53 Best Multiple Sclerosis Podcasts to Listen to (2026)

On this podcast, Christina Applegate and Jamie Lynn Sigler get vulnerable about the curveballs that life can throw…theirs just happens to be MS. Join them each week as they self-reflect, learn, laugh, and grow through their own raw and often-times hilarious conversations with each other, friends, co-stars, and the people that keep them going through the messiness of life. more

Jon Strum cuts through all the jargon and breaks down the latest multiple sclerosis news. You'll meet the scientists who are creating tomorrow's MS treatments today. You'll hear from the experts discussing how the latest tweaks and changes to our healthcare laws will impact your MS treatment. And we'll be talking to the courageous MS warriors who are out there advocating on behalf of the MS community every day, as well as the men and women who are committed to living their best lives with MS and living their best lives as MS caregivers. If you're dealing with multiple sclerosis in your life -- as a patient, caregiver, family member, or friend -- join us each week for RealTalk MS. more

Barry Singer, MD, Director of The MS Center for Innovations in Care at Missouri Baptist Medical Center, interviews global expert guests about the latest treatments, innovations and tips for people living with multiple sclerosis. more

Do you have Multiple Sclerosis and have goals of improving your mobility, energy, and motivation? On this show, you'll learn MS-specific exercises and symptom management strategies to help you gain control over your life with MS. I also bring in other MS Experts in the healthcare industry to share their insights and advice so you'll be armed with research-driven education. You'll leave each episode feeling empowered and ready to take action! more

A podcast providing information, inspiration and motivation for living your best life with Multiple Sclerosis. Learn to speak to this disease as it deserves - tell it FUMS every day! more

Multiple Sclerosis Podcast, hosted by Brooke Slick and Jodi Feltham: For Living a Life by Design not Diagnosis

Welcome to Living Well with MS, the podcast from the Overcoming MS charity. In each episode, your host Geoff Allix explores a different aspect of the Overcoming MS Program in greater depth by talking with experts and people with MS about health lifestyle changes. New episodes are published on Wednesdays and feature interviews with scientists, neurologists, fitness specialists, diet experts, stress reduction professionals. The podcast also features inspirational, real-life stories from people with multiple sclerosis following the Overcoming MS program, about the challenges and victories of managing symptoms through lifestyle modification. more

We all know that MS is a misunderstood disease that shows up differently for each of us. Each week an episode will be released that'll share the highs and lows of this unpredictable disease. My hope is that these episodes will shed some light for those who are newly diagnosed and those of us who have been living with it for years. Each week we will chat with someone who has been effected by Multiple Sclerosis, whether that be someone who lives with it, a family member, spouse, nurse or friend. more

Information, conversations, and stories from MS experts and people living with MS

A podcast dedicated to better understanding MS and learning to live well with MS. Together, we'll explore a wide range of medical information, lifestyle choices, therapies and other care options that can have a huge impact on our existing MS symptoms, as well as work toward healing to slow our MS progression. MS impacts everyone uniquely, but together, we can all live better with MS. Join the flock! more

Our podcast brings together a range of voices from the MS community to cover all aspects of life with multiple sclerosis. We know that living with MS can be life changing and can feel overwhelming at times. That's why we're here with you at each stage of the journey. Look, we know that we don't have all the answers. But our podcast's aim is to bring you the most up to date, trusted information from experts across the MS space including neurologists, therapists and researchers. Plus, hosts Helena and Nick hear real-life experiences from the MS community and find out your tips, tricks and the things that make you tick. We pose your burning questions to our experts and find out the information that you really want to know. Listen now for helpful information on symptoms, treatments, updates and a whole lot more. more

Move It or Lose It is a podcast about all things that Move the Mind, Body, Spirit and Soul. Your Host, Kathy Chester is an MS Warrior, Certified Personal and MS Fitness Trainer, Prenatal and Group Fitness Trainer. Having MS and Rheumatoid Arthritis and Epilepsy, Kathy brings insight and an inside view to how important MOVEMENT is to the Autoimmune community. We have fun guests and cover things that maybe others don't want to talk about regarding Multiple Sclerosis and other Autoimmune Diseases. more

Illuminating the invisibilities of autoimmune disease.Designed to bring voice to HSCT journeys highlight the snowflakes (individual experiences) and recognize our superpowers because we are as unique in our HSCT journey as we are in our experience with autoimmune disease. more

