Heart-Healthy Salmon & Spring Greens

For a heart-healthy win that feels like spring on a plate, you can’t beat this easy sheet pan Lemon-Herb Salmon & Spring Greens. Salmon is packed with Omega-3 fatty acids that support cardiovascular health.

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Connecting with Kindness and Compassion

Kindness is something we encounter more often than we realize. At some point, each of us has been at the receiving end of someone’s patience, and those moments stay with us. When we choose to be kind, we keep that ripple moving forward. What makes kindness such a powerful virtue is that it costs nothing, carries no expectations, and does not require grand gestures or public displays. In fact, it is usually the small, random, and quiet acts that brighten someone’s day the most. Life is short, and choosing kindness is one of the simplest ways to make a meaningful difference in someone’s life. Sometimes it is as easy as holding the door for someone, letting a parent with restless kids go ahead in line, or offering a smile when someone looks overwhelmed.

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When Strength Makes It Hard to Let Others In

Strength and self-reliance are often worn like a badge of honor. For many people, especially those living with chronic illness or ongoing uncertainty, strength becomes synonymous with survival. It allows us to push through difficult days, but it often comes at the cost of deep exhaustion and a missed opportunity for connecting with others. Being strong and self-reliant is admirable, yet it can also make it harder to receive support from those who care about us. Letting others in and choosing vulnerability can feel uncomfortable or even unsafe when independence has become our default.

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More Than Just the Sniffles: Navigating Colds and Flu with MS

For the average person, catching a cold is a minor inconvenience—a few days of tissues and cough syrup before bouncing back to work. But for those of us living with multiple sclerosis (MS), the narrative is often drastically different. We know that a “simple” bug can feel like a seismic event. As one community member vividly shared, “mundane ailments can knock us down for the count.” What might be a fleeting annoyance for our friends and family can hit us with the force of a freight train, leaving us drained and vulnerable.

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Virtual Friendships and Feeling Less Alone

When living with a chronic illness like multiple sclerosis, building a community for yourself of people who truly get it is incredibly valuable. Having a support network in your life of people who are there for you in easy times and hard can make all the difference. A support network can be made up of neighbors, friends, and family members you see regularly. And, with the variety of digital options, your support network can easily be found in virtual forums, like MSAA’s My MSAA Community.

picture of young african american women at her laptop searching My MSAA Community site
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Know Yourself to Reach Your Goals

Setting goals is easy, but holding ourselves accountable is where the real work begins. We often imagine that achieving a goal is simply about motivation, but it also involves structure, self-awareness, and creating the right environment. Accountability isn’t about pressure or perfection; it is about building habits that support the version of ourselves we are trying to become.

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Easy Overnight Oats

Making overnight oats is simple and doesn’t require any cooking!  This basic recipe can be customized to your liking with various add-ins and flavors.

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Jumpstarting 2026

The wheels have turned again, bringing us to the beginning of a brand-new year. This is the perfect time to reflect on the past year and identify the changes one would like to make this year to bring more growth and fulfillment to their life. Setting resolutions for yourself can give a sense of accomplishment and boost your self-esteem when positive results are achieved.

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Wrapping Up

2025 has been a memorable year.  As the year sped by, it is worth reflecting and remembering both the good and the bad moments. It gives me an opportunity to assess the flaws on my side and a chance to examine the areas I can possibly improve for the next year. Looking back, it was a year filled with interesting experiences and valuable life lessons. 


One of the most valuable lessons I’ve been reminded of this year is the importance of holding onto hope, even when everything around me feels overwhelming. Hope means moving forward one step at a time, celebrating small victories, and embracing setbacks as part of the journey toward the life you envision and the goals you want to achieve. It is a calm assurance that, no matter how bleak things may seem at times, there is always light waiting at the end of the tunnel.

Looking back on this year, I am grateful for the opportunities I got to learn and grow personally as well as professionally. I am grateful for the family that stands by me and appreciative of friends that value our connection.  I have come to accept the fact that life is most fulfilling when it is welcomed with open arms, irrespective of the countless obstacles along the way. As I navigate this journey, it continues to be unpredictable and exhilarating at the same time. Here’s to moving onward and forward!

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Highlighting the MS Community This Holiday Season and Always

As we approach the season of giving, the Multiple Sclerosis Association of America (MSAA) would like to bring special attention to the many wonderful community members that we serve. With our mission of Improving Lives Today, MSAA genuinely strives to advocate for and prioritize the well-being of all individuals who have been affected by multiple sclerosis. Over the years, we have collaborated with so many inspiring people, and we are honored to be able to highlight their stories.                                             

In the spirit of the holiday season, we would like to share the heartfelt story of mother and son, Monica and Brian, who both live with multiple sclerosis.

“I’ve learned that in any situation, if you are not advocating for yourself, you’re not going to get anything. My name is Monica Proctor Wilson, and I was diagnosed with multiple sclerosis on my 40th birthday after spending several years seeking answers to my symptoms. For four or five years, doctors kept saying that it was fatigue, and that I was overworked and needed to take a break. I believed it was multiple sclerosis, and I started asking about it. People would ask me, ‘Why would you want MS?’ I did not want MS. I just wanted to know what was going on with me,” Monica shared.

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