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Monday, April 28, 2008 |
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Our interview went well this morning,other than there just wasn't enough time. I think it would take at least an hour for me to talk about AS,lol. Anyway,Brady was good,a bit active as usual. Just before we went in, I realised that his ear was draining,uhhh... He hasn't complained at all and hasn't really been all that fussy til today. So after our interview we went to see the doc,he confirmed that Brady has a nasty ear infection,so hes on meds for that now. I feel so guilty for not noticing that something was going on sooner. If it had been anyone else,they would have been in agony. Brady just amazes me each and every day,at how strong he really is. I just wish that everyone would have got to see how happy he is. He was pretty blah this morning,not many smiles.
Oh,one last bit of news,Brady has learned to shoot a watergun!!! He totally loves it,he finally learned how to push the trigger and he was squirt everyone and everything,lol. Were going to have a blast in the pool this summer. We always buy super soakers for the kiddos,but up until now,Brady hasnt been able to join in the the fun. Im looking so forward to seeing him be able to play with everyone.
Anyway that's about it for now. I will post more later. |
posted by angelwings
@
8:31 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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