multiple sclerosis thrivers leaning into our core values to live our best lives

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Thriving Over Surviving

Listen to Season Two of Thriving Over Surviving, Now!

Listen to Season Two of Thriving Over Surviving, Now!

Listen to Season Two of Thriving Over Surviving, Now!

Listen to Season Two of Thriving Over Surviving, Now!

Listen to Season Two of Thriving Over Surviving, Now!

Listen to Season Two of Thriving Over Surviving, Now!

This Week's Podcast Episode

Listen to the Top Podcast Episodes From Season Four

Episode 96: MS Challenges Are An Opportunity To Learn About Yourself

Episode 96: MS Challenges Are An Opportunity To Learn About Yourself

Episode 96: MS Challenges Are An Opportunity To Learn About Yourself

Ah, the optimist's perspective is one many strive to achieve. When dealing with challenges brought on by MS, it is a lot more work to stay optimistic. But the work is well worth it! Matt Knaggs possesses all the qualities of an optimist. He is self-motivated, always around the most motivated people, he believes in possibilities, he is full of joy and finds ways to express gratitude in all things. Yup, we can all learn a thing or two from Matt.  

Let's chat it up with matt

Episode 92: Living An Adventurous Life With Multiple Sclerosis

Episode 96: MS Challenges Are An Opportunity To Learn About Yourself

Episode 96: MS Challenges Are An Opportunity To Learn About Yourself

What is the biggest risk you have ever taken? Was it one that led you on a grand adventure to far-off places you never dared to go before? For many, that is a bit extreme. For some, life would be boring without an unexpected twist or turn. For Melissa Cook, the author of The Call of the Last Frontier, blogger, and YouTube star there is never a dull moment. It is not an option for MS to put her down, even after over 20 years of living with the disease.  

Let's chat it up with melissa

Episode 91: Owning The Diagnosis of Multiple Sclerosis With the MS Stage

Episode 86: How MS Hope and the Best Bet Diet Changed One Man's Perspective on Living Well

Episode 86: How MS Hope and the Best Bet Diet Changed One Man's Perspective on Living Well

Getting a diagnosis is one thing. Owning a diagnosis is another. With Relapsing Remitting Multiple S

Getting a diagnosis is one thing. Owning a diagnosis is another. With Relapsing-Remitting Multiple Sclerosis, for some, it is easy to ignore it. But when it creeps back in and reminds us that MS is still there, that's when we begin to pay attention. Megan from The MS Stage chats with Edie about owning her diagnosis and taking action to improve her own life and the lives of others. Let's chat it up!  

let's chat it up with Megan

Episode 86: How MS Hope and the Best Bet Diet Changed One Man's Perspective on Living Well

Episode 86: How MS Hope and the Best Bet Diet Changed One Man's Perspective on Living Well

Episode 86: How MS Hope and the Best Bet Diet Changed One Man's Perspective on Living Well

 Matthew Embry and his father, Dr. Ashton Embry, created MS Hope for people who have been newly diagnosed or currently living with MS. Their goal is to provide the science-based strategies that have enabled Matthew and many others with multiple sclerosis to live a drug-free, healthy life. Lee joins Edie to chat it up about how following the Best Bet Diet has enhanced his life since his MS diagnosis. 

let's chat it up with lee

Listen to the Top Podcast Episodes From Season Two

Episode 77: Being Present, Prompt, and Prepared With MS

Episode 76: Adapting To Life With MS By Speaking Your Truth

Episode 76: Adapting To Life With MS By Speaking Your Truth

 We all see Damian Washington on TV commercials and MS Views & News. Maybe you have perused his YouTube Channel or Website. Wherever you have absorbed his fantastic energy, it was bound to be entertaining and full of great information about multiple sclerosis. Do you try to be present in the current moment and in your given circumstance?  

