We talk about the journey of coping with a chronic illness, the importance of support systems, and practical strategies for managing health challenges.

When Vik received her diagnosis in 2011, she felt as if her life was over. Her initial reaction was filled with fear and uncertainty, a common response among newly diagnosed individuals. She recalls thinking, "That's it, I'm finished," as she grappled with the overwhelming information available online.

Vik's experience with disease-modifying therapies (DMT) is a testament to the importance of being proactive and engaged in your treatment. She was initially prescribed **Tysabri**, which, while effective, came with its risks. Understanding the balance of potential benefits and side effects is crucial.

Mental health is an essential aspect of living with MS that often gets overlooked. Vik candidly discusses her struggles and the importance of finding coping strategies during tough times. Engaging with the MS Society helped shift her perspective and provided her with resources and community support.

Living with MS poses unique challenges, but it also offers opportunities for growth, resilience, and community support. By understanding your diagnosis, building a solid support system, and engaging actively in your treatment, you can navigate this journey with strength and hope. Remember, MS is just a part of your story—not the whole narrative.

Connect with Vik on TikTok :

https://www.tiktok.com/@vikb816?_r=1&_t=ZP-94a0bg0TbA6

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on these social media platforms:

https://www.tiktok.com/@msmichiganman64?_r=1&_t=ZP-94Zzr9lDHyg

https://www.facebook.com/share/18YNrBxYQF/?mibextid=wwXIfr

https://www.instagram.com/msmichiganman64?igsh=MXVma2p3emQzaDg0ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #32 - Jen - MS BADASS

distribution@podgo.io (Brian Wallace) — Sun, 8 Mar 2026 12:00:00 +0000

Today I'm talking with Jen, a return MSer I recorded with in episode 89 of my original channel before I partnered with HailMediaGroup. Jen was diagnosed in 2023 and was forced to file for disability and she wanted to talk about her experience.

Ever felt like the system is working against you? Jen's journey with MS and disability is a powerful reminder.

💪 Tag someone who needs to hear this!

Navigating life with a chronic illness can feel like an uphill battle. Jen was diagnosed with MS just three years ago, and her fight isn’t just with the disease, but also with the bureaucratic maze of disability claims.

From misunderstandings about her condition to the challenges of the hearing process, Jen’s story sheds light on the frustrating reality many face.

It’s not just about the paperwork—it’s about the human experience behind it. Every denial, every appeal, it all adds up to a journey that can be overwhelming.

But Jen's resilience is inspiring. She reminds us that sharing our stories can create awareness and support for those in similar situations.

What have you learned from your own battles?

#MSAwareness #ChronicIllness #DisabilityJourney #Inspiration #FightBack

Jen's first episode with me was episode 89 of my channel. Click here to listen:

https://youtu.be/AYo0QZC1bYg?si=Vf-a1JnMr4Td-vhY

If you would like to donate to Jen's GoFundMe click link below:

https://gofund.me/e89c3c7eb

Connect with Jen on her social media:

https://www.facebook.com/share/1HQNNDVjwA/?mibextid=wwXIfr

https://www.tiktok.com/@thesultrywhisperer?_r=1&_t=ZP-94Wo5pQ00J4

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on these social media platforms:

https://www.facebook.com/share/18CHDKvi43/?mibextid=wwXIfr
https://www.tiktok.com/@speakinglifewithtasha?_r=1&_t=ZT-94JShES0fJG

https://www.instagram.com/life.spoken.tasha_?igsh=MTQwMDY3cmp6dGZ5ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #31 - Dhata - MS BADASS

distribution@podgo.io (Brian Wallace) — Tue, 3 Mar 2026 12:00:00 +0000

Today I'm talking with US Army vet, Dhata, from Georgia diagnosed with MS in 2008 after experiencing numbness and tingling in 2005 during a two mile Army fitness test and his legs turned to jelly. Dhata also had just been bitten by a spider so his first thought was a reaction to the spider bite. After a few weeks of researching the symptoms he realized it probably wasn't from the bite so he started to see specialists that finally told him he had MS.

Dhata explains how he felt elation from being told he had a chronic disease because he finally had an answer after three years of seeing doctors.

We discussed how the diagnosis affects our mental health and how it's not addressed at the diagnosis.

Dhata talks about his DMT journey and how he struggled with finding one he could tolerate and how he participated in an auto injector study for Avonex when it first came out.

In 2011 Dhata stopped working because of MS and filed for disability as an auditor. He then started to take care of his health and got dental implant surgery because of periodontal disease he suffered with. Post surgery within 6-12 months Dhata started to see amazing improvements that he was able to go back to work.

We also talk about how Dhata investigated gut health after going through a gastric sleeve procedure to improve his health. He explains how he dove deep into researching H pylori and the effects on MS.

Dhata talks about his research paper encouraged to get published by his gastric sleeve surgeon Dr Charlie Proctor that is currently going through peer review to be published.

A ton of great information from an MSer that has done the research on his own journey with MS.

