With relationships and MS, it’s the little things that matter
Thanks in part to 2024 being a leap year, I’ve never published a column on Valentine’s Day. That won’t happen anytime soon, either, as the next time the holiday lands on a Thursday is…
Chairborne — Ben Hofmeister
Ben Hofmeister was diagnosed with primary progressive multiple sclerosis in 2014, ending a 22-year career in the U.S. Army, as both a Ranger and Green Beret. He gradually settled into a wonderful retired life in Anniston, Alabama, with his wife and their three boys. He couldn’t be happier. After being inspired by the writing of others with MS, he decided to add his own voice. His column is raw and honest, but sometimes sarcastic and pithy too. MS is a serious disease but a life with it doesn’t always have to be.
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When you have multiple sclerosis, it’s hard to enjoy summer
It’s not as though I do well in winter either, but — with apologies to Mr. Shakespeare — now is the summer of my discontent. It’s a shame, because even though autumn is my…
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In life with multiple sclerosis, you can’t wait until you get around to it
The other day, my kids asked if they could go through the jar of coins on my dresser. It’s been sitting there for a while because, like the majority of people with a jar…
Why judging yourself based on the past is unhealthy
With three preteen boys and one soon-to-be 50-year-old child in the house, we watch a lot of animated television. On the occasion when we watch another genre, it’s usually a nature show or historical…
With MS, my mental health had to get worse before it got better
After today, I have only one more session of therapy for my current bout with depression. I don’t mean to imply that I’m getting chased out the door, or that more therapy won’t be…
MS treatments don’t cure my disease; they just make it quieter
I’ve written several times before about how unpleasant it was to catch giardia while serving in Afghanistan with the U.S. Army, but I wasn’t the only person to get sick from drinking contaminated…
In a life with multiple sclerosis, how do you motivate yourself?
I think cold weather affects me every bit as much as hot does. The difference is that instead of turning into a weak puddle, I stiffen into a rock. It doesn’t get that cold…
In navigating life with multiple sclerosis, words matter
We’ve begun a brand-new year, and normally that would mean resolutions, but as I’ve said before, I’m not exactly a resolution kind of guy. I don’t have anything against them and I do intend…
A comprehensive collective nouns list for multiple sclerosis
For someone like me, who is retired and has three preteen children, the days surrounding Christmas and New Year’s feel like a liminal space. With no school or job to be at and…
With MS, I don’t want to lose control when I should give it away
I’m losing control. I don’t mean that I’m out of control or spiraling in that direction, but I definitely feel like I have a lot less of it these days. That’s a real problem…
If you are living with MS, what are others inheriting from you?
My wife and I both have medical backgrounds. She is a registered nurse and has actual credentials that have to be renewed periodically. At one time I had a card that said…
MS presents some of the toughest challenges, but don’t quit
When I attended the selection process for Army Special Forces, I had a number of obstacles to overcome, among them a psychological evaluation, a handful of physical tests, long-range land navigation, and assessments of…
Not thankful for multiple sclerosis, but thankful for what it’s allowed
As this is published, I’m surrounded by family. Some are cooking with passion and purpose. Some are critiquing and giving advice that always seems to start with the phrase “Now what I like to…
We never see the whole picture of MS, just our own little part
Ever since I learned how, I have enjoyed reading. My tastes have changed a little over the years, as has the way I read. I like the feel and smell of a real book,…
Multiple sclerosis can turn a fun hobby into a dreaded chore
About a decade ago, I got caught up in the home brewing craze. I don’t know that I qualified as crazed, but I had a lot of fun with it and felt that since…
A lesson on the importance of being proactive with my MS care
The first time you try something should not be the moment you absolutely need it. During my time in the military, I often applied this concept to both performing a critical task with my…
I wish I could make multiple sclerosis my costume for Halloween
I had a run-in with a nasty, mostly waterborne parasite years ago in Afghanistan. I managed to catch it by, you guessed it, contact with infected water — not by actually drinking it, but…
With MS progression, allowing yourself time to grieve is vital
The company I keep has changed over the past 10 years. I used to associate with people who were much like me. We had a similar way of thinking and faced many of the…
With MS, wedding anniversaries deserve extra celebration
My wedding band is made of tungsten and rose gold. It’s heavier than most, but I’ve had it on for 15 years today, so most of the time I don’t notice that it’s there.
Navigating depression alongside the losses of multiple sclerosis
Due to the nature of my work in U.S. Army Special Operations, or maybe just because of the nature of me, I had a couple psychological evaluations over the years. Don’t worry, I’m…
When a loss of capability feels like a loss of independence
I stopped driving nearly five years ago. That was probably six months or more after I should have. By that point, I was doing it mainly by using my truck’s cruise control and occasionally…
