This blog is about my 8 year old son Joey and our journey into diagnosing his PDD-NOS and Epilepsy, learning from it and helping others, as well as being a great place to store all the information I gather along the way.
I just got the phone call that Joey has been approved for state services. This will open the door to more therapy and intervention opportunities. It is up to me to get him all the help I possibly can so that he can be the best little Joe he can be.
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