National MS Society’s cover photo
National MS Society

National MS Society

Non-profit Organizations

Denver, Colorado 44,415 followers

We will cure multiple sclerosis while empowering people affected by MS to live their best lives.

About us

The National MS Society's vision is: A World Free of MS. The National MS Society's mission is: We will cure MS while empowering people affected by MS to live their best lives. For more information, please visit nationalMSsociety.org or call 1-800-344-4867. For more information on our career opportunities, visit: https://www.nationalmssociety.org/About-the-Society/Careers

Website
http://www.nationalMSsociety.org
Industry
Non-profit Organizations
Company size
501-1,000 employees
Headquarters
Denver, Colorado
Type
Nonprofit
Founded
1946
Specialties
Human Services, Special Events, Medical Research, Fundraising, Advocacy, Education, Financial Assistance, Multiple Sclerosis, Nonprofit, Bike MS, Walk MS, Community Engagement, and Healthcare Access

Locations

Employees at National MS Society

Updates

  • Staying mobile with MS starts with mindset. If your MS progresses, you may need to make adjustments to stay safe and independent at home, work and community. Changes in mobility don't mean you can't stay active. Incorporating mobility aids, working with your employer on reasonable accommodations, making adjustments to your vehicle and establishing a rehabilitation team are just a few ways to stay mobile and engaged with all aspects of your daily life. Learn how to get started: https://lnkd.in/gbec4_z6

    • A smiling person, Rachel, walks outdoors on a bridge using two walking sticks. Greenery and trees are visible in the background. Text on the image reads "Rachel, Diagnosed in 2018."
    • A person, Regina, sits in a motorized wheelchair on a sidewalk next to a brick and iron fence. Trees and greenery are visible in the background. A label on the image reads "Regina, Diagnosed in 1999."
    • A person, Andrea, using a walker is crossing a city street. The text "Andrea, diagnosed in 2009" is visible in the lower left corner. Cars and a pedestrian crossing are in the background.
    • A smiling person, Vickie, stands outdoors holding a cane. They are wearing an orange top and light blue jeans. In the background, trees, lawns, and a sign with an address are visible. Text on the image reads "Vickie, diagnosed in 2018."
  • Not only are women 3x more likely to be diagnosed with multiple sclerosis than men, women living with MS also experience unique symptoms and concerns. Many women find that their MS symptoms feel worse around their period, may develop bladder problems during menopause and must work with their doctors to determine how to manage DMTs while trying to get pregnant. Learn why MS may be more common in women and which healthy habits and practices can help manage symptoms: https://lnkd.in/gHtNjurH

  • Moms living with MS show up every day with a quiet toughness that often goes unnoticed. They're managing a fussy baby while fighting fatigue, balancing pediatrician visits with neurologist visits and learning that even the smallest wins are worth celebrating. MS touches every part of a mom's life — from pregnancy and parenting to playdates. This month, we're honoring the women who never stop showing up. A gift to the National MS Society helps accelerate research, resources and support for all women living with MS: https://lnkd.in/gJ_a7BUF Video: @keepmovingwithemily (Instagram)

  • Calling all MS healthcare professionals who treat people with MS: The National MS Society is inviting clinicians and healthcare professionals, and their administrative support colleagues from across the country to share their perspectives on the current ICD‑10 MS codes, which went into effect on October 1, 2025. These codes are used for billing and reimbursement, medical data collection, tracking mortality and morbidity, and patient care documentation. Your feedback will help evaluate how these codes are working in practice, how well they reflect the needs of the MS community, and will inform the Society's next steps in discussions with our key stakeholders. The survey takes approximately 10–15 minutes to complete. We greatly value your time and insights. Survey direct link: https://lnkd.in/gKCdYPfk Real‑World Impact of Recent ICD‑10 MS Code Changes Survey