Let's chat it up with damian washington

Episode 76: Adapting To Life With MS By Speaking Your Truth

Episode 76: Adapting To Life With MS By Speaking Your Truth

Episode 76: Adapting To Life With MS By Speaking Your Truth

 I don't know anyone with multiple sclerosis that signed up for it. Nobody stands in line with great expectations hoping that someone will say, "Yes, you have MS".  But if you have this disease, you might as well make the most of it. So how do you do that? Stand up and share your story. As I chatted it up with David Beneby Jr, I realized there is something about him that emotes a positive outlook on life. There is no magic wand, but maintaining a mindset focused on the possibilities in life is a great place to start.    

Let's chat it up with David

Episode 74: The World's Strongest Disabled Man

Episode 76: Adapting To Life With MS By Speaking Your Truth

Episode 67: Coping With Chronic Illness By Taking Time For You

Dave Walsh is a strongman, a dad, a husband, and is hilarious. He won the world's strongest disabled man competition in June 2022. But he is not just all muscles. This is a man who also helps others understand what it is like from his perspective in a wheelchair. 

Let's chat it up with dave

Episode 67: Coping With Chronic Illness By Taking Time For You

Episode 64: Choosing Empathy Over Shame When Needing A Mobility Aid For MS

Episode 67: Coping With Chronic Illness By Taking Time For You

How do you cope with MS? Samantha Bromfield lets it all out, in her own words, no holds barred. Her blog highlights her journey with multiple sclerosis. But there's another side to this thriver. As an avid reader, Samantha knows how to take time for herself to feed her soul. 

Let's chat it up with sam

Episode 65: This Healthy Unicorn Says FU MS

Episode 64: Choosing Empathy Over Shame When Needing A Mobility Aid For MS

Episode 64: Choosing Empathy Over Shame When Needing A Mobility Aid For MS

Perseverance is doing something despite difficulty or delay in achieving success. For me, the words, grit, determination, and tenacity come to mind. Jessica Turner is an MS thriver who found purpose in her diagnosis by helping others take back control of their health and wellbeing.

let's chat it up with jessica

Episode 64: Choosing Empathy Over Shame When Needing A Mobility Aid For MS

Episode 64: Choosing Empathy Over Shame When Needing A Mobility Aid For MS

Episode 64: Choosing Empathy Over Shame When Needing A Mobility Aid For MS

Noelle is a mother of three, a wife, and a licensed social worker whose goal is to help others struggling with chronic illness. Although she has Secondary Progressive Multiple Sclerosis (SPMS), Noelle maintains her independence by taking full advantage of mobility aids. 

let's chat it up with noelle

Episode 62: Claustrophobia And MS Do Not Mix

Episode 62: Claustrophobia And MS Do Not Mix

Episode 62: Claustrophobia And MS Do Not Mix

If you have multiple sclerosis, then you have probably had an MRI. Even though I'm not afraid the walls are closing in on me, I am not excited to get in the tube each year. Lorin shares her experience of getting her brain scanned and what she has to do to get through it. Great convo with this funny lady, teacher, and thriver. 

Let's chat it up with Lorin

Episode 60: Epstein-Barr & MS

Episode 62: Claustrophobia And MS Do Not Mix

Episode 62: Claustrophobia And MS Do Not Mix

Mathew Embry shares his thoughts regarding the future of multiple sclerosis research and the search for a cure. Mathew is the man behind the documentary Living Proof. Cofounder of MS Hope, his goal is to help our community by sharing the science-based strategies that have enabled him to live a drug-free, healthy life for more than 25 years since his diagnosis. Mathew says #nocheatdays!

Let's chat it up with mathew embry

Episode 56: When Steroids Are Not An Option

Episode 62: Claustrophobia And MS Do Not Mix

Episode 56: When Steroids Are Not An Option

Everyone's MS diagnosis story is different. For Rachel, the symptoms came on quickly and her diagnosis just as fast. But Rachel soon realized that the typical treatment of steroids was not going to work for her. In Part I, Rachel and I discuss her journey with HSCT and what led up to the discision to take this course of action.  