Welcome to My MS Podcast! I'm Alene Brennan, your host and fellow MS sister. On this podcast I'll be sharing with you my personal experience living with this unpredictable and invisible disease, along with my professional experience as a Nutrition Coach specializing in Multiple Sclerosis. This podcast is an invitation to elevate your life with MS to start thriving with MS. If you still want to dream big, pursue your passions, or simply find peace with your diagnosis - this is for you. Here, you'll find tools, conversations, and a community dedicated to helping you to reclaim your body, mind, and life from Multiple Sclerosis. Tune in every Monday, Wednesday and Friday and be sure to hit that subscribe button so you never miss an episode. more

The MSAA Podcast shares information, insight, and valuable resources from top medical professionals, MSAA staff members, and more with the goal to educate and spread awareness about MS. more

Kym Sellers, formerly of Cleveland's Radio One, WZAK, 93.1 was diagnosed with Multiple Sclerosis in 1992. The goal of this podcast is to share her personal experiences about this mysterious disease, highlight the experiences of families and friends who are affected by Multiple Sclerosis (MS), & provide outreach, awareness and education to individuals with Multiple Sclerosis and their families. more

Nora Gocking was diagnosed with Relapsing Remitting Multiple Sclerosis in 2015. She and her husband, Brian, decided to make major changes to their health. Listen in as Nora and Brian discuss faith, MS, running, and healthy eating. more

Brain Chat is a podcast with the world-renowned researcher, neurologist and MS specialist, Dr. Mitzi Joi Williams. Each episode, Dr. Williams will feature a special guest and cover all 'matters' of the brain as it relates to life, health, wellness, relationships, and science. more

I reversed a life-threatening and debilitating disease of multiple sclerosis (MS) in 2015 naturally. It's my mission now help others know that they have the power to heal too. Since I've totally healed, I have continued to research and interview other wellness professionals with more evidence that we can all heal and reverse this disease with diet and lifestyle changes. I have found that reversing MS is more than possible without medication. I have become a nutritionist, a certified health coach, speaker, and author to spread the word. This podcast will have tips, resources, and advice with real results. I conduct interviews of different wellness professionals for more healing modalities. I offer my health coaching services for those who need direction and a personalized, proven 12-week program. Let's get you back to the healthy person you're meant to be! Adrienne Scharli nutritionist, certified integrative health coach, author, and speaker Find me to help you reverse your MS diagnosis. https://nourishyourway.com/work-with-me/ Email me if you have questions: ****@nourishyourway.com Books on Amazon: Nourish Your Way to Health - cookbook The Path to Reverse Multiple Sclerosis Naturally - paperback Facebook: MS Support - Heal and Reverse Multiple Sclerosis https://www.facebook.com/groups/1349152931901644 more

Multiple Sclerosis News Today seeks to fill an unmet need in healthcare news journalism by providing patients and their families with a reliable news journal on MS that they can engage with on a daily basis for the latest news and MS resources. more

Brought to you by Bionews and Multiple Sclerosis News Today, this new, physician-led podcast hosted by Susan Payrovi, MD and Mirla Avila, MD, offers a comprehensive approach to managing MS, blending the latest treatment insights with practical lifestyle strategies.From symptom management to mental health and daily living tips, each episode delivers actionable advice and expert guidance, empowering you to confidently navigate your MS journey and take charge of your health. Tune in today and take control!Meet the hosts:Mirla Avila, MDInterim Chair of Neurology / Assoc. Prof. of NeurologyTexas Tech University Health Sciences CenterLubbock, TXDr. Avila is a board certified neurologist and MS specialist, and is the Director of Texas Tech Comprehensive MS Center. She is involved in several ongoing MS research projects and has authored numerous abstracts, book chapters, and peer-reviewed articles on MS treatment and management. A passionate neurologist and music enthusiast, Dr. Avila directs funds from her album sales to support patients in underserved communities and advance MS research.Susan Payrovi, MDIntegrative and Functional Medicine PhysicianStanford Center for Integrative Medicine living with MSSusan Payrovi, MD is a triple board-certified physician in anesthesiology, hospice and palliative medicine, and integrative medicine. She is also a patient who is diagnosed and living with MS. Dr. Payrovi is a clinical assistant professor at Stanford University, where her clinical practice focuses on non-pharmaceutical lifestyle treatments of chronic disease. She holds a bachelor's in Microbiology and Molecular Genetics from UCLA and a medical degree from UC San Diego. Dr. Payrovi is also certified in functional medicine. more

