It looks like it’s time to blow the dust off this blog again. Was the last entry really in November 2005? That doesn’t seem that long ago, but according to my calendar, it was about eight months ago. My, how time flies.

A number of things have come to pass since then, including gainful employment with IBM. In addition, I have a few more ComputorEdge articles under my belt, Keith and Logan are out of school for the year, and I have another writing opportunity taking shape behind this curtain over here.

But the most significant thing to happen in the last few months involves my wife, Lannette. She has been diagnosed with Fibromyalgia Syndrome (FMS), a recognized disability under the Americans with Disabilities Act. FMS is an often misunderstood malady, and some doctors don’t even recognize it as a valid disorder. Personally, I think they would recognize its validity if they had to deal with it from day to day.

I don’t have FMS, but I am familiar with it. I recognize it from when my brother had Fibromyalgia as a corrollary to Sjogren’s Syndrome. Lannette’s situation is a bit different, because FMS is her primary diagnosis; it is the source of unpredictable pain that moves all over her body from day to day. Living with FMS is a crap shoot for her. She just returned from a trip to visit family in the Pacific Northwest, and even though it was supposed to be a relaxing, renewing trip, it wore her out. She was exhausted when she arrived at DIA, and is taking it easy for a few days.

I’m constantly amazed by my wife. She’s the strongest survivor I’ve ever known. She was two blocks away from the Murrah Buiding in Oklahoma City when Timothy McVeigh blew it up on April 19th, 1995. She has been physically abused in ways that would stagger anyone, yet she still had the strength to fight back from all of that to start and administer an Internet newsgroup for women who have survived domestic violence.

I know that she will find her way through this challenge, find her “new normal.” She always has, always will.