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Saturday, January 31, 2009 |
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Well, its been a while since our last update, so thought I would post a quick one tonight. Brady is doing well, but we've all been sick here with Strep Throat. Brady has handled it better than me and his brother, thank goodness. Other than a slight cough and occasional sneeze, hes doing great. His sleeping has been all over the place this past week,and he hasn't made it to school all week. He has been very active, almost manic. He did manage to watch part of a movie, Horton Here's A Who. He stood in front of the tv, and danced around, even putting his face up to the tv a few times,lol. It was adorable. Brady hasn't been out of the house all week, I think hes getting really bored being at home. Hopefully next week he can venture back out into the land of the living :)
We done some renovations here in what used to be the therapy room, making it more suitable for all of us. We put up a new quarter wall, putting all of Brady's toys on one side, and adding all padding to the floor, while the other side actually looks like an adults room. Brady loves the new room/rooms. He spends alot of time on his side of the wall, playing with he toys, occasionally throwing some toys over the top. His daddy got a new tv. But we cant mount it on the wall, until the bracket comes in. Brady has shown lots of interest in the new tv, not a good thing. Hopefully it can survive until we can get it hung up out of his reach. The big screen that was here, has now retired to the living room, with lots of war injuries from Brady,lol. The old tv really has been a good one, when Brady pours something in it, we just unplug it, and it starts back working in a couple of days, but I'm sure its days left were numbered.
Anyways thats about it for now. Will post more later. |
posted by angelwings
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11:43 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 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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