This podcast is about Women of colour living with neurological disorders, such as Multiple Sclerosis, Epilepsy, strokes, stiff body syndrome, etc. Fiddly Chic aims to create an awareness and understanding of the challenges, difficulties, and attitudes we often face. It has been documented that people with MS from BME communities are hard to reach which often leads to isolation, compounded by ignorance, stigmatisation leading to a lack of services and facilities to support them. We also experienced increased discrimination and prejudice within our communities which leaves a knock-on effect of isolation and rejection. We aim to utilise this platform, time, and space, to discuss the impacts living with a neurological condition can have, not only on the one with the illness but also on their friends and family. Disability of any type let alone MS which has no known cause or cure is seen as a taboo or curse so people shy away from talking about it we want to help change this mindset. Additionally, we aim to create a space where W.O.C (or anyone), can share their own experiences without feeling judged, ruining someone else's day, or being a burden. We aim to make this podcast relevant and informative, to anyone living with, or caring for, someone with a neurological condition. Fiddly chic. Email: ****@yahoo.com Instagram: fiddly_chic_woc more

Welcome to the BeeWellWithMS Podcast, hosted by Dr. Agne Straukiene, a full-time neurologist with a special interest in Multiple Sclerosis (MS). Our mission is to empower individuals living with MS, their families, and healthcare professionals with the latest knowledge, expert insights, and practical tools to enhance brain health and overall well-being.Through engaging conversations with leading experts, inspiring personal stories, and evidence-based lifestyle strategies, we explore a wide range of topics including MS management, new treatment guidelines, mental health, lifestyle optimization, and cutting-edge research. From understanding disease-modifying therapies (DMTs) to navigating pregnancy with MS or tackling smouldering MS, we aim to make the complex simple and accessible.Whether you're looking for professional guidance, personal motivation, or a sense of community, the BeeWellWithMS Podcast is your trusted companion on the journey toward living well with MS. Join us as we bridge the gap between science and everyday life, fostering resilience, empowerment, and hope.🎧 Listen, learn, and thrive with BeeWellWithMS! Become a supporter of this podcast: https://www.spreaker.com/podcast/beewellwithms-podcast-by-dr-agne-straukiene--5762905/support . more

Hey everybody my name is John, I'm 44, disabled wheelchair user, husband, parent, community radio DJ, small business owner, podcaster with multiple sclerosis and trigeminal neuralgia. I made the What's The Matter With Me? podcast to share what I'm going through. more

On My Nerves: MS Unfiltered is a candid multiple sclerosis podcast hosted by two Black adult first cousins living with MS, sharing the real conversations that happen between doctor's appointments. This show creates a safe, honest space for people living with multiple sclerosis and the people who support them to talk openly about MS symptoms , chronic illness , treatment decisions , and day-to-day life. Each episode explores what it really means to live with MS , including invisible symptoms like MS fatigue , brain fog , mobility changes, pain, and balance issues, plus the emotional and identity shifts that come with an MS diagnosis or ongoing relapses. Tim and Michelle (MSChelleRX) also talk through practical realities like navigating neurologist visits , understanding MS medications and disease-modifying therapies (DMTs) , managing flare-ups, and building routines that support MS wellness . This podcast is for anyone impacted by multiple sclerosis including newly diagnosed listeners, long-time patients, caregivers, partners, family members, and friends who want to understand what life with MS is like between appointments. Expect unfiltered conversations, lived experience, and encouragement that doesn't rely on toxic positivity. On My Nerves: MS Unfiltered goes beyond basic MS education . It's about patient advocacy , disability awareness , mental health, relationships, and building the language to communicate what you're experiencing physically, emotionally, and mentally. If you're searching for a multiple sclerosis support podcast that feels real, grounded, and relatable with honest talk on MS symptoms , MS diagnosis , MS treatment options , chronic illness life , and caregiver support , you're in the right place. more

An international podcast about living with Multiple Sclerosis. 2 Guys with MS not MS'ing around. Hosted by Nick and Terry, discussing and attempting to normalize the conversation around life with a chronic and invisible illness. more

We are literally—and figuratively—A Couple Takes on MS. We're Dan and Jennifer Digmann, a married couple both living with Multiple Sclerosis, Dan with RRMS and Jennifer with SPMS. For nearly two decades, we've built a life together grounded in love, resilience, and the belief that joy is still possible, even in the face of chronic illness. Through honest conversations and shared experiences, we explore what it means to navigate marriage, caregiving, and everyday life with MS. Some days are heavy. Some days are hopeful. Most are a mix of both. Join us every other week as we chat about the challenges, the victories, and everything in between—because life with MS is real and no one should have to face it alone. more

