Friday, March 9, 2012

Blog changes

It has come to my attention that perhaps I'm not being clear enough about Gage and his "diagnosis" (for lack of a better word). I believed when I was writing about Gage and his prognosis that I was making it perfectly clear that his prognosis is great, it is possible that he will outgrow all of this, he does not have a technical diagnosis at this point as he is too young, etc. Apparently that was not clear enough, and some see fit to behave as if Gage having delayed speech, and the possibility of very minor sensory perception issues make him less of a "normal" two-year-old. Let me be the first to say, there is no normal. BUT, as two-year-old go, Gage is right on track with the exception of speech. He should be treated, loved, and accepted like any other two-year-old. Just because he doesn't speak yet, it doesn't mean he doesn't enjoy everything every other kid his age does.

We will continue to do what we need to do in order for Gage to continue thriving. But I feel it's best if I no longer make it public due to how clearly I'm being misunderstood. If you want Gage updates, email me. I'll share what I feel is appropriate. For the time being, all posts tagged with or mentioning Gage, apraxia, and sensory perception are being pulled. As I have time to weed through them pull specific parts out that I'm comfortable reposting, I will.

I'm sorry it has come to this, but I refuse for Gage to be labeled in a way that paints him in a negative light. He is too awesome of a kid for this level of misconception.

1 comment:

  1. Oh my gosh I can't believe that people would be mean like that. I'm sorry they are taking the chance to talk about your experiences from you, and I hope everything continues to rock in the world of Gage.

    Love you all and we'll see you this weekend.