Understanding Multiple Sclerosis
Start here, with a list of trusted information sources.
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Information, Support and Connection
Living with multiple sclerosis can bring questions about health, wellness, mobility, relationships, work, finances, and everyday life. You do not have to find every answer alone. This resource page is for you.
Find reliable information about multiple sclerosis, community support, wellness and adaptive activities, practical services, local connections, and trusted national organizations — whether you’re living with MS, supporting someone you care about, or preparing for conversations with your healthcare team.
MS is a chronic ne urological and autoimmune condition affecting the central nervous system. Its symptoms and progression can vary significantly from person to person.
Quick Resource Categories
Start here, with a list of trusted information sources.
Learn About MSExplore information that can help you understand a new diagnosis, and connect with others who have experienced a similar journey.
Find Newly Diagnosed ResourcesDiscover resources related to movement, emotional wellness, cognitive health, relationships, mobility, accessibility, and healthy daily routines.
Explore Wellness ResourcesFind guidance for supporting someone living with MS while also taking care of your own health and well-being.
Explore Care Partner ResourcesFor help with insurance, transportation, employment, equipment, financial concerns, and other practical needs, connect with the National MS Society’s MS Navigator® program.
Find a MS NavigatorConnect with free MS Bright Spots of Hope programs offering movement, education, social connection, wellness, and positive shared experiences.
Explore Our ProgramsMS Bright Spots of Hope provides free programs designed to educate, empower, inspire, and enhance wellness for people with MS and their support partners.
Understanding Multiple Sclerosis
Multiple sclerosis affects the brain, spinal cord, and other parts of the central nervous system. In MS, the immune system damages myelin, the protective covering around nerve fibers, which can interfere with communication between the brain and the body.
Because the location and severity of this damage can vary, MS may affect movement, vision, energy, sensation, balance, cognition, mood, and other aspects of daily life.
Recommended resource
The National Institute of Neurological Disorders and Stroke provides medically reviewed information about MS symptoms, diagnosis, treatment, disease progression, research, and symptom management.
Visit the NINDS MS Resource ↗Newly Diagnosed
Learning that you have MS may bring uncertainty, relief, concern, confusion, or many emotions at the same time.
You may be wondering:
You do not have to answer every question immediately.
Begin with reliable information, write down your questions, seek qualified healthcare professionals and connect with other people living with MS.
The National Multiple Sclerosis Society provides information for newly diagnosed individuals, including tools for understanding a diagnosis, wellness worksheets, educational programs, and support resources.
Local connection
MS Bright Spots of Hope offers judgment-free Sharing Socials for people who are newly diagnosed or younger adults living with MS. These gatherings provide an opportunity to:
The Newly Diagnosed Sharing Social is a supportive space specifically for people diagnosed within the last five years or those age 40 and younger. Other programs do not have these restrictions.
Wellness and Daily Living
Living well with MS can include medical treatment, movement, rest, emotional health, social relationships, meaningful activities, and access to supportive environments. Wellness will look different for every person.
The National MS Society organizes wellness resources around physical, emotional, spiritual, cognitive, and social well-being.
Our programs offer opportunities to explore wellness in a welcoming and adaptable environment.
Movement and Adaptive Recreation
Adaptive movement programs make it easier to stay active with support, modifications, and professional guidance. Options may include chair-based movement, yoga, aquatics, cycling, strength, balance, stretching, and relaxation.
Before beginning or changing an exercise program, speak with an appropriate healthcare professional, especially when you have new symptoms, mobility concerns, or other medical conditions.
Family Members, Friends and Care Partners
MS can affect the whole support network. Care partners, family members, and friends may help with transportation, appointments, mobility, medications, household needs, communication, and day-to-day decisions—but they need support, too.
Supporting someone does not mean you must manage everything alone.
Join us together
Friends, family members, and care partners are welcome at many MS Bright Spots of Hope programs.
Explore ProgramsTrusted National Organizations
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Reliable information about MS symptoms, diagnosis, treatment, research, and neurological health.
Visit NINDS ↗Information about MS, educational programs, support, MS Navigator services, healthcare resources, connection programs, research, and advocacy.
Visit the National MS Society ↗Programs and services for people affected by MS, including educational information and support resources.
Visit MSAA ↗Educational and wellness resources focused on helping people with MS and their support partners live full and meaningful lives.
Visit Can Do MS ↗A nonprofit that provides free services to address the critical needs of people with MS and their families, helping them maintain the best quality of life.
MS Foundation ↗Receive updates about MS Bright Spots of Hope programs, community opportunities, educational information, and newly added resources.
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Reliable information can help you understand your options. Community can help you feel supported while you find your way forward. MS Bright Spots of Hope is here to help you discover connection, encouragement, wellness, and hope.