The Joy and Meaning of Caregivers

I’ve realized since my diagnosis that a “life sentence” of MS can be just as hard on one’s partner or caregiver as it is for the person living with MS.

WOD MS: Working Out to Raise Awareness

As each minute of the workout passed, I thought about another year of Demetria’s MS fight, and the increasing fatigue from the workout was a reminder of Demetria’s increasing challenges over the years.

How My MS Diagnosis Inspired My Career

There is a distinct lack of accessible psychological support for people with MS, and this had opened my eyes.

Among Brothers and Sisters

I wanted a safe place where the camaraderie could carry over and continue to strengthen as we help one another navigate through the challenges of living with MS.

Marching on With MS: Lessons From a Veteran

For my active duty comrades. Please get yourself checked out. Don’t let anyone tell you anything different.

Latest Blogs

The Missing MS Face

Being “connected” means that we are all part of the MS community. The battle with… Read More

Man Up vs. Open Up

It was tough trying to show mental toughness while at the same time trying to… Read More

“Drawing” in the Rain

It is so easy for people with disabilities to feel inferior and undeserving, despite what… Read More

Answering Your COVID-19 Questions: Part 2

The National Multiple Sclerosis Society is working with experts across the world to learn more… Read More

MS Allies

The answer to how to help is simple: become an MS ally. Share in the… Read More

Choosing the Appropriate Disease-Modifying Protocol

There are clues your neurologist, or a neurologically trained healthcare provider, can use that may… Read More

My Memorable MS Mentorship in the Midwest

I wanted to find out more about the neurological disease that affects almost a million… Read More

Fearlessness

We take so many things for granted and climbing some stairs without a railing was… Read More

When Does MS Start?

Knowing when MS starts is important. It could allow scientists to discover events that trigger… Read More

Long-Term Care & Multiple Sclerosis

Continuous advocacy at both the state and national levels will be necessary to ensure that… Read More

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Professional Wellness

I never knew that being sick is a full-time job.

Quarantine, Shmorentine

The bottom line is take care of yourself and your health, both mental and physical… Read More

I’m an MS Navigator. Here’s What I Want You to Know About Multiple Sclerosis and Suicide

MS Navigators are here to remind people that they’re not alone on their journey and… Read More

Exercise Your Right to Vote

Ensure that your polling place will be accessible on that crucial day. And then go… Read More

Shot of Courage

My doctors encouraged me to get a flu shot, as they do every year. But… Read More

The Shame Behind Being Chronically Ill

There have been many times since my diagnosis of relapsing-remitting MS in 2015 that I… Read More

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