MS Blog - Momentum Magazine

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MS in Underserved Communities: Where Do We Go From Here?

Improving access to care for diverse populations within the MS community requires multiple approaches that address socioeconomic, cultural, geographic and disability-related barriers.

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Silver Linings Exist: Reflecting on a Decade With MS

10 years after her multiple sclerosis diagnosis, Kristen shares some of the unexpectedly positive side effects of her diagnosis.

How Caregiving as a Child Shaped My Life

A National MS Society employee shares his experiences growing up caring for his mom, who lived with MS, and how that shaped his life.

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Fluffy Ball of Cuteness: My Therapy Dog, Francesca

Francesca the therapy dog brings joy to her owner, Bob, who lives with MS.

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What You Need to Know About Fall Vaccines: Flu, COVID-19 and RSV

Dr. Lisa Doggett explains why people living with MS should plan to get vaccinated this fall.

Latest Blogs

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I get knocked down, but I’ll get up again

Recovering from a fall can be challenging. Read how one person gets up.

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Staying above water with MS

One blogger describes finding support and learning to love life again after his MS diagnosis.

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Breaking the cycle of exclusion: Embracing cultural competence in physical activity research for people with MS

Cultural competence in research involves considering the culture and diversity of a population.

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Still Dancing: Overcoming MS to Become an Atlanta Falcons Cheerleader

An MS diagnosis in college didn’t stop Téa from cheering for the NFL.

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Till MS Do Us Part

For one blogger, an MS diagnosis became a chance to rewrite their story.

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Across the Other Side of the Pond, but Connected Through MS

An activist in the U.K. discusses the challenges that the Black MS community faces here… Read More

A Black healthcare professional examines and MRI brain scan.

Can Black People Get MS?

A blogger debunks the myth that Black people are less likely to have multiple sclerosis.

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The Importance of Friendships

Friendship can bring stability to a life lived with MS, an unpredictable disease.

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“And So It Goes”

This writer describes how the works of Kurt Vonnegut helped him define his own journey… Read More

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My Crutches

Explaining to others why you use crutches can be frustrating if you have MS.

A Reflection 1 Year in: MS and COVID-19

During 2020, we were sometimes confined and isolated from friends and love ones; however, we… Read More

multiple sclerosis community Puerto Rico

Impacting MS Patients in Puerto Rico

There are only about 113 neurologists that care for about 3.3 million people in Puerto… Read More

Accessibility Claps and Slaps

I often find myself doing accessibility assessments. These may range from big, obvious things to… Read More

3 Ways My Tired Is Different from Your Tired

The one thing I find the most annoying though is how other people see fatigue…. Read More

“Are You Fine?”

I’d love to link arms with you on your journey; we no longer need to… Read More

6 Things You Need to Know About MS and the COVID-19 Vaccines

The National MS Society convened a group of MS experts to develop guidance so that… Read More