Multiple sclerosis and speech are not on friendly terms for me
I used to sing — a lot. Don’t worry, I didn’t miss my true calling. I could carry a tune, but that was about it. I was loud, and just like arguing, volume can…
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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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…
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Fatigue from MS is hard to both explain and understand
Everyone’s multiple sclerosis (MS) is unique to them. The different disease types, lesion loads, and lesion locations are a few reasons why our symptoms are so variable. We with MS all…
Our treatments for multiple sclerosis aren’t cures, but vital time-buyers
Note: This column describes the author’s own experiences with Ocrevus (ocrelizumab). Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. Tomorrow morning, I’ll have…
Multiple sclerosis requires a different kind of can-do motivation
I’m pretty good at doing what I’m told. You probably think that’s because I was in the Army for 22 years. You might even think it’s because of all the medical authority figures that…
Multiple sclerosis might be the ‘uncanny valley’ of diseases
I recall a conversation I had with an acquaintance soon after my diagnosis. I hadn’t progressed to a wheelchair yet, but my limp was noticeable, and he’d heard talk from mutual friends.
Being seen is an incredible thing when MS makes you feel invisible
The kids had their spring break last week, so we loaded up and drove to Universal Studios in Orlando, Florida. I promise this column won’t be a review of the theme park and…
There’s no point in playing the blame game after the disease is diagnosed
In a previous column, I wrote about the journey to my diagnosis of multiple sclerosis (MS). In it, I mentioned that the neurologist had praised me for “taking this well.” I suppose…
With multiple sclerosis, it’s hard to stop saying ‘I’m sorry,’ but you should
Even if I resolved to improve my cardiovascular health by taking the stairs more often, I can’t. Mobility problems brought on by my primary progressive multiple sclerosis force me to use a wheelchair. Using…
When multiple sclerosis invades even my dreams
I may not be able to turn in circles like a dog anymore, but I still have a few bedtime routines. Before I had an intrathecal baclofen pump, multiple sclerosis-induced spasticity…
An MS diagnosis can be confusing when it doesn’t fit your lifestyle
A little over three years passed between my multiple sclerosis (MS) diagnosis and my medical retirement from the U.S. Army. Even before the diagnosis, I knew something was wrong and had taken…
The responsibility for raising MS awareness goes both ways
Every once in a while, I wake up prepared to swing my legs over the side of the bed and get moving. That sleep-induced forgetfulness evaporates as soon as the reality of multiple…
Learning to love — and accept — that person in the photograph
We had family portraits made a few days ago. With a family of five, this never goes perfectly, so there was a little pre-photo briefing beforehand. There were some veiled threats, a promise of…
Could decluttering your living space improve life with MS?
I am not by nature a very neat person. I want to be. I like order, but I lack the discipline to maintain it. People tend to think that time in the military makes…
How multiple sclerosis leads to what I call ‘microinjuries’
“scabulous adj. proud of a scar on your body, which is an autograph signed to you by a world grateful for your continued willingness to play with her, even when you don’t feel like…
Eating Comfort Food Can Be Uncomfortable With MS
Summer is one of the cruelest times of year for people with multiple sclerosis (MS). Thanks to Uhthoff’s syndrome, it’s hard to enjoy all the fun that comes with warm temperatures. I…
MS Makes Me Feel Like a Child Again, and Not in a Good Way
The other day, my middle child opened the door while I was in the bathroom. If you have children, a surprise visit in what should be a sanctuary isn’t unusual, but in this case,…
Multiple Sclerosis Memory Issues Force Me to Use New Methods
Before multiple sclerosis (MS), I was pretty proud of my memory. For the most part, I still am, but like many others with this disease, I now have trouble recalling information. For me,…
How I Respond to Typical Questions About MS From Children, Adults
As I’ve probably mentioned before, my wife and I have three boys in grade school. This means that between school events, sports, and play dates, I’m around a lot of kids. Considering I…
This New Year, I Resolve to Let Myself Hope
The new year is just a few days away, so if you haven’t already, you might want to start thinking about resolutions, if you’re so inclined. Although I personally don’t bother these days, about…
”Twas the Night Before Christmas’: A Multiple Sclerosis Parody
The holiday season is one of my favorite times of year. Multiple sclerosis (MS), of course, has a way of sucking the joy out of anything, but it can’t have my…
