tweener8292
New member

Posts: 3
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« on: November 30, 2010, 08:38:32 PM » |
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Does anyone here have to cope with MS and the job? My form is primary-progressive. News about new treatments, etc. are for relapsing forms, not for ours. Any medications that are prescribed are only to cope with the slow, steady advance. So far fatigue is the #1 job related effect, and by the time I get home from work I'm too "cooked" to grade papers, etc. #2 would be how stress exacerbates the feelings of numbness, "blah", fatigue, etc. I find myself hiding from those who would use my condition against me when I do not feel well. This happens often in the afternoon, as well as when I have to deal with them (especially a department Chair and Dean who I KNOW who like to use any excuse to negatively impact on my career).
Some days it just stinks. On the others it's a major factor that impacts on how I feel about myself, my job, how it hurts the marriage (my wife teaches at the same institution in another department and her work conditions are much better and more supportive - stressful in its own right even if illness wasn't a factor. My MS, its effects, and the prognosis makes it all even worse). I know that the prescribed career advice is documentation, etc., but it sure doesn't make the career better and/or enjoyable. It's become one of "grinding and coping", and that at its BEST.
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