He can't really see things in fine detail, so there wasn't much he could see with the eclipse, but that didn't stop us from taking him outside to experience the eclipse with us. It took a lot of explaining to him what was happening - mom and dad are the original audio subtitles to the world around him. He liked it when it got shady and when the birds started singing. It was also very quiet outside and cooler than usual.
Towards the end of the eclipse, his teacher arrived and he was ready for school! She brought a cool book for him from vision services so he could feel the eclipse through tactile pictures. They watched some videos about the eclipse and read another book too.
Tuesday was another busy day with physical therapy and school. Max was having a little bit of a rough afternoon on Tuesday, and ended his school time with a headache and needing to have a rest in his room. He was able to tell me and his teacher than he was hurting and needed bed without getting very upset. But the best part of his school time is Max met one of his goals of using his switches for his communication device by himself for most of school. This is huge as last year he refused to use his talker without someone holding his hand for support.
Wednesday was his busiest day of the week, and he was exhausted! He started with music and slept through most of it. Then was school which he did great with. He got through all his subjects and again worked hard at using his communication device by himself. By the time his art therapist got here he told her he needed to do "easy", and she agreed!
He wanted to paint all by himself this week, and then wanted to name his art.
|He only needed a little support for his arm this week.|
|Loving his artwork.|
|"I'm Max" with blue and yellow water colors|
|"Ice In Hot" purple and yellow paint pens|
Thursday was a little more relaxed, but we got out for a drive after the daddy got home to go get tacos as a reward for a great first week back to school. We walked around outside after we ate our tacos and Max got to play around a fountain. (Sorry, no pictures.)
Friday morning started with an early morning trip to the hospital for a lab draw. We're checking his testosterone levels to see how we're doing with the new dose. Changing the dose, and frequency has helped some things but has made some other side effects show up. We wish he didn't need it at all, but he will have to have testosterone replacement for life so we just have to find the right dose for him.
We spent the rest of the day watching movies and kicking back. Something Max has down to an art form. Lately, he wants to be all cuddled up with one foot hanging out of his cover being blasted by his portable air conditioner.
Being an 8th grader takes a lot of energy!
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