We have been really busy the last couple of weeks getting in all of our halloween activities. We went to another pumpkin and hayride event last weekend. We went with Sarah’s friend Marissa and her family. Logan’s soccer is keeping us hopping. I could start a blog just on all of his soccer activities. Kim and I went on a Treasure Hunt last night with some friends. It was a great time and it raised money for the Epilepsy Foundation of Western Ohio. It was a nice adult night out that we really needed.

I noticed today when we were leaving a soccer game that Sarah is not overcompensating her walk as much. The best way I can explain it is that she wasn’t lifting her knee unordinarily high. It could have been because she was tired, but her walk was looking more normal. She is doing the e-stim or her electroshock therapy (I love the reaction when I tell people that we are giving her electroshock therapy) at home now. It doesn’t hurt her, but she gets impatient having to sit in one spot while she is doing it.

Here is a picture of Sarah on the e-stim and some pictures from last weekend.

Sarah getting electroshock therapy

Sarah on the wooden train

Ava, Sarah, and Marissa on the wooden ship

Ava going down the slide on the wooden ship

Marissa, Sarah, and Ava on a really big tire

Photo op

Sarah is going to take the controls

Ryan, Logan, Ava, Marissa, and Sarah on what I guess is the Pumpkin King

Sorry, Michelle I just couldn’t resist posting this