
If I were to level with y'all and be completely, unflinchingly honest (which ... well, is kind of what I DO, here on the Internet, so hardly a novel occurrence), I would have to admit that three years ago, when my son was first diagnosed as speech delayed and the first red sensory flags were waved .... I never, ever could have imagined that we'd "still" be dealing with "this stuff."
One of my very first blog entries about it -- in which I tried wildly and desperately to temper my panic and fear lest I draw out the Pain Olympic players who like to talk about perspective and childhood cancers -- I assured my readers that I understood that a speech delay was "no big thing." Something we'd face head on and conquer and dust our hands of in no time.
A "blip," I believe I called it. Does three years (plus change) still count as a blip?
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Mere hours after I posted a 

Noah came home from school yesterday with bright blue fingers. At first, I thought it was paint. And my heart soared.
So I've sung the praises of our school district's special education and early intervention services quite a bit, haven't I? Sure, we've had some problems, some arguments, some skeptical looks shot across the conference table, but for the most part, our experiences have been primarily positive.
If you had been in our house on Saturday morning -- possibly in the vicinity of the upstairs bedrooms -- I would not have blamed you for hearing the ensuing ruckus and jumping to the conclusion that my husband and I were very possibly setting our 5-year-old on fire.