Connect with Dhata on his social media:

https://youtube.com/@usvsms?si=vURJ1CMEFRjZOr-P

http://www.enitiative.org/

https://www.facebook.com/share/14Wcjx6YbcW/?mibextid=wwXIfr

https://www.instagram.com/theenitiativegroupinc?igsh=MTQwbThoZm41ZTU1cg==

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on these social media platforms:

https://www.facebook.com/share/18CHDKvi43/?mibextid=wwXIfr
https://www.tiktok.com/@speakinglifewithtasha?_r=1&_t=ZT-94JShES0fJG

https://www.instagram.com/life.spoken.tasha_?igsh=MTQwMDY3cmp6dGZ5ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #30 - Tasha - MS BADASS

distribution@podgo.io (Brian Wallace) — Sun, 1 Mar 2026 12:00:00 +0000

Today I'm talking with Tasha from Utah, diagnosed with MS in 2021 but actually had symptoms back in 2003 that went undiagnosed for almost 20 years. Tasha explains how she was diagnosed with optic neuritis at the age of 17 but multiple sclerosis was never brought up.

Tasha explains how she had multiple MRI's leading up to her diagnosis but never the for the spine which is where her lesions were that took her ability to walk in 2020 leading to the MS diagnosis in 2021.

Tasha explains how she was told by doctors for almost 20 years that her symptoms were mental and not believing what she was telling them about her body.

We discuss what Tasha knew about MS and how she learned about her new diagnosis and the struggle she hsd getting medical professionals to help her.

We discuss her DMT journey with Mavenclad and how she had to go to the Cleveland Clinic for med management and how her body rejected multiple DMT's so her neurologist shut her down and she will start them back up soon.

We also discuss the importance of exercise and committing to finding ways to improve how your body feels.

We have an awesome discussion about the mental part of the journey and how we have developed ways to keep going.

We also talk about the importance of the chronic disease community and how we connect with other MSers on social media, especially those that don't have family support.

Connect with Tasha on her social media links below:

https://www.instagram.com/life.spoken.tasha_?igsh=MTQwMDY3cmp6dGZ5ZA%3D%3D&utm_source=qr

https://www.tiktok.com/@speakinglifewithtasha?_r=1&_t=ZT-94JShES0fJG

https://www.instagram.com/life.spoken.tasha_?igsh=MTQwMDY3cmp6dGZ5ZA%3D%3D&utm_source=qr

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on these social media platforms:

https://www.tiktok.com/@speakinglifewithtasha?_r=1&_t=ZT-94JShES0fJG

https://www.instagram.com/life.spoken.tasha_?igsh=MTQwMDY3cmp6dGZ5ZA%3D%3D&utm_source=qr

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #29 - David - MS WARIOR

distribution@podgo.io (Brian Wallace) — Tue, 24 Feb 2026 12:00:00 +0000

Today I'm talking with David Lyons from California, diagnosed with MS in 2006 at the age of 47. David is a US Marine veteran and was a former bodybuilder and a health club owner when he started his journey. We have an awesome discussion about how he went from living a fast paced active life to having partial paralysis from his initial symptoms. David went through multiple tests and was tested for brain cancer trying to figure out what was causing his symptoms.

We talk about how he didn't understand MS and how he thought he had Muscular Dystrophy and how he was told he was going to be in a wheelchair in six months by his doctor.

Dave made the decision immediately he didn't want to take a drug so he dove deep into the exercise part of fighting the disease. It wasn't an easy road to go down and Dave talks about the year he spent shut down and how he shriveled up physically.

Dave actually started training again and competed in a bodybuilding competition after diagnosis but he learned that type of training wasn't good for his MS.

We talk about how Dave spent the next 15 years doing his own research on how to train his body in the best way possible to live his best life.

We talk about motivation and commitment when attacking anything in life especially being diagnosed with a chronic disease.

We talk about the program he developed with Matt Rowe, Optimal Body Optimal Mind, that lays out a plan of how to take care of your body and mind fighting the fight of chronic disease.

David Lyons is an amazing badass that understands what it's like living with this disease and has incredible knowledge he wants to share. Knowledge is power and ignorance is a choice!

Connect with David Lyons on his social media links below:

https://optimalbodyfitness.vhx.tv/

http://www.msfitnesschallenge.org/

https://www.facebook.com/share/16vCN6VYyT/?mibextid=wwXIfr

http://www.optimalbody-optimalmind.com/

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #28 - Jonathan - MS BADASS

distribution@podgo.io (Brian Wallace) — Sun, 22 Feb 2026 12:00:00 +0000

Today I'm talking with a return guest, Jonathan from Massachusetts, diagnosed with MS in 2022. Jonathan is the Director of Operations for the Department of Mental Health Inpatient hospital system in the state of Massachusetts.

We have an awesome conversation about the 5 stages of grief and how we manage them.

We break down denial, anger, bargaining, depression and acceptance talking about our own personal experiences with them all.

We discuss how the stages are linear and how we manage the changes with our journey.

We also have a great conversation about the tools we developed and use to motivate our mind.

We talk about tools and how Jonathan found scuba diving as one of jis most important tools he uses for his mental health.

We talk about the importance of finding a community of people that can relate like we did with TikTok.

