It can be so exhausting to be patient with your special needs child :(
It's heartbreaking but I have to reel in some of Gavin's independence:( Gavin's current capacity is such that I have no choice but to start taking away some of the independence he has earned over the last year. I've said a few times recently that I'm seeing regression once again. This is kind of the status quo for Gavin. He will do really well and then begin to regress again. Clearly this is an ongoing issue. For most of the last year, I've had Gavin responsible for his medications, for the most part anyway. He would take them when it was time and most often remembered to do so on his own. Last night he informed me that he had not taken his inhaler while at his Mom's house because…
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August 23, 2015