let's chat it up with rachel

Episode 55: Life Adjustments After PPMS

Episode 54: Creativity, Faith, And Family

Episode 56: When Steroids Are Not An Option

Less than 15% of the people diagnosed with Multiple Sclerosis are said to be in the Primary Progressive Phase. Folake Taylor shares the difficult journey of misdiagnosis and how she leans into her core values to ensure she is living her best life. From scooters to walking, we learn from Dr. Taylor that it's a lot of hard work, but it can happen.  

let's chat it up with folake

Episode 54: Creativity, Faith, And Family

Episode 54: Creativity, Faith, And Family

Episode 54: Creativity, Faith, And Family

Allison is a wife & mother of two, lawyer, and abstract artist. Living with MS since 2008, she doesn't try to be perfect but she tries to do her best.  

let's chat it up with allison

Episode 52: A Best Life Cocktail For MS

Episode 54: Creativity, Faith, And Family

Episode 54: Creativity, Faith, And Family

In some cases, MS can try to steal your identity. Karen Dwyer shares how she leaned into her core values to "heal" her MS and live her best life. She now helps others to do the same.  Karen's TEDx talk, What's Your Shoe Size Got to do With Chronic Illness? has thousands of views. Karen is thriving! 

let's chat it up with karen

Listen to the Top Six Podcast Episodes From Season One

Episode 29: Getting Back on his Feet After MS Knocked Corey Down

Episode 15: From Tragedy to Triumph, How September 11 Impacted the Journey of This MS Warrior

Episode 27: An MS Journey From Bedbound to Wheelchair to Ballerina

Corey Mitchell, diagnosed with MS, developed The Corey Mitchell Multiple Sclerosis Foundation. His mission is to support other people with MS when they arrive home following diagnosis. The motto of the foundation is... For a dog fears nothing, that's why we take a bite out of MS. Corey lives by this as he will not give up and is working hard every day to get back on his own two feet again. 

Let's chat it up with corey

Episode 27: An MS Journey From Bedbound to Wheelchair to Ballerina

Episode 15: From Tragedy to Triumph, How September 11 Impacted the Journey of This MS Warrior

Episode 27: An MS Journey From Bedbound to Wheelchair to Ballerina

Alexandria was a science teacher and a realtor. Typical MS overachiever. One day she completely lost her ability to walk, speak, and see. How does she go from this to being on point shoes? 

Let's chat it up with alexandria

Episode 15: From Tragedy to Triumph, How September 11 Impacted the Journey of This MS Warrior

Episode 15: From Tragedy to Triumph, How September 11 Impacted the Journey of This MS Warrior

Episode 15: From Tragedy to Triumph, How September 11 Impacted the Journey of This MS Warrior

Kerri Kiefer-Viverito lost her brother, FDNY Firefighter Michael Kiefer, on 9/11/2001. But her story does not end there. Although this was a significant loss to her family, the FDNY, and so many more, Kerri finds strength in her brother's memory and uses this to battle her multiple sclerosis.  

Let's chat it up with kerri

Episode 9: The Body of a Warrior, the Mindset of a Thriver

Episode 2: HSCT Warriors Growing Community One Stem Cell at a Time

Episode 15: From Tragedy to Triumph, How September 11 Impacted the Journey of This MS Warrior

Angela Gensler has fought countless battles and overcome so many obstacles in her journey to live her best life. In this episode, Angie chronicles how her mindset has helped her achieve her goals. 

Let's chat it up with angie

Episode 2: HSCT Warriors Growing Community One Stem Cell at a Time

Episode 2: HSCT Warriors Growing Community One Stem Cell at a Time

Episode 2: HSCT Warriors Growing Community One Stem Cell at a Time

These ladies share their powerful story of courage participating in stem cell therapy. And they wouildn't have had it any other way.

let's chat it up with Cassidy and julie

Episode 1: Navigating My New Normal Multiple Sclerosis Life

Episode 2: HSCT Warriors Growing Community One Stem Cell at a Time

Episode 2: HSCT Warriors Growing Community One Stem Cell at a Time

Melissa shares her journey and how she thrives despite her diagnosis. She bikes, she runs a school, she leads a group of MS'rs. What doesn't she do? Surprise, someone has some new news. 

let's chat it up with melissa
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