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.

Driving My MS

I need to keep revving my body and mind, resting and refueling with energy, avoiding… Read More

Not Pre-Existing

Remember the person behind the label. They are more than their pre-existing condition, and they… Read More

The Road Ahead

I find that optimism is valuable therapy in my battle against MS. But sometimes, I… Read More

If That Day Comes

If a day does come when my disability shows, I’ll handle it then. Not just… Read More

When You Have MS, Politics is Personal

I live with the omnipresent threat that the health care which keeps me functioning, which… Read More

Helping Others to Understand

How many times have you been stumped in describing how you’re feeling, simply because you… Read More