PATIENT RESOURCES

There is a lot of information about multiple sclerosis (MS), but not all of it is easy to understand. This section of the MS Atrium connects people with multiple sclerosis and their care partners to helpful information about multiple sclerosis.

  • My MS Story

    Everyone touched by multiple sclerosis (MS) has a different story. Here you can watch 5 people tell theirs.
    Learn more

    MS stories change based on where people are in their lives.
    Meet 5 people with unique experiences and perspectives on living with MS.

     
    MELISSA
    Married, raising twins
    Diagnosed 14 years ago
    NICOLE
    Planning her wedding
    Diagnosed 3 years ago
    DARREN
    Taking on MS every day
    Diagnosed 5 years ago
    CRYSTAL
    Married with 2 kids
    Newly diagnosed
    ERIC
    Supporting his wife
     






     
  • The Truth About Multiple Sclerosis (MS)

    There is a lot of information about multiple sclerosis (MS)
    Learn more

     

    How does multiple sclerosis happen in the body?

    MS is thought to start as a reaction where the immune system attacks the central nervous system (CNS) by mistake

     

    Is there only one type of MS?

    Everyone experiences MS differently. For a doctor’s purposes, there are 4 types of MS:

    • Relapsing-remitting (RRMS)
    • Secondary-progressive (SPMS)
    • Primary-progressive (PPMS)
    • Progressive-relapsing (PRMS)
     

    Who gets MS?

    "Who gets MS" is more complicated than separating people into race and gender.

    Statistically, MS is most often diagnosed in:

    • People in their 20s and 30s
    • Women
    • People of Northern European descent

    MS affects different types of people in different ways:

    • Men may progress faster than women
    • People of African descent may experience more severe MS
    • MS affects people of all genders and races differently
     

    Is MS a genetic condition?

    Genetics likely play a role in MS, but genes don’t tell the whole story

    • Greater risk of getting MS if a parent or sibling has it
    • Only 2% of parents with MS have a child with the condition
     

    Does where I live affect my risk of getting MS?

    MS is not common worldwide, but it is more common in people farther away from the equator

    • MS is not common worldwide, but it is more common in people farther away from the equator
    • Current research suggests there is a link between vitamin D deficiencies and MS
      • Sunlight is a source of vitamin D
      • Current research suggests a link between MS and not having enough vitamin D
    • More research is needed to understand the relationship between geography, vitamin D, and MS
     

    What is the Epstein-Barr virus?
    Does it cause MS?

    Epstein-Barr virus (EBV) may be associated with MS but is not a
    direct cause

    • 99% of people with MS have been exposed to EBV
    • 95% of everyone else has, too
    • More research is needed to determine the relationship between MS and EBV
     

    Why is MS so hard to diagnose?

    There is no single symptom or test that can properly diagnose MS. Some MS symptoms:

    • Are not clear signs of MS
    • Change over time

    Because MS is different for everyone, doctors follow the McDonald criteria to diagnose it. The criteria look at:

    • Medical history
    • Neurological exam
    • MRI
     

    What can magnetic resonance imaging (MRI) tell doctors about MS?

    MRI is the best way to detect lesions in the brain and spinal cord that almost all people with MS have. MRI can:

    • Show “clinically silent” lesions
    • Find disease activity that doesn’t cause symptoms

    MRI does have limitations. Scans can sometimes:

    • Look like other conditions
    • Fail to show the cause of certain symptoms

    MRI is not a complete diagnosis

     

    Is MS fatal?

    Most people with MS can expect to live as long as their peers who don’t have MS.

     

    Does everyone with MS end up in a wheelchair?

    Living with MS is much different today than it was 20 years ago

    • Symptom management improves quality of life
    • The majority of people with MS do not become severely disabled

    Doctors describe disability using the Expanded Disability Status Scale

     

    When can MS affect memory and concentration?

    • Cognitive problems affect 30%-70% of people with MS
    • They can happen at any time of the disease
    • Cognitive problems can occur early in the disease even when someone doesn’t have signs of physical disability
    • Cognitive symptoms are invisible but can be hard for people with MS to deal with
    • Practical, effective ways to help manage problems with cognition:
      • Support from friends and family
      • Programs focused on ways to cope with cognitive symptoms
     

    If someone with MS is tired, does it mean that her or his disease is severe?

    Fatigue is one of the most common symptoms of MS. It does not mean a person’s MS is severe

    • Fatigue affects about 70% of people with MS
    • Ways to manage fatigue include regular exercise and conserving energy
     

    Is it normal to have more than one relapse per year?

    Because MS affects everyone differently, there is no “normal” MS disease course

    • How often relapses happen varies from person to person
    • More than one relapse per year may be a sign that the MS could be better controlled
     

    When you don’t feel symptoms, does it mean MS has stopped?

