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Thursday, January 24, 2008 |
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Well,we spent the day at my grandmothers house today,thank goodness shes used to Brady being into everything!! She is making our little Chip and Dale stripper some strip proof outfits,its great to have a grandmother that can sew anything:) Anyway,Brady was such a big helper. He was trying to play with the needles,scissors,yanking the patterns away and playing keep away with them :O He was going from room to room,and while getting into one thing,eye balling the next thing he was going to get into. He is walking,or running around should I say,like a little mad person.
He really is doing great though,he has had the appetite of a grown man tonight!!! He has eaten two suppers so far,lol. For some reason Brady and his brother have decided to argue like true siblings,and they both get the biggest kick out of it,lol. Peyton does things just to get a rise out of Brady,and of course Brady stands there and tells him off in Swahili language and just giggles about it. Peyton said tonight,oh mama,I think Brady is calling me bad names,guess its good we cant interpret Swahili,lol.
Sheesh,Brady is so manic tonight. Its after midnight here and hes energized as if he had just got up from a big nap. Hes standing next to me,really telling me something atm,but hes very serious about whatever it is hes saying,lol.
Anyways just thought I would post a short update,gotta get back to the manic boy. |
posted by angelwings
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12:24 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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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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