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
National MS Society
Non-profit Organizations
Denver, Colorado 44,414 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
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http://www.nationalMSsociety.org
External link for National MS Society
- 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
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Primary
Get directions
900 S Broadway
2nd Floor
Denver, Colorado 80209, US
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Get directions
733 Third Avenue
3rd Floor
New York, New York 10017, US
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Get directions
1100 New York Avenue, N.W.
Suite 660
Washington, D.C. 20005, US
Employees at National MS Society
Updates
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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
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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)
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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
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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
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"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
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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.
I'm excited to share issue 2 of Decoding MS with Tim Coetzee. In this newsletter I share a commentary co-authored with Timothy Chou exploring General AI models and healthcare. There's a lot to be excited about, and cautions to consider. Thank you for reading!
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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.
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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
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"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