We talk about an MS event we are both going to be speaking at, MS Rising Summit, in Louisville, Kentucky in May trying to spread awareness about living with chronic disease.

When it comes to knowledge of mental health and being he has a chronic disease himself, Jonathan is incredible to speak to.

Check out Jonathan on TikTok and the badass scuba diving videos he puts out from his dives. They are amazing!

Jonathan is on TikTok @ms.mursenarry.solja. Find him and give him a follow!

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #27 - Gina - MS BADASS

distribution@podgo.io (Brian Wallace) — Tue, 3 Feb 2026 12:00:00 +0000

Today I'm talking with Gina from the UK, diagnosed with MS in 2009 but experienced symptoms ten years prior when she had numbness in her hands and feet. Gina went to doctors but was told it was stress related and didn't get an MRI until she advocated for herself and was told she had MS.

We talk about how she didn't understand MS but was relieved she didn't have a brain tumor because she knew she wouldn't die from MS.

We talk about her DMT journey and her decision to stop taking them in 2017 and take control of her journey.

Gina is now a life coach now helping others to customize their journey their way.

Exercise, meditation, stress management and coping tools are discussed and the importance of taking care of your mind.

We also talk about keeping your independence with various mobility aids.

Connect with Gina on her social media links below:
https://www.facebook.com/gina.dallison.5
https://www.youtube.com/@GinaDallisonCoaching

and Gina is on TikTok @gina.dallison.coa

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #26 - Matt - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 1 Feb 2026 12:00:00 +0000

Today I'm talking with Matt from Indiana and a former ironman competitor., diagnosed with PPMS in 2017 but had symptoms years prior. In 2013, Matt was driving with his family when he experienced vision issues. Matt explains how it was isolated and he gained his vision back but spent the next four years with unexplained symptoms he later found out was the MS.

We talk about the understanding of the disease and how we both attacked our disease with attitude and got to work.

We get into an awesome discussion about the mental part of our training we both experienced being athletes and how we understood the power of our minds with our journey.

We talk about how we can repair our bodies with thought and mental preparation and the tools we use to get there.

Matt is an author and we talk about his book "Belief to Heal" that talks about how to use your mind to heal your body through changing the way we think.

We also talk about Symptom Free MS Summit that Matt is the founder of now in its fifth year where Doctors and healers get together to discuss ways to attack multiple sclerosis.

We also talk about his partnership with Dr David Lyons who is also an MSer that has been fighting the MS fight for 15 years himself and is huge in the fitness world to create Optimal Body Optimal Mind and launched it a year ago worldwide to help people mentally and physically fight the diagnosis and take control of it.

Check out all of Matt's tools to help with the most important part of the journey. You're mind!

http://www.optimalbody-optimalmind.com/
https://www.facebook.com/groups/symptomfreems
https://www.facebook.com/groups/optimalbodyoptimalmind

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #25 - Jamie - MS & EPILEPSY WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 27 Jan 2026 12:00:00 +0000

Today I'm talking with Jamie from Illinois, diagnosed with epilepsy at the age of 18 and then diagnosed at 25 with MS in 2000. Right after graduating from high school, Jamie experienced a seizure that hospitalized her and she was diagnosed with epilepsy. Jamie was put on medication to help control her new condition and went on with life going to college and graduating. Soon after graduating and working a high paced job Jamie was diagnosed with MS.

We talk about stress and the role it played bringing out our disease and the journey of finding a doctor that will listen to us.

We talk about the decision of having a child after a diagnosis for men and women.

We talk about her medications for epilepsy and the path she took after her MS diagnosis.

Jamie gets very descriptive about explaining her seizures and how she has learned how to manage having multiple conditions

We talk about the mental health part of the journey and her support system of her husband, who has been going through the battle with her from day one, and her children who learned as they grew up.

We also have a great conversation about how we use marijuana to manage disease and the benefits we get using THC.

Jamie is a warrior! You can connect with Jamie on TikTok @lovewarriorhugs.

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #24 - Maria - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 25 Jan 2026 12:00:00 +0000

Today I'm talking with Maria from Ohio, diagnosed with PPMS in 2012. Maria actually had symptoms for 10-12 years prior she went to doctors but couldn't get any answers. Finally, she advocated for herself to her general practitioner who ordered an MRI which lit up like a CHristmas tree, giving her an MS diagnosis.

We talk about how she made the decision to not go the traditional DMT route and attack her disease by taking better care of what she put into her body.

We talk about the benefits she gets from Gonstead chiropractic techniques and how it has improved her mobility.

We talk about her son Steven who is in his residency to become a neurologist and how they have different approaches but he accepts his mom"s choice to not use DMT's.

Maria talks about how she hopes her son expands his knowledge beyond what he is learning in med school and will understand there is more than one way to approach things.

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #23 - Phoebe - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 20 Jan 2026 12:00:00 +0000

Today I'm talking with Phoebe from Florida, diagnosed with MS in 2001 after having left side hemiataxia while she was in college. Phoebe spent months of testing and was even told she probably had MS but couldn't be diagnosed because of not having "multiple" lesions.

Phoebe has a family history of MS but still struggled getting doctors to give her the diagnosis.

