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Thursday, July 12, 2007
Bradys day,.
Well we went for Brady's Upper GI today. He done really well. I gave him an empty sippy cup just before the test,and he handed it to the technician,for her to put something in it. I just laughed and said yep,she is going to put something in it alright,lol. So she put the chalky mess in it and he actually drank it. He didn't even stop to taste how bad it was,he waited til he had nearly drank the entire cup,to stop and taste. Of course he then handed the cup back to me and started telling me off,lol. I did give him some pediasure to wash down the nasty chalky stuff. He held really still for the first test. They started turning him on his sides to take xrays and he got a bit frustrated,but he really wasn't that bad. We managed to get all the xrays done,and he only kicked the poor lady a couple of times. One of the ladies kept telling Brady to turn on his side,then told him ok now,hold your breath. I said oh he doesn't know how to do that and she well he just did,hm mm I think it might have been luck,lol.
We then went to pick up his pediasure and his new acid reducer. Of course everyone there had to come out and play with Brady. He played peekaboo and just showed out for them,hes such a little monkey!
I hope I didn't look to terribly bad,Brady had been turning the lights on and off while I was getting ready. Imagine trying to do makeup while using a strobe light,lol. So its a good possibility I looked like a clown,lol.
Anyway Peyton has been going to bible school this week and Brady goes with us to pick him up. He is so amazed at all the kids dancing and singing. He stands on the pew and does his own little dances,lol. During the prayer tonight,he started yelling,"Bubba,Bubba,my Bubba',lol. Bubba was sitting up in the front with his class. We tried to quieten Brady down,but he was so hyped up,to much stimulation I think.
Well that's about it for now.Hope to hear from the tests tomorrow,will let yall know. Gotta go,Bradys got the remote,turning the channels on the tv.

posted by angelwings @ 11:33 PM
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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.

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