The Anti-Myelin Society Podcast features women of color from the Black and Latino communities who have been diagnosed with Multiple Sclerosis (MS). The hosts, Jojo, Taty, and Brika (introduced as new additional co-host in season II) share their experiences of navigating motherhood and building their careers, and health challenges while living with MS. In their discussions, they address various topics, including mental health, symptoms, and more. more

Welcome to The Raw Nerve the official Podcast of MS Australia a conversation space for all things multiple sclerosis.Join us for news and views on the latest research, treatments, and advocacy efforts, as well as candid and informative interviews with our community; those living with MS and their families and carers, together with leading clinicians, researchers, and advocates.www.MSAustralia.org.au/podcast more

This podcast is for anyone with Multiple Sclerosis. My intention is to show you that this condition does not have to 'become you', we are not defined by MS & we all have so much more to offer the world. I have had MS for 19 years, and feel inspired to spread a message of hope, to show you through my own story and that of others,that we CAN still LIVE a vibrant life. My message is always, MS may be a life changing condition,but it does not have to be a life ending one! Listen along and hopefully be inspired & encouraged to beat MS on your own terms. more

Listen to Medscape InDiscussion: Multiple Sclerosis, a podcast series where thought leaders and clinical experts share their diverse insights and practical ideas for optimizing patient care. Relevant disclosures can be found with the episode show notes on Medscape (https://www.medscape.com/viewarticle/977030). The topics and discussions are planned, produced, and reviewed independently of advertisers. This podcast is intended only for US healthcare professionals. more

Rolling Home is a podcast produced by residents and staff of The Boston Home in Dorchester, Massachusetts, which is a residential community for people living with neurological disorders, primarily multiple sclerosis, all of whom are wheelchair users.Here, we share of stories of community, friendship, resilience and adaptability as we strive to thrive with the support of The Boston Home's skilled staff along with the assistive technology that helps us continue to pursue our individual interests. more

The Wheels & Shaky podcast is presented by two people sharing their friendship and their lives with MS and Parkinson's disease. They take an irreverent look at the demands of daily activities, offer helpful product reviews, navigate public spaces, and highlight how their friends and families help them overcome everyday challenges with humor and humility.     more

In the MS-Perspektive Podcast, I present my view of multiple sclerosis and show you how you can make the best of the diagnosis. Because a beautiful and fulfilling life is also possible with multiple sclerosis.Here you will find information and strategies on how you can actively influence your course. In addition, I publish solo articles with my experiences, interview experts and on various topics related to living with MS as well as other affected people. In addition, there are a few episodes that serve the relaxation, positive attitude and stimulation. more

The ECTRIMS Podcast is a sounding board for MS experts & advocates to discuss innovative work in MS research, treatment and care with the greater MS research community, while offering a collaborative platform for MS and healthcare experts to promote & nurture the advancement of research. more

The Other Side of MS isn't here to inspire you—it's here to tell the truth. This podcast gives voice to the raw, unfiltered stories of people living with multiple sclerosis—the ones you rarely hear. Hosted by longtime MS advocate Casey Murphy, each episode pulls back the curtain on the emotional, invisible, and often uncomfortable realities of MS. From navigating public spaces with incontinence, to losing careers, marriages, or mobility, these aren't just stories of strength—they're stories of being human. We don't chase silver linings. We hold space for pain, for humor, for grief, for resilience—and for the voices that deserve to be heard without being sanitized or simplified. If you're ready for a podcast that doesn't sugarcoat the experience of living with MS, this is it. This is The Other Side of MS. more

A podcast about multiple sclerosis hosted by Justin Loizos. Each episode will explore the world of MS. This will either be done through interviews with MS stakeholders or with Justin providing information about the illness. Thank you for listening.  more

Welcome to MS Minute with DCND. Your podcast for understanding Multiple Sclerosis. Every month, our MS experts tackle a different topic to help you manage your disease and live a better life. more

