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Tuesday, April 08, 2008 |
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Just wanted to post a quick update. Brady is doing really well. He has done several things today,that I am so proud of. The first is that he put his legs in the right holes of each pants leg,without even being prompted. Another thing he done was when asked if wanted a bath,he didnt want to answer,but I said if you want a bath you have to use your words,so he quickly started shaking his head yes,yes,yes. Another thing he has learned is to open the doors on my van and his daddys truck. He pulls the handles and pulls the doors open,he is so proud of himself,lol. I had to lock the doors when we were outside today,he kept opening the doors and trying to climb in,lol. The other cool thing he has learned is how to blow the horn on his riding toy. This is an outside toy,that he insisted on bringing in,like we really have the room.... Anyway he climbs in this toy and toots the horn and just giggles,he loves it.
His skills and comprehension continues to improve on a daily basis. We still have not seen any seizures since getting the VNS. He is still sleeping through the night. I know that the absense of seizures and the fact that hes finally getting some rest,has really played a key role in his development these days.
Anyway thats about it for now,I will post more later. |
posted by angelwings
@
7:53 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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Brady playing.
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Interactive Seizure Diary |
This
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Angelman
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The AS Forum was created in April
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Cure Angelman Syndrome |
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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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