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Monday, July 23, 2007 |
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Well Brady has been up to lots of things lately. He has become interested in climbing the spiral stairs,hmmm. He has never been interested in the stairs before,but thanks to big brother agging him on,he is now. He got 4 steps up today then was fussing cause he couldn't figure out how to get back down. Of course I was right there watching him,just wanted to see how far up he could get. He has also figured out how to work the MP3 player,dad wont be to happy about that one,but Brady sure is. Hes kicked back in dads recliner,listening to music,lol. If course he keeps tasting of the headphones,lol. Brady has also been walking a lot today. He just decided to take off and walk from the chair to the TV today. I cant help but jump up and run behind him. I just cant stand the thought of him falling,guess I'm going to get real busy running huh. He of course just thinks its so funny to give his mom a heart attack,lol. We went school shopping this weekend,got mostly Peyton's school clothes,because we have most of Brady's already. This is the first year that we have had to buy Brady school clothes,it almost made me cry. I really do hope that he gets to go to school this year though. If we don't get this sleep straightened out I'm not sure how it will all work out. He did however sleep all night last night,first time in a long,long time,whooo hooo. I wish I could say that I thought it was the beginning of a new trend for him. But its 1:22 am and hes going strong,so no such luck I guess. He still isn't eating a lot these days,but did eat part of a hot dog,some potato soup,and a bite of a candy bar today,so hey,that's better than usual. Hopefully things will get better soon. Anyway that's about it for now,I will keep ya ll posted. |
posted by angelwings
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1:14 AM
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What is Angelman Syndrome?
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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