We've recently updated our podcast cover — same show, new look! Welcome to MSMS: The Many Stories of Multiple Sclerosis Here, you'll hear real stories from real people—Australians and occasionally others from around the world—sharing their experiences of life with Multiple Sclerosis (MS). The podcast began with Colleen's hope to build greater understanding of Hematopoietic Stem Cell Transplant (HSCT), by spotlighting the stories of Australians living with MS who had undergone this intense and often misunderstood procedure. What started as a focus on HSCT has since grown to include a range of conversations relevant to Australians living with MS—honest, heartfelt stories that speak to the reality of this progressive disease. By sharing our experiences, we support one another, reduce the isolation that so often comes with MS, and foster a sense of community—while also raising much-needed awareness. The first series of MSMS centres on HSCT—the decision-making process, the challenges faced, and the individual outcomes that follow. In Episode One, you'll meet your host Colleen and her husband Kel, as they take you on their extraordinary journey to Moscow, Russia. It was there, just 5 years married and desperate to stop the rapid progression of her MS, that Colleen underwent HSCT. What followed was an ordeal of unexpected challenges—physical, emotional, and logistical. Through it all, Colleen the patient, and Kel her steadfast champion. Their story has been shared in Australian newspapers, radio and TV—but here, in their own words, Colleen and Kel share even more of their remarkable story, behind the headlines. --- Disclaimer: This podcast is not intended to replace professional medical advice. The views expressed in this podcast are those of the host or guest(s). No story told, view expressed or opinion voiced, written or otherwise shared in any episode of this podcast is to be taken as medical advice, including when related in an episode as a professional opinion or professional advice given. Always seek the guidance of your doctor or other qualified health professional with any questions regarding your health or medical condition. Content Warning: Multiple Sclerosis is an unpredictable condition and the conversations and stories in all episodes of this podcast will contain reference to MS symptoms as well as situations experienced before, during or after HSCT - some of which may be disturbing or upsetting for some. In Australia https://beyondblue.org.au and Lifeline on 13 11 14 or https://www.lifeline.org.au are organisations which provide assistance - do please look after yourself. more

I am a Physician Assistant working in Lifestyle Medicine and Multiple Sclerosis research. I also have MS, so I offer a rare and valuable dual perspective that can deeply resonate with both patients who have MS, as well as medical professionals treating MS patients. I wanted to create a safe place to discuss things related to MS and other autoimmune conditions. The views and opinions expressed on this podcast are my own and is provided for educational and informational purposes only. This is NOT intended as medical advice. Please consult your healthcare provider for further guidance. more

MS Ireland's New Podcast series 'Living with MS'.The Living with MS Podcast series aims to give a voice to the Irish MS community as our guests share their own personal multiple sclerosis story from diagnosis to today.Every person with MS has different symptoms, different reactions to being diagnosed, different journeys and this series aims to share those stories every month to hopefully help you get a better understanding MS.For more information on MS Ireland and multiple sclerosis go to our website here https://www.ms-society.ie Hosted on Acast. See acast.com/privacy for more information. more

It's the monster you can't see. The exhaustion that feels like concrete. The pins and needles that are anything but a joke.For over 20 years, Jenny has wrestled with Multiple Sclerosis. She knows the fear, the struggle, and the courage it takes to survive.Forget the clinical definitions. Get ready for the real talk. The raw, scary, and surprisingly hilarious truth of what it's like to live with The Demon Within. more

The Ch* ill* Chats: Two Halves of a Chronic Sh!t Show is for anyone living with chronic illness or loving someone who does and wanting real deal conversations from people who get it. Hosted by Ashleigh Rose and Jenna, it's giving big/little sister advice… from two women navigating a wildly unpredictable chronic condition together. We promise you won't be bored with lectures or unsolicited advice. Just honest conversations about navigating life with Multiple Sclerosis, managing visible and invisible symptoms, relationships, mindset, everyday life, and learning how to flow with the violent ups and downs of chronic illness. We share real stories, gentle insights, and lessons we've learned the freaking hard way. We're not here to pretend we have all the answers. We're two women living with MS and figuring it out in real time… sometimes calm, sometimes chaotic, always honest. If you're in the thick of it too, we hope these conversations feel like something you can settle into. Two halves of a chronic shit show, figuring it out as we go. more

Tune in for expert lectures on current hot topics in clinical care for MS. 