We talk about the mental part of her journey and how she feared for her future having a family with the disease. In 2006 Phoebe lost her vision completely and talks about how she was completely alone because her husband was active in the military.

Phoebe gained her eyesight back after a year of darkness, which she explains by her faith in God and she has lived the rest of her life her way.

Phoebe earned her master's degree in 2014 and then was diagnosed with breast cancer.

Amy is an award winning author and is also a competitive ballroom dancer now after stopping her DMT's in 2015.

We talk about the attitude of fighting our disease and how we have to customize our journey live our best life.

We talk about the importance of community and connecting with people that live with MS and other chronic diseases.

Connect with Phoebe, her books and all these social media:

https://a.co/d/5PikLMO
https://a.co/d/djZLt0W
http://damms411.org/
https://www.facebook.com/groups/danceamyelinmyshoes/?ref=share&mibextid=NSMWBT

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #22 - Becca - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 18 Jan 2026 12:00:00 +0000

Today I'm talking with Becca from New Mexico, diagnosed with MS in 2000, after having numbness on her right side. Her mom told her to see a doctor right away so Becca did and the doctor immediately ordered an MRI. Three days later Becca was told she had MS at 25 years old.

We talk about the understanding of the disease being so young and the importance of exercise when we got diagnosed.

We talk about fatigue and how that affects her and also how this disease can affect so many different things like vision, speech and the ability to walk.

Becca talks about how living with her disease affected her ability to work and the mental part of living with MS

We talk about tools, DMT's, family support and the importance of finding a community on TikTok.

Connect with Becca on TikTok @rebeccaortiz64.

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. FaceBook @Brian Wallace Brunswick Ohio. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #21 - Millie - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 13 Jan 2026 12:00:00 +0000

Today I'm talking with Millie from New York, diagnosed with MS in 2006, but had symptoms four years earlier as she was getting ready to graduate from college. Millie had vision issues but she was uninsured so she couldn't receive the care she needed to get diagnosed sooner and also.

We talk about how she got denied for medicaid coverage and then she ended up working for the US Department of Health and Human Service as an auditor for 20 years after diagnosis.

Millie and I talk about everything from being diagnosed young and how we had to figure our MS out and get an attitude as early as we could.

We talk about DMT's and also get into the system she spent 20 years of her life working in and how it's broken for people with disabilities and elderly people.

Connect with Millie on TokTok @camillenobrady.

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #20 - CMae - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 11 Jan 2026 12:00:00 +0000

Today I'm talking with CMae from Kentucky, diagnosed with Multiple Sclerosis in 2011 at the age of 54. CMae started with vision issues, drop foot and numbness which made her see a doctor in 2009 but she received no answers for two year while doctors did crazy testing until she found a doctor that listened to her.

We talk about dating mid life with a chronic disease and how she met her husband and made sure he understood what he was getting into.

We talk about the rollercoaster of DMT's, mobility aids, motivations and how we use comedy to cope with our progression.

We also discuss the importance of our support whether it's family, friends and even TikTok.

Follow CMae on TikTok @ms_granny8. She is amazing with helping people understand living with MS better.

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on YouTube, Apple and Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #19 - Adam - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 6 Jan 2026 12:00:00 +0000

Today I'm talking with Adam from Michigan diagnosed with PPMS in 2019 returning to follow up from our first episode on my original channel Ep 43 about a year ago.

Adam and I talk about everything from meeting up in person last year and how his MS has been treating him. We also discuss all the events he has participated and organized for awareness.

We talk about the importance of exercise and taking care of the mental part of fighting this disease along with having an attitude.

Adam talks about the importance of not giving up and explains how he went from wheelchair to walking to riding a bike because he didn't give up.

Adam also talks about how he was chosen by the MS Society to highlight his journey in 2026 and the awesome sleeve he found by a company called https://www.cionic.com.

Follow Adam on Instagram and TikTok @msd_with_the_wrong_mfr and on FaceBook @Adam Powell.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify, Youtube and Apple - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #18 - Jeff - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 4 Jan 2026 12:00:00 +0000

Today I'm talking with Jeff from Colorado, diagnosed with MS in 1996 after having vision issues. Jeff worked for Mercedes as one of the best auto techs in the country and we talk about how he handled being told he had a chronic disease at 30 years old.

We talk about the mental part of the diagnosis and how his dad lived with MS and Jeff didn't want to follow in his footsteps.

We have a conversation about how we attacked our disease early in our diagnosis and how Jeff became a body builder, competing on stage after his diagnosis winning the competition and how he adapted throughout his life never letting mS define him.

Jeff is an amazing artist and poet, a talent he never knew he had until he that outside the box figuring out ways to continue through life. Jeff has been featured in news stories about living with MS and always looks at life as what he can still do instead of what he can't and how MS (My Situation) has to be the best you can make it.

