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Friday, April 04, 2008 |
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Well,we just got back from Chucky Cheese. We had a good time,but Brady was more interested in socializing,than in playing. He made a lot of new friends,lol. He sat in the highchair at the table and grabbed everyone that walked by. Everyone was super nice,they all stopped and played with him,it just amazes me,the effect that he has on people.
Anyway when we first got there,Peyton went up in the slide,while me,Craig and Brady ordered our food. Peyton came rushing back to us saying that some kid,like middle school age, bit him! My first instinct was to snatch this kid out and confront him. I questioned Peyton a little more about it,and he explained that he thought this kid had special needs. He said that he kept following Peyton around in the tunnels and after he bit peyton,he giggled and kept pointing to his mouth,but he never spoke a word. I was really proud of Peyton for recognizing that this child was different,and not retaliating against him. Brady really has taught Peyton so much. Just before Peyton came up to us telling us this,Brady grabs some poor little boys hair. The little boy turns around and yells hey,but sees Brady and quickly calms down,of course I apologized. So when Peyton comes up to me telling me about the boy that bit him,I realized just how easily that could have been Brady biting someone,and that I would hope if he bit some other child,they would react just as Peyton did. Anyway Peyton didnt have any other run ins with him the rest of the night. Craig seen him later on though,and said that he did have special needs. Im so thankful that we didnt say anything to this child.
Brady has been really sweet today,but wide open of course. We have had a good day,all in all. His incisions look really good,where they took out the stitches. I dont see any signs of stitches left in,but were going back to the doc next week,just to be on the safe side. Anyways,I will keep you posted on any changes. |
posted by angelwings
@
11:50 PM
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| About Brady |
Read Brady's Story Here
I am 11yrs old and I have Angelman Syndrome. I may have this syndrome, but I dont let it hold me back. I love life and live it to the fullest every single day.
My mom says that our research organization, Foundation for Angelman Syndrome Therapeutics, is working really hard on a treatment or even a cure for me and my friends. I am thankful to have 25 words but I look forward to the day that I can carry on long conversations and talk so much that everybody has to ask me to please be quiet for a few minutes :) Anyway, mom says Im awesome and super funny and I have to agree,lol.
See my complete profile
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