Sometimes the MiSery is Not MS

Over the past year or so, I’ve joined several MS Facebook groups, mostly out of curiosity regarding what MS “looks like” in other folks, in hopes of getting some needed perspective.  In some cases, the collective advice and wisdom have been somewhat helpful. On the flip-side, I have also noticed an alarming tendency to attribute every ache and problem under the Sun to MS.  At one point, I was even advised by a member of one of these groups to “just blame everything on MS because it’s easier that way”.   Maybe, but the scientist in me ain’t buying it.  Even more importantly, sweeping everything under the “MS rug” has the potential for doing considerable harm. Take my hand, for instance…

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Data, diagnosis, and the Scientific Method

My previous emails have been an attempt to provide a 15-year background and quickly catch up to the present-day.  I’m almost there!  When I last posted, I was discussing my Copaxone treatment, and mentioned that one reason that I had fallen “off the wagon” for a couple of days was because of an unusually stressful week that got me home late each evening and really just too tired to deal with the hassle and pain.

Well, there was another reason for temporarily stepping off the wagon… Continue reading