Check out some of Jeff's art her and on my FaceBook.

https://a.co/d/foVEr4N

Follow Jeff on TikTok @jefftuttoilmondo

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64 and on FaceBook @Brian Wallace Brunswick, Ohio Original podcast on Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #17 - Hollie - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 30 Dec 2025 12:00:00 +0000

Today I'm talking with Hollie from Maryland, diagnosed with MS in 2017 because of vision issues. Her journey started years before with symptoms leading to the hereditary angioedema diagnosis in 2016 and she explains how she battled for that diagnosis for years prior as an adolescent.

We talk about the mental part of the diagnosis and how she had to understand her new life and how she was going to navigate her way through.

We have a conversation about the role of our family and supports in the community and how she is on a mission as an advocate and how she meets with politicians on Capitol Hill to try to make changes in healthcare.

Check out Hollie's column about angioedema she had published here

https://angioedemanews.com/living-rare-speaking-loud-hollie-amadio/

Follow Hollie on TikTok @holllucille

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64 and on FaceBook @Brian Wallace Brunswick, Ohio Original podcast on Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #16 - Amy - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 28 Dec 2025 12:00:00 +0000

Today I'm talking with Amy, a pharmacist from Georgia diagnosed with MS in 2012 right after she graduated from the University of Georgia with her Phar-D. Amy explains how she was diagnosed with Vitiligo at the age of 17 and how that was her first experience with autoimmune disease. Later at the age of 25 she was also diagnosed with a thyroid autoimmune disease. Amy knew enough to realize that she had issues that could be signs of what was yet to come. Two years later Amy started to experience drop foot while out running which set off the alarm something wasn't right.

Amy went to her doctor and after multiple tests including an MRI and a lumbar puncture she was told that she had PPMS at the age of 27. We talk about the fear and uncertainty after being told you have MS and how she handled her new norm.

Amy and I talk about the mental part of the diagnosis and how we had to learn how to manage the ups and downs of our journey living with MS and preparing for other life issues like divorce and other health issues we deal with throughout life.

Amy gives me her opinion of DMT's being a pharmacist and how she manages that part of her journey and also how she readjusted her path and now helps coaching people through their chronic disease journey.

If you want to connect with Amy, please check out her coaching website with amazing information and tools to use to keep yourself the best you that you can be.

https://amybehimercoaching.com/join and also https://podfollow.com/autoimmune-health-secrets

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64 and on FaceBook @Brian Wallace Brunswick, Ohio. Original podcast on Spotify, YouTube and Apple - MS Michigan Man 64.

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #15 - Meagan - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 23 Dec 2025 12:00:00 +0000

Today I'm talking with Meagan from California, diagnosed with MS in 2000, at the age of 20. Her journey started with numbness on her left side and a couple weeks later her vision became distorted. Meagan went to an eye doctor and they right away told her they suspected MS. After testing Meagan was told she had multiple sclerosis not having any knowledge of the disease.

We talk about her DMT journey and the mental part of her diagnosis and how she had to learn about her new life after hearing she was going to be dead in 20 years by her doctor.

Meagan talks about her struggles with cognitive issues and how it's the invisible part of the disease.

We also have an awesome conversation about having a family with her chronic disease and how she went through her fibromyalgia diagnosis at 30 years old and how she managed that. Meagan is also a breast cancer survivor being diagnosed and treated in 2020.

We talk about divorce, family, TikTok and how we have to find something to occupy our mind to keep fighting the fight. Meagan is very talented with craft making and we have a great conversation about her "she shed" where she works on her art.

Connect with Meagan on TikTok @meagan_mommyshobbys and check her craftwork https://www.mommyshobbys.com/.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64 and on FaceBook @Brian Wallace Brunswick, Ohio. Original podcast on Spotify, YouTube and Apple - MS Michigan Man 64.

Keep fighting. Go Blue!
_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #14 - Darren & Destiny - MS WARRIORS

distribution@podgo.io (Brian Wallace) — Sun, 21 Dec 2025 12:00:00 +0000

Today I'm speaking with Darren and his wife Destiny from Michigan known as the MS Duo. I recorded with Darren and Destiny on my original YouTube channel Episode 35 earlier this year and they shared their journey with their MS diagnosis and how they found each other and are battling life together as MS warriors.

We catch up with how their wedding went and how special of a day it was for both of them and their families. Destiny explains how they rode their amigos together after they were married and how they celebrated their new chapter of the journey.

We also catch up on Darren's journey with the VA and the services he was finally able to get after 7 years of trying being a veteran and how he is finding good results from Botox treatments he recently started for mobility.

We also have a great conversation about how they continue fighting their MS together and how they use each other for motivation to keep pushing. Darren and Destiny are absolutely amazing with their positive attitude and how they continue to support each other.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64 and FaceBook @Brian Wallace Brunswick, Ohio. Original podcast on Youtube, Apple Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #13 - SWAB - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 16 Dec 2025 12:00:00 +0000

Today I'm talking with the SWAB, an MSer from the UK that was diagnosed with his MS in 2009. Before his diagnosis the SWAB was a heroin addict that thought he had a stroke during an episode. We talk about the mental health part and the fact that he was sexually abused while he was a child and how that affected his mental health.

SWAB explains his path of being diagnosed with PPMS and how it took his ability to walk rapidly and how his mind started to swirl into dark thoughts of suicide.

