living with MS

Assessing multiple sclerosis (MS) disease activity using Octave Bioscience’s MS Disease Activity (MSDA) blood biomarker test can help guide clinicians’ decisions about care, a study showed. “Our goal is to empower both providers and patients with precision tools that transform MS care,” Doug Biehn, CEO of Octave, said…

Some exercises are better than others at easing certain problems associated with balance in people with multiple sclerosis (MS), and the most effective type may depend on a patient’s specific issue, a small study suggested. The findings “provide valuable insights into the long-term effects of these exercises,” the researchers…

Aranzazu Calzado, known to friends as Zazu, has lived in Houston, Texas, since 1996 after moving from Spain. She was diagnosed with primary progressive multiple sclerosis in 2021 and faces the challenge with resilience, relying on God, family, and friends as her support network. She finds joy in helping…

People with multiple sclerosis (MS) who live in rural areas are 17% less likely to receive disease-modifying therapies (DMTs) than those in urban regions, a study involving people from the Canadian province of Alberta suggested. The likelihood was lower when considering therapies that are highly effective at controlling…

I’m sure the same thing happens in a lot of professions, but combat medics, which I was, often zoom in on the job at hand and lose sight of everything else. I know that when I was treating a casualty, I’d sometimes get in the zone and lose track of…

Medicaid coverage for people with multiple sclerosis (MS) in the U.S. is associated with worse disease outcomes — including more clinical relapses and greater disability progression — compared with private insurance, according to a new study that investigated the impact of insurance type and socioeconomic factors on patient care. In…

In recent months, I’ve attended a couple events in large stadiums. Last December, I went to the Music City Bowl college football game in Nashville, Tennessee, where Mizzou (the University of Missouri) beat the Iowa Hawkeyes. I also saw a Justin Timberlake concert at the T-Mobile Center in Kansas City,…

When I learned to cook, I didn’t attend a class or have formal lessons. I learned the basics as a child from my mother in our home kitchen. At first, everything was structured: follow the recipe to the letter, precisely measure everything, and use only the recommended tools for a…

I remember the day of my relapsing-remitting multiple sclerosis diagnosis, when I didn’t understand the weight of what I’d been told. I was only 17 years old and didn’t know what questions to ask, what the future held, or what I should’ve felt after hearing those words. Aside from feeling…

People with multiple sclerosis (MS) in Austria spend an average of €136 (about $149) per month on nondrug therapies such as dietary supplements and therapeutic interventions like physiotherapy, a study found. These complementary and alternative medicines (CAMs) are generally not fully covered by Austria’s public healthcare system, leaving many…

In an Army surveillance course I took in the spring of 2010, which I wrote about last year, I learned more than just the fact that I had a noticeable limp. For instance, on the first day, we had a class on simple ways to alter your appearance when…

The patient support program Cycle Vita, which assists patients throughout the process of medical prescriptions, is now available for people taking the multiple sclerosis (MS) medication Bafiertam (monomethyl fumarate). That’s according to Cycle Pharmaceuticals, in an announcement a few months after the company acquired Banner…

I knew that starting my college journey in a a different city, less than a year after receiving my relapsing-remitting multiple sclerosis (RRMS) diagnosis, would be challenging because I didn’t fully understand what was happening in my body. Even though my college, the University of Texas at Austin,…

Recently, my work-life balance felt off, so I took the opportunity to house-sit a family farm. I needed the solitude — the peace and quiet — to recharge. While there, I watched a flock of 50 to 60 goldfinches gather at the bird feeders daily. Their communal nature fascinated me,…

From left, Adela Puente and her niece, Desiree Lama, spend time together in downtown San Antonio. (Photos courtesy of Desiree Lama) Day 31 of 31 This is Adela Puente’s story: Lama and Puente share a hug at Desiree’s college graduation. Being the youngest of six, I always wished…

Sheila Hofmeister and her husband, Rick, stand behind the wheelchair of their son Ben Hofmeister, whose three sons, Sterling, Jule, and Monte, are pictured from left to right. (Photos courtesy of Ben Hofmeister) Day 30 of 31 This is Sheila Hofmeister’s story: Note: Multiple Sclerosis News Today columnist…