    • Relapsing-remitting MS symptoms come and go
    • It is possible for someone with MS to feel better
    • Symptoms aren’t the only signs of MS
    • Signs of MS may be "clinically silent"
    • Stress, fatigue, heat, and infection can make MS symptoms temporarily worse
    • Treating MS is a marathon—not a sprint
    • MS treatments focus on managing MS for life
     

    Is there a cure for MS?

    Although there is no cure for MS, there is progress toward effectively managing it

    • A number of therapies are approved to reduce relapses
    • Symptom management options aim to improve quality of life for people with MS and their families
    • Research continues to expand our understanding
     

    Can stem cells stop relapses and even
    reverse MS?

    Stem cells are both a new frontier and a highly controversial field

    • More research is necessary to understand their promise
      and dangers
    • No stem cell treatment is currently approved by the FDA
     

    Can women with MS have children?

    Many women with MS can and do have children. It’s important
    to consider:

    • There is only a 2% chance of passing MS to a child
    • Risk of relapse goes down during pregnancy
    • Risk of relapse goes up for 3 months after delivery
     

    Is it true that people with MS cannot exercise?

    When done correctly, exercise can benefit people with MS

    • Improve symptoms, disability, and quality of life
    • Possible activities include walking, cycling, yoga,
      and weight training
    • Precautions make exercise safer
     

    Is it true that people with MS cannot work or go to school?

    • MS does not necessarily mean an exit from the workplace
      or from school
    • MS treatments and symptom management strategies are available to make working easier
    • Disclosing MS is a personal choice

    People with chronic illnesses like MS who are considered to have a disability are guaranteed certain rights in the workplace

     
  • "What You Need to Know About Magnetic Resonance Imaging (MRI)" Video

    This video shows you what to expect from an MRI.
    Learn more

    It will take you step by step through what happens during an MRI.

    Watch now to learn:


    • What an MRI is and how it works
    • How to get ready for an MRI
    • What an MRI can tell you about MS
    • What to do after an MRI

    CHAPTER 1:
    What you need to know about MRI
    CHAPTER 2:
    What MRI tells your doctor
    CHAPTER 3:
    How to prepare
    CHAPTER 4:
    What to expect
    CHAPTER 5:
    Discussing your results
    CHAPTER 6:
    Things to remember
     
  • Additional Resources

    Below are links to useful multiple sclerosis (MS) resources
    Learn more

    American Academy of Neurology logo

    American Academy of Neurology (AAN) Patient Site

    The American Academy of Neurology's website helps you and your family understand neurology and the science behind neurologic disorders, including multiple sclerosis, and available treatments.
    Go to the site

    Can Do MS logo

    Can Do MS

    Can Do MS is an innovative provider of lifestyle empowerment programs for people with MS and their support partners. Go to the site

    MS World logo

    MS World

    MSWorld.org is managed by volunteers all diagnosed with MS and provides online support to more than 65,000 people worldwide living with MS. We have been providing chat and message boards for the National MS Society since 2001. MSWorld, where wellness is a state of mind! Go to the site

    Multiple Sclerosis Association of America logo

    Multiple Sclerosis Association of America (MSAA)

    The Multiple Sclerosis Association of America (MSAA) is a national, nonprofit organization dedicated to enriching the quality of life for everyone affected by MS. MSAA provides informative publications, online videos, Helpline, equipment distribution, educational events, MRI funding, and more. Please visit www.msassociation.org or call (800) 532-7667. Go to the site

    Multiple Sclerosis Foundation logo

    Multiple Sclerosis Foundation (MSF)

    The Multiple Sclerosis Foundation offers a wide array of free services, including national toll-free support, homecare, support groups, assistive technology, and more, to improve the quality of life for those affected by MS. Go to the site

    National Family Caregivers Association logo

    National Family Caregivers Association (NFCA)

    The National Family Caregivers Association (NFCA) empowers family caregivers to act on behalf of their loved ones and themselves and remove barriers to health and well-being. NFCA helps hundreds of thousands relieve their isolation, develop skills for finding help, and advocate for themselves and their loved ones in healthcare settings. Through print publications, the Web, phone, media, and face-to-face interactions, NFCA is there for family caregivers. Go to the site

    National Multiple Sclerosis Society logo

    National Multiple Sclerosis Society (NMSS)

    The National MS Society, through their 50-state network of chapters, helps people with MS and their families move their lives forward by funding research, driving change through advocacy, facilitating education, and providing programs and services. Go to the site

     

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This website is intended to be an educational resource for U.S. residents and does not constitute medical advice.

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