Sunday, July 17, 2011

It's been a rainy Summer

Since the end of school, we have gone camping, gone to the movies, had the kids playing in the back yard...well when it's not raining. What a pitiful summer it has been! We got the kids a little pool, and they love it....when they can enjoy it that is! I think that mother nature has been PMSing lately.

We leave for a two week camping trip on monday. Well not really a full two weeks. I will be back and forth with the kids through out the first week. Joe still has tutoring and sportball soccer, and Kenny has IDP etc. The second week, I only need to come back once. But the kids are just as happy to go for the nights anyways.

Kenny has received his new stander. He's liking it. We saw the neurosurgeon this week. He's happy with the lack of brain pressures as of now. So we don't have to see him for another year now.

It's just been busy as usual...with a bit of sleeping in! September will kill me with that one...lol!

Monday, June 13, 2011

Kristen, Kristen, Kristen!

Well my little CHERUB is growing up. Last week we had her intergration meeting with the school. And believe it or not, I left feeling good! I feel like Kristen, and myself are going to be supported to the fullest. She is doing amazing things this little girl of mine.

We had a CI mapping today. We were taken into the booth, and she did her listening. She did such great conditioned play. She even hit the button when there was nothing even being presented....well, I figured out pretty quickly it was because I didn't hear it! But she did! Uh Oh, time for mommy to have a hearing test!

She was then presented with an assesment of vocabulary for 5 year olds. She quickly got bored, because she was getting it! And so the audiologist moved up to the 6 year old assessment. WOW. She did really well with that one too! I am just so proud of where she was, and where she is!

Wednesday, June 8, 2011

Friday, June 3, 2011

A blog to follow

This blog is of a 23 year old man, who has PDD-NOS, and is giving insight into what he feels and see's. So very interesting, and nice to have a voice as to what we may be dealing with with Joe. I thank him for allowing me to share!

http://voicefromthespectrumop.blogspot.com/

Thursday, June 2, 2011

Water proof hearing aids.

http://talkingtwentyfourseven.blogspot.com/2009/03/water-aids.html

this person has allowed me to share this post with you. I felt that it was a nice way to let people see this too!

http://talkingtwentyfourseven.blogspot.com/2010/06/prepping-for-water-fun.html

This one was for short tuerm spraying!

Thanks so much for letting me share!

Friday, May 6, 2011

Neonatology followup

Kenny had a Neonatology Follow-up Clinic on Tuesday. The PT felt bad bringing us in for the visit. She knows that we are well supported in the community. Of course they saw lots of change in him and were happy. It's slow for us to watch daily though. But the last time they saw him, he was only about a month post-op for the hydrocephalus. So of course there were tonnes of change since then. They have classified him as a level 4 maybe 5 on the CP scale. There are only 5 levels, one being maybe walks with a limp. I said, that's nice, no one will be able to predict his future and every baby has a different early intervention stage, and really since he has only been without brain pressure for 8/9 months, that took him right to almost a newborn stage again, he is doing well. Now don't think that I'm burying my head in the sand in denial. I do believe that Kenny will need a wheel chair. I do believe that he will have some mobility. How much, that I don't know. But I like to think postitive. I do know the reality too. But it doesn't change who he is.

The pediatrician there has put in a referal for full genetic counselling and work up for the whole family. It's just so curious how we have won the lotto on our kids, and why. Is there a genetic componant? Who know's? Again, doesn't change anything or anyone, but will just give us more information.

Wednesday, April 27, 2011

Sand....yep!

I think that we have officially hit all of the tactile issues with Kristen! She has been through all of it! I think it has to do with her vision as well. So we started with cement, grass, gravel, bark mulch, and now we have achieved sand. If you saw her last year, taking her to the beach...yikes...it was like putting a cat in a bag! She would scream and dig her heels in and refuse to go! I'd pick her up and just sit her on a chair beside me. Well we went camping at Camperland in Bridal Falls last weekend. And she walked on the sand on the first day. Shoes on...but did it. No screaming, and on her own free will. The next day it was shoes with no socks and dumping the shoes every 5 minutes. Then out of no where...shoes off...thrown to the side and walking! Barefoot! HUH??!! And then the kicker, she started kicking her toes in the sand! How far she has come!