Multiple Sclerosis Information (MSi) Video Library
On-Demand Videos, Webinars, and Webcasts
Welcome to MSAA’s video program initiative, Multiple Sclerosis Information (MSi). Through the MSi initiative, MSAA offers an extensive library of on-demand video programming, webcasts, and webinars that bring information and empowerment right into the privacy and comfort of a person’s home.
Most Recent Videos
▷ Keys to Adapting Your Environment
▷ Understanding Progression in MS
▷ Exploring the Landscape of MS in Black Americans – February 2022
Understanding MS
▷ Understanding MS: Full Video
▷ What is MS?
▷ Possible Causes
▷ The MS Process
▷ Who Gets MS
▷ MS Diagnosis
▷ Types of MS
▷ Relapse Management
▷ Treatment Importance
▷ MS Treatments
▷ MS Symptoms
▷ Wellness Tips
▷ How MSAA Can Help
Disease and Symptom Management
▷ Understanding Progression in MS
▷ The Science Behind MS
▷ Approaches to Managing MS in 2022: A Research Update – January 2022
▷ What’s New in MS Research: A Look Into the Future of Multiple Sclerosis Treatment – July 2021
▷ Managing Depression and Anxiety in MS
▷ Support for the Newly Diagnosed
▷ A New Diagnosis: Is What I’m Feeling Normal?
▷ Building Your Healthcare Team
▷ Best Practices in MS: What We Know, What We Don’t Know, and What We Hope
▷ Measuring Brain Health – MS On Your Mind Part 2
▷ The Science of Brain Health – MS On Your Mind Part 1
▷ Clarifying the Confusing World of Clinical Trials in Underserved Populations
▷ Helpful Tools for MS Relapse Management
▷ A Closer Look at Managing MS Fatigue
▷ A Closer Look at The Value of MRIs
▷ A Closer Look at Clinically Isolated Syndrome
▷ A Closer Look at Multiple Sclerosis Symptoms – Part 1
▷ A Closer Look at The Importance of Treating and Managing MS Relapses
▷ How to S.E.A.R.C.H.™ for the Right MS Therapy For You
▷ Understanding Depression and Multiple Sclerosis
▷ Latest MS Research Updates: A Review of the Most Promising MS Research Happening Now
▷ Why Do I Cry or Laugh Inappropriately? featuring Daniel Kantor, MD
Lifestyles and Meeting the Challenges
▷ Keys to Adapting Your Environment
▷ What’s for Dinner? Let’s Talk About Nutrition and MS
▷ Close to Home: How to Leverage Your Relationship with Your PCP
▷ Rural Perspectives on Living with MS
▷ The Medical Road Trip: Seeking Care and Resources Outside of Your Hometown
▷ Creative Communities: Taking Advantage of Unconventional Resources
▷ Stretch and Strengthen
▷ Healthy Relationships and Living with MS
▷ Helping Those That Help Us: A Program for Care Partners
▷ How We Talk to Ourselves and The People That Support Us
▷ Managing Depression and Anxiety in MS
▷ Finding Purpose in Life
▷ What Now? 2020 Post-Election Update
▷ It’s a Generational Thing: Creating an Understanding of MS Between Parents and Their Children (Part 2)
▷ It’s a Generational Thing: Creating an Understanding of MS Between Parents and Their Children (Part 1)
▷ Losing Connection: Difficult Discussions in a Virtual World
▷ Mind, Body, and Spirit: A Comprehensive Overview of Wellness in MS
▷ An Integrated Approach to Wellness for MS Patients and Care Partners
▷ Employment and Disability Benefits for People Living with MS
▷ Unlocking the Keys to Health and Wellness in MS
▷ Keeping it Simple: Everyday Mindfulness for People Living with MS
▷ The Importance of Wellness Care in MS
▷ Creating Healthy Habits for a Healthy Lifestyle
▷ The Partnership of Care: Redefining Caregiver to Care Partner
▷ Intimacy and Family Planning with MS
▷ What Happened to My Copay Assistance? How Copay Accumulators Are Affecting You
▷ MS Nutrition: A Four-Part Series with touchNEUROLOGY
▷ Yoga and MS: Start Where You Are
▷ Introduction to MS Aquatic Fitness
▷ A Closer Look at The Benefits of Exercise
▷ Making Your Home Work For You – Improving Home Safety and Accessibility
▷ A Closer Look at MS and Complementary and Alternative Medicine
▷ A Closer Look at Managing Stress and MS
▷ A Closer Look at the Emotional Impact of MS
COVID-19 and MS
▷ What You Need to Know About COVID-19 and MS – Program 9
▷ New Directions: How to Navigate the COVID-19 Pandemic as a Person of Color Living with MS
▷ What You Need to Know About COVID-19 and MS – Program 8
▷ What You Need to Know About COVID-19 and MS – Program 7
▷ What You Need to Know About COVID-19 and MS – Program 6
▷ What You Need to Know About COVID-19 and MS – Program 5
▷ Understanding the COVID-19 Impact on MS in People of Color
▷ What You Need to Know About COVID-19 and MS – Program 4
▷ What You Need to Know About COVID-19 and MS – Program 3
▷ What You Need to Know About COVID-19 and MS – Program 2
▷ What You Need to Know About COVID-19 and MS – Program 1
Health Equities and Diversity
▷ Exploring the Landscape of MS in Black Americans – February 2022
▷ Close to Home: How to Leverage Your Relationship with Your PCP
▷ Rural Perspectives on Living with MS
▷ The Medical Road Trip: Seeking Care and Resources Outside of Your Hometown
▷ Creative Communities: Taking Advantage of Unconventional Resources
▷ Lo nuevo en EM: A dónde ir desde aquí
▷ How We Talk to Ourselves and The People That Support Us
▷ Mujeres Fuertes: Viviendo con Esclerosis Múltiple como Latina
▷ Making Sense of “Me” and My MS Diagnosis
▷ El Poder del Cerebro: Mantener una Mente Sana Mientras se Vive con EM
▷ New Directions: How to Navigate the COVID-19 Pandemic as a Person of Color Living with MS
▷ Understanding the COVID-19 Impact on MS in People of Color
▷ The Many Faces of MS: Exploring Diversity and Differences
▷ MS Research Mythbusting
▷ Clarifying the Confusing World of Clinical Trials in Underserved Populations
▷ The African American Experience and Multiple Sclerosis
▷ Hispanic American MS Experience
▷ Experiencia Hispanoamericana sobre Esclerosis Múltiple
▷ Women Living with MS
