De la comunidad

Se muestran 10 de 328 resultados

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  10 de septiembre de 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.

  • De la comunidad
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  3 de septiembre de 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.

  • De la comunidad
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  13 de agosto de 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.

  • De la comunidad
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  13 de agosto de 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.

  • De la comunidad
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  4 de agosto de 2025

  Impacto de encontrar un neurólogo que habla español

  Cuando recibí el diagnóstico a los 24 años, me pregunté cómo se lo explicaría a mis padres hispanohablantes.

  • De la comunidad
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  28 de julio de 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.

  • De la comunidad
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  23 de julio de 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.

  • De la comunidad
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  30 de junio de 2025

  Disability Law Handbook: Know Your Rights

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

  • De la comunidad
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  24 de junio de 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.

  • De la comunidad
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  24 de junio de 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.

  • De la comunidad