By the end, I will probably decide I typoed and it was evilness.
But, we’ll have some answers, about ten thousand more questions, but we will have our start.
I’ve heard a lot of good things about this psychologist. I’ve been told he’s good at working with the family unit, seeing PX as part of a bigger picture, and helping to customize our goals and tactics to best fit all of us. I like that. Because as much as I am a “my kids come first, I will cut out an organ or pinkie toe to benefit their quality of life!” I know that some things might just not fly with a sensory sensitive one-year-old who has some *mild* separation anxiety in our family portrait.
I’m really excited to get a diagnosis. That probably sounds fucked, but it’s true. I have made peace with the fact my son is most likely on the autism spectrum. I know I won’t be able to look on the bright side 24/7 and sometimes, I’ll get sad and downright pissed about how hard he has to work as compared to NT kiddos. And that’s okay; emotions are human. I’m excited that plans will be able to be focused, we’ll know what options we have and what we have to do to get there.
Only 4 months of total waiting, and we’ll know. We will have some answers for Gus Gus.
