Living with M.S.

"Living with M.S. is sort of like training for a long race. The harder you try, and the longer you keep at it, the stronger you become.
Eventually, looking back, you may be amazed at the power you possessed, even when you had no idea it was within your reach." (Linda Ann Nickerson)

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Monday

Zoning Out - Facing MS symptoms from A to Z



Yesterday, I rode in a car through a raging thunderstorm. The clouds were so low to the road that they blocked most of the visibility. The driver had to follow the brake lights of the vehicle in front of us for several miles until we had passed through the stormy area.

Cruising through the foggy stretch was disorienting and uncomfortable. It took all of the focus the driver had, just to keep our car moving forward safely and on-route. Even so, it was a struggle to focus and stay on course.



Sometimes multiple sclerosis feels sort of like that.

People call it “brain fog.” Similar symptoms can accompany other medical conditions.

Folks report attention issues, focus problems, memory challenges, and multi-tasking difficulties with chemotherapy, chronic fatigue syndrome, chronic stress, depression, exposure to toxins, long periods of physical inactivity, lupus, menopause, nutritional deficiencies, pregnancy, sleep deprivation, when taking certain medications, and during the grieving process after a loved one’s death.

Anyone can zone out a bit when overtired, overburdened, or overloaded. MS just tends to tip the scales in that direction much of the time.

Despite our earnest efforts to pay attention (especially when we’re viewing programs and presentations or when someone is speaking to us), we may zone out for a moment. We might miss a piece of something a person just said, take a few extra moments to answer a question, or forget an appointment.

Sensory overload can do that to us. So can MS fatigue, pain, or any number of other MS-related symptoms that interrupt our daily functioning and ability to concentrate.

MSers join the countless crowds who keep daily calendars, to-do lists, and other reminders, just in case they zone out. We might ask others to help us remember something important (although we cringe at the idea of inviting nagging). We set up notes on our smart phones.

And we try like heck to stay in the zone.



Note to loved ones: Beware of telling an MSer that he or she has brain fog or is zoning out. It’s much safer, more tactful, and wiser to let us tell you about it, if we feel like sharing.

Images:
Word cloud generated by Kicking MS to the Curb - All rights reserved
Series title graphic adapted from public domain artwork.



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