.
First off ... ignore my laundry in the background. Secondly - this is Nathan checking out his Personal section of his NC7 ... we are avoiding the buttons with - say - address, phone number, etc... that is why I have some covered up and am directing him around them. Otherwise he would have to play them in order. Ha ha....
Today when I took him to school, he did NOT want to go ..... this is him saying "I'M SICK!!!!!"
He's telling me "MY TUMMY HURTS" ... ha ha... he's faking.
This was outside his room today ... had to take a picture of it......
We have a routine. We drive him to school (if he took the bus he would be on it for probably OVER AN HOUR - at least 45 minutes - and for him, that would NOT be okay - he would spend the whole time crying.) He eats breakfast at school. So we go in his room, drop off his stuff (he's usually unwilling and sad if not crying) .... we take his breakfast back to his room because it's quiet in there there... there isn't that many people and he can focus on eating. He might be extremely pokey puppy about it all - but he eats.
Here he is sporting his noise cancelling headphones at school. We need some at home - the definitely help him relax.
Later that day - we went to pick up Nathan from school! He had taken his NC7 with him and we heard the speech therapist was THRILLED and wanted to know how to get it for the other kids. LOL... it was a long long process....
And I say - even though insurance hasn't agreed to pay for it - and we're "renting" it .. and trying to raise money to buy it..... I say... now that we have it... they are going to have to come knocking on my door and pry it from my cold dead hands (and Nate's) to get it back....
When we left school, Nathan HAD to carry his NC7 ... course, he's busy shooting me with his M&M tube that Kaedyn picked up for him as a treat.
Parenting Unique and Differently Abled Children with a wide variety of medical issues. ADHD/ODD, Allergies, Aspergers, Autism, Brain Malformations, Cleft Palate, Dysgraphia, Dyslexia, Eczema, Hearing Loss, Hypothyroidism, Mosaic Trisomy 16, Russell Silver Syndrome, Sensory Issues, Speech Issues...just to name a few...
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Showing posts with label Nova Chat 7. Show all posts
Showing posts with label Nova Chat 7. Show all posts
Friday, October 11, 2013
Thursday, October 10, 2013
Nathan got his A.C. DEVICE!!!!!!!!!
.
Nathan got a box in the mail today!!!
We opened it up and it was his NOVA CHAT 7 ..... Woohoo!!! He was so excited!
We are just doing a rental basis right now - which is $75 a week ... but it's better than not having it!
Nathan got a box in the mail today!!!
We opened it up and it was his NOVA CHAT 7 ..... Woohoo!!! He was so excited!
We are just doing a rental basis right now - which is $75 a week ... but it's better than not having it!
Labels:
Communication Boards,
Dyspraxia,
Nathan,
Nova Chat 7,
Speech
Friday, December 7, 2012
Nathan's I.E.P - 2012
.
Actually - I can't say that I have to fight for much with Nathan. I had to fight more for Cal and Noah than I have with Nathan. I'm pretty happy with his team at his school.
He has improved in a lot of areas however .. his speech goals are the same since his speech hasn't changed much. He's attempting to say a lot more, and is being more of a parrot - but the quality of his speech hasn't changed much. His teacher commented on how she can understand him but others can't. I said "Welcome to my world!" LOL...
He's getting longer Occupational Therapy time.... and they were thinking ahead to next year and gym... and how much more .... ah the only word I can think of is violent - but that's not really true... forceful maybe? Anyway - they started to talk about how gym in 1st grade changes to a lot of throwing balls and such.... and I start shaking my head no. LOL... .... they are going to keep him in the kindergarten gym class until he's more size appropriate and ready to be playing with flying balls and kids who aren't paying attention to the tiny kid. Otherwise OT is going to be working on writing letters, cutting with scissors, and doing things like zipping and snapping and such which is really hard for him. She also said that with it getting colder here now, he doesn't like to go outside. Ha ha. So they make them go outside for at least 5 minutes and she says that he just stands at the door and stares at her. I couldn't help but to laugh.
He's made some improvement from last year where he's not spinning a lot. His Occupational Therapist (who was with him at the preschool) said that. She also said he's a bit more engaged with the other kids. They said that he knows when Matthew (one of his classmates who is in a wheelchair) gets frustrated and he goes over to his desk to help him out - and they are back there working on stuff together. I love hearing stuff like this. She also said he's not staying in the beanbag/papasan chair all the time either, like he was the beginning of the year. He lasts about 5 minutes or so in the regular classroom before he gets overwhelmed. In the inclusion room he can go at his own pace and get up and do other things too, if he needs to - and he can go in the other room and jump on the balls or what not ... and he does so on his terms... Over all he's doing well and he's working on the kindergarten curriculum - in the inclusion room - so YAY!! Everyone agrees that he's super smart he just can't communicate. :)
They said that they are going to be working with him on doing things like - asking for help, or asking to go to the bathroom. I want, I need, etc. They are making him talk and pointing doesn't get him anywhere - and I said "good, cuz it doesn't get him very far at home either."
They say he's a super slow eater... LOL... but he does good, he usually only eats half his meal, but at breakfast he LOVES bananas and he will eat several... which is very typical of him. He loves his fruit and he loves his veggies. He's drinking his Pediasure at school, so yay! She says sometimes he doesn't drink it all - and I told them that's nothing abnormal.
We also talked about his P.O.D.D. and how Nathan lost it at home (or Kaedyn did) ... and how I haven't been able to find it for about a month now (sigh) .... and how the Nova situation is going.
