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

Crutches leaning against a light grey wall.

My Crutches

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

The Wheelchair

Ah, the wheelchair. That’s what I most want to talk about. For years I resisted… Read More

Dizziness

Dizziness is the bane of my existence. It’s my most persistent and irritating MS symptom.

A Double-Edged Sword

Understanding the role of central nervous system MRIs in diagnosing and managing the treatment of… Read More

The Long Walk to the Coffee Shop

As with most workplace accommodations, a little thought and sensitivity could have changed everything–they could… Read More

The Importance of Preventive Care

But preventive care should be a top priority for everyone with MS, adding quality and… Read More

On the Chopping Block

Honestly, I don’t think that I would have had the perspective on life and happiness… Read More