So I have a piece of exciting news... I'm going to be a contributor to another blog. For a wonderful person whom I just happen to love! I love their blog too, so it's win-win! I'm going to be filling in the role of "free printables" so I can't wait to show you all what I've been working on. I'm really excited for it. As soon as it's up I'll let you guys know so that you can go check it out for yourselves.
Anyway, today is Link's first parent-teacher conference. I can't wait to get some feedback. I know that he's been learning a lot (colors, shapes, numbers, etc.) but I want to know more. Since he doesn't have all the words to tell me, our typical ride home consists of me asking how his day was, "Good," and what he did, "Um...play...paint."
Yesterday, for the first time I think, he used an adverb. We were snuggling on the couch watching Polar Express (that movie creeps me out, anyone else?) and it was snowing. He turned to me and said, "I really want snow." I was blown away! This kid hardly ever forms complete sentences and hardly ever uses I and then even threw in an adverb. If it had been within my power I would have made it snow right there and then for the kid! I'm excited to see all of his progress.
Showing posts with label speech delay. Show all posts
Showing posts with label speech delay. Show all posts
Wednesday, November 14, 2012
News
Labels:
design
,
dysarthria
,
family
,
graphic design
,
speech delay
,
speech disorder
,
the boys
Wednesday, November 7, 2012
Back into the Fray
So a lot, and I mean A LOT, has happened these past few months. I've been incredibly busy and preoccupied but here's a rundown of things:
1. I quit my daytime job so I can devote more time to my family, including my son who has speech dysarthria and has numerous doctors / therapy appointments
2. My dysarthric son had ear tubes in/adenoids and tonsils out. They seem to be working wonders. I know some people are on the fence about tonsillectomies, but this child no longer has sleep apnea nor snoring. It's improved the quality of the sounds he can produce as well. Win-win!
3. We went to Disneyland Paris and Legoland Deutschland. They. Were. Amazing. Love the memories that we created and maybe one of these days I'll post some information/tips/photos.
4. I realized that I'm frustrated by the lack of information out there about children with speech dysarthria (if you google it you'll find it's mostly in older patients, particularly stroke patients, who have had some sort of head trauma). I'm frustrated that we're not sure what we're in for, nor how far Lincoln can go, and that there's just NO ONE out there. Then I realized, hey, I can blog about it. I can be the start. There might some other mother out there that's just getting the dysarthric diagnosis for her child and she might want to find some answers (I have none) or atleast some camaraderie (I have plenty). So if I start rambling about my child and his speech / motor delays, you know why. :)
Well, those are the main points, I think. I do plan on becoming more active in my blog. I really enjoy reading other blogs, reading comments, etc. so I hope that I can get back into it. Like everything else in life, I think I'll just have to make time for it.
1. I quit my daytime job so I can devote more time to my family, including my son who has speech dysarthria and has numerous doctors / therapy appointments
2. My dysarthric son had ear tubes in/adenoids and tonsils out. They seem to be working wonders. I know some people are on the fence about tonsillectomies, but this child no longer has sleep apnea nor snoring. It's improved the quality of the sounds he can produce as well. Win-win!
3. We went to Disneyland Paris and Legoland Deutschland. They. Were. Amazing. Love the memories that we created and maybe one of these days I'll post some information/tips/photos.
4. I realized that I'm frustrated by the lack of information out there about children with speech dysarthria (if you google it you'll find it's mostly in older patients, particularly stroke patients, who have had some sort of head trauma). I'm frustrated that we're not sure what we're in for, nor how far Lincoln can go, and that there's just NO ONE out there. Then I realized, hey, I can blog about it. I can be the start. There might some other mother out there that's just getting the dysarthric diagnosis for her child and she might want to find some answers (I have none) or atleast some camaraderie (I have plenty). So if I start rambling about my child and his speech / motor delays, you know why. :)
Well, those are the main points, I think. I do plan on becoming more active in my blog. I really enjoy reading other blogs, reading comments, etc. so I hope that I can get back into it. Like everything else in life, I think I'll just have to make time for it.
Labels:
boys
,
children
,
disneyland paris
,
dysarthria
,
legoland
,
motor delay
,
speech delay
,
speech disorder
,
the boys
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