living with MS

I’m back in my happy place. My wife, Laura, and I, along with our Yorkie-poo and our Maine Coon cat, have made it back to our Florida home after 16 hours and about 1,000 miles of driving over two days. There were no traffic jams, we had a comfortable motel…

Halloween is five days away, and if you have kids, you’re running out of time to have your costumes ready. My wife and our three boys have everything figured out, minus some finishing touches — unless I want to dress up, of course. Fortunately, I wasn’t planning on it because…

A patient’s ability to cope with and recover from adversity — called psychological resilience — was found to impact the observed relationship between fear of relapse and life quality among people with multiple sclerosis (MS) in a new study. Essentially, MS patients who had…

Multiple Sclerosis News Today is chronicling MS advocate and podcaster Mike Parker’s journey, leading up to a skydiving jump he’ll make Oct. 29 to benefit the MS Society U.K. Learn more about Mike at mikesmsjourney.com. You can also donate to his fundraiser.  Third in a…

Neural Sleeve, a bionic piece of clothing by Cionic designed to help with walking and strength, is among the 200 devices on Time magazine’s annual list of best inventions, under its accessibility category. The lightweight, leg-worn device, which combines continuous motion analysis with functional electrical stimulation,…

Nabiximols, the cannabis-based oral spray sold as Sativex, is available for reimbursement as an add-on therapy for moderate to severe spasticity in adults with multiple sclerosis (MS) in Ireland who failed to respond as intended to other spasticity medications. Marked by muscle stiffness and involuntary spasms or twitches,…

A few columns back, I wrote about my lack of time to get anything done. Sure, the way around it would be to get up infernally early — well, early for me. But I’m most certainly not going to pay to be punished. And that’s the story I’ve always…

“I’m so tiredThe hammer’s coming down againI’m hardwiredAll the signals cross and double backBroken insideThere’s no fixing anythingHow do i explainI’m fighting every day to do the simple things?” The lyrics to “Hammer,” written by singer Susie Ulrey and the band Pohgoh,…

The overall financial impact of changes in treatment and delayed diagnoses for people with multiple sclerosis (MS) in Canada due to the COVID-19 pandemic likely will be in the hundreds of millions of dollars between 2020 and 2024 in terms of extra healthcare costs and lost productivity, as well…

I try not to let my life revolve around multiple sclerosis (MS), but there’s no escaping the fact that the disease affects every part of it. That’s a bit of a conundrum and often frustrates me to no end. If there’s a bright side to be found, it’s that…

Multiple Sclerosis News Today is chronicling MS advocate and podcaster Mike Parker’s journey leading up to a skydiving jump he’ll be making Oct. 29 to benefit the MS Society U.K. Learn more about Mike at mikesmsjourney.com. You can also donate to his fundraiser.  Second in…

Obese people with multiple sclerosis (MS) had faster disability accumulation, greater cognitive declines, and worse quality of life in the 15 years after diagnosis relative to patients with normal weight, according to an analysis of Swedish data. While it’s been known that obesity was a risk factor for developing…

About a month ago, I embarked on what might have been my last-ever solo outing. You can file it away with my other lasts: sitting down and getting off the sofa on my own, walking without mobility aids, doing a controlled Frankenstein’s monster stumble into my bedroom, putting myself to…

My mobility scooter died last week. I can walk 100 feet or so using a pair of canes, but my wheels are usually my legs. So when I turned the key and discovered those “legs” were powerless, I was in a bind. This breakdown couldn’t have happened at a worse…

With my kids in school, me being retired, and, of course, the limitations of my multiple sclerosis (MS), I have a lot of free time on my hands. I’d like to say that I always use it productively, but that’s far from the truth. I putter — if you…

Multiple Sclerosis News Today is chronicling MS advocate and podcaster Mike Parker’s journey leading up to a skydiving jump he’ll be making on Oct. 29 to benefit the MS Society U.K. Learn more about Mike at his website mikesmsjourney.com and click here to donate to his fundraiser.

Socioeconomic factors, specifically income and education levels, and marital status, were identified as risk factors for multiple sclerosis (MS) severity in a new study in Sweden. In fact, the study found that earning a higher income and having more years of education before being diagnosed with MS are associated with…

MS Bike‘s cycling fundraiser events have raised at least $4.3 million over the last four months to support MS Canada and people with multiple sclerosis (MS) in a country with one of the highest rates of the progressive neurodegenerative disorder. The organization predicts up to $4.6 million…

Welcome to “MS News Notes,” a column where I comment on multiple sclerosis (MS) news stories that caught my eye last week. Here’s a look at what’s been happening: ‘Silent’ MS progression Readers of the MS News Today website and Facebook page sometimes wonder why their MS…

The original title for this week’s column wasn’t so much of a headline, but more of an essay. I had to shorten it. I’d also better write a bit more here so that my opening paragraph is a tad longer. Ah, being all meta about it has saved my vegan…

You’d think that people with multiple sclerosis (MS) and other disabilities would have easy access to healthcare services. That’s not always so. A small study in the journal Health Affairs that I wrote about last year said many physicians “expressed explicit bias toward people with disabilities and described…

Most disability worsening events happen independent of relapse activity across all types of multiple sclerosis (MS), including clinically isolated syndrome (CIS) and early relapsing-remitting MS (RRMS), a new study reports. The findings challenge the idea that relapses are the main driver of disability worsening in early relapsing…

People with multiple sclerosis (MS) who experience a greater number of more severe flare-ups, also known as relapses, are more likely to take their medications regularly, but less likely to keep taking them over time, a review study has found. Other factors associated with better treatment adherence and persistence…

Back in spring, I wrote about the fatigue that accompanies multiple sclerosis (MS) and how difficult it was to describe and for others to understand. That’s true, of course, but really, the entirety of MS is difficult to explain. Factor in the variety of symptoms and the…

Problems with sexual dysfunction are a concern for multiple sclerosis (MS) patients of all ages, but the issues tend to have distinct causes as people age, a new study highlights. The study, “Age-Related Differences in the Severity of Sexual Dysfunction Symptoms and Psychological Distress in Individuals with…

People with multiple sclerosis (MS) in the United Kingdom are less likely to be on disease-modifying treatments (DMTs) compared with MS patients in other countries in Europe, a new study reports. “We know that getting early treatment with disease-modifying MS therapies can improve long term health and wellbeing.

A cognitive behavioral therapy (CBT) program delivered virtually — using self-paced remote modules — significantly eased depressive symptoms and improved life quality in multiple sclerosis (MS) patients with depression, according to new research. A Phase 3 trial testing the remote program had aimed to determine if an internet-delivered platform…

Among multiple sclerosis (MS) patients treated with Ocrevus (ocrelizumab), most of the disability worsening they experience is not associated with any relapse activity, according to an analysis of real-world data. “We present real-world data from our multiple sclerosis center underlining that in a typical population of relapsing MS…

I haven’t seen my mate Nige for years. Actually, to his face I call him Nigel, but it’s Nige when I, or anyone else, talk about him in the third person. It’s weird — I’d never thought about that before typing his name just now. And it’s not like he…

My wife and I got the latest COVID-19 vaccine the other day, the first of three vaccines we’ll be getting this fall. The others are the seasonal flu vaccine and the respiratory syncytial virus (RSV) vaccine. This was my sixth COVID-19 vaccine, and I’ve received a…