The Nova Chat 7 is his electronic communication device. He was evaluated in May and determined he would benefit from one... so the process started and we were told we'd get it in about 5-6 months. So I called prior to Thanksgiving to see how things were going - and found out that our amazing Marci who's dealing with it all had turned in the paperwork, she got an email confirmations back saying they had gotten it - but come to find out - there was not record of the paperwork. So we're basically starting back at square one there..... ugh....
So - that's about it ....... :) IEP is done until next December.
He has improved in a lot of areas however .. his speech goals are the same since his speech hasn't changed much. He's attempting to say a lot more, and is being more of a parrot - but the quality of his speech hasn't changed much. His teacher commented on how she can understand him but others can't. I said "Welcome to my world!" LOL...
He's getting longer Occupational Therapy time.... and they were thinking ahead to next year and gym... and how much more .... ah the only word I can think of is violent - but that's not really true... forceful maybe? Anyway - they started to talk about how gym in 1st grade changes to a lot of throwing balls and such.... and I start shaking my head no. LOL... .... they are going to keep him in the kindergarten gym class until he's more size appropriate and ready to be playing with flying balls and kids who aren't paying attention to the tiny kid. Otherwise OT is going to be working on writing letters, cutting with scissors, and doing things like zipping and snapping and such which is really hard for him. She also said that with it getting colder here now, he doesn't like to go outside. Ha ha. So they make them go outside for at least 5 minutes and she says that he just stands at the door and stares at her. I couldn't help but to laugh.
He's made some improvement from last year where he's not spinning a lot. His Occupational Therapist (who was with him at the preschool) said that. She also said he's a bit more engaged with the other kids. They said that he knows when Matthew (one of his classmates who is in a wheelchair) gets frustrated and he goes over to his desk to help him out - and they are back there working on stuff together. I love hearing stuff like this. She also said he's not staying in the beanbag/papasan chair all the time either, like he was the beginning of the year. He lasts about 5 minutes or so in the regular classroom before he gets overwhelmed. In the inclusion room he can go at his own pace and get up and do other things too, if he needs to - and he can go in the other room and jump on the balls or what not ... and he does so on his terms... Over all he's doing well and he's working on the kindergarten curriculum - in the inclusion room - so YAY!! Everyone agrees that he's super smart he just can't communicate. :)
They said that they are going to be working with him on doing things like - asking for help, or asking to go to the bathroom. I want, I need, etc. They are making him talk and pointing doesn't get him anywhere - and I said "good, cuz it doesn't get him very far at home either."
They say he's a super slow eater... LOL... but he does good, he usually only eats half his meal, but at breakfast he LOVES bananas and he will eat several... which is very typical of him. He loves his fruit and he loves his veggies. He's drinking his Pediasure at school, so yay! She says sometimes he doesn't drink it all - and I told them that's nothing abnormal.
We also talked about his P.O.D.D. and how Nathan lost it at home (or Kaedyn did) ... and how I haven't been able to find it for about a month now (sigh) .... and how the Nova situation is going.
The Nova Chat 7 is his electronic communication device. He was evaluated in May and determined he would benefit from one... so the process started and we were told we'd get it in about 5-6 months. So I called prior to Thanksgiving to see how things were going - and found out that our amazing Marci who's dealing with it all had turned in the paperwork, she got an email confirmations back saying they had gotten it - but come to find out - there was not record of the paperwork. So we're basically starting back at square one there..... ugh....
So - that's about it ....... :) IEP is done until next December.
Monday, June 11, 2012
Alternative Communications....
.
So in May, a few days prior to Nathan's surgery, we had a very long awaited and exciting appointment. Nathan has been working with his Pod (communication book) for awhile now. He is finally learning to to navigate through it a little better but it's still very hard for him (and for us) ...
We've had our hearts set on an iPad and ProLoQuo2Go Software....... (you can read more about at iPAD & AUTISM) It was the first software that I became aware of .... so of course, I thought it MUST be the best.
It's not.
Nathan's appintment started out simple enough - working with the Pod book just to get a feel on if he could identify photos and use them for his needs - which he did very well using both balloons and bubbles....
Then she switched to using different electronic devices to see which one (with program) he worked well with best ...... (there was a lot of bubbles going on!)
Nathan was very proud of his "Taxi" Ride of the day ....
*BEEP*BEEP*BEEP* Move out the way!
Here he is practicing on the device he will end up getting in 4-6 months (depending on when insurance gets it's head out of it's behind) ....
So in May, a few days prior to Nathan's surgery, we had a very long awaited and exciting appointment. Nathan has been working with his Pod (communication book) for awhile now. He is finally learning to to navigate through it a little better but it's still very hard for him (and for us) ...
Nathan's Pod (communication book)
We've had our hearts set on an iPad and ProLoQuo2Go Software....... (you can read more about at iPAD & AUTISM) It was the first software that I became aware of .... so of course, I thought it MUST be the best.
It's not.
Nathan's appintment started out simple enough - working with the Pod book just to get a feel on if he could identify photos and use them for his needs - which he did very well using both balloons and bubbles....
Then she switched to using different electronic devices to see which one (with program) he worked well with best ...... (there was a lot of bubbles going on!)
He is getting a Nova Chat 7 System ... it is lightweight, has a built in handle and stand, amazing program that will actually predict what you might want to say next and put those options up for you .... you can put together sentences .... and the program with GROW WITH HIM ....
Nathan was very proud of his "Taxi" Ride of the day ....
*BEEP*BEEP*BEEP* Move out the way!
Here he is practicing on the device he will end up getting in 4-6 months (depending on when insurance gets it's head out of it's behind) ....
We are SOOOOOOOOOOOOOO very Very VERY EXCITED!!!!
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