We also discuss how even after all the battles he endured mentally and physically he still never game up. SAWB also tells me the beautiful story of how he met his wife, Layla, who is also an MS warrior.

Together, SWAB and Layla have created a team and have a beautiful 3 year old son Zane they are bringing up together showing him how to love unconditionally!

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64 and FaceBook @Brian Wallace Brunswick, Ohio. Original podcast on Youtube, Apple Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #12 - Tilly - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 14 Dec 2025 12:00:00 +0000

Today I'm talking with Tilly from British Columbia, Canada - a returning guest diagnosed with MS in 2020. When we first met, she was newly diagnosed and scared, could only stand for two minutes and dragged her left leg. She was into CrossFit and running before MS, but didn't quit. She started with sitting exercises and built herself back up. Within two years, she returned to work doing Tabata workouts daily.

Tilly is a single mom fighting to get daughter Addie diagnosed on the autism spectrum - currently on a two-year waitlist. She works a physical job with weight restrictions and balance issues. After leaving an abusive relationship, she went through therapy and tough relationships before recently meeting someone who supports her journey.

We talk about the TikTok MS community keeping her motivated, using meditation for mental health and pain management, "dancing it out" on bad days, and fighting this disease. Tilly's message: rest when you need to, find your community, and never give up hope.

Follow Tilly on TikTok @metillyca and on FaceBook @Tilly Elliot.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64 and on FaceBook @Brian Wallace Brunswick, Ohio. Original podcast on Spotify, YouTube and Apple. - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #11 - Brandon - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 9 Dec 2025 12:00:00 +0000

Today I'm talking with Brandon, an Army veteran who served 15 years including deployment to Afghanistan. Diagnosed with MS in 2016 while 12 years into his military career, Brandon's journey started with pelvic numbness and leg paralysis. The ER dismissed it as back-related, but a familiar doctor performed an exam and suspected MS based on inflamed nerves. Brandon went through 45 days of testing including a robotic spinal tap and multiple MRIs before getting his 2016 diagnosis.

Brandon went through divorce shortly after diagnosis. He hit rock bottom but found support from phenomenal military leaders at the Pentagon who told him to take care of himself. He tried multiple DMTs - Tecfidera caused severe flushing and bowel issues, Copaxone created massive injection site welts. A coworker nicknamed "Nurse Amy" helped with injections.

After failing three DMTs, Brandon researched Ocrevus and brought documentation to his neurologist. Got approved same day and all nine lesions went inactive after first infusions.

We discuss the mental game of diagnosis, hoops to jump through for medication changes, and finding support when you need it most.

Connect with Brandon on TikTok @orangefighter_msf

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify, YouTube and Apple - @BrianWallace-p6f - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #10 - Maytee - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 7 Dec 2025 12:00:00 +0000

Today I'm talking with Maytee from North Carolina, diagnosed with MS in 2015. Her diagnosis came suddenly - started with pain on her right side and tripping, then complete right-side paralysis. She went to the ER on Friday night, by Sunday she was bedridden and diagnosed with MS. It was December - she begged to leave the hospital after days of relearning basic skills to be home for Christmas with her children. She finished her Christmas tree and wrapped gifts with one arm until 3:30am.

We talk about some of the struggles within the Hispanic community. Maytee was a medical interpreter for years and witnessed the barriers Hispanic patients face - language issues, cultural differences, providers rushing through appointments, and patients staying quiet because they're embarrassed or don't understand medical terminology.

We talk about why MS has the highest depression rate among chronic diseases, learning to honor what your body asks for, being unapologetic about disability, and accepting mobility aids. We discuss the mental toll being harder than physical symptoms and how MS reminds you every morning from the minute you open your eyes.

Follow Maytee on all her social media's @M_S_Positive!

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify, YouTube and Apple - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #9 - Cassandra - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 2 Dec 2025 12:00:00 +0000

Today I'm talking with Cassandra from Connecticut, diagnosed with MS in 2024 after experiencing vertigo while backing out of a parking space at her gym. A walk-in clinic dismissed it as vertigo, but her PCP got her into a neurologist fast. Cassandra got her diagnosis over the phone after an MRI - she had mentally prepared for a brain tumor, not MS.

Two years before diagnosis, Cassandra started hitting the gym to lose weight and get healthy for her two kids. When her neurologist saw she'd been training, he told her to thank her past self - staying physically fit is the best thing she could do for MS. Now she's a competitive powerlifter who's done three competitions in six months, deadlifting 210 pounds and white-dotting despite her leg muscles spazzing mid-lift.

We talk about movement being medicine, having coaches who adapt training for MS, refusing to let the diagnosis define you, and dealing with people questioning if you really have MS because you're "doing too much." Cassandra discusses toxic positivity accusations, the TikTok MS community support, and how her husband and daughters (18 and 9) are learning to understand the disease.

Her attitude: even if it doesn't count, she's not dropping the bar.

