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Thursday, July 17, 2008 |
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Were heading out to the ENT to have Brady's nose and ears checked again,hopefully everything will be fine. He hasn't had a nose bleed in a while,so it is better for sure.
But I had to share what he just done,it is sooooo cool. I have some pieces of colored construction paper,laminated,with the color listed on each piece. Brady was playing with a green one and I said to him "green", he holds up the green card and starts slapping it with the other hand,then starts clapping for himself, he knew that he was holding the green card,he associated the word green with it,how cool is that!!!! Its so fun to see him doing all these new things. I know that he is so teachable,its just finding the right technique. It just seems like the possibilities are endless, all these new doors are opening. It gives me hope that we will one day teach him to read, he is so capable!
Anyways just wanted to share. Gotta get going here. I will post when we get back and let yall know how it goes at the doc. |
posted by angelwings
@
12:42 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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Interactive Seizure Diary |
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The AS Forum was created in April
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The Foundation for Angelman Syndrome Therapeutics (or FAST) is an organization of families and professionals dedicated to finding a cure for Angelman Syndrome and related disorders through the funding of an aggressive research agenda, education, and advocacy.
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