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.
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.
There is a lot of information about multiple sclerosis (MS) Learn more
MS is thought to start as a reaction where the immune system attacks the central nervous system (CNS) by mistake
Everyone experiences MS differently. For a doctor’s purposes, there are 4 types of MS:
"Who gets MS" is more complicated than separating people into race and gender.
Statistically, MS is most often diagnosed in:
MS affects different types of people in different ways:
Genetics likely play a role in MS, but genes don’t tell the whole story
MS is not common worldwide, but it is more common in people farther away from the equator
Epstein-Barr virus (EBV) may be associated with MS but is not adirect cause
There is no single symptom or test that can properly diagnose MS. Some MS symptoms:
Because MS is different for everyone, doctors follow the McDonald criteria to diagnose it. The criteria look at:
MRI is the best way to detect lesions in the brain and spinal cord that almost all people with MS have. MRI can:
MRI does have limitations. Scans can sometimes:
MRI is not a complete diagnosis
Most people with MS can expect to live as long as their peers who don’t have MS.
Living with MS is much different today than it was 20 years ago
Doctors describe disability using the Expanded Disability Status Scale
Fatigue is one of the most common symptoms of MS. It does not mean a person’s MS is severe
Because MS affects everyone differently, there is no “normal†MS disease course
Although there is no cure for MS, there is progress toward effectively managing it
Stem cells are both a new frontier and a highly controversial field
Many women with MS can and do have children. It’s important to consider:
When done correctly, exercise can benefit people with MS
People with chronic illnesses like MS who are considered to have a disability are guaranteed certain rights in the workplace
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:
Below are links to useful multiple sclerosis (MS) resources Learn more
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 is an innovative provider of lifestyle empowerment programs for people with MS and their support partners. Go to the site
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
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
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
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
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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