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Timothy L. Vollmer, MD
Department of Neurology
University of Colorado Health Sciences Center Professor

Co-Director of the RMMSC at Anschutz Medical Center

Medical Director-Rocky Mountain MS Center
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Timothy L. Vollmer M.D.
Department of Neurology
University of Colorado Health Sciences Center
Co-Director of the RMMSC at Anschutz Medical Center
Medical Director-Rocky Mountain MS Center

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Fighting the MS Cold

Catching a cold is no fun for anybody. But when you live with MS, it can really be disruptive. Just a few days ago, I succumbed to the common cold that has been making the rounds.

One of the first things I noticed, even before the cold really set in, was that my legs were feeling heavy and my body was all a-buzz. My legs are still heavy and about half of my skin is still doing the jumping bean dance just under the surface.

Next to settle in was the increased spasticity. As my body temperature rose slightly, my ever-present MS symptoms grew to an un-ignorable level. For the last two days, the pain, tightness, achiness, and heaviness has been keeping me from wanting to do much. I actually went back to bed yesterday in the middle of the day to try to shake it off.

It’s like what they call a “man cold”
Then this morning, I was feeling particularly whiny….and that’s when it hit me. I was experiencing what others have described as a “man cold.” No longer was I the self-sufficient, strong, determined person that I usually am regardless of the challenge ahead. I had become a sniffling, stuffy, stay under the covers, only able breathe through maybe 1/3 of one nostril, moaning pile of flesh and bones.

All joking aside. Catching a cold when you have MS can really put you done for awhile. Old symptoms return, current symptoms get worse, and you generally feel like a pile of…well…the gunk that you keep trying to unsuccessfully blow out of your nose.

This temporary increased amount of symptoms is called a pseudoexacerbation. It feels like a relapse, but symptoms will typically return to “normal” once you’re over being sick. Probably what I hate the most about my “MS cold” is that it turns my brain into sluggish mush, too. I can’t quite think clearly and I usually lose most motivation to get things done, even simple things.

It can feel like you’re having an MS relapse
The good thing about a pseudoexacerbation is that you know it will eventually pass. You may feel like crap, but you will survive. Whenever I feel like this, I try to remember to take something to bring my body temperature down. For me, that is a common OTC medication.

If I begin to feel all of the above symptoms, but I definitely don’t have a cold, I start to suspect a different underlying cause. Frequently that cause may be something like a urinary tract infection, overexertion, or exposure to heat.

There have been times when I seem to lose the ability to think clearly and start to feel frustrated that I need to figure out what’s going on. Surprisingly, it often takes a while before I think to go check the thermostat in the house. When the heat has kicked on and the temps outside grow, I need to make sure that I can keep my body cooler. More often than not, just a couple of degrees can make a huge difference in how I feel and function.

But for now, I just need to drink lots and lots of fluids, stay warm, and attempt to keep from becoming a whimpering mess while I surreptitiously fight the cold with vitamins, rest, fluids, and good food.

So the next time you come down with a virus, try not to be hard on yourself. Although it’s not as socially understandable as a man cold, an “MS cold” can literally make it hard to function, physically and mentally

Story Source: The above story is based on materials provided by MULTIPLESCLEROSIS.NET
Note: Materials may be edited for content and length

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