"hmmm...I've never had a hand massage before! Are these for boys or grills?" -Logan
"hmmm...I've never had a hand massage before! Are these for boys or grills?" -Logan
My patient boy got rewarded with frozen yogurt after our shoe shopping trip!
Corn on the cob...the one veggie we can get Logan to eat!
The Portland Children's Museum is always a favorite! Mom and I took the kiddos on Saturday...

Mason and Mya's new thing is to make anything and everything into a hat. Baskets, buckets, bowls...you name it, and they will wear it. It is pretty hilarious because they will wear them for a long time....almost like it's a real hat that they they are supposed to be wearing. The very funniest part is that Mya has excellent posture and can keep things (even quite small things) on her head for a relatively long time. I get such a kick out of all their crazy antics!
Yesterday I took Miss Mya to Legacy Emanuel to get her developmental asessment and review. I haven't even been worried about it because she is doing SOOO well. She still has the diagnosis 'dissociation of maturation' but she is far surpassing their expectations developmentally so we will just have to wait and see (as far as I'm concerned). The very best thing that can be done for a kiddo with a motor planning issues (mentally and physically getting from point A to point B...swallowing, rolling, babbling, etc.) is to have lots and lots of modeling and practice. Typically that means lots and lots of therapy and practice at home. They suspect that the primary reason Mya has progressed so rapidly is that she has had Mason as a constant model of all the tiny steps that piece together to create task mastery. So having Mason just a few skills ahead of her has really given her the edge in taking off. She is constantly striving to do what he does and how he does it. She watches him like a hawk and copies what he does. It has also provided some stimulation and motivation for her to keep trying. She has Logan but it is a lot different than having someone right at your level to follow and copy. Currently Mya is in an informal study on dissociation of maturation as there isn't much literature about it available. That was a really LONG way to say that God knew Mya needed Mason. He knew the special needs that she had and He provided for them in His loughty wisdom and understanding. In my narrow perspective I thought I had it all figured out. I felt like our parental insight was going to be what gave Mya that leg up. Little did I know that God was caring for His precious daughter in a way that I didn't know anything about. I am so grateful for the Lord's mighty hand in the lives of our kiddos.

We got these for a couple of bucks at a garage sale...good find, huh?