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Wednesday, May 14, 2008 |
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Well I have good news and bad news. The bad news is Brady had his first bad night last night,since his surgery. No seizures,thank goodness,but he did stay up playing until 3:30am. I was wore out,I have gotten out of practice,lol. He slept til 9am and was cranky so I told him to go back to sleep,we weren't acting like that all day. So he slept til sometime after 11am and got up feeling happy and refreshed.
The good news is,Brady said some new words today! I was calling the cat a big baby,because he was sitting at the door meowing. Well Brady blurted out "big baby"! It was so funny,thank goodness we had company here that heard him say it to,so we had a witness,lol. We managed to get him to repeat it 2 more times after that,he said it so clearly! I tried to get him to call his dad a big baby when he came in,but he only managed to call him a baby,which was pretty funny,lol. Anyway were excited,he has never said either of those words,let alone put them together like that,its so cool!
I also forgot to tell you guys,Brady walked in beach sand over the weekend. He walked all the way down to the water,I was very impressed! He has never been able to do that,we have always had to carry him,so our backs are finally getting a rest!
Anyways thats it for now. I will post more later. |
posted by angelwings
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9:32 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 |
This
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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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