Guest Post: The Real, Real Deal with Exercising and MS

Oh no. No, no, no, you’re thinking. Not another Barts MS Blog lecture on the importance of exercising when you have multiple sclerosis. Especially a guest blog from that Dave guy who runs ActiveMSers.org and who thinks he is funny and has no professional medical or physical fitness credentials—just a dude who runs a blog, ruffles feathers like Gavin, and works out.






I get it. I mean, I could point you to a collection of scientific abstracts covering virtually every competent exercise study done on MS over the past decade—I’ve painstakingly gathered almost 150—with nearly all pointing to the same conclusion: it’s a seriously big deal. Yawn, you already know.

I also could direct you to the largest collection of exercise tips and tricks for MSers on the internet—vetted by physical therapists and MS experts—including the five ultimate MS exercise hacks so that you can get started ASAP on how to maximize your life with MS. But that would be folly.

And I could steer you to motivational stories of fellow athletic MSers, gear advice that makes exercise easier, and a host of articles about everything from cycling with this disease to the critical importance of stretching. But no, let’s not go there.

The real reason I wanted to post today is to discuss the ongoing and unsettled debate concerning a salty potato-derived snack: are they potato crisps or potato chips? (For now let’s not address the term “chippies” sometimes used in the southern hemisphere, because seemingly every other word gets an “ie” added to it. So happy! But so unnecessary.)

On the surface, potato chips seem to make the most sense, as it is more commonly used worldwide. But then again, “crisp” seems to better convey the sound made when you bite into one. And it doesn’t muddy the waters with a dozen other uses like “chip” does. Cow chip. Chip off the old block. Poker chip. Chip shot. Chocolate chip. Chip on your shoulder. Computer chip. Confusing as all get out, right? Thankfully there isn’t such a thing as a cow crisp. Plus, the English aren’t going to serve fish and french fries, that’s just wrong on so many levels.

Now if you are thinking this is a deviously clever way of connecting exercise with potato chips/crisps using classic psychological conditioning techniques to reframe neural pathways in order to establish learned associations so that every time you consume a bag of chips/crisps you ponder exercising, you would be wrong. I got a B in Psychology 101; I have absolutely no clue what I am talking about.

But as author of arguably the longest-running MS blog and with gobs of first-hand experience with just about every aspect of this disease (and, sigh, treatment, including even HSCT), I do know a thing or two about multiple sclerosis. And exercise. I crank it, hard, daily, even though these days I mostly roll in a wheelchair.

Well pardon me, gotta run, I’ve got a case of the munchies. Oh damn, that reminds me it’s also time to work out. (With a shaking first in the air, I curse me and learned association!!!) Oh, I’ll still enjoy those crisps/chips and so will you. Besides, the salt sure tastes yummy after working up a good sweat. Be active, stay fit, and keep exploring! 

Those links again:

Exercise studies: http://www.activemsers.org/exercisesstretches/studiesexercisems.html
Exercise tips: http://www.activemsers.org/exercisesstretches/tipsexercisingwithms.html


Exercise hacks: http://www.activemsers.org/exercisesstretches/bestmsexercisehacks.html
Stories: http://www.activemsers.org/yourstories.html
Gear: http://www.activemsers.org/gear.html
Cycling: http://www.activemsers.org/exercisesstretches/cyclingwithms.html
Stretching: http://www.activemsers.org/exercisesstretches/advicestretchoften.html


By Dave Bexfield

Dave Bexfield is the founder of ActiveMSers, a website designed to help, motivate and inspire those with multiple sclerosis to stay as active as possible—physically, intellectually and socially—regardless of physical limitations. Established when Dave was diagnosed in 2006, ActiveMSers has helped hundreds of thousands of people with MS from around the world through its encouraging website, blog, Twitter feed, Facebook page, Instagram pics, YouTube videos, and discussion forum. An Albuquerque, NM, resident and longtime professional writer, Dave’s efforts have been championed by The New York Times and many other publications have spotlighted his journey and stubborn defiance with MS. He is active in the larger MS community, volunteering for iConquerMS as well as the National MS Society (USA). Armed with attitude, a wheelchair, and a pair of forearm crutches, Dave continues to travel the world with his wife of 25 years, Laura.