    • A person in a lab coat and gloves works in a laboratory setting. Surrounding them are various lab equipment pieces. An orange banner reads: "Calling All MS Researchers - Real-World Impact of Recent ICD-10 MS Code Changes Survey." The MS Society's logo is in the corner.
  • Women are disproportionately affected by MS – diagnosed three times more often than men – and experience unique challenges related to pregnancy, menopause, gynecologic cancer and more. Despite this fact, research that guides care for women is still limited. To address these knowledge gaps, the Society is investing in eleven new research projects that focus on priority issues identified in global surveys of more than 5,000 women living with MS. Just a few of these projects will... — Study how to modify immune cells to make them more effective in women — Explore how pregnant women's use of disease-modifying therapies affects their children — Understand the impacts of MS on women going through menopause including how hot flashes affect MS symptoms and how menopause can contribute to loss of muscle strength. — Examine the effects of ovary removal on MRI results Investing in research that prioritizes women's health can improve how MS is understood, treated and managed for the millions of women who live with its effects every day. A gift to the National MS Society accelerates the research and support these women urgently need: https://lnkd.in/gJ_a7BUF

  • "Living with MS has reshaped my life, but also revamped my purpose. When I was first diagnosed in 2019, I made a promise to myself that MS might change how I move, but it will never stop me from showing up, thriving, and helping others do the same. I started a community committed to empowering Black women living with chronic illnesses to embrace resilience. We exist to create a safe and inclusive space where HER story, HER strength, and HER voice are amplified, celebrated, and supported. Through sisterhood and a strong network, we transform pain into purpose, challenges into victories, and create opportunities for women to live authentically and unapologetically. This journey has taught me that MS doesn't mean putting life on hold — it means learning to live it more intentionally, surrounded by love, community, and joy." — Rachel The MS movement is fueled by inspirational women like Rachel. This May, we're celebrating their unwavering strength. Learn how to rally your community in support of women impacted by MS: https://ntlms.org/smttlh

    • A person is seated in a white chair, surrounded by floral arrangements, with a backdrop reading "We are ill" in an indoor setting. They are wearing glasses, a jacket, a printed shirt, ripped jeans, and sneakers.
    • A group of people smiling under an orange "LET'S GO!" arch at a "Walk MS" event. They are standing on a city street with buildings and a large digital screen in the background. Some are wearing blue outfits or volunteer shirts, and one person is in a bright orange top.
    • A person smiles and laughs in a professional portrait. She is wearing glasses, a blue, orange, and tan shirt. and orange statement earrings.
    • The image shows a group of five women smiling and standing closely together. They are wearing bright, colorful clothing with logos and text related to multiple sclerosis.
  • Can we trust AI for medical advice? In the latest edition of Decoding MS, Tim Coetzee and Dr. Timothy Chou explore the role of AI in healthcare — including where it falls short and what it will take to get it right. As AI becomes more embedded in how people seek health information, this is an important conversation for the future of MS care and beyond.

  • What does it take to “decode” multiple sclerosis? Our President and CEO, Tim Coetzee, explores just that in Decoding MS, a new LinkedIn newsletter exploring the latest in research, care, innovation and the future of MS. This is just the beginning — follow for more!

    I’m excited to share Decoding MS with Tim Coetzee, a new newsletter where I’ll explore the many dimensions of multiple sclerosis, from scientific progress and innovation to access, care, and what’s next in the field. In each issue, I’ll share insights, perspectives, and occasional conversations with leaders advancing this work. I look forward to your thoughts and perspectives.

  • MS affects everyone differently, and for Hispanic individuals and families, that journey can come with unique experiences and challenges. The Hispanic MS Experience Summit creates space for connection, learning and community — bringing people together to hear from experts, access valuable resources and connect with others who understand the journey. Join us for this empowering program and be part of an MS movement where every story matters and every voice is heard. Register today: https://ntlms.org/hmses

  • "Strength is showing up with hope every single day." — Elsa Mendoza For her sons and husband, Elsa Mendoza is an inspiration and a foundation — a reminder that toughness doesn't have to be loud, that showing up can make all the difference and that a diagnosis does not define the future. Mothering with MS is uniquely challenging. It means being there for the people you love despite uncertainty, fear and pain. Taking on the school run even though your body is fighting you. Adjusting each day around unpredictable and often invisible symptoms. To all moms and mother figures living with MS: You carry more than most people see and show quiet, steady strength that often goes unnoticed. This Mother's Day and every day, we honor that strength. Learn more: https://lnkd.in/eY2cGfgu

Similar pages

Browse jobs