Battling Multiple Sclerosis

I have been posting each month a “THANK-YOU” post, like this one, to all the advertisers from the previous month listed as at month end. That’s a permanent link in this blog, under the category heading which I call .. “Sponsor Appreciation”. I know it’s hard out there trying to figure out where to spend your advertising dollars .. and well .. THANKS for considering the Battling Multiple Sclerosis Blog.

I have compiled a new advertising page for the HART-Empire Network of sites for your perusal.

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By Jon Wegner

I would like to say first that I’m not a doctor so I don’t know all the technical words for what I describe in the following paragraphs. But I speak in layman’s terms that I think most people understand. I have secondary progressive multiple sclerosis and as I sit here I’ve been thinking what my life is going to be like in a year, five years and 10 years from now? I’m 49 years old and I suppose I’m getting set in my ways. My MS is only going to get worse. That’s not a very cheerful thought but I try to never feel sorry for myself. I was dealt this hand of cards and I have to deal with it the only way that I know how, with laughter and a never say die attitude! I was diagnosed in 1991 but now that I know what the symptoms of MS are I can easily trace it back to 1980 and maybe even earlier. It’s ironic but I managed health clubs in southern Minnesota from 1980 until May of 1987. It’s ironic because I used to be able to run a couple of miles per day and also bicycle 20 miles the same day. Now I can hardly get out of bed and when I do I’m reaching for my electric scooter or my walker.

The first symptom that I clearly remember is from 1980. Obviously, I didn’t know it was a symptom back then but I do now. I was working at a racquetball club in my hometown of Rochester, MN. I remember sitting in the whirlpool after work or working out and when I got out of the whirlpool I would feel strange. I thought I just didn’t like the hot water because the whirlpools were at least 105 degrees. I couldn’t explain the feelings then and I can’t explain them now but I just didn’t feel right! I was sort of lightheaded, a little dizzy, and sort of wobbly. Thinking back now I was at the clubs for almost 7 years and I bet I wasn’t in the whirlpools more than six times! I also remember having that feeling when I sat in the saunas or the tanning beds. Now I know that it was the beginning of my sensitivity to heat. When I think back I can’t believe that my MS was in my body just waiting to get out. I did a lot of activities in the 80’s that made me warm and I always drank extra beer and blew it off that I just didn’t like heat! Who would ever imagine that it was multiple sclerosis? I know I didn’t.

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