We’ve all heard comments from people who aren’t educated about multiple sclerosis (MS). Some that I’ve heard include “My friend had that and is fine now,” “Eating better will fix you,” and “Try a parasite cleanse.” I have to chuckle at these statements. With March not far away,…
Columns
Just three years before I was diagnosed with multiple sclerosis (MS), I was on what was to be my last overseas tour with the U.S. Army. One day while dozing during a lull in a mission, I was awakened by the sensation of someone standing over me.
Last month, I told you that while I’m not a psychologist, I’m fascinated by the subject. I should probably make a list of things I don’t do but still find interesting. One of those professions we can add to the list is historian. I enjoy reading and learning about…
As those of us with multiple sclerosis (MS) know, every so often a call comes or a letter arrives telling us we have a date with an extraordinary friend: the magnetic resonance imaging (MRI) scanner. For me, it seems that time has arrived again. Just a few days…
Valentine’s Day is less than a week away. If you haven’t gotten anything for your significant other yet, let me add to the holiday’s commercialization by reminding you that time is running out. It really wasn’t my foremost intention to spur anyone into panicked action. This column isn’t even about…
Summer planning has started for my family, which means trying to arrange trips and time together. Before I was diagnosed with multiple sclerosis (MS), we could simply book an excursion that looked enjoyable. But now, thanks to my mobility issues, planning is slightly tricker. In the…
I feel like I’ve written a lot of negative, maybe even depressing, columns lately. While multiple sclerosis (MS) can be a pretty negative and depressing subject, I’m normally a bit more upbeat. We’ve been having cold and gloomy weather lately, and I’d like to blame my low spirits on…
Because multiple sclerosis (MS) has changed much of my life in a short amount of time, I’m now fighting mental health issues. Things have been especially tough since the start of the new year. Usually, I’d spend January working, planning holiday time, and looking at my calendar to…
My name is Dave and I’m Beth Shorthouse-Ullah’s husband. We had spoken about the possibility of writing a column that looks at the experiences of partners of people who have multiple sclerosis (MS). But instead of sharing a thought-provoking piece from another perspective, today I sadly announce that Beth…
My father taught me to play chess when I was barely old enough to say the names of the pieces. I wasn’t a child prodigy or anything like that. I never joined a chess club or competed in a single tournament. I simply enjoyed the game…
I’m not a psychologist, but if you’re a regular reader of my column, you know that I’m intrigued by the subject. I seem to be particularly drawn to unusual conditions and making amateurish comparisons to multiple sclerosis (MS). In my defense, MS has odd symptoms, so…
About four years before I was diagnosed with multiple sclerosis (MS), someone else inadvertently “diagnosed” me. This person wasn’t medically trained, probably had no personal knowledge of MS, and didn’t actually use the words “multiple sclerosis.” Still, they gave me one of the best clues in my quest…
The new year is nearly upon us, so if you’re planning to make any resolutions, you should probably narrow down the list. As I said last year, I’m not in the habit of making any, but I did resolve to foster a sense of hope. I still have what…
When my general practitioner first spoke about the possibility of a diagnosis of multiple sclerosis (MS) in February 2022, I walked out of his office. I broke down in tears; I was terrified. At that instant, my first thought was, “OK, so how long do I have left?”…
I’m not very good at this sort of thing, but depending on whether or not you count today and the 25th itself, we’ve got about four days left until Christmas. If I still needed to get my wife anything, I’d be entering shopping panic mode about now. Fortunately, I don’t…
Where has the year gone? As we move closer to Christmas and a new year, I’ve pondered what the past 12 months of change have brought to my life. At the beginning of the year, I was working full time and still coming to terms with the diagnosis of…
When I was in the military, I wore several different hats. A U.S. Special Forces team has only 12 soldiers, so we couldn’t afford for anyone to know just one trick, no matter how good that trick might be. In addition to each person’s primary job, everyone had to know…
This is my 823rd column for Multiple Sclerosis News Today. It is also my last. Over the past seven and a half years, I’ve written about multiple sclerosis (MS) fatigue and frustration, about treatments and travel, about neurologists (good and bad), stress,…
Counting today, there are only 18 shopping days left until Christmas. Unless you’re one of those annoying people who did all their gift buying months ago and won’t stop talking about it, the clock is ticking. I guess that makes me one of those annoying people who reminds you of…
Many years ago, I had an MRI scan on my right knee, and it didn’t go well. In fact, panic set in when I first looked at the scanner, as the tube seemed small. After I lay down and the operator started moving the table, I faced a…
I encountered multiple sclerosis (MS) for the first time in a Valdosta High School math class. Before my geometry teacher was diagnosed, I had never known anyone with the disease and, in all likelihood, was completely ignorant about it. I would hear the name again about 10 years…
Let me introduce myself: I’m Mike, and if you don’t mind, I’d like to share my story. I was diagnosed with multiple sclerosis (MS) in August 2022. Since then, a lot has changed, including the loss of a 20-year career, worsening mobility problems, and the start of…
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 some of what’s been happening: A good report for Vumerity Final results are in from the EVOLVE-MS-1 clinical trial for patients with…
For someone with multiple sclerosis (MS), going to a venue to see a concert or sporting event can be an experience filled with uncertainty — especially if, like me, they’re using a mobility aid. For me to do it, I have to ask myself several questions: How will I…
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 some of what’s been happening. MS relapses and COVID-19 Since COVID-19 became a concern over three years ago, I’ve read many comments…
It wasn’t a good morning. I was dragging my cement-pillar legs around the kitchen and grew frustrated as I lurched from the refrigerator to the counter to feed the cat and the dog. I’d propped my two canes against the counter, but they’d slid to the floor — not once,…
I’ve warned you in previous columns that you might have to endure a rambling story or two from my military past. It’s just that there are so many lessons from the experience that pertain to my multiple sclerosis (MS). It was supposed to rain later that evening, so…
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: ATA188 fails a big test ATA188 is an experimental cell therapy developed by Atara Biotherapeutics aimed at easing MS…
As I’ve mentioned a time or two, my wife and I have three boys. Although they’re all under the age of 12, they’ve started to talk like the budding teenagers they are. As they mingle with peers more than their parents, their vocabulary in particular becomes less like ours every…
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: Lemtrada or stem cell transplant? While the U.S. Food and Drug Administration has not yet approved stem cell transplants…