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

Apoyo a la familia y al cuidador / Family and Caregiver Support

Navigating Employment Changes

Living with MS as an LGBTQIA+ Person

Introducing the Ultimate MS Treatment Guide: Expanding Your MS Shared-Management Tool Repository



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

Disease and Symptom Management

Living with MS as an LGBTQIA+ Person

Introducing the Ultimate MS Treatment Guide: Expanding Your MS Shared-Management Tool Repository

Understanding Your MRI

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

Lifestyles and Meeting the Challenges

Navigating Employment Changes

Yoga and Mindfulness for MS

Working to Destigmatize Mental Health and MS

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 and MS

COVID-19 and MS

COVID-19 Vaccines and MS: The Importance of Getting Vaccinated

COVID-19 Vaccines and MS: Why Get a Booster Shot?

COVID-19 Vaccines and MS: The Detrimental Impact of COVID-19 on the African American MS Community

COVID-19 Vaccines and MS: The Cultural Context of Vaccine Hesitancy

Vacunas COVID-19 y EM: La Importancia de Vacunarse

Vacunas COVID-19 y EM: El Contexto Cultural de la Vacilación de las Vacunas

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


Diversity

Health Equities and Diversity

Apoyo a la familia y al cuidador / Family and Caregiver Support

Living with MS as an LGBTQIA+ Person

MS, Spirituality, and Health

COVID-19 Vaccines and MS: The Detrimental Impact of COVID-19 on the African American MS Community

COVID-19 Vaccines and MS: The Cultural Context of Vaccine Hesitancy

Vacunas COVID-19 y EM: La Importancia de Vacunarse

Vacunas COVID-19 y EM: El Contexto Cultural de la Vacilación de las Vacunas

Participating in Clinical Trials: Your Opportunity to Make a Difference

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


Covid and MS

Personal Stories

Changing Lives Monday to Sunday

Swim for MS – How to Get Started

Photographer Anna Webber – My MS Manager Ambassador

Tim’s Story – MSAA Board Member

Meet Cathy – Cooling

Meet Sara – MRI

Meet Simone – Swimming

Kristen’s Story – Swim for MS

Ginny’s Story – Swim for MS

Mary’s Story – Swim for MS

Mandy Iris’ Story – Swim for MS