I like to look up. No, I’m not referring to my disposition, although I do consider it to be an improvement over what it once was. I’m actually pretty sunny, if you happen to think of “sunny” as burning, harsh, and damaging when you’re exposed to it. What I…
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Neuro Night, a philanthropic event set for October in Scottsdale, Arizona, is raising funds for the Barrow Neurological Institute and its mission of supporting the lifesaving care, medical education, and research for neurological diseases. The star-studded night of music, dancing, and fundraising, hosted by the Barrow Neurological Foundation,…
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: Neurologists comment on DMTs available for RRMS There are 20 disease-modifying therapies (DMTs) available to treat MS in the…
I was never a hypochondriac until multiple sclerosis (MS) whacked me. A catastrophic fall while playing tennis in 2007 resulted in a shoulder separation that took two operations to fix. The pain was so bad that, at the time, MS was just something else I had. To be accurate,…
“Will you still need me, will you still feed me/ when I’m 64?” Could Paul McCartney have imagined what life would be like at 64 when he wrote that iconic lyric as a teenager, or when the Beatles recorded it in their early 20s? I never could’ve imagined…
This morning, at an unholy hour, our family awoke to the sound of alarm bells. Well, not bells, but rather the gentle yet insistent sound of one of Alexa’s alarms. Actually, we changed the name of our bedroom device to Ziggy, so we can’t simply roll over, still…
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: Could MS be predicted by an artificial intelligence tool? Wouldn’t it be great if there was a way to predict…
Long ago, I acquired a pair of speakers for my laptop. In fact, they’ve survived many, many iterations of the things. Laptops become outdated quickly, their inbuilt fans fail, or, as in my latest version, the installed RAM is only 8 gigabytes. I’ve been made aware that RAM, or random-access…
My wife hates to cook, except for a big Thanksgiving turkey. I don’t know how to cook, except for scrambled eggs or meat on a grill. So for many years, our meals have pretty much been restaurant (eat-in or carry-out), ready-to-heat from the grocery store, frozen (lasagna or pizza), and,…
I’m not a doctor, just a patient. And depending on whom you ask, I’m not a very good one, either — unless you happen to be fond of lots of questions. I was a medic in the U.S. Army — a time buyer, as I refer to it…
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: Are DMTs useful and safe for older MS patients? The MS News Today story “Can elderly MS patients…
As last week’s column ended, I’d just negotiated with my ambulance driver and paramedics to take me to any London hospital other than the one where I’d spent the Christmas months. They offered me St George’s Hospital, which I knew to be the major trauma center ’round these…
Note: This column describes the author’s own experiences with several disease-modifying therapies for multiple sclerosis. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. Times, they’ve been a-changing for disease-modifying therapies (DMTs). When I was diagnosed with multiple…
About three years before my multiple sclerosis (MS) diagnosis and subsequent retirement, I found myself in Iraq preparing for a mission. I was going out with a different team from another branch of the U.S. military, and the planning and briefing process wasn’t as detailed as I was…
Editor’s note: “MS News Notes” will return to its regular Monday morning schedule next week. 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: A 10-minute injection of…
There was no column from me last week, and here follows the reason why: “In the wee small hours,” as Frank Sinatra so eloquently crooned, I, too, was abruptly awake. Only I hadn’t drunk my way there. Instead, my wee was indeed a real one, though painfully…
I’m drinking again, more than I have in years. It’s not the hard stuff, though; not even beer or wine. It’s just plain water. That may sound crazy for someone like me who has bladder problems due to multiple sclerosis (MS). For many of us with MS, we…
I am not left-handed! No, I’m not channeling Westley or Inigo from “The Princess Bride,” just clarifying a common — and fair — assumption. While I now do nearly everything left-handed, including eating, drinking, and even typing this column, my right hand was dominant for most of…
Welcome to “MS News Notes,” a Monday morning 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: Testing a new MRI contrast agent One concern that some people with MS have when getting an MRI…
I nearly jumped for joy — well, I would’ve if I could’ve — when I saw a new TV commercial for the Expedia travel company the other day. It shows a woman in winter who’s obviously had enough of the cold, ice, and snow. She is desperate to…
I must look like I need help all the time. I don’t own a shirt or any other article of clothing that says so, and I don’t think I have a helpless look on my face, either. I smile often, sometimes genuinely and sometimes with my mouth formed in…
The director of the Multiple Sclerosis Center of Catalonia (CEMCAT) has been recognized with the 2023 Charcot Award, a prestigious prize that honors researchers for their lifetime work toward understanding multiple sclerosis (MS). Xavier Montalban, MD, PhD, has contributed to several areas of MS research and clinical care…
Welcome to “MS News Notes,” a Monday morning 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: Another study shows positive results with stem cell therapy Yet another study has concluded that autologous hematopoietic…
It’s only day one, but my eyesight has already improved. It may not be that of a hawk’s, but at least I can tell the difference between a lumbering pigeon and a bird of prey. The world seems brighter — and not just because of that vision thang, peeps. If…
It’s been almost two and a half years since my first COVID-19 vaccine — eight months since my most recent booster — and my COVID-19 antibodies seem to still be doing their thing. I know this because, after having nine test tubes of blood drawn, the lab results…
A few — OK, many — years ago, I played the lead in a production of “Oklahoma!” Don’t get excited; it wasn’t on Broadway or anything like that. It was a high school production, and I suspect I only landed the role because I could sing — and probably…
The government of Canada soon will provide new income benefits designed to help Canadians living with a disability — including people with multiple sclerosis (MS). Applauded by MS Canada, a nonprofit that actively advocated for these benefits, the announcement follows the passing of the Canada Disability Benefit Act,…
Welcome to “MS News Notes,” a Monday morning 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: MS experts offer more than 50 vaccine guidelines I know there are different opinions about vaccines, and I’ve…
Nobody’s life is eternal, but let’s face it, peeps: Much of the psyche of a multiple sclerosis (MS) patient is internalized. I spend an inordinate amount of time, physical and mental, on my illness. Yer, OK, I’m not turning this into a therapy session. Or am I? A serious…
“What can Dr. Crayton help you with today?” I was starting my annual multiple sclerosis (MS) checkup with my neurologist, and before I met with her, I got this question from her MS nurse. I was stumped. I’d never been asked that before. I think most people with MS…