Wednesday, August 29, 2012

August Update


ALEX

Alex is doing really well and is coming right along with his therapy. Still no Gait Trainer, it has been almost 5 months since we ordered it and we continue to have set back after set back. I am trying to stay optimistic, but it’s hard because I am so frustrated with the whole process.

He got fitted last week with some new shoes as I like to call them. They are AFO’S which are a type of Orthodic to help the position of his feet and toes as well as keep his foot flat while learning to walk. The pair he has now, were to stabilize his ankles, but the new pair will be taller and go up onto his calves more. They should be in soon so we will have to see how well he does with them.

Last Friday he received Lidocaine Injections in his legs per recommendation of his Physiatrist. The shots are administered behind the knee while lying on his stomach. The purpose of the injection is to block his nerves going to his calf muscles to keep them from tightening. So far, it is working well. I am amazed at how squishy his calves are – but in a good way. I am so used to them being tight that it’s a nice change and he seems to be adjusting well. We really aren’t sure how long the effect will last but we are happy with the results so far. He is a trooper. He did so well the day he got the shots.

On top of all of that, he got casted as well – poor little guy! His OT decided last week to cast his left arm in hopes of him utilizing his right arm more. That is the whole purpose of his OT sessions. He doesn’t seem to mind the cast. He still bangs on his toys with his left hand - cast and all. He also thinks he can hold his cup and pick up foods with it! It is super cute. He is doing alright with his right hand, but it’s going to take a lot of casting to break him away from his left hand. He favors it so much!


 
Next Tuesday Alex will be going to “school”. He will be attending class for an hour and a half on Tuesday mornings as part of the Early On program through the state. He will be in class with 6 other children with special needs and they will participate in circle time where they will read and story and sing songs. Then they will move onto different stations where he will be able to play. He will see an OT and an SLP while his is there as well. I think it will be a great change for him rather than them coming to the house. Evan is also welcome as a sibling to come and participate which I am sure he will.
 
Alex has enjoyed his summer by swinging, playing in the sandbox and listening to his favorite songs. (He LOVES music!). He also likes when we blow bubbles out on the deck!


 
 
 
 
 
EVAN
"Best Summer Ever” is how Evan would have to describe his summer so far. This kid has had a blast with everything this summer from his new sandbox, to his swing set, to the pool. His new thing is going down the slides at the park. He can’t get enough of it!
 
He has learned to use a fork and a spoon very well in the last couple of months and actually throws a fit if I try to feed him. He likes to do it himself and I have to say, he does a pretty darn good job.
He is into EVERYTHING – and I mean EVERYTHING! I used to have him barricaded in the family room and he decided he would start scaling the couch to get out. He is a little stinker!
Evan is all boy. He loves to get dirty, always has bumps and scrapes on him and he is non-stop from the time he gets up until he goes to bed. He is exhausting but fun all at the same time. I could do without the yelling, screaming and tantrums though.
 
His favorite toys right now are puzzles, wooden blocks and crayons. He could care less about the colorful, flashy toys that make all the noise. He’s a pretty simple kid as long as he gets his way!


 
 
 

1 comment:

  1. Carter has had his right arm casted three times for three weeks at a time to help improve the use of his left arm and hand. He had it done at 18 months, 2 years and 3 years. I find it to be a very effective therapy. Sounds like Alex is doing great!

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