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Welcome to “The Other Side of MS,” a podcast dedicated to amplifying the voices and stories of those whose lives are deeply affected by Multiple Sclerosis (MS). Through honest conversations and heartfelt stories, we shed light on the strength, resilience, and challenges of the MS community. Each episode goes beyond awareness; it’s about action, whether that means learning, supporting, advocating, or simply listening with an open heart. This podcast is not just a platform for stories—it’s a movement fueled by everyone who believes in a brighter future. Together, let’s make a difference—one conversation, one story at a time.
Tuesday May 09, 2023
Tuesday May 09, 2023
Jason DeRoo: Supporting a Loved One with Multiple Sclerosis In this episode, we talk with Jason DeRoo, husband of Sarah DeRoo, who was diagnosed with multiple sclerosis (MS) and a previous guest on our podcast. Jason shares his experience as a caregiver and how he has had to adjust his expectations for his life with Sarah since her diagnosis. We discuss the impact of MS on their family life, the financial burden of the illness, and how they manage to balance caring for two children while also managing the demands of the illness. Jason also shares some of the challenges he has faced as a caregiver and how he has overcome them. This episode is a must-listen for anyone who is supporting a loved one with MS or any chronic illness.
Donate to Sarah DeRoo's Bike MS Fundraiser
Tuesday Apr 11, 2023
Tuesday Apr 11, 2023
Tuesday Apr 11, 2023
Sarah DeRoo: "I Bike with MS" We are thrilled to introduce you to Sarah DeRoo, an exceptional individual who is part of the "I Ride with Multiple Sclerosis" program through the National MS Society's Bike MS Event. The "I Ride with MS" program celebrates and recognizes the resilience of our cyclists who are diagnosed with multiple sclerosis and shines a light on what it means to live with this disease.
Sarah is a member of Team Left Hand, a team that is dedicated to finding a cure for Multiple Sclerosis, a chronic disease that affects the central nervous system. In this edition, Sarah will share her inspirational story of riding with Multiple Sclerosis, including the challenges she has faced and the triumphs she has achieved. She will also discuss the importance of family dynamics and how her family provides support in her fight against the disease. Furthermore, Sarah will talk about her fundraising efforts for this year's Bike MS: PGA Bike to the Shore, an event that aims to raise awareness and funds for Multiple Sclerosis research.
Sarah's story is one of strength, resilience, and determination, and we are honored to have her on our podcast.
Donate to Sarah DeRoo's Bike MS Fundraiser
Sara also raises funds through her business, "I Dye Yarn". Each year, Sarah creates a special BikeMS yarn and she put all the proceeds from sales of it to my fundraiser.
Sarah's "I Dye Yarn" Bike MS Fundraiser
Friday Mar 10, 2023
Friday Mar 10, 2023
Friday Mar 10, 2023
Welcome to "The Other Side of MS" where our passion is to share the remarkable stories of individuals deeply affected by Multiple Sclerosis (MS) and to pedal together towards a world free from this condition. As a cyclist for Bike MS, I understand the power of the journey, and it's our collective 'why' that drives us.
Our 'why' is clear and unshakeable: To make MS a thing of the past. Through heartfelt interviews and authentic conversations, we aim to shed light on the untold aspects of MS, the resilience of those living with it, and the impact it has on their lives, as well as those who support them.
This podcast is not just about me; it's about you, the listeners, and the diverse voices that join us. Whether you're a seasoned cyclist, a family member, a passionate community member, or anyone who shares our dream of a world without MS, you're part of our community.
Join us on this journey as we cycle towards a future where MS is a distant memory. This podcast is more than just stories; it's a movement. Together, let's amplify the 'why' that fuels us and work towards a world where MS is nothing but a part of history.
Comments / Want to share you MS story: cmurphy@sjmalaw.com