I'm supporting National MS Society! (2024)

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A cure is on the line.

Walk MS unites the MS community in the largest gathering of its kind to raise funds and make a difference for everyone living with MS.

Whether you live with MS, love someone who does or are part of the wider community, at Walk MS you can proudly display your role in the movement and be celebrated for the important part you play.

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Walk to End MS

Learn how Walk MS brings us together to rally for those affected by MS because a cure is on the line.

How Walk MS Works

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Register for one of our in-person events or participate virtually through our Walk MS: Your Way option.

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Your Impact

No one has to face MS alone

Funds raised through Walk MS support programs and services – like MS Navigator® – so everyone has what they need to take back control from MS.

No one has to face MS alone

Our compassionate, highly skilled MS Navigators ensure no one faces this disease alone. Each year, 50,000 people affected by MS receive in-depth, personalized support from MS Navigators to help them tackle the unique challenges of MS – including finding healthcare providers, prescription assistance, emotional support resources and crisis intervention in times of need.

Darrin, Diagnosed 2007

"Yes, I have this condition. Will you help me fight it? Can you help me raise funds? Can you help me spread the word?" Walk MS has allowed me to reach out to a circle that I never knew that I had. When you just ask the question, it's amazing how people just rally around you and uplift you, and make you just feel like, "Let's go do some more."

Darrin, Diagnosed 2007

As men, we're taught to be strong, rub it off, not talk about things that may be affecting us in an adverse way because we may be seen as weak or can't handle it. The circles of support, as I started reaching out to other people about what I was going through, it's amazing how people rallied around me to support me.

Building on more than 75 years of progress

The National MS Society has paved the way for all MS treatment options that exist today and funded over $1.1 billion in research since 1946.

Building on more than 75 years of progress

Walk MS participants have played a critical role in fueling research and treatment by raising over $1 billion since the event’s inception. See how this passionate community continues to bring us one step closer toward a cure. Learn more >

Rosa, Diagnosed 2021

My circle of support is important because it makes me feel safe. It makes me feel secure. It makes me feel like somebody has my back. My circle of support is actually my family, my very close friends and I rely on them a lot.

Rosa, Diagnosed 2021

Walk MS is like walking into a world that you belong to. I feel like I walk in a world where I don't belong because not everybody around me has MS. I feel like not everybody understands. So, walking into Walk MS, it's a whole different world, and you feel like you belong, you feel like you can connect with everybody else and it's a great feeling.

Pathways to Cures

Pathways to Cures is the biggest, most collaborative MS research effort of our time with MS organizations and scientific leaders from across the globe agreeing that this is the way forward to stop MS, restore lost function and end MS forever.

Pathways to Cures

Just as the experience of living with MS is different for every person, every person’s cure for MS may look different. The National MS Society is uniting the brightest minds – including MS organizations, scientists, donors and people living with MS across the world – to pursue the most promising research to reach these cures as fast as possible.

Heidi, Diagnosed 2009

I'm very blessed with my circle of support. From day one, I've had a tremendous amount of friends, family and coworkers who have been there, who have lent an ear, donated money, stood beside me and been there no matter what.

Heidi, Diagnosed 2009

I find so much joy giving back to others and helping to bring awareness of MS because there's so much that people don't know. Where it is now from where it was 20, 30, 40 years ago is so vastly different.

Together We Are Stronger

Thank You to Our National Sponsors

I'm supporting National MS Society! (1)

Bristol Myers Squibb is proud to support the MS community and return as a National Sponsor in 2024.

I'm supporting National MS Society! (2)

EMD Serono is committed to supporting the MS community and proud to return as a National Sponsor of Walk MS!

I'm supporting National MS Society! (3)

We thank Genentech as they proudly return for the 9th year as a National Sponsor of Walk MS!

I'm supporting National MS Society! (4)

Proud to walk with the MS Community for the 13th consecutive year!

I'm supporting National MS Society! (5)

Fundraising made easier with our NEW DonorDrive App

We have a brand-new app this year! Download the NEW DonorDrive app to connect to Walk MS and access exclusive features that will level-up your fundraising. Quickly deposit checks, easily create and share QR codes, track your fundraising progress, ask for donations and more from the palm of your hand.

I'm supporting National MS Society! (6)DonorDrive Charity Fundraising App

I'm supporting National MS Society! (9)DonorDrive Charity Fundraising App

I'm supporting National MS Society! (2024)

FAQs

Is National MS Society a good charity? ›

The National MS Society meets all 20 BBB Wise Giving Alliance Standards.