Natasha Quariab relaxes in her garden in Amman, Jordan, in 2023. (Photos courtesy of Natasha Quariab) Day 29 of 31 This is Natasha Quariab’s story: I woke up and tried to move my right leg. Nothing. My heart pounded. This couldn’t be happening. Not here, alone in a snowy…

I despise theme parks, and I feel zero guilt about depriving my kids of Disneyland, Six Flags, and the general horror of standing in long lines to be terrorized. Why do I hate theme parks? It’s not the shameless commercialism, the overpriced food, or the fact that the tickets for…

Denise Schneiders embraces her role as an MS advocate. (Photos courtesy of Denise Schneiders) Day 28 of 31 This is Denise Schneiders’ story: My life changed on March 12, 2024, with three words: “You have MS.” As an athlete, wife, mother, teacher, coach, and business owner, I had always…

Just before a deployment, all the teams in my military unit received a large supply of medical gear that included two medical backpacks, or aid bags. As the team’s medic, I elected not to bring them, because I already had a bag that I liked, and the new ones looked…

  Hollie Amadio meets with Stefanie Barone, a staffer for U.S. Rep. Steny Hoyer, D-MD, to advocate for the Safe Step Act. (Photos courtesy of Hollie Amadio) Day 27 of 31 This is Hollie Amadio’s story: “Hollie, you’re having a stroke from eating all those chocolate eggs!” my dad…

Dimika V. Cavalier is shown in a photo she uses for advocacy work. (Photos courtesy of Dimika V. Cavalier) Day 26 of 31 This is Dimika V. Cavalier’s story: My journey with multiple sclerosis (MS) began in my early 30s. I was having episodes of vertigo that would…

A 3-year-old Chris Delemater smothers his aunt, Jenn Powell, on the couch, along with Toby the dog. (Photos courtesy of Jenn Powell) Day 25 of 31 This is Chris Delemater’s story: What is it like to know someone with multiple sclerosis (MS)? Have I learned anything from someone…

Karly Isaacson’s mother, Donna Ball, laces up Karly’s dress for her wedding last summer. (Photos courtesy of Karly Isaacson) Day 24 of 31 This is Karly Isaacson’s story: When I think of empowerment and multiple sclerosis (MS), I think of my mom. I had my first MS…

More Stamina, a gamified mobile app, helped a small group of people with multiple sclerosis (MS) better manage their fatigue by becoming more aware of their energy levels and planning their activities more effectively, according to a study from Finland. “Fatigue is an invisible but life-altering symptom…

Michelle Lesmeister posed for this headshot in February 2025. (Photos courtesy of Michelle Lesmeister) Day 23 of 31 This is Michelle Lesmeister’s story: “You’re the strongest person I know — you will be OK.” Lesmeister takes her dog Barrett for an afternoon walk. Who wants to be just…

Ena Salcinovic celebrates her birthday three years after her MS diagnosis. (Photos courtesy of Ena Salcinovic) Day 22 of 31 This is Ena Salcinovic’s story: Saturday. Finally. A good day. I still believe that even though I overslept and missed the Red Cross and our weekly international cooking. I…

Sacral neuromodulation (SNM), in which an implanted device delivers mild electrical pulses to the nerves that control the bladder, led to sustained improvements in urinary function in half of people with multiple sclerosis (MS) who underwent surgery to have the device put into place, according to a review of…

Kevin Byrne grew up in Bronx, New York. A graduate of the U.S. Military Academy at West Point, he was struck by multiple sclerosis (MS) in 1999 while commanding an Army Air Cavalry Troop overseas. Now medically retired, he lives with his daughter, Rogue, in Portland, Oregon. Kevin works…

Ross smiles for a photo. (Photos courtesy of Ross) Day 21 of 31 This is Ross’ story: I was diagnosed with relapsing-remitting multiple sclerosis (RRMS) in 2007 when I was a senior in college. I had been very sick with vertigo and gastrointestinal issues for a year…