Angelman Syndrome, Life as an Angel

Monday, July 28, 2008

Well were doing good here. Brady has had a busy weekend, getting into to something the entire time. The first thing he done,was to bad to even mention here,but it was a heck of a party! We all went out to the camper,per Peyton's request. Craig,Peyton and me decided to play a game of monopoly while there,while Brady ran wild. He decided to take a head dive from the top of three steps,leading up to the bedroom,all the way to the bottom. Of course it nearly scared me and Craig to death,and Brady was very stunned at first. He cried just a bit and then was up looking for something else to get into. His brother thought he had to get out the marshmallows,which we don't usually do around Brady. Of course Brady managed to steal one from his brother and had it nearly down his throat before me and Craig could hold him down, prize his mouth open and pull it out of his throat. Well we got back to our game where Brady continued to steal his brothers monopoly money and take off running with it. He also had a floor full of popcorn by this point. Then he decided to go under the table,where he found yet,another piece of a marshmallow and nearly got choked on it as well. We finally admitted defeat to Peyton so that we could take the manic boy back inside, after he had taken years off our lives of course! Yeah it was a wild night,but we did have fun,and it satisfied Peyton,most importantly.
Anyways everything else is good here. My step dad seems to be back on the mends,but has a very long time to go. I finished up clothes shopping for the boys,to go back to school,glad to have it over with. Not sure if I posted about Peyton's doctors appt or not,but he was diagnosed with migraines. We go back in two weeks for an MRI with contrast,to make sure that everything looks ok.
Not much else going on here. Brady just got out of bed,yikes!!!!! He is petting the puppy at the moment. He does occasionally have to pull its hair to make sure it still cries,lol. Well thats about it for me. I will post something more interesting later. Maybe even get a video on here,if I can get it to work :)

posted by angelwings @ 12:37 PM 1 comments

1 Comments:

At 11:44 PM, Emma said…

I so love reading about Brady's adventures and accomplishments now that he is free of seizures. I'll say a prayer the migranes are solved for Payton. Hope your summer continues to go well.

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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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