We got an official diagnosis today by DD's speech therapist. I am not even remotely surprised and have been waiting for this for almost a year now. Everyone was very quick to dismiss DD's lack of speech due to tubes/hearing loss, but I was always skeptical. With good reason! haha.
So, even though I am not surprised I am still trying to wrap my head around what this means for the future. We do not qualify for services through EI. In our area you have to have less than 10 words to get help, and approximations count. Will a diagnosis change that? What about help through the school district? Will a diagnosis help that come November when DD turns 3? I'm sure it varies by area, but I'd love any insight anyone can offer.
Final question: Any books or other websites you would recommend?
One of my IRL friends has a son wiith apraxia. They are in ST 5x a day. If that is the path we are on I think I am about to get very overwhelmed very fast.
Re: Talk to me about apraxia.