She's getting him to put pressure through his feet and
touch the musical touch activated toy
He did so well last visit!
Its astounding really. We went to Alberta on a road trip and truly it was a holiday in more ways than one. I mentally decided to take a break and chill out from all the physiotheraphy, speech theraphy, and calorie pushing that I tend to do on a daily basis. I wondered if I'd regret it in the long run as I was concerned he may back track a tad from the lack of consistancy. But it seems to have done the complete opposite! On the trip he decided it was time to feed himself a mum mum cracker (a quickly disolvable cracker) which is huge as he basically has only put a spoon in his mouth. He also decided he'd start grabbing his feet which has been an endless daily routine in trying to make him aware that they exisit. Now he has decided he can grab them with both hands! Anyhow after we got home he suddenly starts rolling over three times before we even get out of bed...........mind you its starting at 4 in the morning....but who's complaing? We can't believe it really...its just wonderful that he's at this stage. He seems so determined to no longer lie soley on his back. So thats making this mama and papa pretty proud. Its not limited to just the above though. He is also starting to eagerly drink from a glass, do some weight bearing through his feet, and interact with musical cause and effect toys. So just as I was coming to terms with a lack of progression my little man decides to surprise his ma prior to his first birthday. Needless to say this is quite the treat.
We have also started to wean him off his old anti-seizure med as the otherone is up to its max dose. So fingers crossed that is uneventfull. So far so good. Some nights he has a lot of extra movement but that was even prior to reducing his meds. It'll be so nice to be down to two rather than three meds. But whenever I think of complaining about having to give him anything I remember this mom and her 10 month old babe in the x-ray department at Children's. A month prior to that meeting she had been informed her daughter had Cystic Fibrosis and she was having to give her 31 yes THIRTY ONE meds A DAY! So if you ever get on the poor me band wagon ...think of that little darling having to scoof down all those meds EACH DAY.
Cheers Dears! Jules!
Hi Julie:
ReplyDeleteGreat news on Alistairs progress. All the best to you all and have a great day.........Love, Anita
Julie,
ReplyDeleteJoelle said look baby Alistair as soon as she seen the video. She also got a good giggle from watching. Glad to see the progression. Can't wait to come down and visit.
Valerie
hi julie, love those videos . looks like alistair is coming along just fine. tell jason he used to be handsome, but now alistair is the most handsome and sooooooooo cute.i can't wait til you can come and visit use here.
ReplyDeletelove gramma polly
Yay Alistair!!!!
ReplyDeleteI am so thrilled and can't get over the change in him!
Thaks for the visit the other day, we will have to come out again! Rocco sure loved it.
I will call you when we are back in town. Have a great week!
xx