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Tuesday, May 20, 2008 |
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Well first off,Brady is standing here sniffing my feet,lol lol. Either that means they smell pretty good or they really stink,lol. I dont know whats gotten into him with his new sniffing fetish. I caught him sniffing his dads socks this weekend,lol.
Today has been a pretty good day,all in all. Brady slept in this morning,so hes not sleepy at all right now. Hopefully his magic pill will kick in real soon. He has been really destructive tonight. I have cleaned this room up at least 4 times today,but he immediately starts back to work on it when I'm done. He has managed to rip up two books tonight,little stinker!! We of course had to throw a poop party into that mix,yippeee! We have got to get our potty chair,he cant stand to mess up his diaper,but wont sit on toilet either,he just has to many other things he would rather be doing :0
OH,I got an estimate on how much money the Angelman Walks raised for the foundation this year,but of course the numbers are still coming in. The estimated total at the moment is $850,000,whooooo hooooo!!! I think its a little less than last year,but hopefully the numbers will keep going up.
Anyways thats it for now. I will post more later. Gotta go chase my little monkey,hes into something! |
posted by angelwings
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1:12 AM
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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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