David is off being allergy tested as I type this. I can't wait to see what his results are. He was so nervous when he left here.
Ryan seems to be communicating more recently. I think it is the meds. I am happy. We go back to psych doctor in 2 weeks. In about 4 weeks, I should hear something from local school district about help for Ryan.
Liam is still wild and sometimes a bully towards Ryan. Ryan says to Liam, "Don't bully!" a lot. Liam likes Mickey Mouse, The Wiggles, and Barney.
When your baby is born, you make sure they have 10 toes and 10 fingers and all the right body parts in the right places. But what about the parts you can't see, the invisible pieces. Those become more visible as the child grows up. This blog is about my two sons' invisible pieces and how we are dealing with them as a family. I hope you follow along in the discovery of Our Invisible Pieces.
Subscribe To
Posts
All Comments
Monday, February 13, 2012
Wednesday, February 1, 2012
January 2012
January was busy for us. Ryan had 2 appts with a new doctor and another school evaluation.
The eval went smoothly and lasted about an hour. I could see where Ryan was lacking and not doing what they wanted him to do. I will know in March what programs the school district will offer Ryan. I am hoping he will be able to go a preschool for special needs children in our school district. If he doesn't do that, he will try Pre-K.
I am still waiting for TX Children's to call me back to get Ryan eval there for his Autism.
Ryan's new doctor is a psych one. She said that Ryan was mild/moderate Autistic with SPD. She started him on a med that made him walk around moaning and he would throw up. We have changed him to a new med, but I am leery of trying it while David is at work. We go back in 4 weeks.
The rest of us are doing fairly well.
I lost my voice for 3 days over New Years. My voice is still not back to normal. Ugh! I need to get a filling.
David got a raise at work. We have filed our taxes.Since David got a raise the boys can no longer get Medicaid and they are now on CHIP.
Liam is growing like a weed. He is pointing and saying - mama, dada, up, down, kitty, baba, bye, hi, and night night. He can blow kisses and wave. Liam can sign - more and milk. He will show you where his milk is for his cup. He will tell you through non-verbal signals that he wants to jump in his jumper.
The eval went smoothly and lasted about an hour. I could see where Ryan was lacking and not doing what they wanted him to do. I will know in March what programs the school district will offer Ryan. I am hoping he will be able to go a preschool for special needs children in our school district. If he doesn't do that, he will try Pre-K.
I am still waiting for TX Children's to call me back to get Ryan eval there for his Autism.
Ryan's new doctor is a psych one. She said that Ryan was mild/moderate Autistic with SPD. She started him on a med that made him walk around moaning and he would throw up. We have changed him to a new med, but I am leery of trying it while David is at work. We go back in 4 weeks.
The rest of us are doing fairly well.
I lost my voice for 3 days over New Years. My voice is still not back to normal. Ugh! I need to get a filling.
David got a raise at work. We have filed our taxes.Since David got a raise the boys can no longer get Medicaid and they are now on CHIP.
Liam is growing like a weed. He is pointing and saying - mama, dada, up, down, kitty, baba, bye, hi, and night night. He can blow kisses and wave. Liam can sign - more and milk. He will show you where his milk is for his cup. He will tell you through non-verbal signals that he wants to jump in his jumper.
Subscribe to:
Posts (Atom)