Follow Cassandra on TikTok @cass_gymbrat.1122.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok and Instagram @msmichiganman64 also FaceBook @Brian Wallace Brunswick, Ohio. Original podcast on YouTube, Spotify and Apple - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #8 - Eric - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 30 Nov 2025 12:00:00 +0000

Today I'm talking with Eric from Texas and his wife Neomy. Eric, a lifelong athlete and runner, was diagnosed with MS in 2017 at 44 after waking up with numbness from knees to feet. His high school nickname was "Walkie Talkie" - he loved to talk. Now MS affects his speech, but Eric refuses to give up his voice.

We talk about why mental health is crucial - your brain never shuts off with this disease. We discuss Eric's progression from cane to walker to power chair, and how MS affected his esophagus and speech. Neomy shares her journey from hovering to giving Eric space to figure things out, and how she can now tell by looking at him if he's having a bad day.

Eric shares how the TikTok MS community helped him fight to keep his voice - a year ago he could barely speak, now he's talking for hours. We discuss his DMT Ocrevus and how after his last treatment his voice dramatically improved overnight. Neomy talks about their home health team, physical therapy, and how family moved in to help.

Eric's attitude: you have to fight mental, because this disease is a fight every day.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #7 - Johnny - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 25 Nov 2025 12:00:00 +0000

Today I'm introducing MS Warrior Johnny - artist and member of my team handling all art for the MS Michigan Man 64 Podcast. Johnny's full story is on my original podcast channel Episode 74 and this is his catch-up and introduction.
Johnny has always been an artist but had his dream paused because of a pituitary tumor diagnosis in 2017 and then being diagnosed with MS in 2019. Johnny and I talk about how we met an collaborated together to come up with cover art and a t-shirt design.

We talk about building a team of chronically ill people and giving them opportunities to show the world that even though they can't live life as intended, they can still do what they love. We discuss connections we've made and how people with chronic illness overcome and adapt to challenges.
We discuss the community and all the badass warriors we have met since being on TikTok and the talents they have even though they live with chronic disease and how we just want to be understood by society.

Hit subscribe, but more importantly hit that share button and help me bring awareness to chronic illness and disease.

Follow Johnny on TikTok @artistic_wolf_prints and check his art at https://awp-art.carrd.co/

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify, YouTube and Apple - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #6 - Juliann - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 23 Nov 2025 12:00:00 +0000

Today I'm talking with Juliann, diagnosed with MS at 15 years old back in 2014. Her symptoms started with hand numbness while playing guitar, then progressed to leg dragging while pitching softball. After seeing her pediatrician who initially thought it was a pinched nerve, Juliann's mom got her an MRI that showed abnormal results and she was sent to the hospital immediately.

We talk about why mental health should be addressed at diagnosis - Juliann turned down therapy at 15 but wishes she'd said yes. We discuss losing friends after diagnosis, hiding the disease in high school, and eventually opening up about it through songwriting. Juliann shares how Montel Williams responded to her on Twitter with a quote that still carries her through bad days: "You have MS and it will never have you unless you let it."

We talk about her incredible husband Garrett who stood by her through her worst flare and pushes her wheelchair when needed. Juliann is also mom to Mason, a three-year-old autistic warrior, and we discuss the fight to get his diagnosis and dealing with judgment in public when he's having sensory episodes.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #5 - Lynnie - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 18 Nov 2025 12:00:00 +0000

Today I'm talking with Lynnie from Seattle, diagnosed with MS in 2009 after dealing with nine surgeries from broken feet. After her last surgery, she experienced symptoms like word confusion, numbness, and tingling. Her physical therapist suspected something else was going on, and MRIs revealed MS. She got her diagnosis over the phone while at work.

We talk about why mental health counselors should be in the room when MS diagnoses are delivered. We discuss losing our work identity, facing discrimination despite ADA laws, and the struggle to prove we're sick just to get disability benefits approved. We dive into MS as an invisible disease and that frustrating comment "you look good for being sick."

Lynnie is also grandmother to a grandchild that has autism and who teaches her positivity every single day. We talk about autism awareness and the broken disability system.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify, Apple and YouTube - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #4 - Amber - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Sun, 16 Nov 2025 12:00:00 +0000

Today I'm talking with Amber from Rhode Island, diagnosed with MS in 2022. She's also a mother to an autism warrior. Amber is an absolute fighter and badass managing both challenges.

Amber's diagnosis came during intense stress - moving back to her mom's house, struggling to find an apartment. She experienced numbness across her entire upper torso for a month, got dismissed by doctors who treated her like a pill chaser. Then came visual disturbances, severe headaches, and unequal pupils. After initially leaving the hospital due to wait times, she was eventually admitted when a nurse practitioner suspected a brain bleed. MRIs revealed MS, and she found out through her MyChart app - we both agree that's no way to deliver life-changing news.

We talk about why mental health counselors should be in the room when MS diagnoses are delivered. We discuss MS as an invisible disease, how stress triggers relapses, and the isolation that comes when people don't believe you're sick because "you look fine."

Amber also shares her fight getting her daughter's autism diagnosis and the crucial ABA services she needs.

Hit subscribe and share to help bring awareness.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify, YouTube and Apple - MS Michigan Man 64.