Welcome to 'Let's Talk MS' a podcast series created by young minds for young minds and proudly presented to you by the European Multiple Sclerosis Platform. In this podcast, we unpack the intricacies of living life as a young adult while navigating the challenges that come with Multiple Sclerosis (MS) and MS-related disorders (like NMO and MOGAD). From dating to nutrition or dealing with the MS stigma, we navigate it all through expert insights and personal stories. This podcast is a project of the European Multiple Sclerosis Platform. This episode if co-funded by Sanofi, Merck, Roche, Novartis, Alexion and Amgen who do not have any influence on the content of the project and their financial support does not constitute endorsement by EMSP of any of the companies' products or services. We thank them for their generosity and support. You can support our Podcast at https://www.patreon.com/emsp more

Lunch talk dives into the daily life of someone living with an autoimmune disease. The host Dominic Toupin goes into greater detail about his life after being diagnosed with RRMS (relapsing-remitting multiple sclerosis) over 2 years ago, being a voice for someone living with an autoimmune disease, someone who's newly diagnosed, or someone who's nervous or afraid to talk about their disease with others. Note: I am not a health care professional, what I do for myself might not work for others. Consult with your doctor before starting any new things that are discussed on this podcast. #MSWarrior more

At the age of 20, Sigurd Hartkorn was diagnosed with the serious and incurable disease multiple sclerosis. Now, 16 years later, he is ready to talk about it — not about the disease itself, but about what it has done to his way of being in the world. We will travel all the way from Moroccan nightclubs and endless drinking binges to depression and the fear of dying before his parents. This is a series about living in hiding from, despite, and because of the thing you cannot change. The podcast is produced and edited by Sigurd Hartkorn in collaboration with Danish MS Society. All the music is by Daniel Vognstrup. Read more and support at www.ifyoucry.com more

My Chronic Adventure is an honest, human podcast about living with MS, navigating healing, movement, and life when your body changes the rules — and choosing to expect more than just OK. more

A show about all things Multiple Sclerosis. Having MS for 15 years, I want to share my experience and hopefully inspire others! more

The life's journey of an MS Warrior: documenting a life of persistent faith and resilience while navigating Aggressive Relapsing-Remitting Multiple Sclerosis.Join me as I share the raw realities, the victories, and the strength found in the struggle.Welcome to The life's journey of an MS Warrior: beyond the curtains documenting a life of persistent faith and resilience while navigating Aggressive Relapsing-Remitting Multiple Sclerosis.Applause to myself and my persistent strength as I share the raw realities, the victories, and the strength found in the struggle.@MSWarrior@ResilientFaith@MultipleSclerosisAwareness@FaithOverFear@ChronicIllnessJourney@NewPodcast@InsomniaWarrior more

Welcome to MS is Chronic. If you have Multiple Sclerosis, are on a journey that is leading to an MS diagnosis or know someone with MS this podcast is for you. Having MS impacts people emotionally and physically. These episodes are with people living with, the often unpredictability, of MS day to day. Telling their story with honesty, openness, humour and stoicism. Sometimes the language can be a little blue. And the topics covered are from the heart, intimate and very personal. This is not science, medical or health advice. It is regular folk sharing their own experience and from time to time the chat moves from MS into the normal humdrum day to day of life. As the series develops guests will include perspective of family and friends of those with MS. I'll have professionals share their knowledge insight and advice too. If you'd like to be a guest in future series please get in touch. Thanks, Barney Black more

My Solo Journey with MS is a deeply personal and powerful documentary-style podcast chronicling Timothy Brien's experience living with relapsing-remitting multiple sclerosis (RRMS). Through candid reflections, medical milestones, and emotional insights, Timothy shares the reality of navigating life with MS—alone, but not without purpose. Whether you're newly diagnosed, a long-time multiple sclerosis warrior, or a caregiver seeking understanding, this podcast offers an honest look into the day-to-day challenges and victories of living with RRMS. Each episode explores the physical, emotional, and mental toll of multiple sclerosis, from the unpredictability of relapses to the journey toward remission and resilience.Join Timothy as he documents his evolving relationship with MS symptoms, treatment options, and personal growth, offering support and solidarity to others on a similar path. If you're searching for authentic stories about managing MS, overcoming isolation, and finding meaning through adversity, My Solo Journey with MS is your companion on the road. more

MS Compass: Guiding Clinical Care is a NeurologyLive podcast led by Lindsay Ross, MD, a board-certified neurologist specializing in multiple sclerosis and neuroimmunology at the Cleveland Clinic's Mellen Center. The series centers on the unique clinical considerations facing women with MS, from emerging research and evolving treatment strategies to gaps in care that are gaining renewed attention. Through conversations with expert guests across neurology and related disciplines, Dr Ross examines how science, advocacy, and real-world practice are shaping the next era of MS care for women. more