What does the MS Society do for people with MS? ›

We fund world-leading research, share the latest information and campaign for everyone's rights. Together we are a community and together we can stop MS. We understand what life's like with MS. And we know together we are stronger.

What is the goal of the National MS Society? ›

The National MS Society's vision is: A World Free of MS. The Society's mission is: We will cure MS while empowering people affected by MS to live their best lives.

What to say when someone tells you they have MS? ›

What to say to someone who has MS
  • I am here for you.
  • I care about you.
  • I'd really like to help as best as I can. ...
  • You can always lean on me.
  • It's okay to show your emotions to me. ...
  • I want to give you a great, big hug because I care.
  • Let's talk about how you really feel.
May 17, 2017

How much of the National MS Society goes to charity? ›

Programs
Client and community services$46,140,446
Public education$40,534,925
Research and scientific studies$30,400,823
Professional education and training$6,791,475
Total Program Expenses:$123,867,669

What is the best charity for multiple sclerosis? ›

Founded in 1986, the Multiple Sclerosis Foundation, known in the MS community as MS Focus, is a nonprofit organization focused on providing free services that addres ...

Who runs the National MS Society? ›

Cyndi Zagieboylo - National MS Society | LinkedIn.

What are the common complaints of people with MS? ›

Multiple sclerosis (MS) is a disease of the central nervous system that can affect the brain, spinal cord and optic nerves. Common symptoms include fatigue, bladder and bowel problems, sexual problems, pain, cognitive and mood changes such as depression, muscular changes and visual changes.

What should people with MS not do? ›

It's recommended that people with MS avoid certain foods, including processed meats, refined carbs, junk foods, trans fats, and sugar-sweetened beverages. Other tips to manage MS symptoms include: making meals in bulk. using “ready-to-use” grocery items.

Which type of MS is the least common type of the disease? ›

A small percentage of individuals are initially diagnosed with a less common form of MS known as progressive-relapsing MS (PRMS). This type of MS steadily worsens from the onset, but symptom flare-ups – with or without remissions – are also present.

What does the MS Society stand for? ›

Brief from the Multiple Sclerosis Society of Canada.

What is the most common type of MS? ›

Relapsing Remitting MS is the most common form of MS. About 85% of people with MS are diagnosed with RRMS. It is caused by flare ups or exacerbations of the neurological symptoms of MS, also known as relapses, followed by periods of recovery or remission.

Who is the most famous person with multiple sclerosis? ›

Famous Faces of Multiple Sclerosis
  • John King. 1/18. CNN anchor John King announced he has MS during a panel discussion on the topic of COVID-19 vaccinations. ...
  • Christina Applegate. 2/18. ...
  • Selma Blair. 3/18. ...
  • Art Alexakis. 4/18. ...
  • Montel Williams. 5/18. ...
  • Jamie-Lynn Sigler. 6/18. ...
  • Jack Osbourne. 7/18. ...
  • Trevor Bayne. 8/18.
Mar 9, 2024

What is the divorce rate for people with multiple sclerosis? ›

In one Australian study, the most severely disabled patients with multiple sclerosis were four times more likely to have been divorced than the less disabled; but even among the most disabled the prevalence of divorce was only 13%-18% of all prevalent patients.

What is multiple sclerosis life expectancy? ›

Many people with MS live for as long as the general population. Studies on the effect of MS on life expectancy have been carried out in several countries. The results from these studies suggest that, on average, having MS reduces your life expectancy by six to seven years.

How long has the National MS Society been around? ›

The National MS Society (the MS Society) was founded in 1946 by Sylvia Lawry “to end the devastating effects of multiple sclerosis.” Her brother had been diagnosed with MS and doctors told her there was nothing they could do for him. In response, she established a foundation that would be devoted to research on MS.

What is the life expectancy of a person with MS? ›

MS isn't a fatal condition in most cases, and most people with MS have a close-to-normal life expectancy. But since the disease varies so much from person to person, it can be difficult for doctors to predict whether their condition will worsen or improve.

Who is the CEO of the National MS Society? ›

Cyndi Zagieboylo

Cyndi ensures we live our Cultural Values to inspire confidence so that people engage with the Society and take action.

Is National MS Society a 501c3? ›

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