From the Community

Displaying 10 of 328 results

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  September 10, 2025

  Accessible Rideshare Apps May Be Imperfect, But They Are Worth Trying

  And the more of us with mobility impairments who get out and use rideshare apps, the better these services will become.

  • From the Community
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  September 3, 2025

  I Can’t Run a Marathon — But My Progressive MS Story Still Matters

  As someone with progressive MS, it can be hard to see and hear from people with MS who are “fine.” Because I’m not fine.

  • From the Community
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  August 13, 2025

  My RRMS Diagnosis Doesn’t Feel Like the Right Fit Anymore

  The current descriptors may have worked well 30 years ago, but they just don’t accurately describe MS today.

  • From the Community
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  August 13, 2025

  Understanding MS Begins With the Words We Choose

  Commonly, when seeing people with MS, I see that our current descriptors of the disease fall short in capturing everything that MS is.

  • From the Community
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  August 4, 2025

  Finding a Spanish-Speaking Neurologist Made All the Difference

  When I was diagnosed with MS at 24 years old, I wasn’t sure how I was going to translate my diagnosis to my Spanish-speaking parents.

  • From the Community
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  July 28, 2025

  How Pediatric MS Impacted My Career Goals

  Ever since I was a child, I knew I wanted to become a doctor ... Following my diagnosis, I knew I wanted to specialize in neurology.

  • From the Community
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  July 23, 2025

  The Benefits of Adaptive Ballet for MS

  Learn about the benefits of dance for people living with MS and get tips for adaptive ballet.

  • From the Community
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  June 30, 2025

  Disability Law Handbook: Know Your Rights

  You should know your rights as you navigate a world filled with barriers.

  • From the Community
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  June 24, 2025

  A Message From Our CEO: New & Upcoming MS Advances

  Whatever the challenges ahead, we will face them together, and we will not stop until we have cured this disease for every single person living with MS.

  • From the Community
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  June 24, 2025

  When Life with MS Feels Like Playing Jenga

  Jeffrey Gingold explains how living with MS can be a lot like a game of Jenga.

  • From the Community