Follow Amber on TikTok @honeynsug and also has a headstone cleaning service @lexani.dontcare

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #3 - Ronald - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Tue, 11 Nov 2025 12:00:00 +0000

Today I'm talking with Ronald, diagnosed with MS in 2024 after symptoms like falling, slipping, and tremors. He was seen in February 2024 and diagnosed March 19th, 2024 with about 30 lesions found in his brain and spine. Here's the kicker - Ronald had been experiencing symptoms for almost 20 years and knew nothing about Multiple Sclerosis. He also has osteoporosis.

Ronald's husband Rod had a steep learning curve. Ronald went from using a walker in early 2024 to a power chair by year's end.

We talk about learning to accept that MS is with us every day and how Rod is learning to accept it too. They're using couples therapy to work through this life-changing curve ball - that's real relationship work right there.

We discuss mental health awareness, the loneliness and isolation that comes with this diagnosis, and how thankful Ronald is for connections he's made through this journey, like meeting Holly. We talk about the healthcare system and how different it can be region to region, MS specialists, Disease Modifying Therapy, and Ronald's experience with Ocrevus.

Hit subscribe and share this episode to help bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #2 - Amber K - MS WARRIOR

distribution@podgo.io (Brian Wallace) — Mon, 10 Nov 2025 12:00:00 +0000

Today I'm introducing MS Warrior Amber K - singer, songwriter, and newest member of my team handling original music for this podcast. Amber's full story is on my original podcast Episode 56 (funny MS moment - I said it is 54), but this is her catch-up and official introduction.

Diagnosed in 2021, Amber had a 2024 flare-up that sparked her drive to express herself through music. You'll hear her song "I Hate That It's For Me" during this episode. PRO TIP - bring tissues.

I share about my friend Dave, a high school football coach with primary progressive MS who still coaches. Even cooler - he coached Will Campbell, the #4 pick of the 2025 season with the Patriots. That's badass!

Hit subscribe, but more importantly hit that share button and help me bring awareness to chronic illness and disease.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #1 - MY Story Pt 2

distribution@podgo.io (Brian Wallace) — Wed, 5 Nov 2025 12:00:00 +0000

In Part 1, I covered my football journey and 1997 MS diagnosis. Now we're diving into living with Multiple Sclerosis - struggles nobody talks about and mental health battles.

I dealt with drop foot and optic neuritis that messed with my vision. Stress triggered MS episodes. In 2015, I went on disability retirement, which destroyed my mental health. I ignored depression for years - big mistake.

My wife pushed me to get help. I addressed mental health, returned to work, found jobs I loved, but faced employment discrimination when MS vision problems caused mistakes.

Football taught me to take hits and get back up. MS taught me the hardest opponent is inside your body. But you adapt, fight, and find community.

This podcast brings awareness to chronic illness and MS. Shows athletes can face disability and still have purpose. Helps people know they're not alone.

Find me on Instagram and TikTok @msmichiganman64. Original podcast on Spotify - MS Michigan Man 64.

Keep fighting. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.

WARRIOR #1 - MY Story Pt 1

distribution@podgo.io (Brian Wallace) — Sun, 2 Nov 2025 12:00:00 +0000

Welcome to Hail Media I'm Brian Wallace, MS Michigan Man 64, Left Tackle for the Michigan Wolverines 1988-1991 finishing my career at the 1992 Rose Bowl. This is where a former Wolverine gets real about life after football - battles you don't see coming and training that prepared me for my toughest opponent. Hail to the Victors. Go Blue!

Before Michigan, I was 1987 Offensive Lineman of the Year DIV II in Ohio and won the 1988 Ohio State Championship for hockey at Padua Franciscan High School in Parma, Ohio. I made my dream come true by earning an athletic scholarship to play for the winningest college football program in HISTORY, the Michigan Wolverines! During my time, we won 4 Big Ten Championships, played 3 Rose Bowls and 1 Gator Bowl. Sophomore year, I fractured vertebrae in my back and missed most of the season. Senior year I made Victor's Club for my performance against Minnesota. I was never a regular starter but learned that hard work and determination will lead you to great opportunities in life as long as you NEVER give up! I became the Wolverine from Ohio who NEVER lost to Ohio my entire college football career! My career ended in 1992, but the discipline, mental toughness, and fight never left.

Five years later in 1997, I got blindsided - Multiple Sclerosis. A disease that attacks your nervous system, mobility, vision. But everything football taught me about pushing through pain, adapting, and never giving up set me up for managing my MS.

This podcast exists because I refuse to let chronic illness win. I'm bringing awareness to MS and disability, showing Wolverines don't quit when the game gets hard. Whether you remember the Maize and Blue or dealing with your own battles, this is our locker room.

Find me on Instagram and TikTok @msmichiganman64. Original podcast with 99+ episodes on Spotify - MS Michigan Man 64, on YT @HailMediaGroup

Let's get into it. Go Blue!

_____________________________________________________

Hail Media is proud to add the MS Michigan Man 64 Podcast to the Hail Media family!

Hail 〽️edia
Our Stories.
Our University.
Our Team.

Hosted by Simplecast, an AdsWizz company. See pcm.adswizz.com for information about our collection and use of personal data for advertising.